Chemist Jobs in Newark, DE

We are seeking a motivated and detail-oriented Analytical Scientist to join our team. The ideal candidate will have a Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field, with at least 1 year of hands-on experience in analytical testing using techniques such as High-Performance Liquid Chromatography (HPLC) and other modern instrumentation. This role supports the analysis of raw materials, intermediates, and finished products to ensure compliance with regulatory and quality standards. Key Responsibilities: Perform analytical testing using HPLC, UV-Vis, FTIR, dissolution, and other relevant techniques. Support method development, validation, and routine sample analysis in compliance with cGMP regulations. Document all laboratory activities and results accurately in laboratory notebooks and electronic systems. Assist in investigations, OOS (Out of Specification) results, and laboratory deviations as required. Maintain and calibrate laboratory instruments according to SOPs and regulatory standards. Qualifications: Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field. Minimum 1 year of experience in a pharmaceutical laboratory environment. Hands-on experience with HPLC is required; familiarity with other techniques like GC, UV, FTIR, and dissolution is a plus. Working knowledge of cGMP, ICH, and FDA regulations. Strong attention to detail, organizational, and documentation skills.

10 Days of PTO / 6 Sick Days / Paid Holidays Compensation: $35.76/hr to $45.87/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Healthcare benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, financial protection benefits, as well as HSA, FSA, and DCFSA account options. 401k retirement account access is offered starting on the 90th day with employer matching after one year of service. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Required Skills & Experience -Minimum 2 years of relevant GMP work experience in a lab setting -Minimum 1 year of experience working with mammalian cell culture -Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA -Bachelor degree in Biology or Chemistry -Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs) -Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols -Proficient with Microsoft Office applications (Outlook, One Note, Teams, Excel, Word, and PowerPoint) Nice to Have Skills & Experience -CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience -Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC -Ability to complete equipment and software qualification protocols -Experience developing and setting long-term objectives -Experience working in Biosafety Level lab (BSL 2, BSL2+) or aseptic facility -Knowledge of EU/FDA guidance Job Description The QC CRS Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor. Key Responsibilities: -Conduct analytical biological testing of clinical and commercial drug product/drug substance samples -Perform peer reviews and approvals of laboratory data -Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data -Support of New Product Initiatives (NPI) including owning a project and perform project management functions with limited to no coaching from supervision/management -Perform Instrument Calibration and Preventative Maintenance -Update CRS-owned documents using the Document Management System (DMS) -Order/receive supplies and manage inventory -Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities -Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight -Act as a peer subject matter expert in assessing talent by participating in panel interviews for job -Complete invalid assay and general laboratory investigation records -Complete corrective and preventative actions (CAPA) as assigned -Assist in the execution of internal audits

About Us: At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the worlds largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs. Position Summary: Design, plan, and execute complex organic synthesis reactions to support research and development goals, with a focus on improving process efficiency, yield, and product quality. Job Accountabilities: * Design and Optimize Synthesis Routes: * Develop and implement efficient synthetic routes for complex organic compounds. * Scale-up and Process Development: * Scale up small-scale reactions to large-scale production, ensuring process consistency, efficiency, and safety. Quality Control and Assurance: * Collaborate with the quality assurance lab to develop and implement robust analytical methods for monitoring product quality and purity. Troubleshooting and Problem-Solving: * Troubleshoot complex synthesis issues, identify root causes, and implement corrective actions to improve process efficiency and product quality. Purification Techniques: * Develop and implement efficient purification techniques, including distillation, crystallization, chromatography, and extraction methods, to isolate and purify target compounds. Characterization Techniques: * Utilize characterization techniques such as NMR,MS, IR, and HPLC to identify and confirm the structure of synthesized compounds, ensuring high purity and quality. Collaboration with Cross-Functional Teams: * Work closely with R&D, manufacturing, and commercial teams to ensure seamless integration of new products and processes. Documentation and Record Keeping: * Maintain accurate records of experiments, results, and synthetic routes, ensuring compliance with regulatory requirements. * Maintain equipment glassware and workspace in order to keep them clean and well-functioning. Properly dispose of all laboratory waste. Participate in ensuring good management of laboratory equipment and storage spaces for chemicals and raw materials. Comply with housekeeping rules. * Ensure that all equipment and machines in your area of control are managed with regards to safety, maintenance, calibration, and availability. Education/Experience: * A bachelor's degree in chemistry and 3+ years of organic synthesis experience OR a master's degree in chemistry with an organic synthesis focus is required. Masters degree preferred. * At least 3 years of relevant experience in organic synthesis, with a strong background in laboratory techniques, reaction mechanisms, and spectroscopic methods. What's in it for you: * Competitive pay programs with excellent career growth trajectory * Hybrid work environment in Conshohocken, PA * Opportunities to see your efforts contribute toward the success of the business. * Work for a global leader in the industrial process fluids industry EEO STATEMENT: It is Quaker Houghton's policy 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. Houghton International will also provide reasonable accommodations for qualified individuals with disabilities. This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

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 (******************************************* At DuPont, and within the Electronics and Industrial (E&I) organization, we are looking to reinforce our Research and Development Team to support the HD Microsystems business. HD Microsystems is a joint venture between DuPont and Resonac and is a global leader in our market space providing high-performance coatings that are used in the semiconductor and related industries. The successful candidate will be a DuPont employee on-loan to the joint venture. Our US R&D Team is based at the **Experimental Station in Wilmington, Delaware, US.** We are currently seeking an **Associate Investigator (AI) Organic Polymer Chemist** . The successful candidate will perform hands-on laboratory work under the direction of a technical Principal Investigator. The candidate is expected to apply scientific skills and expertise regarding the research project(s) which involve all aspects of polymer chemistry with emphasis in the areas of polyamide and polyimide synthesis, analytical characterization, formulation, and coating processes. While the candidate is expected to work as a part of an interdisciplinary team, the candidate is also expected to be able to work independently in the laboratory, and to occasionally design and execute their own sub-team projects. Your Key Responsibilities: + Independently conducting synthetic reactions, including reaction system assembly, monitoring, product work-up/analysis/characterization, and experimental documentation using an electronic laboratory notebook system. - Conducting polymerization reactions at scale ranging from a few grams to a few kilograms including assembling glassware, weighting reagents, monitoring reaction progression and controlling reaction rate. - Isolating and purifying polymers. + Preparing photosensitive formulations of polymers + Coating formulations in a clean room and evaluating effect of process conditions on final film properties. + Analyzing polymer, liquid formulations and cured film samples through instrumented methods (including NMR, FT-IR, GPC, DSC, viscosity, TGA, TMA, etc.) - Operation and maintenance of such laboratory instrumentation. + Contributing to all phases of project development including planning, execution, data collection, and analysis of lab experiments **Qualifications:** + B.S in Chemistry or related fields with 2-4 years of hands-on wet chemistry / practical laboratory experience. + Knowledge of organic chemistry, general polymerization processes and basic functional group transformations. + Experience with crosslinking reagents such as acrylics, phenolics or epoxy resins + Knowledge of methods for polymer synthesis and characterization. + High level of creativity and productivity + Exceptional knowledge of and hands on experience with NMR, GPC, FT-IR as well as interpretation of the respective data. + Commitment to laboratory safety, including adherence to best practices, PPE usage, proper disposal of chemicals, and managing chemical inventories. + Experienced in maintaining a laboratory in good working condition as well as ordering supplies and chemicals. + The aptitude to effectively collaborate with interdisciplinary teams of scientists and to communicate research directions within the R&D community. + Initiative, aptitude, and willingness to learn a new fields of research. + Knowledge about polymer chemistry + Experience working in clean room environment. + Experience with UV or thermal crosslinking chemistries such as acrylic, phenolics, or epoxy and related analysis + Knowledge about formulation and handling of photosensitive materials + Knowledge of materials for microelectronics applications + Familiarity with various coating methods such as spin, slot-die, spray, and roll coating processes. 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 (****************************************************** .

Precise Systems seeks an Analytical Chemist to perform headspace analysis on explosives and other substances that could be relevant to canine scent detection (e.g., drugs, biomedical samples, novel training aids, etc. Position Responsibilities: Deliver analytical chemistry technical experience and expertise, hands-on laboratory work, and programmatic support for applied research, technology evaluation, methodology development and systems development to support headspace (odor) characterization and analysis Perform in areas of chemical, biological, and explosives detection, chemical analysis via gas chromatography and mass spectrometry, and other military life cycle programs Provide qualified laboratory, technical, programmatic, and administrative services Conduct untargeted analytical chemistry - headspace analysis (required) Deliver Good Laboratory Practice (GLP) skills Provide excellent communication, documentation, and attention to detail Write standard operating protocols, test plans, and analyzing results Conduct hands on chemical surety work on chemical/biological warfare agents, emerging threat agents, experimental agents, and toxic industrial compounds Conduct experimental design Provide laboratory test support Develop, modify and/or install new applications as required. Education Master of Science Degree from an accredited college or university in Chemistry, Biochemistry, or related discipline and 5 years of laboratory experience in analytical chemistry Bachelor of Science Degree from an accredited college or university in Chemistry, Biochemistry, or related discipline and 9 years of laboratory experience in analytical chemistry Experience: Must meet be able to meet Chemical Personnel Reliability Programs (CPRP) requirements M.S. and 5 years or B.S. and 9 years' experience Physical Demands: Requires sitting and standing associated with a normal office and laboratory environment Manual dexterity is needed for conducting laboratory work while wearing personal protective equipment May require standing for long periods of time Must be able to lift at least 50 pounds. Must be able to obtain and maintain a Secret security clearance. Due to the sensitivity of customer related requirements, U.S. Citizenship is required. Precise Systems values employee contributions, promotes diverse opportunities for professional growth, and prioritizes overall well-being. Our comprehensive professional services benefits package includes health insurance, life and accidental death and dismemberment coverage, disability insurance, retirement plans, holiday pay, employee-managed leave, and professional growth opportunities. We recognize exceptional performance and alignment with our core values through our STAR Award recognition program. Compensation at Precise Systems is determined by various factors, including education, experience, skills, competencies, and contract-specific requirements. The salary range for this position is $78,433.26 to $129,258.60 (annualized USD). This range represents the standard pay for this role and is just one component of Precise Systems' total compensation package. Precise Systems is committed to fair and equitable pay practices in alignment with applicable pay transparency laws and equal employment opportunity standards. Precise Systems and its subsidiaries are committed to an inclusive and diverse workplace that values and supports the contributions of each individual. This commitment and shared Vision and Values of Integrity, Respect, and Responsibility allow us to leverage differences, encourage innovation, and expand our success in the global marketplace. Precise Systems and its subsidiaries are Equal Opportunity /Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, protected veteran status, status as an individual with a disability, or any legally protected status under federal, state, or local law.

Agilent Technologies is seeking a Production Chemist for its manufacturing facility in Newport, Delaware. The Newport site is part of Agilent's growing Consumables and Supplies Division (CSD), with a focus on liquid chromatography products. Agilent's product quality and technological innovation lead the market. As a leader, we are entering new phases of product transformation with increased emphasis on new product and process innovation, process standardization and production efficiency. This is a high-visibility and growing product line where you will have the opportunity to make a real difference to one of Agilent's key consumables businesses. Plus, we embrace 6-Sigma and Lean Manufacturing methodologies making for an engaging and rewarding mix of scientific discovery, process improvement, and employee growth and development. Key responsibilities include working individually or as part of multi-discipline, cross-functional teams to: Evolve existing chemistries and design new chemistries Provide support for and/or represent the site on new product introduction projects Scale existing chemistries in support for a rapidly growing line of liquid chromatography consumables Lead project teams to develop and deploy product and process improvements, which include capital projects and continuous improvement projects Support and actively pursue Lean, 6-Sigma, and Safety Improvement projects Provide daily support for the production of silica-based packing for high-performance liquid chromatography columns Resolve yield and scrap issues Execute and support the Management of Change control process, determine the disposition of nonconforming product, and create and execute corrective and preventive action plans to improve safety and quality Maintain SAP data accuracy (bills of materials, recipes) Qualifications Bachelors or Masters Degree in Chemical Engineering, Chemistry, Material Science or equivalent 1+ years of experience in a chemistry based working environment Demonstrated technical and problem solving skills Demonstrated communication skills; written, oral and listening Demonstrated leadership skills Computer and digital skills Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least April 16, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $79,200.00 - $123,750.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing

Wilmington PharmaTech (WPT) is seeking self-motivated Research Scientists to join our dynamic chemistry process department for active pharmaceutical ingredient (API) synthesis in clinical phase drug development. Key Responsibilities: Participates in the production of APIs in a kilolab or pilot plant setting by following batch records under cGMP environment. Records precisely all critical observations and documents all results during the production accurately. Diligently follows company SOPs to clean equipment for production and maintains appropriate cleaning records. Disassembles reactors for cleaning as necessary and reassembles them after the cleaning complete. Ensures and maintains kilolabs and related storage areas are in good condition. Performs routine qualifications for production equipment and maintains related records. Understands cGMP requirements of WPT and strictly follows all company policies, SOPs and best practices. Adheres to safety standards. Potential to conduct hands-on organic research with supervision for process optimization, and collect data to support the production of intermediates/APIs. Participates in the hazard operations (HAZOP) discussion and provide suggestions and solutions as necessary. Assists in trouble shootings and investigations of processes. Maintain good, clear laboratory records. Desired Qualifications: Academic or industrial research experience in organic chemistry. This position offers benefits, competitive salary and an opportunity to advance in a growing company.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Performs qualitative and quantitative chemical analysis of raw materials . Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non-conformances and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance. Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Qualifications The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Who are we, and what do we do? At Corteva Agriscience, you will help us grow what's next. No matter your role, you will be part of a team that is building the future of agriculture - leading breakthroughs in the innovation and application of science and technology that will better the lives of people all over the world and fuel the progress of humankind. We are seeking a Senior Associate Investigator to develop and apply various modern analytical techniques to support toxicity testing for agricultural products, intermediates, metabolites, and impurities, under the supervision of a Principal Investigator. What You'll Do: Conduct routine and non-routine analyses of toxicity testing study samples (diet and dose, in vitro and in vivo matrices), including sample extraction and purification to meet project quality and timing needs Operate, maintain and be technically competent in various types of analytical instrumentation (e.g. LC/UV, LC-MS/MS, etc.) including calibration and systems qualification in order to provide accurate and reliable data Develop chromatographic methods to separate, identify, and quantify actives and metabolites in toxicity testing samples and utilize them for GLP studies and reports Perform and document work under GLP and other appropriate regulatory guidelines Custodial duties for laboratories and various analytical equipment What Skills You Need: B.S. degree in chemistry or related fields, preferably with at least 5-years experience in a GLP laboratory or M.S. with at least 1-year experience Experience with method development and analysis using chromatography (HPLC, UHPLC) with DAD and modern mass spectrometric (LC/MS, LC-MS/MS) techniques Highly organized, with attention to detail and ability to work independently or with minimal supervision in several projects; good interpersonal skills, demonstrated problem-solving and troubleshooting skills Good written and oral communication skills; familiarity with (or ability to rapidly learn) computers and software packages from various instrument manufacturers VISA Sponsorship is not available for this position. Relocation assistance is not offered for this position. Benefits - How We'll Support You: • Numerous development opportunities offered to build your skills • Be part of a company with a higher purpose and contribute to making the world a better place • Health benefits for you and your family on your first day of employment • Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays • Excellent parental leave which includes a minimum of 16 weeks for mother and father • Future planning with our competitive retirement savings plan and tuition reimbursement program • Learn more about our total rewards package here - Corteva Benefits • Check out life at Corteva! ************************************* Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team. Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! The Translational Medicine (TLM) department of QPS is comprised of three laboratory operations units: Biomarker Analysis (BMA), Gene & Sequence Analysis (GSA), and Immunobioanalysis (IBA). An Associate Scientist in any of these units will be a fully-supervised trainee, responsible for gaining mastery of GCP and GDP, conducting assigned studies according to study protocols, and recording study results and observations. Our TLM department is continuing to expand, and has positions available in most of the above units. If you have a Bachelor's degree in Biology, Biochemistry, Immunology or other related disciplines, we would like to hear from you. QPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (************ for more information and to see all current openings. The Job Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies Assist supervisor in performing analysis of drug or other targets in complex biologic matrices Set-up, use and maintain complex instrumentation Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Perform routine mathematical & chemical calculations Work Location This job will be 100% QPS-office/facility based Requirements The successful candidate will hold an undergraduate degree in Biology, Molecular Biology, Biochemistry, Immunology, Pharmacology, Medical Technology, or a related field as follows: Bachelor's Degree Associate's Degree plus 2 or more years relevant experience Desire to learn and grow professionally Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals. Structured Career Ladders that provide excellent growth based on your personal aspirations. Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance. Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance Park-like setting in Newark, Delaware Internal committees designed with the needs and enjoyment of QPS employees in mind. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Since 1869 we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Michael Angelo's, Pace, Pacific Foods, Prego, Rao's Homemade, Swanson, and V8. In our Snacks division, we have brands like Cape Cod, Goldfish, Kettle Brand, Lance, Late July, Pepperidge Farm, Snack Factory, and Snyder's of Hanover. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. Campbell's offers unlimited sick time along with paid time off and holiday pay. If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. Giving back to the communities where our employees work and live is very important to Campbell's. Our “Campbell's Cares” program matches employee donations and/or volunteer activity up to $1,500 annually. Campbell's has a variety of Employee Resource Groups (ERGs) to support employees. How you will make history here… The R&D Technician, under general supervision, is responsible for the safe and efficient operation of Pilot Plant machinery. Responsibilities include a wide variety of assignments as scheduled by immediate supervisor including but not limited to ingredient and component preparation, blending, mixing, filling, laminating, depositing, baking, cooking, packaging, cleaning and sanitizing, and any other duties as assigned. Working in a fast-paced environment with continuously changing requirements and procedures, the ability to apprehend, adapt, and deliver results with precision will be key in successfully delivering job requirements. What you will do… Principal Accountabilities 50% - Operation of equipment and processes to produce safe and wholesome food 15% - Execute documentation requirements accurately for all product executions per food safety and quality programs and procedures 10% - Conduct work activities in accordance with all safety and quality requirements 10% - Support manual production processes of manufacturing executions 10% - Sanitation and general cleaning in adherence to Standard Sanitation Operating Procedures 5% - Responsibility for Health & Safety program Job Complexity Participate in food manufacturing process and complete required documentation in a satisfactory manner - Communicate clearly with Product Development and Process Engineering partners to troubleshoot issues and deliver expected results - Execute critical process procedures to deliver expected production results in a timely manner - Ensure work is done in accordance with Food Safety and Health & Safety guidelines - Maintain in-depth understanding of equipment and process operation/execution - Safely handle and utilize cleaning chemicals to administer sanitation procedures Who you will work with… You work with all functions in the R&D Pilot Plant. What you bring to the table (must have) … High School Diploma or equivalent 5 years' experience in operations It would be great to have… Associates or Food Science Degree Bakery experience Ability to work well with other under moderate supervision, detail oriented, mechanical aptitude, and ability to multitask Strong interpersonal communication skills including ability to read, write, speak, and understand English language Must be comfortable communicating to immediate team members, maintenance personnel, and leadership staff Ability to push and pull up to 700 pounds with and without mechanical assistance and lift/carry up to 50 lbs Basic Math and computer skills Compensation and Benefits: The target base salary range for this full-time, salaried position is between $42,900-$61,600 Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package. The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.

SCM is committed to a workplace that values and promotes diversity, inclusion and equal employment opportunity by ensuring that all employees are valued, heard, engaged and involved at work and have full opportunities to collaborate, contribute and grow professionally. We are currently seeking a highly driven, well organized, and motivated candidate to join our team. SCM offers the opportunity to work in person, remotely or in a hybrid work environment. Primary Responsibilities: * Develop, implement and evaluate quantitative trading models in the global equity markets. * Continuously improve trading models and modeling techniques. * Identify orthogonal factors to enhance overall portfolio performance. Requirements: * 5+ years quantitative hedge fund or proprietary trading experience. * Experience utilizing statistical modeling techniques to develop quantitative trading models. * Keen focus on achieving outstanding risk adjusted returns. * Strong interest in the financial markets. * Exceptional economic intuition. * Degree(s) in statistics, mathematics, computer science or other technical disciplines. The base pay for this position is anticipated to be between $150,000 and $300,000 per year. The anticipated annual base pay range is current as of the time this job post was generated. This position is eligible for other forms of compensation and benefits, such as a bonus, health and dental plans and 401(k) contributions, which includes a discretionary profit sharing program. An employee's bonus and related compensation benefits can be a significant portion of total compensation. Actual compensation for successful candidates will be carefully determined based on a number of factors, including their skills, qualifications and experience.

**Analytical Associate Scientist** **Exton, PA** The Analytical Associate Scientist will assure that dsm-firmenich Biomedical products are of consistent and high quality by: Assuming responsibility for duties related to the research, development, testing and manufacturing of medical device materials, products or technologies in compliance with GMP and ISO standards and participating on project teams consisting of R&D, Commercialization, Advanced Engineering, Manufacturing, Quality, Regulatory, Business Development and Finance within the PMP/project management process. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work to not only benefit our People, Customers & Communities but also drive business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. **Key Responsibilities:** + Develop a solid IP track record (patents, trade secrets, freedom to operate) for the business based on unique concepts that provide DSM Biomedical with a freedom to operate well beyond the normal standard. Stay up to date with competitor IP and contribute to patent searches and IP justifications. + Generate and process Device Master Record documentation, including process routers, drawings, preventative maintenance procedures, and other written documentation in accordance with GMP requirements to support product development, process development, validations, and manufacturing. Prepare relevant technical sections for product or regulatory submissions. + Identify, evaluate, and implement improvements (productivity, efficiency, reliability) to existing processes or products. Assist production and quality personnel in the training, initial launch, and validation of new products and processes. Provide technical interface for internal and external stakeholders and customers. + Develop and fabricate novel biomedical materials and processes from lab-scale level through manufacturing scale-up for the development and production of biomaterials and/or related implants or devices. Assist or take a lead role in the transition of acquired products, processes, and/or equipment into laboratory, manufacturing, or production environments. + Plan, construct, and implement Design of Experiments (DOEs) and Risk Management Documentation as required to develop or validate new or existing products. Develop testing methods and complete Test Method Validation (TMV). Prepare protocols and reports, and provide recommendations based on completed experiments and/or tests. Develop and maintain design control systems and procedures that comply with all US/OUS medical device regulations. + Perform analytical, mechanical, and biochemical assay testing, as well as polymer synthesis, polymer processing, natural materials manufacturing and characterization, according to dsm-firmenich Quality Systems protocols for raw materials, intermediates, and finished products while maintaining a laboratory notebook and other associated documents. Independently plans, prioritizes, and conducts research. + Participate in project teams, taking responsibility for assigned tasks and ensuring their completion on time and within budget. **We Bring:** + A competitive compensation package, with comprehensive health and welfare benefits + A place to grow and develop. + A company that is purpose-led and performance-driven in a corporate culture that values people and planet. + The opportunity to work on growing brands and build on a strong foundation. + The chance to make improvements and make an impact on the business. **You Bring:** + Ph.D., Master's, or Bachelor's degree in analytical chemistry, chemistry or polymer science with a minimum of 4 years of experience. + Highly skilled in two or more analytical techniques. + Inorganic analysis experience is a plus with knowledge of techniques such as ICP, XRD, Surface area, particle size analysis, etc. + Experienced with analytical method development, validation, and implementation. + Demonstrated skill in analytical instrumentation trouble shooting and repair. + Understanding of polymer and natural materials science. + Knowledge and experience working with Engineering & Quality tools (Statistics, Six Sigma, DFM, DOE, etc.). + Computer literacy (i.e. Word, Excel, Project, PowerPoint, Outlook, Pro/E or similar CAD system). + Understanding of Engineering concepts. + Understanding of anatomy and surgical procedures. + Good written and oral communications skills. + Ability to function or lead as a part of a team. dsm-firmenich is fully dedicated to inclusion because when people feel engaged and empowered, their creativity and innovation drives unprecedented progress. We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate: there's a place for everyone at dsm-firmenich. As a committed equal opportunity employer, we ensure our recruitment practices are inclusive and fair. We encourage the recruitment of a diverse workforce, representative of the communities in which we work, by using inclusive language, diverse interview panels, diversified sourcing strategies. Selection is based on qualifications, competency, experience, performance history and fit with the team to advance fair and equitable opportunity. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, ethnicity, national origin, religion, gender, gender identity or expression, sexual orientation, age, disability, backgrounds, genetic information, protected veteran status, or any other status protected by law. We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know. Please note this is a direct search led by dsm-firmenich. We only accept applications from candidates, not from agencies nor subject to agency's fees, percentages or similar.

Scientist/Associate Scientist aids in the development of bioanalytical methods. Responsibilities: Conduct method validation for bioanalytical methods and conduct sample testings Complies with all relevant GLP and/or cGMP regulatory requirements while carrying out assigned tasks Utilizing various types of instrument including LC-MS, SIMOA, MSD, SP-X, ELLA, etc Assist principal investigator and responsible scientist to perform the projects Requirements: * Scientist B.S. level with 1+ year experience or M.S. level or above * Associate Scientist- B.S. level without experience

Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Responsibilities: Coordinate study activities with Responsible Scientist to ensure efficiency and quality Aid in the preparation of study summaries and/or reports Maintain the proper level of regulatory compliance for each study, helping to address QA audit findings Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities Follow safety precautions Requirements: Ability to successfully work in a team environment. Excellent oral and written communication skills Bachelor's degree or Master's degree in a related scientific discipline Salary and Benefits: Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Who We Are: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. Role Overview: The purpose of the Quality Control Chemist is to perform chemical testing of in-process, raw materials, intermediates, and finished product samples in support of GMP production and stability testing. They execute standard analyses with regular supervision. Core Responsibilities: Able to perform standard quality control laboratory techniques such as: HPLC, GC, UV, LC-MS, KF, FTIR, NMR, and wet chemical methods such as titrations. Conducts analyses and reports results. Sets up, troubleshoots, and adjusts laboratory equipment, as necessary. Reviews other team member's analytical data for accuracy. Works with other chemists on shift to support product campaigns. May prepare written documents including generation and revision of SOPs and other GMP documents. Contributes to the technical growth and continuous improvement of the department. Supports laboratory investigations through testing under the direction of quality control supervision. Executes safety initiatives in the laboratory that maintain and improve the work environment. Qualifications: Must be able to work Night Shift (7:00 pm - 7:00 am). Shift rotation is a 2/2/3. Bachelor's Degree in Chemistry or related field Minimum one (1 year) experience in a quality control environment Able to operate standard QC laboratory equipment (HPLC, GC, FTIR, UV, KF, etc.) desirable Proficiency in Microsoft Office is desirable Our Commitment: Health & Wellness: Comprehensive health & Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match. Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs. Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career. How to Apply: At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit **************** to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team. For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to ****************************** in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Additional Information: Applicants for this role must be authorized to work in the United States without further employer sponsorship. Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here. Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com. Legitimate LinkedIn communications will only come from active Veranova employees. Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number). Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks). If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: ********************* (US) or ***************** (UK). All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Who We Are: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. Role Overview: The purpose of the Quality Control Chemist is to perform chemical testing of in-process, raw materials, intermediates, and finished product samples in support of GMP production and stability testing. They execute standard analyses with regular supervision. Core Responsibilities: Able to perform standard quality control laboratory techniques such as: HPLC, GC, UV, LC-MS, KF, FTIR, NMR, and wet chemical methods such as titrations. Conducts analyses and reports results. Sets up, troubleshoots, and adjusts laboratory equipment, as necessary. Reviews other team member's analytical data for accuracy. Works with other chemists on shift to support product campaigns. May prepare written documents including generation and revision of SOPs and other GMP documents. Contributes to the technical growth and continuous improvement of the department. Supports laboratory investigations through testing under the direction of quality control supervision. Executes safety initiatives in the laboratory that maintain and improve the work environment. Qualifications: Must be able to work Night Shift (7:00 pm - 7:00 am). Shift rotation is a 2/2/3. Bachelor's Degree in Chemistry or related field Minimum one (1 year) experience in a quality control environment Able to operate standard QC laboratory equipment (HPLC, GC, FTIR, UV, KF, etc.) desirable Proficiency in Microsoft Office is desirable Our Commitment: Health & Wellness: Comprehensive health & Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match. Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs. Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career. How to Apply: At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit **************** to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team. For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to ****************************** in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Additional Information: Applicants for this role must be authorized to work in the United States without further employer sponsorship. Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here. Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com. Legitimate LinkedIn communications will only come from active Veranova employees. Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number). Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks). If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: ********************* (US) or ***************** (UK). All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Sirius Staffing is seeking a Lab Tech for the Newark, DE area for a contract. We are seeking someone to develop, validate, and apply various modern analytical technologies and approaches for the development and commercialization of agricultural products, including intermediates, metabolites, and impurities. This is a day shift, working Monday – Friday, 8 to 5. $26.00/hr + benefits offered PTO & Holiday pay The scope of the assignment includes analytical support to process and formulation development, product chemistry, regulatory science, operations, and discovery. The role also includes data and report generation, both GLP and non-GLP, in support of registration, re-registration, and quality assurance of agrichemicals in their portfolio. The successful candidate is expected to be a strong team player, flexible, and responsive to change to meet project quality and timing needs. Responsibilities: Develop new methods for qualitative and quantitative analyses under the direction of a Principal Investigator to meet business needs in a timely manner. Conduct routine and non-routine analyses of discovery, process, technical, and formulation samples to meet project quality and timing needs. Collect data, generate summaries and reports under GLP and other appropriate regulatory guidelines Operate, maintain, and be technically competent in various types of analytical instrumentation (LC/UV, GC, IC, MS), including calibration and systems qualification to provide accurate and reliable data. Manage lab safety and industrial hygiene aspects, including proper waste disposal procedures, to maintain a highly efficient and productive laboratory. Interact with a diverse customer base on a variety of projects/tasks. Provide oral and written presentations of technical and business-related work within the work team. Qualifications: Bachelor’s degree in chemistry/biochemistry or equivalent experience with basic knowledge of analytical and organic chemistry. 2+ years of experience in an industrial research laboratory setting, translating oral and/or verbal directions into empirical realities. Experience with method development and analysis using chromatography (HPLC, IC, GC) with modern mass spectrometric (LC/MS, GC/MS) and spectroscopic (UV) techniques Track record of delivering on-time, quality results Experience in working independently with minimal supervision Strong interpersonal skills, demonstrated problem-solving and troubleshooting skills Good written and oral communication skills Experience managing multiple demands in a timeline-driven environment Familiarity with (or ability to rapidly learn) computers and software packages from various instrument manufacturers. Sirius Staffing is an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to characteristics such as race, color, national origin, religion, gender, age, marital status, disability, veteran status, citizenship status, sexual orientation, gender identity, or any other status protected by law.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst - 12hr Rotational Day Shift position at its facility in West Deptford, NJ. Ideal candidates will possess the following: * A BS or BA in the biological sciences or related field (required) * Proficiency with data entry and computer applications * Ability to multitask and work in a fast-paced environment * Strong written and verbal communication skills * Strong attention to detail * Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. This is a full-time position and is eligible for standard benefits after a brief waiting period. The schedule for this position is on a rotating shift basis: the first week is Wednesday-Thursday, from 7:00am to 7:00pm; the second week is Monday, Tuesday, Friday, Saturday, and Sunday, from 7:00am to 7:00pm. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from