Associate Scientist Jobs in Jersey City, NJ

Coatings R&D Scientist A fast growing PE-backed company in the Advanced Materials manufacturing space is looking for a Coatings R&D Scientist to develop innovative coatings, dispersions, and chemical formulations for diverse applications, including industrial lubricants, high-temperature release, conductive, and corrosion-resistant coatings. This is a hands-on, fast-paced role where you'll lead research initiatives, collaborate with cross-functional teams, and contribute to groundbreaking product development efforts at a state-of-the-art R&D facility. Responsibilities Include: Designing and formulating novel coatings and dispersions tailored for various industrial applications. Conducting experiments, analyzing data, and providing clear insights and next steps. Leading a safe, clean, and well-organized laboratory environment. Guiding and supervising junior chemists in performing experiments and presenting results. Developing standard operating procedures (SOPs) and ensuring compliance with safety protocols. Researching and testing new raw materials to enhance existing products or create new ones. Identifying and evaluating advanced laboratory instrumentation to expand R&D capabilities. Presenting data and findings to internal stakeholders and collaborating with marketing and new business development teams to align research with market opportunities. Supporting production scale-up at manufacturing plants and ensuring a seamless transition from R&D to commercialization. Required Skills and Experience: Education: Ph.D., MS, or BS in Chemistry, Chemical Engineering, Materials Engineering, or related fields. Experience: 3-5+ years in industrial chemical-based manufacturing: coatings, sealants, adhesives, or dispersions. Expertise in rheology, coating application techniques, adhesion principles, and DOE (Design of Experiments). Strong data analysis and presentation skills, with proficiency in statistical tools like Excel and DOE software. Effective communication skills to interface with cross-functional teams and stakeholders, including C-suite executives. Adaptability and problem-solving skills to thrive in a fast-paced, growth-oriented environment. What the role Offers: A chance to work in a newly built, state-of-the-art R&D facility equipped with cutting-edge technology. A culture focused on innovation, collaboration, and transparency, supported by a growing, forward-thinking organization. Opportunities to engage in exciting market development efforts, particularly in high-temperature coatings, aluminum applications, and conductive coatings for thermal and electrical use. Physical Requirements: This onsite position requires the ability to stand for extended periods and occasionally lift up to 50 lbs. Salary and Benefits: The salary range for this role takes into account the wide range of factors that are considered in making compensation decisions, including but not limited to skill set; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. It is not common for an individual to be hired at or near the top of the range for their role, and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the base range is $100,000.00 to $ 125,000.00 per year + 15% company performance bonus and benefits.

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Biology who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented accounting and tax experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by…Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to BiologyEvaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise:A bachelor's or higher degree in Biology or a related subject Experience working as an Biology professional Ability to write clearly about concepts related to Biology in fluent EnglishPayment:Currently, pay rates for core project work by Biology experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Title: Senior Scientist Work Schedule: Mon -- Fri, Business Hours Duration: 06+ Months Pay rate: $50 - $53/hr on W2 Hybrid role Hybrid = 2 days onsite 1 week, 3 days onsite the next week, subject to change based on the needs of the business. Top Must Have's for candidate to be Considered for this role: Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Summary Report creation/Review in support of CPV (Continuous Process Verification) and APQR (Annual Product Quality Review). Must be detail oriented and proven track record of impeccable time management, to meet timelines. Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. Job Description: The Senior Scientist of Biostatistics is a member of the MSAT team, with focus in CPV (Continued Process Verification) and APQR (Annual Product Quality Review) reporting. Position Summary: The incumbent will support the monitoring/trending of production and release testing parameters, in support of product of personalized cell therapy products for both global commercial and clinical trial supply. The Incumbent will trend CPV parameters, including but not limited to Manufacturing process parameters and Quality Control Release attributes for the MSAT organization, to support the Summit, NJ Cell Therapy facility. The purpose of a CPV program is to provide evidence that a process is running under a state of control. The incumbent will monitor/trend, alerting stakeholders of any drifts and supporting the data reporting of process parameters to the global MSAT organization, while meeting established timelines. The CPV program includes supporting the APQR, as required by regulatory agencies. The incumbent will support the CPV and APQR reports and approvals. The organization being supported is a 24x7x365 manufacturing facility. Work scope will include commercial manufacturing and clinical manufacturing for all cell therapy products manufactured in Summit, NJ Building S12. This role will work with Supply Chain, Manufacturing, Quality Control, Quality Assurance, Project Management, and MSAT. Duties/Responsibilities: Provides support to maintain the site Statistical Process Control (SPC) program, manufacturing performance trending and reporting. Provide multivariate analysis (MVA) modeling for improved process understanding and robustness Continuously monitor CPV parameters, evaluate Statistical Alert Events (SAEs), and take needed actions. Collaborate and support investigations by providing data and analysis Meet CPV and APQR timelines Establish and support predictive process monitoring analytics Supporting any proactive initiatives or investigations related to drift in product performance Represent the site MSAT CPV team in cross-functional forums Performing review and approval of site documents within the scope of CPV and APQR Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness; actively supporting regulatory inspections Interacting with other teams including Operational Excellence, PMO (Project Management Organization), site MSAT, Global MSAT, Quality Assurance, Process Support/Engineering and Manufacturing Support, Manufacturing Operations, Supply Chain Operations Staying current with industry trends and BMS standards and participating in best practice forums consistent with function responsibilities Identify key Opex opportunities, using data driven evaluations Qualifications Specific Knowledge, Skills, Abilities: Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Must be detail oriented and proven track record of impeccable time management, to meet timelines. Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. Expert knowledge of cGMP's and multi-national biopharmaceutical/cell therapy regulations. Experience of facility/clean room design, process, equipment, automation, and validation. Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities. Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies. Experience with Operational Excellence and Lean Manufacturing Education, Experience, Licenses, Certificates: Bachelor's Degree required (science or engineering is preferred); Graduate or higher-level Degree is preferred 8 or more years of work experience in the biopharmaceutical or related Industry 8 or more years of manufacturing support or related experience in the biopharmaceutical industry Experience in CPV and/or APQR reporting preferred. May be substituted for relevant experience in monitoring/trending performance of Quality attributes Experience in cell therapy, biologics, or vaccine manufacturing/support required Experience with Operational Excellence and Lean Manufacturing is a plus

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment". Job Title: Senior Associate Scientist Duration: 12 months Pay rate: $51.97/ hr on W2 Job Description: 4-7 years experience with CAR-T cell therapy Cellular biology techniques, flow cytometry, ELISA Mammalian cell experience Bench level experience, they have to be 100% lab based and looking to stay in the lab. Cell based assays 10+ years CAR-T experience would be overqualified Minimum bachelor's degree with 4+ years experience Comfortable with master's degree with 2+ years' experience About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

We're seeking an experienced Senior Scientist/Head Chemist with proven expertise in formulation development, troubleshooting, and innovation across skin care, hair care, and body care. In this role, you'll work closely with Marketing, Product Development, and Manufacturing to deliver high-performance, market-ready products that align with consumer trends and business goals. The Role In this role, you will be responsible for: Developing innovative formulations for skin care, hair care, and body care, ensuring technical excellence, consumer appeal, and market relevance. Leading reformulation efforts to optimize product performance, improve stability, and align with regulatory or market needs. Troubleshooting technical issues related to stability, viscosity, pH, compatibility, and texture, delivering solutions that meet quality and performance standards. Collaborating with Marketing and Product Development to translate concepts into viable, on-trend products. Scaling up formulations from bench to pilot and full-scale manufacturing, ensuring process feasibility and consistency. Identifying and integrating new raw materials and technologies to drive product innovation and differentiation. Monitoring stability testing and analyzing results to maintain formula integrity under multiple conditions. Acting as the technical lead in cross-functional projects, bridging communication between R&D, Regulatory, QC, and Manufacturing. Providing mentorship to junior chemists, fostering growth, and promoting lab efficiency. Ensuring formulations meet global regulatory compliance and internal quality standards. Essentials 10+ years of experience in formulation development for skin care, hair care, or body care. Bachelor's degree (or higher) in Chemistry, Chemical Engineering, or related scientific discipline. Expertise in formulating emulsions, serums, creams, gels, cleansers, and treatments with a proven ability to resolve technical challenges. Experience scaling formulations to full-scale production and working with Manufacturing teams. Strong understanding of raw materials and their functionality, with a focus on performance-driven applications. Comprehensive knowledge of global regulatory standards and compliance for beauty and personal care products. Exceptional problem-solving, technical leadership, and project management skills. Proven success working cross-functionally with Marketing, Product Development, and Regulatory teams to bring concepts to market. Excellent technical documentation and communication skills. Preferred not necessary Bilingual English and Spanish

Job Title: Associate Cell Scientist Compensation Range: $70,000 - $80,000 Join Us in Revolutionizing Women's Ovarian Health We are seeking a motivated and detail-oriented Associate Scientist to join our innovative team at Gameto. This role offers a unique opportunity to contribute to cutting-edge research at the intersection of cell biology, biotechnology, and women's health. As part of a collaborative team, you will focus on maintaining and expanding cell cultures to support the development of a cell therapy for menopause, a revolutionary approach that aims to reshape the future of endocrine care for women. If you are passionate about scientific discovery and thrive in a dynamic research environment, this is your chance to make an impact. You'll apply your technical expertise in cell culture techniques and laboratory best practices to maintain high-quality cell lines while contributing to multiple areas of research and development. About the Role In this role, you will serve as a key contributor to a high-impact program developing cell therapies for menopause treatment. Your work will directly support our mission to advance women's health and contribute to Gameto's innovative platform. We are looking for a self-motivated, detail-oriented individual who enjoys working in fast-paced and translational research settings, evolving with the demands of multiple concurrent projects. Key Responsibilities As an Associate Cell Scientist, you will support research and development activities across several exciting initiatives. Specific responsibilities include: Performing routine and advanced cell culture techniques, including passaging, expansion, and cryopreservation of human induced pluripotent stem cells (hi PSCs) and other mammalian cell lines. Ensuring cell quality and viability through regular monitoring, assessment, and troubleshooting of culture conditions. Maintaining and optimizing cell culture protocols to improve reproducibility and efficiency. Characterizing cell lines using flow cytometry, PCR, ELISA, and immunofluorescence to assess phenotype and functional attributes. Performing cell banking, mycoplasma testing, and other quality control procedures to ensure high standards in cell culture practices. Supporting differentiation and functional assays by preparing and maintaining high-quality cell populations. Recording detailed experimental data, analyzing results, and preparing reports for internal and external stakeholders. Collaborating with cross-functional teams to meet project goals and milestones efficiently. Qualifications Bachelor's degree in a biology discipline is required (fields such as cell and molecular biology, biomedical engineering, or related fields preferred). 2+ years of research experience in a laboratory setting, either academic or industry, with a strong emphasis on mammalian cell culture. Proficiency in aseptic technique, media preparation, and routine maintenance of stem cell cultures. Experience with microscopy, cell counting, and viability assessments. Knowledge of laboratory assays such as ELISAs, flow cytometry, PCR, or immunostaining is preferred. Excellent communication skills with a proven ability to work collaboratively within research teams. Strong organizational skills with a focus on precision, efficiency, and accuracy in experimental execution. A proactive, problem-solving attitude, with the ability to thrive both independently and within a team in a fast-moving research environment. How to Apply If you are excited about advancing women's health through cutting-edge science and want to be part of a mission-driven team, we encourage you to apply today! Please apply on LinkedIn and with the following materials together in a single PDF document: A cover letter that: Describes how your experience aligns with our needs Highlights which aspects of the role in which you will excel Explains what interests you about Gameto and your potential start date Includes anything else you'd like to share with us to help us get to know you better CV/resume Why Join Us? As an Associate Scientist at Gameto, you will work alongside world-class scientists, pushing the boundaries of research in women's health. Your work will play a pivotal role in transforming the treatment of menopause and contributing to innovations that impact women globally. You will have the opportunity to shape new frontiers in cell therapy and develop your career within a vibrant and mission-driven organization. About Gameto Gameto is a pioneering biotechnology company in women's health, co-founded by Dina Radenkovic, a physician-turned-entrepreneur, and Martin Varsavsky, a leader in fertility innovation and founder of the Prelude Network. With our groundbreaking cell engineering platform-developed through a collaboration with Harvard University's Wyss Institute and Professor George Church's lab at Harvard Medical School-we aim to create treatments for menopause and infertility affecting the female reproductive system. Our scientific approach surpasses traditional therapeutic modalities and sets a new gold standard for research and development in the field. Backed by $73 million raised in Series A and B funding from Insight Partners, Future Ventures, RA Capital, Two Sigma Ventures, Lux Capital, and others, Gameto is committed to transforming women's healthcare through bold innovation. Read about us in: MIT Technology Review, The New Yorker, The Boston Globe, and Stat News. Our Values and Commitment to Diversity At Gameto, we value kindness, collaboration, authenticity, and diversity. We are an equal opportunity employer and are committed to creating an inclusive environment. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Support of analytical testing and chromatography data collection on samples from small molecule development/characterization. Other activities include method screening, and optimization using liquid chromatography modelling software. Qualifications BS (2+ yrs) or MS/PHD (1+ yr) of relevant experience in analytical chemistry or small molecule testing lab. Industry experience preferred. Required Skills and Experience Must have separations experience for small molecules Experience in analyzing small molecule formulation development samples and/or other therapeutic modalities using at least one of the following techniques: Liquid Chromatography (HPLC / UPLC) Such as: Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX, AEX, CEX), Reverse Phase (RP), or Hydrophobic interaction chromatography (HIC) Spectroscopic techniques (UV, Mass Spectrometry) Desired Skills and Experience General knowledge of analytical chemistry Making accurate reagent preparations (dilutions / solutions / buffers / mobile phases) Good documentation practices & utilization in electronic lab notebooks (ELN) Analytical software including Empower and/or ChemStation or OpenLab Familiarity with Microsoft Office Applications (Outlook, Excel, Word, PowerPoint, OneNote, Teams, etc.) Knowledge of ACD Labs tools such as LC-SIM or any computer coding language is a plus Responsibilities Analysis of analytical samples. Results processing and documentation by following appropriate methods / protocols / procedures Sample & data management following best practices Following all appropriate laboratory safety and hygiene procedures

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are seeking a talented and dedicated Scientist to join our team. The successful candidate will be responsible for developing and preparing beverage formulations, syrups, or beverage concentrates at lab and pilot plant scale, following direct customer specifications. Key responsibilities Develop and prepare beverage formulations, syrups, or beverage concentrates at lab and pilot plant scale. Test and establish beverage formulations according to specific taste profiles and regulatory requirements. Customize beverage ingredients independently or within a cross-functional team environment. Calculate calories and understand sweeteners and nutrients in formulations. Facilitate the shipment of samples for internal and external customers. Support beverage and taste development under proper GMPs and safety standards. Maintain flexibility to meet deadlines and handle multiple tasks with speed and high accuracy. Master beverage formulation for sparkling, still, juice and functional beverages. Exceptional sensory skills to define and discriminate flavor profiles in short timelines. Ability to work on RTD and RTM formats at different concentration levels. Deep understanding of beverage processing techniques and nutritional value calculations. Good communication skills to explain formulations at a commercial setting with customers. Good mathematical skills to work with dilutions, percentages and ppm on ingredients. Self- motivated to find a solution to complex problems. Qualifications and skills Degree on Food Technology, Biology, Chemistry, or a related Applied Science. Scientific and analytical aptitudes. Basic computer and mathematical skills. Prior CPG or flavor application experience is preferred. The typical hiring range for this role is $73,758 to $108,755 annually and is based on several factors including but not limited to education, work experience, certifications, location, etc. In addition to your pay, Kerry offers benefits such as a comprehensive benefits package, incentive and recognition programs, equity stock purchase and retirement contribution (all benefits and incentives are subject to eligibility requirements. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at: Know Your Rights: Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a “starter kit,” investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.

Title: (Senior) Scientist, Cardiovascular Diseases Salary: $125,000-$145,000 EPM is currently partnered with clinical stage biopharmaceutical company with an exciting pipeline that shows preclinical promise in a broad range of clinical indications. Two lead assets are currently in early phase clinical developments, and on track for further clinical development this year. The leadership team brings over 25 years of success, with FDA-approved therapies, IPO launches, and multiple strategic biotech exits, along with deep connections across life sciences and venture ecosystems. Backed with resourceful funding and high-value partnerships in biotech and top-10 pharma, the company is well-positioned to reinvest into R&D, while advancing their current clinical pipeline in CNS and Fibrotic indications. They have identified that their platform naturally aligns with cardiovascular biology and are expanding into this area to drive the next wave of first-in-class therapies Key Responsibilities: Lead target discovery, identification, and validation efforts focused on cardiovascular and cardiometabolic diseases, leveraging a cutting-edge small molecule discovery platform. Design and execute in vitro and cell-based assays to interrogate target biology, disease-relevant pathways, and compound activity across cardiovascular indications (e.g., atherosclerosis, vascular remodeling, heart failure, and fibrosis). Collaborate cross-functionally with chemistry, translational, and clinical teams to ensure alignment between discovery biology and downstream development strategies. Apply deep knowledge of vascular biology, endothelial dysfunction, inflammation, and metabolic signaling to guide biological validation of new targets. Analyze and interpret complex data sets, integrating findings into broader disease biology and drug discovery programs. Contribute to the development of the cardiovascular research strategy, incorporating new technologies, disease models, and biomarker approaches to support target prioritization and lead optimization. Stay current with emerging science and competitive landscape in cardiovascular and cardiometabolic drug discovery, providing scientific insights to shape pipeline expansion. Key Skills & Qualifications: PhD in Cardiovascular Biology, Vascular Biology, Pharmacology, or a related discipline, with 3+ years of relevant industry experience(open to strong postdocs looking to transition). Deep expertise in cardiovascular disease biology, including knowledge of vascular dysfunction, endothelial biology, cardiomyocyte biology, cardiac fibrosis, and metabolic signaling. Hands-on experience with target discovery techniques such as: CRISPR screening RNA sequencing & omics data interpretation Biochemical and cellular assays to study target function (reporter assays, phenotypic screening, pathway modulation). Strong foundation in in vitro pharmacology- assay development, compound profiling, and mechanism-of-action studies for small molecules. Ability to work in a highly collaborative environment, communicating effectively with medicinal chemists, translational biologists, and external partners. Experience working within a small to mid-sized biotech environment is a plus - comfort operating in a fast-paced, evolving R&D setting. Passion for cardiovascular discovery and desire to play a hands-on role in shaping pipeline strategy in an innovative biotech setting.

Opportunity for an experienced Upstream Manufacturing Scientist (multiple levels) to continue their career in downstream/upstream manufacturing. This role will be with our client who has a global footprint in both R&D and manufacturing within the biopharma industry. Location- Middlesex County, NJ Terms: Direct Hire Salary: $80-100k/yr. What you will be doing: Work closely with manufacturing associates and engineers to execute upstream batch processes. Perform cell culture and bioreactor operations (single-use fed-batch bioreactors) across various scales. Carry out harvest clarification processes using centrifuges and depth filters at multiple scales. Ensure timely execution of engineering and clinical batches. Develop equipment specifications and optimize manufacturing techniques. Leverage programs to collect and analyze operational data, making real-time adjustments to products, instruments, and equipment. Interpret and follow instructions in written, oral, diagrammatic, or scheduled formats. Adhere to GMP standards in the manufacturing area and lead compliance with environmental health and safety regulations. Review completed manufacturing and packaging batch records and supporting documentation. Coordinate investigations and implement corrective actions for any issues identified during batch execution. Perform additional duties as assigned. Comply with all company policies and standards. What you bring to the company: Bachelor's or Master's degree in Chemical, Biological, or Biochemical Sciences, with at least 3 years of relevant experience in the biopharmaceutical industry. Proven expertise in independently designing, executing, analyzing, and documenting all phases of process development. Strong foundational knowledge and subject matter expertise in executing both engineering and clinical batches. Hands-on experience in GMP and aseptic manufacturing environments. Familiarity with single-use manufacturing consumables, such as bags, tube sets, columns, and process manifolds. Proven ability to work both independently and collaboratively within a team; excellent interpersonal skills. Strong verbal and written communication skills, with advanced computer and organizational abilities. High attention to detail and proficiency in basic software, including Word, Excel, and spreadsheets. In-depth understanding of GMP batch manufacturing and packaging documentation, including audit and review procedures. Knowledge of cleaning verification and validation processes. ** This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**

Work Schedule: Mon -- Fri, Business Hours Hybrid = 2 days onsite 1 week, 3 days onsite the next week, subject to change based on the needs of the business. The Senior Scientist of Biostatistics is a member of the MSAT team, with focus in CPV (Continued Process Verification) and APQR (Annual Product Quality Review) reporting. Position Summary: The incumbent will support the monitoring/trending of production and release testing parameters, in support of product of personalized cell therapy products for both global commercial and clinical trial supply. The Incumbent will trend CPV parameters, including but not limited to Manufacturing process parameters and Quality Control Release attributes for the MSAT organization, to support the Summit, NJ Cell Therapy facility. The purpose of a CPV program is to provide evidence that a process is running under a state of control. The incumbent will monitor/trend, alerting stakeholders of any drifts and supporting the data reporting of process parameters to the global MSAT organization, while meeting established timelines. The CPV program includes supporting the APQR, as required by regulatory agencies. The incumbent will support the CPV and APQR reports and approvals. The organization being supported is a 24x7x365 manufacturing facility. Work scope will include commercial manufacturing and clinical manufacturing for all cell therapy products manufactured in Summit, NJ. This role will work with Supply Chain, Manufacturing, Quality Control, Quality Assurance, Project Management, and MSAT. This position is based in Summit, NJ. Travel up to 10% of time may be required within US. Duties/Responsibilities: • Provides support to maintain the site Statistical Process Control (SPC) program, manufacturing performance trending and reporting. • Provide multivariate analysis (MVA) modeling for improved process understanding and robustness • Continuously monitor CPV parameters, evaluate Statistical Alert Events (SAEs), and take needed actions. • Collaborate and support investigations by providing data and analysis • Meet CPV and APQR timelines • Establish and support predictive process monitoring analytics • Supporting any proactive initiatives or investigations related to drift in product performance • Represent the site MSAT CPV team in cross-functional forums • Performing review and approval of site documents within the scope of CPV and APQR • Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness; actively supporting regulatory inspections • Interacting with other teams including Operational Excellence, PMO (Project Management Organization), site MSAT, Global MSAT, Quality Assurance, Process Support/Engineering and Manufacturing Support, Manufacturing Operations, Supply Chain Operations • Staying current with industry trends and client standards and participating in best practice forums consistent with function responsibilities • Identify key Opex opportunities, using data driven evaluations Working conditions: • The incumbent will be required to adhere to the current client policies and procedures. • The incumbent will be required to gown to access classified manufacturing areas when needed. • This is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. • This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management. Qualifications Specific Knowledge, Skills, Abilities: • Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. • Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. • Must be detail oriented and proven track record of impeccable time management, to meet timelines. • Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. • Expert knowledge of cGMP's and multi-national biopharmaceutical/cell therapy regulations. • Experience of facility/clean room design, process, equipment, automation, and validation. • Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities. • Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies. • Experience with Operational Excellence and Lean Manufacturing Education, Experience, Licenses, Certificates: • Bachelor's Degree required (science or engineering is preferred); Graduate or higher-level Degree is preferred • 8 or more years of work experience in the biopharmaceutical or related industry • 8 or more years of manufacturing support or related experience in the biopharmaceutical industry • Experience in CPV and/or APQR reporting preferred. May be substituted for relevant experience in monitoring/trending performance of Quality attributes • Experience in cell therapy, biologics, or vaccine manufacturing/support required • Experience with Operational Excellence and Lean Manufacturing is a plus

81828 **Please ONLY local candidates to Summit NJ with extensive Pharmaceutical and Manufacturing experience. Experience in cell therapy, biologics, or vaccine manufacturing/support required. TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading pharmaceutical company is hiring a Senior Scientist for a contracting role. Location: Summit NJ MUST have Required skills: Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Summary Report creation/Review in support of CPV (Continuous Process Verification) and APQR (Annual Product Quality Review) Expert knowledge of cGMP's and multi-national biopharmaceutical/celltherapy regulations Experience of facility/clean room design, process, equipment, automation,and validation Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies Experience with Operational Excellence and Lean Manufacturing Bachelor's Degree required (science or engineering is preferred); Graduateor higher-level Degree is preferred 8 or more years of work experience in the biopharmaceutical Experience in CPV and/or APQR reporting preferred Pay: $51-52/hour W2 Responsibilities: Focus in CPV (Continued Process Verification) and APQR (Annual Product Quality Review) reporting Will support the monitoring/trending of production and release testing parameters, in support of product of personalized cell therapy products for both global commercial and clinical trial supply Will trend CPV parameters, including but not limited to Manufacturing process parameters and Quality Control Release attributes The purpose of a CPV program is to provide evidence that a process is running under a state of control The CPV program includes supporting the APQR, as required by regulatory agencies Travel up to 10% of time may be required within US Provides support to maintain the site Statistical Process Control (SPC)program, manufacturing performance trending and reporting Provide multivariate analysis (MVA) modeling for improved process understanding and robustness Continuously monitor CPV parameters, evaluate Statistical Alert Events (SAEs), and take needed actions

Jefferies is seeking a senior associate for its New York-based Life Insurance Equity Research team. The candidate will support the Life Insurance Equity Research team in delivering extensive company and industry research, constructing detailed company and industry financial models, creating written and analytical content for publication and marketing written research recommendations to clients and institutional salespeople. Responsibilities will include: Creation and maintenance of earnings and valuation models Analysis of industry trends and compilation of findings Production of written research publications Creation of marketing materials for clients Development of relationships with management teams and industry contacts Over time, communication of stock views and industry themes to institutional investors, trading desks, and other internal constituencies within Jefferies Key qualifications: Strong work ethic with a focus on teamwork Fluency in accounting and financial statement analysis Superior financial statement modeling skills with demonstrated self-auditing abilities Highly detail-oriented Strong verbal and written communication skills Intellectual interest in equity markets CFA / MBA a plus Prior equity research or life insurance corporate / industry experience (e.g., FP&A, Corporate Treasury, business unit finance) preferred Primary Location Full Time Salary Range of $135,000 - $165,000.

Full-time position Competitive compensation (Salary, Benefits & Options) 180 Varick Street, New York, and 430 E 29th Street, New York Waypoint Bio is a venture-backed biotech startup building the next generation of cell therapies for solid tumors and autoimmune diseases. Traditional cell therapy development faces a trade-off between in vitro approaches that are fast but inaccurate, and in vivo approaches that are accurate but slow and expensive. Using our proprietary platform combining spatial biology, pooled screening, in silico protein engineering, and machine learning, we can obtain both depth and breadth when screening cell therapy candidates - speed without compromising on in vivo accuracy. Our team is highly collaborative, interdisciplinary, and shares the mission of developing novel immune cell therapies to benefit patients' lives. Position Summary: We are seeking a highly motivated, creative scientist who thrives in a fast-paced and collaborative environment. The ideal candidate will have extensive expertise in immunology, including a deep understanding of either regulatory T cells (Tregs) or the design of engineered T cell therapies (e.g. CAR-Treg, CAR-T, TCR-T, or others). Their primary tasks will be to apply their knowledge of the immune system to design novel T cell therapies, optimize the manufacturing of these cell therapies using multiplexed cloning and T isolation & genetic engineering approaches, and then test their function using in vitro and in vivo models of diseases. In this role, you will work collaboratively with our team of computational and wet-lab scientists to develop cutting-edge technologies and new therapeutic options for patients. Duties and Responsibilities Apply your knowledge of immune-related signaling pathways & protein domains to improve the efficacy of existing T cell therapies. Generate hundreds of innovative designs for cell therapies that address the challenges in different disease indications, with a focus autoimmune diseases and solid tumors. Work independently to optimize the manufacturing conditions for Treg and CAR T cell therapies, and implement these strategies to generate libraries of T cell therapies. Develop in vitro assays and in vivo models of Treg function, and work collaboratively to implement these assays to compare the function of different Treg cell therapy designs. Implement existing strategies for highly multiplexed cloning, using either pooled cloning or arrayed cloning approaches. Introduce new technologies and improve the performance, throughput, and accuracy of existing assays Actively engage in prioritizing key milestones and developing appropriate timelines Provide conceptual input on experimental design and interpretation in a team setting Required Qualifications Ph.D. in Immunology, Cancer Biology, Protein Design, Cell Biology, or a related field. Alternatively, M.S. or B.S. degree with 5 years or 7 years of equivalent experience, respectively. 4+ years of academic or industry experience working on immunology and T cell biology. Experience culturing T cells ex vivo and using these cells for downstream assays. Strong molecular biology skills for cloning (e.g. Gibson Assembly) and genetic engineering of mammalian cells (e.g. viral approaches, CRISPR systems). Knowledge of the interplay between the immune system and either healthy tissues or the tumor microenvironment. Practical knowledge of the immune cell therapy field. An excellent scientific track record with published papers or recent experience in immunology or cell therapy. Superb written and oral communication skills, and the organizational abilities to pursue several projects on tight timelines. Preferred Qualifications Deep expertise in the design and testing of engineered Treg cell therapies (e.g. CAR-Treg, armored T cell therapies) for autoimmune and inflammatory indications. Knowledge of the mechanisms used by Treg cells to dampen immune responses in a variety of tissue contexts. Experience designing novel in vitro assays or animal models for autoimmune and inflammatory indications. Send CV and cover letter to apply: ********************

Current HHMI Employees, click here to apply via your Workday account. HHMI is focused on supporting and moving science forward in a variety of different ways ranging from conducting basic biomedical research, empowering educators, inspiring students, developing the next generation of scientists - even stretching into film and media production. Our Headquarters is in the greater Washington, DC metro area and is home to over 300 employees with expertise in investments, communications, digital production, biomedical sciences, and everything in between. The work housed here supports and augments the groundbreaking research conducted in HHMI labs across the nation. As HHMI scientists continue to push boundaries in laboratories and classrooms, you can be sure that your contributions while working here are making a difference. We are always open to finding self-motivated and highly organized Postdoctoral Scientist candidates for potential opportunities within our labs in the greater New York City area. Applications are accepted on a rolling basis. You will be contacted by a member of our Recruitment team if your skills and experience appear to be a match when a role opens. The Postdoctoral Scientist performs a variety of research and/or laboratory tasks and experiments under general supervision. Analyzes data and records the results and conclusions of laboratory experiments. Interprets analytical data and prepares research reports. May assist in the establishment of experimental protocols. Scientist appointments are tied to a research program advised by the Investigator. Principal Duties and Responsibilities Performs research and/or development in collaboration with others for projects. Makes detailed observations, analyzes data, and interprets results Exercises technical discretion in the design, execution, and interpretation of experiments that contribute to project strategies. Prepares technical reports, summaries, protocols, and quantitative analyses. Maintains familiarity with current scientific literature Contributes to project process within their scientific field. Investigates, builds, and develops new methods and technologies for project advancement. Maintains high level of professional expertise through familiarity with scientific literature. May participate in scientific conferences and contribute to scientific journals. Uses professional concepts in accordance with HHMI's objectives to tackle complex problems in creative and effective ways. May determine methods and procedures on new assignments and may provide mentorship to staff in the laboratory. QualificationsEducation Ph.D. degree in a scientific field or MD degree Skills and Abilities Proven understanding of scientific principles Exercises independent judgment in developing methods, techniques, and evaluation criteria for acquiring results Ability to perform highly complex experiments with high levels of reliability and accuracy within time constraints Operational knowledge of sophisticated lab equipment Ability to provide work and supervise directions to others Ability to initiate and compose communications for various purposes in an appropriate style Ability to work successfully within a collaborative and congenial environment and foster this ability in others. Ability to review goals, analyze processes vital to achieve those goals, and develop techniques and systems required to meet those goals. Often explores new areas and seeks opportunities to apply new knowledge to work. Physical Requirements Remaining in a normal seated or standing position for extended periods of time; reaching and grasping by extending hand(s) or arm(s); dexterity to manipulate objects with fingers, for example using a keyboard; communication skills using the spoken word; ability to see and hear within normal parameters; ability to move about workspace. The position requires mobility, including the ability to move materials weighing up to several pounds (such as a laptop computer or tablet). Persons with disabilities may be able to perform the essential duties of this position with reasonable accommodation. Requests for reasonable accommodation will be evaluated on an individual basis. Please Note: This job description sets forth the job's principal duties, responsibilities, and requirements; it should not be construed as an exhaustive statement, however. Unless they begin with the word "may," the Essential Duties and Responsibilities described above are "essential functions" of the job, as defined by the Americans with Disabilities Act. Compensation Range: Postdoc 00 - $70,000.00 (minimum) - $91,000.00 (maximum) Pay Type: Annual HHMI's salary structure is developed based on relevant job market data. HHMI considers a candidate's education, previous experiences, knowledge, skills and abilities, as well as internal equity when making job offers. Typically, a new hire for this position in this location is compensated between the minimum and the midpoint of the salary range. Compensation and Benefits Our employees are compensated from a total rewards perspective in many ways for their contributions to our mission, including competitive pay, exceptional health benefits, retirement plans, time off, and a range of recognition and wellness programs. Visit our Benefits at HHMI site to learn more. HHMI is an Equal Opportunity Employer RequiredPreferredJob Industries Other

Our client, a skincare brand, is looking to hire a Senior Chemist to join the team at their corporate office onsite in Edison. Candidates must be able to work a 5 day, in office schedule. Job Duties Include: Lead reformulation initiatives to enhance product performance, stability, and to ensure alignment with regulatory and market demands Develop skin, hair, and body care formulations that prioritize technical excellence, consumer appeal, and market relevance Serve as the technical lead on cross-functional projects, facilitating communication between R&D, Regulatory, QC, and Manufacturing teams Troubleshoot and resolve technical challenges related to stability, viscosity, pH, compatibility, and texture to meet quality and performance standards Collaborate to transform concepts into feasible, trend-driven products Scale formulations from bench prototypes to pilot and full-scale manufacturing Oversee stability testing and analyze results to ensure formula integrity across varying conditions Mentor junior chemists, fostering skill development and enhancing lab efficiency Job Qualifications Include: 10+ years of experience in formulation development for skin care, hair care, or body care products Bachelor's degree (or higher) in Chemistry, Chemical Engineering, or a related scientific field Demonstrated success in cross-functional collaboration with Marketing, Product Development, and Regulatory teams to bring innovative concepts to market Expertise in formulating emulsions, serums, creams, gels, cleansers, and treatments Proven track record of resolving complex technical challenges Strong knowledge of raw materials and their functionalities, focusing on performance-driven applications Understanding of global regulatory standards and compliance requirements for beauty and personal care products Excellent problem-solving, technical leadership, and project management capabilities Salary: $115k - $120k annually *While PCG appreciates all applicants, only those qualified will be contacted. Thank you for your application. We look forward to hearing from you! If you believe you are a great candidate for this position, and the salary listed does not meet your expectations, we would still love to speak to you! PCG, in good faith, believes that this posted range of compensation is the accurate range for this role at this location at the time of this posting. PCG and our clients may ultimately pay more or less than the posted range depending on candidate qualifications. This range may be modified in the future. Pyramid Consulting Group, LLC is an Equal Opportunity Employer that takes pride in a diverse environment. We do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status. Please refer to our website: ***************** for access to our Right to Work and E-Verify Participation Posters.

What we're looking for: We're seeking a dedicated and detail-oriented Analytical Chemist to join our dynamic team, supporting both Production and R&D operations. In this role, you will perform critical analyses using HPLC, GC-MS, NMR, and other analytical techniques, ensuring the success of kilo-scale production and small molecule development. This position provides an exceptional opportunity to leverage your expertise in analytical chemistry to support the production and development of high-quality materials. Join our team and take a pivotal role in shaping innovation, advancing precision, and driving excellence in our laboratory operations. About Us: Mironova Labs, Inc. is a small, fast-paced, manufacturing company with a successful history in the discovery and development of specialty ingredient technologies. With a thirty-year heritage in process innovation, our research and development capabilities deliver process technologies for breakthrough ingredients used in the cosmetic industry. Responsibilities Analytical: Update and optimize methods for HPLC/MS analysis, ensuring accuracy and compliance with established protocols. Perform routine and advanced analyses using HPLC-MS, NMR, GC-MS, and other analytical instruments as required. Maintain, calibrate, and troubleshoot analytical equipment to ensure operational efficiency and reliability. Ensure the analytical laboratory remains clean, organized, and fully operational. Accurately document all analysis results in logbooks, laboratory notebooks, and digital systems. Troubleshoot and resolve issues with analytical methods or equipment to minimize downtime. Production: Support kilo production processes by assisting with chemical reactions, distillation, extraction, filtration, chromatography, crystallization, and related tasks. Help maintain cleanliness and organization of work areas while ensuring all documentation and logbooks are accurately completed and up-to-date. Research and Development: Conduct laboratory experiments (wet chemistry) to support process chemists in method development and process optimization. Maintain accurate and detailed experimental records and laboratory notebooks. Qualifications: Education: Minimum of Bachelor's Degree (required) in Chemistry, Biochemistry, or a related scientific field. Preferred Masters or Ph.D. in Analytical Chemistry or related field. Skills: Proficiency in using analytical instruments (e.g., HPLC-MS, GC-MS, NMR, UV-Vis, FTIR, etc.). Strong communication, time management, organizational skills, and attention to detail. Experience: 3-7 years of experience in a laboratory environment, preferably in a regulated industry. Experience managing multiple projects and ensuring timely delivery of results. Compliance: Familiarity with industry-standard EHS protocols and regulatory requirements (FDA, ISO, GMP).

Insight Global is looking for an Analytical Chemist to join the R&D organization of a large animal health pharmaceutical company. This individual will be supporting the small molecule portfolio specifically for a liquid formulation project. The Chemist will be responsible for hands on laboratory activities including executing analytical tests and techniques. On a daily basis, they will be utilizing HPLC, UPLC, Density Meters, and Karl Fisher instrumentation. 90% of the role will be based within the laboratory and the other 10% will be dedicated to documentation within the Electronic Laboratory Notebook. The idea candidate will have 3+ years of industry experience within an analytical lab REQUIRED SKILLS AND EXPERIENCE - Bachelor's Degree in Chemistry, Biology, or Scientific Field - 3+ years experience within pharmaceutical industry - Experience with UPLC or HPLC instrumentation - Empower software experience - Strong communication and collaboration skills NICE TO HAVE SKILLS AND EXPERIENCE - Experience with liquid product formulations

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Biology who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented Biology or related fields expert to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by…Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to BiologyEvaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise:A bachelor's or higher degree in Biology or a related subject Experience working as an Biology professional Ability to write clearly about concepts related to Biology in fluent EnglishPayment:Currently, pay rates for core project work by Biology experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.