Serologist Jobs Near Me

About Us: How many companies can say they've been in business for over 177 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team! Location/Region: This position is located in Philadelphia, PA. What's the role? The Applications Development Scientist - Biotech & Pharma holds a pivotal role, leveraging advanced technical expertise to develop novel applications tailored to the unique demands of the life sciences industry. The outcomes of their work are integral to our growth strategy within this sector. Sound Interesting? Here's what you'll do: The Applications Development Scientist - Biotech & Pharma holds a pivotal role, leveraging advanced technical expertise to develop novel applications tailored to the unique demands of the life sciences industry. The outcomes of their work are integral to our growth strategy within this sector. Supporting customers at our partner site and enabling their success, Designing and conducting experiments using ZEISS imaging solutions, either independently or through collaboration with customers, and Effectively communicating findings to drive impact with the target audience. Work with business development managers to generate applications notes and other customer facing marketing content. Customer training activities include resolving implementation problems and conducting user training. Develop and deliver training to educate customers on the features of the product or service they have purchased. Respond to very complex customer questions and troubleshoot, investigate, and resolve technical problems that arise during or after implementation. Lead trainings for internal sales and service professionals. At all times, conduct in accordance with company guidelines and standards is expected. Must embody the ZEISS values at all times. Do you qualify? Masters or higher in Cancer Biology/ other Biological Sciences, preferably from an accredited college or university 3+ years of working knowledge is on high-end microscopy. Experience may include widefield, automation microscopy, laser scanning microscopy, and advanced imaging techniques such as automated time lapse with Z-stack, etc. Working knowledge of or prior work experience overseeing a shared instrumentation (Core) lab or experience of working with multi-faceted groups in the industry Sample preparation skills like cell culture, transfection, organoid culture and tissue staining is valuable Spatial biology experience is advantageous. Strong knowledge of ZEISS software solutions such as ZEN Software, Intellesis, Connect, arivis etc. are advantageous Knowledge of microscopy workflow solutions including image analysis, data visualization and coding skills is a plus Solution oriented problem solver with excellent verbal and written communication skills Implementation of MS Office, related software and strong presentation skills is required Positive “can do” attitude coupled with a willingness to continuously acquire product and application knowledge independently To excel in this position, you must possess the following attributes: Excellent communications & time management skills, along with the ability to learn quickly and thrive in a highly collaborative environment, A deep understanding of at least one of the key areas within life sciences, such as cell biology, oncology, immunology, metabolic disorders, or neuroscience, and Previous hands-on experience with light microscopy sample preparation, operation and image analysis. Ideally with expertise in high throughput scanners, high content screening or confocal and associated image analysis. Position will be based at our customer partner site or a ZEISS Microscopy Customer center Willingness and ability to travel domestically and overseas, up to 30% Capable and willing to engage customers in their workspace/environment, including BSL -2 and BSL-3 facilities. In addition to applications development function, maybe asked to work in assigned teams on defined projects as directed by management. Must have driving record in good standing and a valid driver license. Must have valid employment authorization to work in the United States. We have amazing benefits to support you as an employee at ZEISS! Medical Vision Dental 401k Matching Employee Assistance Programs Vacation and sick pay The list goes on! The annual pay range for this position is $112,000 - $140,000 The pay offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, & complexity/specialization/scarcity of talent. This position is also eligible for a performance bonus or sales commissions. ZEISS also offers robust benefits, including medical plans, retirement savings plan and paid time off. Your ZEISS Recruiting Team: Tina Eilerman Zeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).

The mission of the Allen Institute is to unlock the complexities of bioscience and advance our knowledge to improve human health. Using an open science, multi-scale, team-oriented approach, the Allen Institute focuses on accelerating foundational research, developing standards and models, and cultivating new ideas to make a broad, transformational impact on science. The mission of the Allen Institute for Immunology is to advance the fundamental understanding of human immunology through the study of immune health and diseases where excessive or impaired immune responses drive pathological processes. The Institute employs a multi-disciplinary team approach in collaboration with academic centers of human immunology to generate novel mechanistic insights into the immune synapse in health and in diseases such as autoimmunity or oncology. The Institute aims to simultaneously provide a foundational data set and tools for future immunological research as well as a novel collaboration portal for the broader scientific community. The Allen Institute for Immunology is looking for an exceptional Scientist I to join its newly formed Innovation Center, an initiative aimed at facilitating collaborative science and disseminating technological capabilities both within and outside of the broader institute. This individual will be supporting the development and application of cutting-edge molecular technologies for the institute and in collaboration with outside partners to derive new insights into immune function both within the periphery and tissues. This role includes novel technology development and application across a variety of platforms, including single cell and spatial platforms. Good judgment and problem-solving skills are required for assessment of the current tools & gaps in the market, in-house technology development, participating in troubleshooting, and operation of complex laboratory instrumentation. Strong interpersonal skills will be an asset to the highly collaborative nature of the position. A successful candidate possesses excellent attention to detail and the eagerness to work in a Team Science, deadline-driven atmosphere. Key deliverables will include contributions to technology development & application, publications and patents. At the Allen Institute, we believe that science is for everyone and should be open to everyone. We are dedicated to combating biases and reducing barriers to STEM careers more broadly. We also believe that science is better when it includes different perspectives and voices. We strive to make the Allen Institute a place where everyone feels like they belong and are empowered to do their best work in a supportive environment. We are an equal-opportunity employer and strongly encourage people from all backgrounds to apply for our open positions. Essential Functions * Support the development and adoption of novel technologies to drive biological insight. Examples include enhancing existing platforms through the addition of novel modalities and/or implementing perturbations of immune samples ahead of readout with a variety of technologies * Participate in discussions to identify key research areas and gaps in existing technologies where novel solutions would have high impact. Keep current on technologies and identify potential gaps and opportunities to drive novel insight * Design, perform experiments and analyze data to push forward technology development forward and derive new biological insights * Collaborate with immunologists to develop and apply technologies or adapt workflows for novel mechanistic understanding in a variety of contexts * Keep excellent experimental records and communicate progress in technology development Note: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This description reflects managements assignment of essential functions; it does not proscribe or restrict the tasks that may be assigned Required Education and Experience * Ph.D. or equivalent combination of degree and experience in a life sciences discipline Preferred Education and Experience * 0 5 years post Ph.D. experience in immunology including profiling immune cell function * Experience working with fixed and live tissues and/or mammalian cell culture * Proven success in troubleshooting and innovation on existing single cell omics platforms (for example 10x, Parse) * Background in molecular biology with a working knowledge of assays to probe gene regulatory networks (for example, reporter screens, genetic manipulation [e.g. CrispR], in vitro perturbations, single cell technologies, spatial transcriptomics) * Demonstrated impact in technology development and/or application of relevant technologies through publications or patents * Working knowledge of spatial omics platforms (10x Visium, Xenium, Nanostring) * Experience with in vitro immune cell manipulation (i.e stimulation, enrichment, cytokine mediated lineage specification, conditioned media or feeder cell co culture) * Demonstrated ability to independently analyze data through coding languages (R, python, bash, version control) * Experience with a LIMS system Work Environment * Working in a laboratory environment with potential exposure to lasers, biohazards Physical Demands * Occasional lifting to 30 pounds * Fine motor movements in fingers/hands to operate computers and other office equipment; repetitive motion with lab equipment * Stooping, bending, crouching Position Type/Expected Hours of Work * May need to work outside of standard working hours at times * This role is currently working onsite and is expected to work onsite for the majority of working hours. The primary work location for this role is 615 Westlake Ave N., with flexibility to work remotely on a limited basis. We are a Washington State employer; any remote work must be performed in Washington State. * This is a limited term position expected to last through December 2025 based on business needs and funding Additional Eligibility Qualifications * All employees who work with live animals must complete an Occupational Health medical history form and/or consultation with an Occupational Health Provider and receive clearance to work with animals. Depending on your health history and job responsibilities, an annual respiratory health screening and clearance to use a respirator may also be required. Additional Comments * Please note, this opportunity offers relocation assistance Annualized Salary Range * $84,900 - $105,050 * * Final salary depends on required education for the role, experience, and level of skills relevant to the role, along with work location, where applicable. Benefits * Employees (and their families) are eligible to enroll in benefits per eligibility rules outlined in the Allen Institutes Benefits Guide. These benefits include medical, dental, vision, and basic life insurance. Employees are also eligible to enroll in the Allen Institutes 401k plan. Paid time off is also available as outlined in the Allen Institutes Benefits Guide. Details on the Allen Institutes benefits offering are located at the following link to the Benefits Guide: ******************************************** It is the policy of the Allen Institute to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, the Allen Institute will provide reasonable accommodations for qualified individuals with disabilities.

#KeepGrowing with Nutrafol We're a growing company. Everything we do, we do to help people grow into the best version of themselves. As the pioneers of hair wellness, we create clinically tested products for hair growth and provide support for people at every step of their hair journey. Our multi-factorial approach targets key root causes of hair thinning using a patented blend of standardized vitamins, minerals and natural ingredients -- and is recommended by over 7,500 physicians and hair professionals for trusted, reliable results. We never settle, and are continuously challenging existing treatments and methodologies to advance the frontier of hair science. As we help our customers grow, we grow too -- by embracing individuality and differences, leading by example, and empowering ourselves and others with our passion for wellness and innovation. Keep growing. It's our mantra. Our commitment to helping anybody and everybody committed to realizing their own potential to grow. About You Nutrafol is seeking a scientific expert in hair/skin biology to help us maintain our competitive edge as innovators in hair wellness. This role will be part of the R&D Innovation team and will design/lead preclinical hair biology research programs between our company and numerous research partners, including identifying/vetting new labs/collaborators, designing experiments, managing research collaborations, maintaining records/databases, data analysis and reporting, scientific communication, allocation of resources, and working collaboratively, internally & externally. The successful candidate will be an expert in Hair/Skin Biology, especially in basic research/preclinical research focus, with relevant expertise including but not limited to pigmentation modulation, exosomes, biomarkers, and preclinical (in vitro & ex vivo) models. You are a creative problem-solver, highly organized and proactive, as well as able to consider the big picture. This person will build, design, and manage research & innovation projects including developing overall project plan, phases, workstreams, activities, deliverables, timelines, and milestones. You are unafraid to ask bold questions and propose new experiments to investigate novel/unknown territories, and highly motivated to create solutions that do not exist today. Responsibilities Build and lead research & innovation projects in hair biology, including pigmentation modulation Identification of & coordination with labs/external partners to conduct analytical testing, in vitro, “omics” and ex vivo studies, and project progression for new ingredients, botanicals processing and/or manufacturing technologies Lead and execute the experimental design, work plans, data analysis and reporting Communication of data, including preparation of presentations, scientific posters and manuscripts for publication Track and manage progress on laboratory projects, managing timelines to ensure deadlines are met and roadblocks are solved for as necessary Create action plans for new projects generated by internal and external requests, including requests for proposals (RFPs) and/or statements of work (SOW) Responsible for coordination across labs, including requesting samples/supplies and documents, item coordination, and shipments, and managing timelines Communicate directly with various internal and external partners to research, define, and communicate progress on projects Develop firm understanding of internal lab/company processes and databases High level of organization and responsiveness for record keeping/data management for reports, NDAs/CDAs, supplier/external materials and internal presentations/data Build and maintain effective relationships which create a high level of trust across multiple functions Respond to inquiries by phone, email and in person quickly and professionally Participate in meetings with internal/external teams to evaluate and interpret the validity of data, determine methodologies, and evaluate lab procedures impacting the quality and timeliness of research. Analyze data using statistical methodologies & ability to showcase data/results in a variety of formats Communicate with researchers in other laboratories; share ideas and research methodologies to improve the effectiveness of the research. Track & keep abreast of research techniques, methodologies and literature/IP that may facilitate designated research projects (current or future) Monitor the performance of both the Investigator(s) and/or the Laboratory as applicable. Manage the initiation, draft revision, completion and maintenance of contracts, NDAs, SOWs, invoices/payments in a timely manner. Support maintenance of project documentation files and internal databases with project information/updates, as directed and if applicable. Requirements PhD preferred. Bachelor's and/or master's degree; Biology, biotechnology, biochemistry or similar field preferred 3-6 years of post-graduate research experience with an expertise in cell and molecular biology Publication/patent/external presentation track record and preparation of scientific decks Experience with in vitro and ex vivo research related to bioactives utilized in dietary supplements and/or topical/personal care applications a plus Exceptional communication and interpersonal skills Strong organizational skills and R&D project management experience Attention to detail and ability to complete tasks on time with a high degree of accuracy Show initiative and ability to work as part of a high-level team while working independently Proven ability to learn new skills quickly and adapt to new processes smoothly Open innovation experience a plus Nutrafol takes into consideration a wide range of factors in final compensation decisions, including but not limited to: skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. The listed range is applicable only to the annual base salary and does not include additional perks, benefits, or applicable bonus eligibility comprising the total compensation package.Salary Range:$120,000—$140,000 USDPerks & Benefits Fully remote work experience Comprehensive medical, dental, and vision package, including FSA program 401K with 50% match Quarterly Bonus Program Flexible PTO Two company-wide wellness breaks every day Free lunch on us every Tuesday and Thursday via Seamless/Grubhub Monthly wellness stipend Monthly internet stipend Monthly cell phone stipend Annual learning & development stipend Wellness Program, including virtual Wellness Sessions & No-Meeting Wednesdays Free meditation app membership (Headspace) Free Nutrafol subscription Pet insurance and benefit programs California residents may review our CCPA notice here.

**\#KeepGrowing with Nutrafol** We're a growing company. Everything we do, we do to help people grow into the best version of themselves. As the pioneers of hair wellness, we create clinically tested products for hair growth and provide support for people at every step of their hair journey. Our multi-factorial approach targets key root causes of hair thinning using a patented blend of standardized vitamins, minerals and natural ingredients -- and is recommended by over 7,500 physicians and hair professionals for trusted, reliable results. We never settle, and are continuously challenging existing treatments and methodologies to advance the frontier of hair science. As we help our customers grow, we grow too -- by embracing individuality and differences, leading by example, and empowering ourselves and others with our passion for wellness and innovation. Keep growing. It's our mantra. Our commitment to helping anybody and everybody committed to realizing their own potential to grow. **About You** Nutrafol is seeking a scientific expert in hair/skin biology to help us maintain our competitive edge as innovators in hair wellness. This role will be part of the R&D Innovation team and will design/lead preclinical hair biology research programs between our company and numerous research partners, including identifying/vetting new labs/collaborators, designing experiments, managing research collaborations, maintaining records/databases, data analysis and reporting, scientific communication, allocation of resources, and working collaboratively, internally & externally. The successful candidate will be an expert in Hair/Skin Biology, especially in basic research/preclinical research focus, with relevant expertise including but not limited to pigmentation modulation, exosomes, biomarkers, and preclinical (in vitro & ex vivo) models. You are a creative problem-solver, highly organized and proactive, as well as able to consider the big picture. This person will build, design, and manage research & innovation projects including developing overall project plan, phases, workstreams, activities, deliverables, timelines, and milestones. You are unafraid to ask bold questions and propose new experiments to investigate novel/unknown territories, and highly motivated to create solutions that do not exist today. **Responsibilities** + Build and lead research & innovation projects in hair biology, including pigmentation modulation + Identification of & coordination with labs/external partners to conduct analytical testing, in vitro, "omics" and ex vivo studies, and project progression for new ingredients, botanicals processing and/or manufacturing technologies + Lead and execute the experimental design, work plans, data analysis and reporting + Communication of data, including preparation of presentations, scientific posters and manuscripts for publication + Track and manage progress on laboratory projects, managing timelines to ensure deadlines are met and roadblocks are solved for as necessary + Create action plans for new projects generated by internal and external requests, including requests for proposals (RFPs) and/or statements of work (SOW) + Responsible for coordination across labs, including requesting samples/supplies and documents, item coordination, and shipments, and managing timelines + Communicate directly with various internal and external partners to research, define, and communicate progress on projects + Develop firm understanding of internal lab/company processes and databases + High level of organization and responsiveness for record keeping/data management for reports, NDAs/CDAs, supplier/external materials and internal presentations/data + Build and maintain effective relationships which create a high level of trust across multiple functions + Respond to inquiries by phone, email and in person quickly and professionally + Participate in meetings with internal/external teams to evaluate and interpret the validity of data, determine methodologies, and evaluate lab procedures impacting the quality and timeliness of research. + Analyze data using statistical methodologies & ability to showcase data/results in a variety of formats + Communicate with researchers in other laboratories; share ideas and research methodologies to improve the effectiveness of the research. + Track & keep abreast of research techniques, methodologies and literature/IP that may facilitate designated research projects (current or future) + Monitor the performance of both the Investigator(s) and/or the Laboratory as applicable. + Manage the initiation, draft revision, completion and maintenance of contracts, NDAs, SOWs, invoices/payments in a timely manner. + Support maintenance of project documentation files and internal databases with project information/updates, as directed and if applicable. **Requirements** + PhD preferred. Bachelor's and/or master's degree; Biology, biotechnology, biochemistry or similar field preferred + 3-6 years of post-graduate research experience with an expertise in cell and molecular biology + Publication/patent/external presentation track record and preparation of scientific decks + Experience with in vitro and ex vivo research related to bioactives utilized in dietary supplements and/or topical/personal care applications a plus + Exceptional communication and interpersonal skills + Strong organizational skills and R&D project management experience + Attention to detail and ability to complete tasks on time with a high degree of accuracy + Show initiative and ability to work as part of a high-level team while working independently + Proven ability to learn new skills quickly and adapt to new processes smoothly + Open innovation experience a plus Nutrafol takes into consideration a wide range of factors in final compensation decisions, including but not limited to: skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. The listed range is applicable only to the annual base salary and does not include additional perks, benefits, or applicable bonus eligibility comprising the total compensation package. Salary Range: $120,000-$140,000 USD **Perks & Benefits** + Fully remote work experience + Comprehensive medical, dental, and vision package, including FSA program + 401K with 50% match + Quarterly Bonus Program + Flexible PTO + Two company-wide wellness breaks every day + Free lunch on us every Tuesday and Thursday via Seamless/Grubhub + Monthly wellness stipend + Monthly internet stipend + Monthly cell phone stipend + Annual learning & development stipend + Wellness Program, including virtual Wellness Sessions & No-Meeting Wednesdays + Free meditation app membership (Headspace) + Free Nutrafol subscription + Pet insurance and benefit programs _California residents may review our CCPA notice here (******************************************************************************************************************* ._ As set forth in Nutrafol's Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.

COMPENSATION: $95,000 to $105,000 per year. You are eligible for a Short-Term Incentive with the target at 5% of your annual earnings; terms and conditions apply. Variant Assessment Scientist I: WGS - Development (REMOTE-US) The primary responsibilities of this role include leading cross-functional projects to drive scientific innovation and excellence in variant classification, gene-disease validity, computational biology, and clinical data analytics. As a member of the Genomic Science Development team, the variant scientist will evaluate the latest scientific advancements to continuously improve the Ambry Classifi™ program and implement new analytical methods and automation tools. The successful candidate will focus on high impact data-driven outcomes to support business goals. Essential Functions: Rigorous analysis of scientific data, evaluating external published literature and designing internal validation studies Leadership of cross-functional groups at the team, department, and enterprise level Demonstrate scientific expertise in molecular genetics, variant science, and gene-disease validity Develop innovative technologies, software tools, AI/ML to improve the quality and efficiency of variant, gene, disease, and clinical data curation and classification Develop robust processes to implement scientific advancements meeting all quality assurance standards and documentation requirements while maintaining operational efficiency Develop educational training modules and methods to ensure broad adoption of all scientific advancements in a high-throughput laboratory environment Other duties as assigned. Qualifications: PhD, MD, or MS (with min. of 3 yrs experience) in scientific analysis and expertise in biological sciences, molecular genetics, human genetics, or related field Thorough and ongoing knowledge of current theories and principles of human genetics Whole Genome Sequencing experience Excellent written, verbal, and interpersonal communication skills to engage stakeholders and socialize success Ability to adapt to significant change that is inherent in development and innovation Ability to work in and contribute to a fast-paced, highly collaborative environment Preferred: Post-doctoral fellowship or minimum +2 years of experience in clinical variant science preferred Experience in project, program, and change management preferred #LI-AC1 #LI-REMOTE About Us: Ambry Genetics Corporation is a CAP-accredited and CLIA-licensed molecular genetics laboratory based in Aliso Viejo, California. We are a genetics-based healthcare company that is dedicated to open scientific exchange so we can work together to understand and treat all human disease faster. At Ambry, everyone is welcome. A career at Ambry Genetics is a chance to be part of a dynamic company that aims to improve health by understanding the relationships between genetics and human disease. We earned our reputation as industry leaders by responsibly introducing cutting-edge genetic testing solutions and continually sharing what we learn with the global scientific community. At Ambry you will be learning, challenging yourself, and having fun while collaborating with teammates through the open exchange of ideas. Our outstanding benefits program includes medical, dental, vision, FSA, paid sick leave and generous paid time off (PTO) program. You can learn more about the benefits here. Ambry Genetics is an Equal Opportunity Employer (EOE) and we maintain a drug-free work environment. The Company believes in second chance employment. Qualified applicants with arrest or conviction history will be considered regardless of their arrest or conviction history, consistent with local laws such as Los Angeles County Fair Chance Ordinance and the California Fair Chance Act. You do not need to disclose your criminal history or participate in a background check until a conditional job offer is made to you. After making a conditional offer and running a background check, if the Company is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report. For the purpose of the above job description, “Essential Functions” are “Material Job Duties”. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. All qualified applicants will receive consideration for employment without regard to race (and traits historically associated with race, including, but not limited to hair texture and protective hairstyles such as braids, locks, and twists), color, creed, religion, sex, sexual orientation, gender identity, gender expression (including transgender status), national origin, ancestry, age, marital status or protected veteran status and will not be discriminated against on the basis of disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. If you have a disability or special need that requires accommodation, please contact us at ******************** Ambry does not accept unsolicited resumes from individual recruiters, third party recruiting agencies, outside recruiters or firms without an executed contract in place. We are not responsible for any fees related to resumes that are unsolicited or are received by Ambry. Such resumes will be deemed the sole property of Ambry and will be processed accordingly. PRIVACY NOTICES To review Ambry's Privacy Notice, Click here: ********************************************* To review the California privacy notice, click here : California Privacy Notice | Ambry Genetics To review the UKG privacy notice, click here: California Privacy Notice | UKG

Advantage Technical is partnering with a leading multinational medical device company to bring on a skilled Medical Device Toxicologist to join their team. This remote position offers an excellent opportunity to work from home while making a meaningful impact in the healthcare field. Location: Remote, 12 months Pay: Up to $33/hr Responsibilities: * Review medical device product documentation to ensure compliance with ISO 10993 standards. * Conduct biocompatibility assessments and studies at a Contract Research Organization (CRO). * Confirm evidence related to product safety and biocompatibility. * Communicate effectively in Mandarin, as many of the documents are written in this language. Requirements: * 1-2 years of experience with ISO 10993 standards. * Prior experience in authoring biocompatibility assessments and conducting studies. * Fluent in Mandarin, both written and verbal. * Strong attention to detail and experience in reviewing medical device documentation. The services you offer are not without uplifting benefits to show our appreciation for your time and energy! Payday every single Friday by direct deposit or pay card. You will have access to a dedicated local team that cares about your success and is here to support you every step of the way. Don't forget about our employee discounts and referral bonus potential. We offer medical, dental, vision, and 401K options to suit you and your family's needs. Ready to take the next step in your career? Click "Apply Now" to join Advantage Technical and be part of a team that values your growth and success. We can't wait to welcome you! After you have applied, download our Staffmark Group WorkNOW App to receive real-time job offers and apply for additional opportunities. You can download it from the App Store or get it on Google Play.

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers We are hiring a Research and Development Scientist to join our Cleveland, Ohio team. The Research and Development Scientist develop polymer-based materials for thermal and EMI management solutions under direction of senior technologist. This position requires background in chemistry, polymer science, or polymer composites, and a strong understanding of materials and structure-property relationships. Your Key Responsibilities: Use solid scientific principles to plan and conduct lab experiments, prepare samples, characterize materials and understand composition and property relationships. Develop, formulate, and characterize new technically advanced materials per product development roadmap with guidance by senior level scientists. Update existing material formulations as needed based on required raw material substitutions or necessary property enhancements Generate technical reports and project progress reports as requested. Interface with process engineer for scale up experiments and/ or process development or improvements. Qualification: Master's degree in polymer science, materials science, or chemistry. 2-5 years' experience in polymer composites/materials development. Experience and knowledge with polymer structure, polymer chemistry, polymer composites, rheology control, instruments. Chemistry, polymer and materials characterization techniques such as TGA, DSC, rheometer, FTIR, SEM, etc. Hands on experience with formulating, polymer-filler system is preferred. Experience with silicone and thermoplastics is a plus. Experience with complex fluids, structure fluids is a plus. Ability to work well in Team environment. Highly motivated with hands-on approach to laboratory work. Join our Talent Community to stay connected with us! On May 22, 2024, we announced a plan to separate our Electronics and Water businesses in a tax-free manner to its shareholders. On January 15, 2025, we announced that we are targeting November 1, 2025, for the completion of the intended separation of the Electronics business (the “Intended Electronics Separation”)*. We also announced that we would retain the Water business. We are committed to ensuring a smooth and successful separation process for the Future Electronics business. We look forward to welcoming new talent interested in contributing to the continued success and growth of our evolving organization. (1) The separation transactions are subject to satisfaction of customary conditions, including final approval by DuPont's Board of Directors, receipt of tax opinion from counsel, the filing and effectiveness of Form 10 registration statements with the U.S. Securities and Exchange Commission, applicable regulatory approvals, and satisfactory completion of financing. For further discussion of risks, uncertainties and assumptions that could impact the achievement, expected timing and intended benefits of the separation transactions, see DuPont's announcement. DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information.

Twist is looking for a scientific development scientist to cover AMER East, with specific experience in the biologics and pharma space. This role offers a unique opportunity to merge scientific expertise with customer-facing responsibilities, driving Twist's innovative Biopharma offerings into the market. In this role, you will be an integral part of our Sales team and serve as a primary scientific field contact for selected pharmaceutical, biotechnology and other related companies. The FAS's primary goal is to help strengthen Twist's market position within these key accounts in the area of our BioPharm services for synthetic biology and the discovery and development of biologics. In this role, you will be responsible for providing pre- and post-sales technical support (field based), developing strategic goals, building key customer relationships, identifying business opportunities, and maintaining extensive knowledge of market needs to increase opportunities and thereby increase Twist's value to our key customers and maximize revenue for Twist Bioscience. You will partner closely with our business development and sales team to create strategies to increase existing customer purchasing and identify new, potential customers of high value (e.g., KOLs). The FAS will report to the Synbio/BioPharma Scientific Development Manager. Prior experience with process development and manufacturing of complex biological products (particularly bio-pharmaceuticals) is desired to enable translation of customer requirements to internal teams. This position will be based in AMER East, with travel requirements of up to 50% locally and across the east coast. Key Milestones and Responsibilities: Training on Twist technology, products and services (BioPharm) will be provided to enable FAS to translate Twist capabilities Provide expert understanding and strong technical competency in discussing Twist's capabilities and product offerings with selected pharmaceutical, biotechnology, and other related companies. Build and nurture relationships with stakeholders and customers to better understand their strategic direction and perspectives. Prospect and generate lists of potential customers, collaborators, and partners that will generate revenues from gene synthesis, variant libraries, and oligo pool sales as well as products in alpha testing phase. Provide application support for pre- and post sales activities for Twist's product portfolio to help support the sales team to achieve quota. Local and regional travel (up to 50% time) to work in the field with Sales, attend meetings with key customers and participate in trade shows. Identify, nurture, and manage collaborations to network and collaborate on leads with the account management sales team. Support sales team in technical discussions, presentations, and meetings with selected pharmaceutical, biotechnology, and other related companies. Generate and drive a continuous deal flow of library sales and antibody development solution contracts with collaborators and partners that will lead to high value commercial agreements, with an emphasis on agreements that cover antibody development services provided by Twist Biopharma. Primary lead to solicit and pitch Twist capabilities (presentations), competencies and offerings (with the support of Twist Pharma scientific resource) to strategically important potential new collaborators and partners in the biologics space Develop strong working relationships with subject matter experts throughout Twist Biopharma and Twist, Inc; assign and coordinate tasks to more qualified co-workers involved in the pursuit of each opportunity. Network with customers and provide feedback to Marketing on customer requirements for new applications or products. Minimum Qualifications: Minimum of 5 years of experience and success within antibody discovery and development within academic/bio-pharmaceutical /biotech/protein engineering segments. Experience developing and cultivating customers and opportunities in the Therapeutic or Biopharma industry organization Advanced degree (PhD or MS) and/or at least 5 years of experience within antibody development, or related scientific profession required. In-depth knowledge and experience within the variant library and antibody engineering space Experience working in a global environment is preferred Experience working in a corporate, global or regional sales and marketing role involving gene mutant library and/or antibody development products/services. Advanced knowledge of, and practical experience in biotechnology product development High attention to detail High self-motivation and must have demonstrated ability to work in a collaborative team environment Excellent verbal and written communication skills Experience of customer support and use of CRM system a plus About Twist Bioscience Twist Bioscience synthesizes genes from scratch, known as “writing” DNA. Just as children learn to both read and write, the next phase of development for the genomics revolution is the ability to write DNA. At Twist Bioscience, we work in service of people who are changing the world for the better. In fields such as health care, agriculture, industrial chemicals and data storage, our unique silicon-based DNA Synthesis Platform provides precision at a scale that is otherwise unavailable to our customers. Twist Bioscience Corporation is an Equal Opportunity Employer. Twist Bioscience Corporation provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic characteristics, or any other category protected by law.

Your Opportunity as the Scientist, Uncrustables Formulations-Frozen Handheld & Spreads Research & Development Team The Scientist practices and encourages creativity to drive innovation and solve technical problems. They will execute projects designed to result in new or improved products by leading technical teams and developing work plans independently. Location: Corporate Offices in Orrville, Ohio Work Arrangements: Ability to work a hybrid model; a typical week in office is 40-50% in office and up to 100% when lab/pilot plant/manufacturing plant support is needed. Start times based on work needs will be before 8 AM on occasion. In this role you will: Lead formulation development of new and existing formulas for Uncrustables and build subject matter expertise Utilize conceptual and practical expertise in formulation and basic knowledge of related disciplines in development Ensure formulations are compliant with regulations such as, but not limited to, nutrient profiles and claims Coordinate and manage laboratory, pilot plant and scale-ups for projects at JM Smucker (JMS) and contract manufacturing locations Work independently, guided by functional processes, with guidance only in complex situations (e.g., when decisions have functional or organizational impact) Develop and publish technical documentation within specification and lab notebook systems Conduct analytical testing, analyze data, and articulate findings through written and verbal summaries Partners with technical team members to develop key tasks and project plans for timely completion of goals; may informally lead teams Actively collaborate and leverage relationships within Research & Development (R&D) and cross functional teams to achieve project goals Provide coaching and function as a resource for colleagues with less experience as part of our Basic Belief and Commitment to Each Other philosophy Assume an advisory role to internal teams such as operations, technical services, and procurement Become fluent and participate in JMS Key Element and Quality programs to support R&D Embrace and actively participate in company's inclusion, Diversity and Equity (ID&E) initiatives The Right Place for You We are bold, kind, strive to do the right thing, we play to win, and we believe in a strong community that thrives together. Our culture is rooted in our Basic Beliefs, and we believe in supporting every employee by meeting their physical, emotional, and financial needs. What we are looking for: Minimum Requirements: A Bachelor of Science Degree or higher (required); Food Science, Cereal Grains Science, or Engineering strongly preferred 5+ years of technical experience in R&D or another technical discipline (required) Strong experience with food formulations or process engineering, and record of leveraging this experience to develop, qualify, and launch product innovation Ability to thrive in a fast-paced environment, managing multiple projects simultaneously (required) Initiative-taking with the ability and desire to work independently (required) Proven success leading projects from benchtop to scale up and commercialization Ability to work a hybrid model; a typical week in office is 40-50% in office and up to 100% when lab/pilot plant/manufacturing plant support is needed. Start times based on work needs will be before 8 AM on occasion. Approximately 20-30% travel annually; concentrated around project scale-up periods and project learning plan deliverables Food safety foundation - PCQI training a plus Additional skills and experience that we think would make someone successful in this role: Candidate must be able to communicate difficult technical concepts and collaborate across functional teams to achieve shared goals Proven troubleshooting abilities in fast paced environment Excellent communications skills (written, oral, group presentations) Maintaining robust documentation in systems of record and supporting IP filings Learn more about working at Smucker: Our Total Rewards Benefits Program Our Thriving Together Philosophy Supporting All Impacted by Our Business Our Continued Progress on Inclusion, Diversity and Equity Follow us on LinkedIn #LI-MR1

Battelle delivers when others can't. We conduct research and development, manage national laboratories, design and manufacture products and deliver critical services for our clients-whether they are a multi-national corporation, a small start-up or a government agency. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. **Job Summary** The Life Science Research Team is seeking an experienced **Toxicologist Chemical** to support our clients' toxicology, and inhalation research programs at our **West Jefferson, OH** lab. Our multidisciplinary integrated approach to providing critical solutions for our pharmaceuticals, biotech, agrichemical, industrial, and government clients increases the speed of the development while maintaining quality and compliance. The Toxicologist functions as a study director within the organization and has oversight of the scientific elements of projects to ensure successful implementation and/or study completion of toxicology studies. This position analyzes and reports results for publication and/or to sponsor, provides scientific instruction to other members of the project team, and collaborates with other senior members of the staff on projects/research. This position may also be responsible for the supervision, oversight, scheduling, training, and mentoring of individuals within Battelle's Life Science Research Center. Individuals filling this position must be and remain knowledgeable of emerging trends and may contribute to and influence best practices within the discipline. This position is responsible for the organization, management, and business performance of non-clinical toxicology studies. This position will be located in **West Jefferson, OH** . **_This position is contingent upon award of work._** **Responsibilities** + Serves as Study Director on toxicology, biodistribution, pharmacokinetic, efficacy, and related studies for commercial and government sponsors. + Interfaces directly with client's scientific staff as appropriate. + Design toxicology studies to develop animal models and then test medical counter-measure efficacy. + Reviews toxicology data and authors toxicology study reports, or portions thereof, as appropriate. + Partners with Business Development, Project Management, and Proposals to ensure successful client engagement, proposal development, study execution, and deliverables upon study completion. + Participates in proposal generation and performs scientific/technical review of proposals. + In collaboration with the business development team and senior toxicology staff, is responsible for new pipeline development; accountable for some level of revenue generation. + Drafts protocols, amendments, departmental notifications, and study comments forms, ensuring correct grammar, punctuation, consistency in format and style, and adherence to regulatory requirements and contract language. + Identifies and incorporates exceptions to GLP conduct into GLP study protocols as applicable (e.g., systems/processes that are not validated). + Reviews and approves Provantis study setups. + Participates in all required training. + Follows FDA GLP and other appropriate regulatory (e.g., OECD, ICH) requirements to ensure all experimental data, including observations of unanticipated findings, are accurately recorded and verified. + Observes appropriate safety and study requirements by reading, understanding, and following SOP's, GLP regulations, and study protocols. + Reviews SOP's associated with study conduct and incorporates language into the protocol describing procedures or processes when necessary. + Authors, updates, and/or reviews area-specific SOP's, ensuring that SOP's reflect current practices. + Manages studies within time and budget constraints. + Oversees the building of new capabilities to bring in new technologies and services. + Within defined policies and procedures, provides resolution to complex scientific problems within a specified program. **Key Qualifications** + PhD degree in life sciences discipline or Master's degree with 2- 5+ years prior experience or Bachelor's degree with 5- 8+ years prior experience. + Expertise in in-vivo design, execution, interpretation of small-molecule toxicology studies. + Effective verbal and written communication skills including correct grammar, spelling, and punctuation. Prior presentation experience. + Ability to obtain and maintain a U.S. government security clearance (U.S. citizenship required). + Additionally, will require ability to obtain and maintain the following: DOJ Security Risk Assessment approval, CDC Approval to work with BSAT material, Chemical Personal Reliability Program (NACLC required) and Biological Suitability Assessment Program. Ability to work in biosafety level 2 (BSL2) (biocontainment) and wear appropriate respiratory protection. Requires participation in random drug screening. Willing to be immunized with FDA licensed vaccines and Investigational New Drugs (IND) recommended for persons at risk to occupational exposure of biological agents. **Preferred Qualifications** + Diplomate of the American Board of Toxicology certified OR DABT eligible - if not already certified, candidate will be required to become board certified within five years of hire date. + Demonstrated competency in regulated environment including prior experience working in a GLP or similarly regulated environment. **Benefits: Live an Extraordinary Life** We care about your well-being, not just on the job. Battelle offers comprehensive and competitive benefits to help you live your best life. + **Balance life through a compressed work schedule** : Most of our team follows a flexible, compressed work schedule that allows for every other Friday off-giving you a dedicated day to accomplish things in your personal life without using vacation time. + **Take time to recharge** : You get paid time off to support work-life balance and keep motivated. + **Prioritize wellness** : Stay healthy with medical, dental, and vision coverage with wellness incentives and benefits plus a variety of optional supplemental benefits. + **Better together** : Coverage for partners, gender-affirming care and health support, and family formation support. + **Build your financial future** : Build financial stability with an industry-leading 401(k) retirement savings plan. For most employees, we put in 5 percent whether you contribute or not, and match your contributions on top of that. + **Advance your education** : Tuition assistance is available to pursue higher education. + **Flexible work arrangements** : You have options for where you work and when you work. **A Work Environment Where You Succeed** For brilliant minds in science, technology, engineering and business operations, Battelle is the place to do the greatest good by solving humanity's most pressing challenges and creating a safer, healthier and more secure world. You will have the opportunity to thrive in a culture that inspires you to: + Apply your talent to challenging and meaningful projects + Receive select funding to pursue ideas in scientific and technological discovery + Collaborate with world-class experts in an inclusive environment + Nurture and develop the next generation of scientific leaders + Give back to and improve our communities **Vaccinations & Safety Protocols** _Battelle may require employees, based on job duties, work location, and/or its clients' requirements to follow certain safety protocols and to be vaccinated against a variety of viruses, bacteria, and diseases as a condition of employment and continued employment and to provide documentation that they are fully vaccinated. If applicable, Battelle will provide reasonable accommodations based on a qualified disability or medical condition through the Americans with Disabilities Act or the Rehabilitation Act or for a sincerely held religious belief under Title VII of the Civil Rights Act of 1964 (and related state laws)._ _Battelle is an equal opportunity employer. We provide employment and opportunities for advancement, compensation, training, and growth according to individual merit, without regard to race, color, religion, sex (including pregnancy), national origin, sexual orientation, gender identity or expression, marital status, age, genetic information, disability, veteran-status veteran or military status, or any other characteristic protected under applicable Federal, state, or local law. Our goal is for each staff member to have the opportunity to grow to the limits of their abilities and to achieve personal and organizational objectives. We will support positive programs for equal treatment of all staff and full utilization of all qualified employees at all levels within Battelle._ The above statements are intended to describe the nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, activities and skills required of staff members. **No statement herein is intended to imply any authorities to commit Battelle unless special written permission is granted by Battelle's Legal Department.** For more information about our other openings, please visit ************************

INEOS Composites US LLC INEOS is a global manufacturer of petrochemicals, specialty chemicals and oil products. Our products touch every aspect of modern life. INEOS comprises 36 businesses each with a major chemical company heritage. Our production network spans 194 sites in 29 countries throughout the world. INEOS Pigments produces TiO2 and TiCI4 via the chloride process with approximately 500 employees at the Ashtabula Complex and 30 employees associated with the Baltimore Administrative and Technical Center (BATC). The T&I group is split between the Ashtabula Complex and the Baltimore Administration and Research Center (BATC). This role is a salaried, exempt position based in either BATC or Ashtabula with regular travel between the two sites. Future relocation to Columbus, OH will be required. The Scientist II receives supervision from T&I VP or Senior Scientist on a fortnightly or monthly basis and works week to week independently or as part of a team as required to apply chemical principles in synthesis and characterization of solid-state metal oxide materials leading to new or improved TiO2 pigment products. Carries out laboratory work on a day to day basis unsupervised. The role exists within the Technology & Innovation Group (T&I) and consists of material synthesis, characterization, and applications testing. The individual should also be able to improve and modify existing test methods that will benefit productivity as well as maintain laboratory equipment and laboratory order and make recommendations to improve laboratory work processes This position will apply good laboratory practices in following standard operating procedures as directed by the VP of T&I. Familiarity with the research tools in product development and quality testing required. The qualified individual should be able to take learning from the lab experiment or plant trial results and apply that to development of ideas for new product or improvement of current product and/or processes. This position will work with other T&I teams as well as the Manufacturing teams to achieve the performance goals needed for scale up at the Ashtabula Complex by conducting lab, pilot, and plant trials. The incumbent should possess critical analytical skills and be adept at utilizing solid decision-making tools coupled with a high level of data analysis skills. Key Activities: · Adhere to INEOS Pigments Safety Principles and Life Saving Rules · Complete Action Items on time · Complete computer-based training on time · Perform specific Safety Audits · Participate in safety improvement efforts including monthly meetings · Receives direction from the VP, T&I but works independently on a day to day basis. · Perform area inspections and keep laboratory chemical inventory current · Performs duties according to established standard operating procedures. · Maintains labs to ensure continued reliability use in development and evaluation efforts. · Understanding and experience in applications testing related to the TiO2 pigment markets helpful. · Will be responsible for ensuring all test procedures are carried out day to day · Order chemicals and supplies for experiments and to maintain inventory · Prepares samples, characterizes products, and formulates into end uses · Maintains good records and regularly reports study results Education and Experience: · A BS/BA degree in Chemistry, Chemical Engineering, or equivalent with 3-7 years industrial experience or equivalent · Good written and verbal presentation skills · Statistical accumen showing ability to organize, analyze, and interpret data · A good knowledge of Health and Safety procedures generally as relates to internal SHE and CHP guidelines · Should be well versed in pigment test methodologies. · Should be adept at performing surface treatments involving corrosive and caustic materials dissolved in water · Should have an excellent understanding of pigment manufacture. · Should have an excellent understanding of material characterization techniques. · Has a basic understanding of the operating principle of, and be able to perform regular maintenance of lab equipment. · Skilled at working with hands · Should be aware of TiO2 pigment market, customers and general regulations related to coatings, plastics and paper applications. · A good knowledge of pigment application testing and product awareness. · An awareness of the latest techniques, applications and analytical techniques for TiO2 pigment. · Should have demonstrated good interpersonal skills with peers · Should be available for plant trial support as required. · Should have a sense of how regulatory rules impact work functions Candidates must be authorized to work in the US and future sponsorship is unavailable for this role.

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers We are hiring a Research and Development Scientist to join our Cleveland, Ohio team. The Research and Development Scientist develop polymer-based materials for thermal and EMI management solutions under direction of senior technologist. This position requires background in chemistry, polymer science, or polymer composites, and a strong understanding of materials and structure-property relationships. Your Key Responsibilities: Use solid scientific principles to plan and conduct lab experiments, prepare samples, characterize materials and understand composition and property relationships. Develop, formulate, and characterize new technically advanced materials per product development roadmap with guidance by senior level scientists. Update existing material formulations as needed based on required raw material substitutions or necessary property enhancements Generate technical reports and project progress reports as requested. Interface with process engineer for scale up experiments and/ or process development or improvements. Qualification: Master's degree in polymer science, materials science, or chemistry. 2-5 years' experience in polymer composites/materials development. Experience and knowledge with polymer structure, polymer chemistry, polymer composites, rheology control, instruments. Chemistry, polymer and materials characterization techniques such as TGA, DSC, rheometer, FTIR, SEM, etc. Hands on experience with formulating, polymer-filler system is preferred. Experience with silicone and thermoplastics is a plus. Experience with complex fluids, structure fluids is a plus. Ability to work well in Team environment. Highly motivated with hands-on approach to laboratory work. Join our Talent Community to stay connected with us! On May 22, 2024, we announced a plan to separate our Electronics and Water businesses in a tax-free manner to its shareholders. On January 15, 2025, we announced that we are targeting November 1, 2025, for the completion of the intended separation of the Electronics business (the “Intended Electronics Separation”)*. We also announced that we would retain the Water business. We are committed to ensuring a smooth and successful separation process for the Future Electronics business. We look forward to welcoming new talent interested in contributing to the continued success and growth of our evolving organization. (1) The separation transactions are subject to satisfaction of customary conditions, including final approval by DuPont's Board of Directors, receipt of tax opinion from counsel, the filing and effectiveness of Form 10 registration statements with the U.S. Securities and Exchange Commission, applicable regulatory approvals, and satisfactory completion of financing. For further discussion of risks, uncertainties and assumptions that could impact the achievement, expected timing and intended benefits of the separation transactions, see DuPont's announcement. DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information.

Vibrantz Technologies (“Vibrantz” or “Company”) is a leading global provider of specialty chemicals and materials solutions whose purpose is to bring color, performance and vibrancy to life. Every day, our employees, the products we make, and our valued customer partnerships are inspired by this purpose. Serving customers globally, our innovations are trusted in a variety of advanced materials, color solutions and performance coatings applications to enhance the hue, functionality, safety and environmental footprint of everyday consumer products. Our key competencies in particle engineering, glass and ceramic science and color technology enable benefits like more durable vehicles and batteries, easier-to-clean appliances, energy efficient roof tiles and bricks, stronger and more decorative glass, and eco-friendly paints. Headquartered in Houston, Texas, Vibrantz has over 60 manufacturing facilities and sales offices on six continents and employs roughly 4,000 individuals. We are building a strong, shared culture that is rooted strongly in our six core values that focus on safety, our people, customers, excellence in all we do, environmental stewardship, and integrity, ethics, and trust. And we are intent upon fostering a workplace that engages employees' heads, hands and - uniquely - their hearts. Vibrantz is owned by American Securities, a leading U.S. private equity firm that invests in market-leading North American companies with annual revenue generally ranging from $200 million to $2 billion and/or $50 million to $200 million of EBITDA. American Securities and its affiliates have approximately $23 billion under management and are based in New York with an office in Shanghai. For more information, please visit **************** and **************************** Job Function Reporting into the Technology Manager, Plastics, the Product Development Scientist will be based out of Ashtabula, Ohio and will be responsible for innovative projects requiring research and development for the Plastics and Coatings markets and provide start-up support to Operations when projects are scaled up to production quantities. Responsibilities Set a positive example with respect to safety and overall professional performance. Prepare project plans, periodic reports, and Gate Review information to allow smooth transition of new products from development through scale up to Operations. Train technical personnel in new processes and procedures as it relates to innovation development. Communicate new technology to Commercial management and Product management in terms of features, benefits, and comparisons to benchmarks. In support of target objectives, prepare exhibits, specimens and presentations that illustrate key characteristics. Accompany commercial sales on customer visits for collaboration opportunities and/or innovation launch opportunities. Work independently and in collaboration with other team members to meet project goals with accelerated schedules and significant commercial impact. Compose presentations and reports to internal/external parties. Plan and conduct developmental/customer support projects that are assigned by the Technology Manager. Issue periodic reports on progress and activities in support of internally determined objectives. Also, purchase supplies for the timely and efficient operation of projects/programs. Determine specification requirements for raw materials as used in new technologies and related applications. Accordingly, make appropriate recommendations to Technology Manager and/or QC/QA Manager(s). Perform laboratory, pilot-scale and manufacturing work involving the development and/or scale up of dispersion products and processes for a multitude of thermoset applications. Establish processing and quality control parameters that are essential to newly developed technologies and provide relevant information to QC/QA Manager(s) and Internal Technical Service. Where assigned, assist in troubleshooting of batches involving significant changes in process and/or chemistry. Comply with safety rules and regulations, lead /support safety meetings and training, inspects work area for hazards/deficiencies and initiates action to correct them. Also, reports injury/illness and/or environmental incidents. Maintain lab notebooks to organize, analyze, and record work product. Perform other duties as assigned. Required Experience Doctor's degree in chemistry, material science or related field with demonstrated knowledge in chemistry and/or chemical engineering, and colloidal/nano particle modification chemistry would be a plus. Understanding of dispersion chemistry effect to the surface treatment of substrates used within the thermoset application area. 5+ years of experience in a scientific field and experience functionalizing nanoparticles. Experience and discipline in hands on experimentation as well as experience with DOE design statistic software is an advantage. Ability to analyze, design and implement projects. The ability to operate in a self-directed manner and make independent decisions as required. Ability to work well in a team environment and lead product development efforts to successfully complete assigned product development projects. Ability to carry out efficient communication with team members as well as internal and external customers. Strong oral and written English communication skills are required. Proficiency in Microsoft Office applications as required. Benefits We offer a comprehensive benefits package including medical, dental, life insurance, paid vacation, and 401K. Physical Requirements and Working Conditions The physical demands and working conditions are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Vibrantz Technologies Inc. (“Vibrantz”) is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. Vibrantz strictly prohibits and does not tolerate discrimination against employees, applicants, or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex, gender, age, physical or mental disability, genetic information, or any other characteristic protected under applicable federal, state, or local law . Location Ashtabula, OH Vibrantz is committed to protecting your privacy. We provide a Website Privacy Policy located on our Vibrantz.com site to explain the type of information we collect and to inform you of the specific practices and guidelines that protect the security and confidentiality of your personal data. Please read that policy carefully. If any term in the policy is unacceptable to you, please do not use the Website or provide any personal data. This policy may change from time to time (see Revisions to Our Privacy Policy on Vibrantz.com). Vibrantz Technologies Inc. (“Vibrantz”) is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. Vibrantz strictly prohibits and does not tolerate discrimination against employees, applicants, or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex, gender, age, physical or mental disability, genetic information, sexual orientation, or any other characteristic protected under applicable federal, state, or local law.

Your Opportunity as a Scientist, Pet Research & Development-Product Development Be responsible for developing product designs and formulations that deliver solutions against the identified unmet consumer needs and business priorities. You will leverage technical expertise and scientific method thinking skills to bring together consumer needs and product possibilities to both winning, and creative innovation, as well as product improvement and maintenance. You will lead several RoadMap projects within Pet Snacks as well as capability projects. Location: Orrville, OH Corporate Offices Working Environment: Supporting our Presence with Purpose Model with a minimum onsite expectation of 30% or as business need require In this role you will: * Initiate and lead formulation development of optimized formulations, new technologies and product innovation, renovation or cost optimization that delivers against the consumer need and design criteria. * Develop and run (in partnership with Process Lab/Plant) experimental designs to test hypotheses in the areas of sensory/palatability, stability, and other key technical project deliverables. * Communicate results, key learnings, and recommendations. Author or contribute to technical proposals, summaries, presentations, and project reports. Maintain technical documentation (eg laboratory notebooks and invention records). * Lead project or functional teams, as needed to proactively meet project needs/timing. * Keep abreast of new ingredients and technologies as well as patent art in and beyond the existing category. * Actively collaborate and partner with team members, both internal and external to R&D, to develop key tasks and project plans for timely completion of goals. The Right Place for You We are bold, kind, strive to do the right thing, we play to win, and we believe in a strong community that thrives together. Our culture is rooted in our Basic Beliefs, and we believe in supporting every employee by meeting their physical, emotional, and financial needs. What we are looking for: Minimum Requirements: * BS degree or higher in Science, Technology, or Engineering * Depending on degree type/level, a minimum of five (5) years of relevant experience in Research & Development * Strong critical thinking and creativity skills. * Ability to work independently, with guidance in only complex situations * Collaboration ability to create and maintain productive relationships * Effective presentation, verbal and written communication skills. * Must be willing/able to drive a company or rental vehicle as needed * Up to 20% Travel required Additional skills and experience that we think would make someone successful in this role: * Pet Food and/or Snacks formulation and product development experience * Experience with food processes, e.g. extrusion, thermal processing, or baking * Experience with commercial formulation software such as Concept 5 Learn more about working at Smucker: * Our Total Rewards Benefits Program * Our Thriving Together Philosophy Supporting All Impacted by Our Business * Our Continued Progress on Inclusion, Diversity and Equity Follow us on LinkedIn #LI-MR1

Your Opportunity as the Scientist, Uncrustables Formulations-Frozen Handheld & Spreads Research & Development Team The Scientist practices and encourages creativity to drive innovation and solve technical problems. They will execute projects designed to result in new or improved products by leading technical teams and developing work plans independently. Location: Corporate Offices in Orrville, Ohio Work Arrangements: Ability to work a hybrid model; a typical week in office is 40-50% in office and up to 100% when lab/pilot plant/manufacturing plant support is needed. Start times based on work needs will be before 8 AM on occasion. In this role you will: Lead formulation development of new and existing formulas for Uncrustables and build subject matter expertise Utilize conceptual and practical expertise in formulation and basic knowledge of related disciplines in development Ensure formulations are compliant with regulations such as, but not limited to, nutrient profiles and claims Coordinate and manage laboratory, pilot plant and scale-ups for projects at JM Smucker (JMS) and contract manufacturing locations Work independently, guided by functional processes, with guidance only in complex situations (e.g., when decisions have functional or organizational impact) Develop and publish technical documentation within specification and lab notebook systems Conduct analytical testing, analyze data, and articulate findings through written and verbal summaries Partners with technical team members to develop key tasks and project plans for timely completion of goals; may informally lead teams Actively collaborate and leverage relationships within Research & Development (R&D) and cross functional teams to achieve project goals Provide coaching and function as a resource for colleagues with less experience as part of our Basic Belief and Commitment to Each Other philosophy Assume an advisory role to internal teams such as operations, technical services, and procurement Become fluent and participate in JMS Key Element and Quality programs to support R&D Embrace and actively participate in company's inclusion, Diversity and Equity (ID&E) initiatives The Right Place for You We are bold, kind, strive to do the right thing, we play to win, and we believe in a strong community that thrives together. Our culture is rooted in our Basic Beliefs, and we believe in supporting every employee by meeting their physical, emotional, and financial needs. What we are looking for: Minimum Requirements: A Bachelor of Science Degree or higher (required); Food Science, Cereal Grains Science, or Engineering strongly preferred 5+ years of technical experience in R&D or another technical discipline (required) Strong experience with food formulations or process engineering, and record of leveraging this experience to develop, qualify, and launch product innovation Ability to thrive in a fast-paced environment, managing multiple projects simultaneously (required) Initiative-taking with the ability and desire to work independently (required) Proven success leading projects from benchtop to scale up and commercialization Ability to work a hybrid model; a typical week in office is 40-50% in office and up to 100% when lab/pilot plant/manufacturing plant support is needed. Start times based on work needs will be before 8 AM on occasion. Approximately 20-30% travel annually; concentrated around project scale-up periods and project learning plan deliverables Food safety foundation - PCQI training a plus Additional skills and experience that we think would make someone successful in this role: Candidate must be able to communicate difficult technical concepts and collaborate across functional teams to achieve shared goals Proven troubleshooting abilities in fast paced environment Excellent communications skills (written, oral, group presentations) Maintaining robust documentation in systems of record and supporting IP filings Learn more about working at Smucker: Our Total Rewards Benefits Program Our Thriving Together Philosophy Supporting All Impacted by Our Business Our Continued Progress on Inclusion, Diversity and Equity Follow us on LinkedIn #LI-MR1

Assumes responsibility for conducting research, developing new products, improving existing products and supporting field evaluations on new products on a global basis. The R&D Principal Scientist recommends new raw materials, equipment and manufacturing procedures. This position provides technical and supervisory support within the laboratory and other MFS departments as required. The R&D Principal Scientist coordinates research and development activities with marketing, manufacturing, laboratory and health and safety departments. The R&D Principal Scientist guides QC and production in dealing with unusual problems related to non-conforming production batches and borderline in-coming raw materials as well as day-to-day production problems providing technical assistance in utilizing and/or disposing of old stocks of raw materials and finished goods.

Department: Laboratory Reports to: Laboratory Manager FLSA Code: Non-Exempt Responsible for performing technical duties in preparation of surgical, autopsy, and cytology specimens for microscopic examination. It may also involve technical instruction of students in an ASCP-approved Histologic Technique program. Position Accountabilities: Receive and accession tissue and cytology specimens and prepare specimens for Histotech processing. Cut sections and stain according to established guidelines for routine and special stains and cover slip and label finished slides for the pathologist's review. Process cytology specimens. Assist the Pathologist with frozen section as needed. Maintain stock of reagents for staining and processing. Maintain equipment, instruments and cleanliness of work area. Retrieve blocks and slides for review as needed. Ordering and accessioning, history card file, patient inquiry, and results reporting. Complete required continuous training and education, including department specific requirements. Comply with universal precautions. Cover Phlebotomy as designed for the position. Ability to interact well with physicians and patient care staff. Highland District Hospital is committed to serving our community by quality healthcare in an atmosphere of safety, compassion and excellence. It is the responsibility of all employees to interact with patients, visitors, and/or co-workers with compassion, dignity, and respect. Employees are to maintain positive behaviors, approaches and attitudes and commitment to interpersonal service. Each employee is to serve as a role model for the organization's Customer Service initiative; A-I-D-E-T; Acknowledge - Introduce - Duration - Explanation - Thank-you; proactively promoting teamwork and a collaborative culture. Responsible for abiding by and adhering to all HDH Corporate Compliance Program initiative and standards. Responsible for compliance with HDH safety standards, policies and procedures. The above statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills of personnel so classified. . Position Qualifications: Education Required: A Bachelors degree and one year of training in an approved program for Histology. Certification Preferred: Must be certified Histologist HLT (ASCP) through the American Society of Clinical Pathologists. Why join the HDH team? Highland District Hospital is a critical access designated, 25-bed acute care facility. We currently employ more than 400 people and benefit from the services of community volunteers. Our medical staff includes over 100 physicians and 15 mid-level providers, representing over 25 specialties and subspecialties. While we are a community-centered hospital, we are also known for our technology and sophisticated healthcare services. Our service area includes over 65,000 residents from Highland County and surrounding counties. At Highland District Hospital we are caring people serving our community by providing exceptional, accessible, quality healthcare in an atmosphere of safety, compassion, and excellence. Our values provide the framework for fulfilling our mission and vision. We value: Quality Teamwork/Collaboration Integrity Patient-First Mind Set Compassion At HDH we are always focused on doing what is best for those we serve and committed to providing a safe, effective, and efficient environment which promotes healing and growth. Benefits Available: Competitive Salary Cafeteria Discounts/Employee Ordering Options Health, Dental and Vision Insurance Company Paid Life Insurance Generous Paid Time Off OPERS and Ohio Deferred Compensation Full-time, Part-time, and PRN schedules available Professional Development and Educational Assistance Opportunities Loan Forgiveness Program Employee Assistance Program Employee Recognition Programs

Method Development Associate Scientist/Scientist Essential Responsibilities Develop and validate HPLC procedures for small molecule drug substances and drug products. Perform forced degradation studies and develop stability-indicating assay and impurities methods Work in a GLP/GMP laboratory. Coordinate the timely and compliant generation of data to support client projects. Perform routine HPLC, GC, NMR, MS, IR, ICP, KF and other analysis and validation studies. Author and review protocols and reports. Review data for technical content and accuracy. Maintain current expertise with relevant ICH, GMP, and FDA guidelines. Requirements Educational Qualifications B.S. to Ph.D. in Chemistry or related field with 5+ years analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good manufacturing practices (GMP) laboratory is required. Specific Skills and Requirements Experience with standard lab instrumentation (HPLC, UPLC, etc.) Experience with LCMS and GC preferred but not required. Be proficient Microsoft Excel and Word Must have basic knowledge chemicals their properties, structure, reactivity, and be able to handle with safe and appropriate techniques. Must have basic knowledge of arithmetic, algebra, and statistics. Must be able to communicate effectively with all plant and office personnel. Must be able to effectively multi task

R&D Meat Food Scientist Salary: $73K and Up (Depending on Experience) Benefits: Full Benefits, Bonus, Health, 401K, Vacation & more. . Contact: *********************************** ******************************************************* Our client, a fast-growing premier food manufacturing company with products sold worldwide, is seeking an experienced R&D Meat Food Scientist for their Research Laboratory. This position will support multiple manufacturing plant facilities. Come join this team of fascinating R&D professionals who are leading the way to outstanding products & exciting innovation. Responsibilities: Create new food formulations and samples through R&D. Identify new ingredients to apply towards new innovative food products. Document product specifications & processes that will be consistent with the production of various manufactured food products. Conduct internal & external audits at multiple locations to measure product quality. Manage food product document control and records, specifications, attaining food safety, verification, product identification trace and incident management. Work with the R&D team to assure all specifications (ingredient specification, formula specification, making specifications, finished product specifications, trade specifications, labeling specification, proper handling specifications) are accurately developed before product launch. Requirements: BS. Degree in a related field of Food Science, Microbiology, Meat Science, Animal Science or Chemistry 2+ years or more experience in R&D or Food Technology from a food manufacturing or food development company. 2+ years of R&D experience with meat products. Knowledge of FDA & US Government regulations, including labeling & nutritional facts with use of Genesis Nutritional Software. Must be detailed oriented with excellent communication skills. Excellent technical writing skills. Experience with MS Office Suite and Excel. Ability to travel regionally with some overnight stays required. Some flexibility to work from home on occasion. Must be currently authorized to work in the USA without the need for visa sponsorship now or in the future. If you are interested, please send me your updated MS Word version of your resume and cover letter. Or if you know of someone that would be a great match, please have them contact - John Marino at *********************************** Or apply directly here online by clicking the “APPLY NOW” link: ******************************************************* #FoodTechnologist #R&D #ResearchAndDevelopment #Meat #MeatScience #SimplyHired #Monster.com #Indeed.com #LinkedIn #ZR #ZipRecuiter #Jobs #pork #poultry #beef #proteins