Associate Scientist Jobs in Morristown, 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.

"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

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

RESPONSIBILITIES: Responsible for developing and optimizing fit-for-purpose analytical methodologies across early through late stage product development for injectable and ophthalmic drug products. Responsible for designing and executing appropriate pre-validation and/or validation studies required to support analytical methodologies. Must test various samples in support of formulation development, subsequently followed by interpretation of results to provide meaningful guidance to the team. Must verify co-workers calculations in notebooks/logbooks and verifies results in reports and/or appropriate systems to check for accuracy and integrity of data. Required to maintain and clean laboratory instruments and equipment. Required to design and/or execute departmental methods, protocols and SOPs Must perform other laboratory related miscellaneous duties as required. QUALIFICATIONS: A M.S. degree in Analytical Chemistry or related field with 7+ years of experience or a Bachelor's degree with 9+ years of experience 3 - 4 years minimum experience supporting Analytical R&D in regulated industry, familiarity with ICH Guidelines, and world pharmacopeias (USP, EP) are preferred

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

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.

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

Job Details: Skin Biology Research Scientist Global Pharmaceutical Company Skillman, NJ Contract, long term (Pay Available for w2 and c2c) We are interested in developing solutions for skin conditions, and are taking multiple approaches to understanding the factors that contribute to healthy skin functioning. This role is global and will have opportunities to partner cross functionally. The Scientist will: Have experience conducting in vitro and ex vivo research in skin biology, using established methodologies and developing new methodologies. The successful candidate will apply knowledge in skin biology and related sciences to assigned projects, ensure project design reviews, analyses, data summary and interpretation, and report and manuscript preparation. Work internally and externally to identify biological targets and technologies to provide skincare benefits. Will develop in vitro as well as ex vivo models and assays to assess functional effects of technologies in order to predict clinical performance. Evaluate cell signaling mechanisms in order to understand mechanisms of action for key technologies. Work closely in a team environment, as well as independently to acquire data, analyze and interpret results. Document results in the form of reports, papers and communicate findings to R&D colleagues and management. Create documentation (technical reports, posters and presentations, etc.). Calibrate and maintain laboratory equipment. Review external literature, data sources and intellectual property to stay current and access competitive threats. Stay current on GXP requirements and ensure compliance with internal SOPs and laboratory requirements. Ability to handle retinoids. Qualifications Bachelor's degree, or Masters' Degree, with minimum of 2 year of research experience, in either Life Sciences, Biology, Biochemistry, and related fields is required. Industry experience is strongly preferred. Research experience in molecular and cellular biology including experience with culturing and handling of cells and tissues, in vitro biochemical (e.g. ELISA, enzymatic activity) and molecular (e.g. QPCR) assays is required. Ability to conduct projects, acquire, analyze, interpret and organize data, write and document research experiments and protocols is required. It is required that the candidate be self-motivated, productive and has excellent communication, leadership and scientific problem solving skills. Demonstrated experience in skin biology or related field is strongly preferred. Working knowledge in transcriptomics, epigenetic and skin biological pathways and techniques are strongly preferred.

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).

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 Biology Evaluating 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 English Payment: 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. PLEASE NOTE: We collect, retain and use personal data for our professional business purposes, including notifying you of opportunities that may be of interest and sharing with our affiliates. We limit the personal data we collect to that which we believe is appropriate and necessary to manage applicants' needs, provide our services, and comply with applicable laws. Any information we collect in connection with your application will be treated in accordance with the Outlier Privacy Policy and our internal policies and programs designed to protect personal data. This is a 1099 contract opportunity on the Outlier. ai platform. Because this is a freelance opportunity, we do not offer internships, sponsorship, or employment. You must be authorized to work in your country of residence. If you are an international student, you may be able to sign up for Outlier if you are on a visa. You should contact your tax and/or immigration advisor with specific questions regarding your circumstances.

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

Chemist III-New Brunswick, NJ Perform analytical testing drug products such as tablets and capsules and liquid products. Operate instruments such as HPLC, GC, Dissolution, Particle size, KF titrator. Perform method transfer and validation. Calibration of analytical instruments. Area Of Responsibility Performs routine analytical tests of pharmaceutical raw materials, in-process samples, blends, finished products, and stability samples using instrumentation such as HPLC, UPLC, GC, UV/VIS, FTIR, dissolution apparatus, particle size analyze, etc. Timely complete the laboratory training. Complete the assign task as schedule and complete the laboratory documentation contemporaneously. Legible and accurate documentation of all the raw data, observations in the worksheets/templates/notebooks. Perform QC testing of exhibit batches Perform the testing of process validation/characterization batches and stability samples. Compile the analytical data and notify the results to supervisor. Perform QC testing of exhibit batches Perform the testing of process validation/characterization batches and stability samples. Adhere to safety, DEA procedures, and department SOPs. Perform calibration of analytical instruments. Perform qualification of working standards. Execute method transfer and method validation. Keep the working place clean and tidy. Create and maintain clear and concise lab records and documentation (notebooks and computer-based) Perform routine maintenance of lab equipment as needed. Education and Job Qualification Minimum BS or equivalent degree in Chemistry or related discipline, MS preferred. Understanding of GMP, ICH and FDA guidelines. Proficient with Microsoft Office applications such as Excel. Excellent written and verbal communication skills. A self-starter with a hands-on approach and a can-do attitude. Excellent project management and problem solving skills Experience Minimum of eight (8) years of experience in pharmaceutical analytical laboratory. Experience with analytical instrumentation, theory and practice. Experience with wet chemistry techniques.

Job Title: Chemist Department: Quality Control This position is responsible for performing various laboratory tests to determine chemical and physical characteristics or composition of solid or liquid materials. Laboratory tests will primarily include wet chemistry and may include basic use of instrumentation such as Gas Chromatography and High Pressure Liquid Chromatography. The Chemist I will also be responsible for supporting the Quality Control laboratory through reagent compounding. This position will also be responsible for performing identification testing using wet chemistry or instrumentation analysis, physical property testing and general laboratory upkeep. The individual will also be responsible for maintaining a laboratory notebook in accordance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). ESSENTIAL DUTIES AND RESPONSIBILITIES: Performs tests on a wide variety of samples of manufactured products to verify their conformity to defined specifications. Such products may be regulated under Good Manufacturing Practices and regulated by government regulatory agencies like FDA. As such the individual is required to have a basic knowledge of GMPs and other pertinent government regulations. Operates basic laboratory equipment such as analytical balances, pH meters, volumetric glassware, and spectrophotometers. Basic operation of advanced instrumentation such as Gas Chromatography and High Pressure Liquid Chromatography may also be required. Responsible for performing tests on a wide variety of materials comprised of powders, granules, gases and liquids to confirm quality attributes such as purity, stability, viscosity, density, absorption, and melting point. Records test results on standardized forms and laboratory notebooks. Writes test reports describing procedures used and uses basic mathematical analysis following Good Documentation Practices. Understands basic statistical concepts that may be required to reach sound scientific conclusions. Participates in Out of Specification investigations to resolve scientific issues in a timely manner. Maintains workspace and common areas for tidiness and cleanliness. SUPERVISORY RESPONSIBILITIES: This position has no supervisory responsibilities. QUALIFICATIONS: To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and EXPERIENCE: A Bachelor's Degree from an accredited four year college or university in chemistry, biochemistry or related scientific field with 3 plus years experience working in a laboratory in a cGMP setting. Or, a Master's Degree from an accredited four year college or university with 3 year's experience MATHEMATICAL SKILLS: The individual is required to have the ability to work with mathematical concepts such as unit conversion, stoichiometry, and basic chemistry formulas. The individual must also be able to apply basic mathematical skills such as fractions, percentages, ratios, and proportions to basic problem solving techniques. Some knowledge of basic statistical techniques is recommended. CERTIFICATES, LICENSES, REGISTRATIONS: None required for this position. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, feel or reach with hands and arms. The employee frequently is required to stand, walk, sit, talk or hear, and taste or smell. The employee is occasionally required to climb or balance and stoop, kneel, crouch, or crawl. The employee may be required to lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Must pass respiratory fitness test as position requires employee to wear a respirator. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee may be frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The noise level in the work environment is usually moderate.

Full-time, Contract Description The Downstream Manufacturing Scientist is a hands-on position responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian based biosimilars. The candidate will be responsible in the purification of 50L to 1000L volumes engineering, clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF and knowledge of initiating batch records, protocols, investigations and other technical documents. Work in a team environment to execute batches and can work independently with minimum supervision. This position requires extensive technical expertise in mammalian cell-based purification processes, cGMP manufacturing and compliance for BLA requirements. Essential Duties & Responsibilities Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis. Provides technical direction in the execution and development of the purification process. Uses programs to collect and evaluate operating data to conduct on- line adjustments to products, instruments or equipment. Ensure that engineering and clinical batches are executed in a timely manner. Establishes operating equipment specifications and improves manufacturing techniques. Works with other teams and outside vendors to resolve technical issues as well as maintenance of production equipment. Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health and safety policies. Coordinate the conduction of investigations and corrections for issues found during the batch execution process. Performs other functions as required or assigned Complies with all company policies and standards Requirements Education: Requires a Bachelor or Master' degree in chemical, biological or biochemical sciences and a minimum of 4- 5 years of related experience in the biopharmaceutical industry. Previous experience working in GMP and aseptic manufacturing environment. Experience working with AKTA Process skids or similar and familiarity of single use manufacturing consumables such as bags, tube sets, columns and process manifolds. Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation. Special Skills: Ability to work with other team members and independently - good interpersonal skills. Good communication skills: verbal and written, good computer and organization skills, detail oriented. Basic computer skills, including knowledge of Word, Excel and spread sheet Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review. Knowledgeable in cleaning verification/validation. Work Environment & Physical Demands: General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines. Some travel may be involved. Supervisory Responsibility, if any: No This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.

We are seeking a Production Scientist for our Manufacturing Department in Warren. The Production Scientist will provide day-to-day operations support in a cGMP manufacturing environment for the production of BeadChip and NGS products including formulation of bead intermediates, bulk reagents,and filled vials. If you are interested in helping to save patient lives, this may be the role for you! This position is not eligible for sponsorship for work authorization . Therefore, if you will requires sponsorship from us for work authorization now or in the future, we cannot consider your application at this time . Responsibilities Key Accountabilities: Perform the following activities in a quality focused cGMP manufacturing environment: BeadChip carrier assembly - involves manual and automated equipment processes. Formulate custom bulk reagents - involves working with pipettes and balances. Bulk and fill reagent manufacturing. Weighing, diluting, measuring and verifying chemicals for in-process solutions. Packaging of carrier and reagent boxes. Ensure materials and equipment are available in inventory for production as required. Follow manufacturing schedule. Report issues and concerns to management. Perform equipment setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency. Follow GMP documents (e.g., SOPs, Work Instructions, Manufacturing Records) with strict adherence to safety and compliance. Create legible written records within batch records/forms. Write, revise and update manufacturing documentation. Maintain a clean and organized working lab environment. Responsible for training on all procedures assigned. Ensure all training is up to date and appropriately documented. The ability to be cross trained to assist in other production areas /departments as needed. Follows OSHA safety regulations for bloodborne pathogens. Qualifications Minimum Knowledge & Experience required for the position: Bachelors Degree in a science related field. Preferred cGMP manufacturing experience and/or training. Basic knowledge of MS Office and software systems used in product support. May be required to work irregular hours and days necessary to meet production schedules. Overtime may be required which may include holidays and weekends.

We are Bentley Labs, a cutting-edge formulation and manufacturing partner to the World's Best Beauty Brands! Our product formulation and production capabilities are wide-ranging and distinctive - with innovative, exciting products across skin care, bath and body, hair, and lip categories. Over the past 16 years, the Bentley team has grown to include some of the industry's brightest stars. Our diverse and talented group are ever and truly a unit -working together toward an all-consuming vision to be the best. In the past 2 years, our formulation team has won over 20 industry awards for best products in wide range of categories. We launch over 200 new products a year, and growing rapidly and seeking new R&D Chemists to join our team! As a valued member of our R&D team, this position will have hands-on responsibility to work with our formulation chemists to produce customer-winning formulas for skin care, sun care and bath & body care products including but not limited to creams, gels, lotions, serums, anhydrous and surfactant systems. This is a place where we create products that matter, relationships that last, and where ambition is supported and rewarded! We know you work hard and we want you to be successful. What will we do for you? Let us help you with tuition reimbursement. Don't know something? Let us send you to classes. Come on in and we will show you what else we have to offer you! Who you are…you celebrate your success and others too. You focus on the right solution with each customer. Your passion for providing outstanding service contributes to our high level of customer satisfaction. Building relationships is your strong suit. You like to have fun at work too! Loud laughing encouraged. Main Responsibilities: The R&D Chemist is a key member of the company's Research and Development Team. The primary responsibilities required for this role are: Review new Product Development Requests (PDR's) and collaborate with SE's for additional clarification; assign tentative project completion dates. Prepare lab batches of formulas needed for submitting samples for customer analysis within lab schedule, and reformulating / resubmitting them based on customer's feedback. Maintain detailed and organized lab notebook with detailed observations while making lab batch. Develop detailed lab scale process for success including order of addition, critical raw materials and processing parameters, bench standard and benchmark, and lab scale preliminary specification and test results Work closely and collaboratively with lab technicians, to teach, coordinate and collaborate on projects leading to well-planned and executed bench work and successful sample submissions Perform and monitor stability with lab technician, utilizing approved stability protocol, and re-formulate if initial formula is unstable. Meet with raw material vendors to learn about new technologies and new raw materials that can be utilized to create/improve Bentley's innovative technology offerings. Collaborate as a key team member across the R&D department, contributing innovative ideas, expertise, knowledge, experiences with strong team spirit, and pride in organization's contribution to the company Perform/Monitor calibration and validation of all lab instruments with Lab Technicians. Maintain clean, safe and well-organized lab working area. Required Outcomes: Stable and compliant personal care, cosmetics and OTC products Timely shipment of lab samples to customers/marketing/testing facilities Documentation of detailed observations and specifications Learning of new technology via researching new raw materials and processes Establishing preliminary product specifications and detailed lab process Education and Experience Requirements: BS in Chemistry 3 + years of R&D experience in Personal Care Excellent lab processing techniques and data management Must have strong analytical, communication and organizational skills Must have a bias for action and initiative to collaborate and contribute value to the overall R&D effort

Bio Analytical scientist Duration: 12+ Months (Extendable) is Onsite Pay Rate: $38.00/hr on W2(Without Benefits included in the pay you will have you buy them separately by paying price for the benefits) Client: Pharmaceutical Bio-Analytical Scientist Warren, NJ- Onsite Work Schedule: Mon - Fri, Business Hours Summary: Executes experiments and analyzes data from flow cytometry analytical assays with limited supervision, as part of the Cell Therapy Analytical Development (CTAD) team. Executes experiments to support on-going method development to support drug product release. Responsible for ensuring compliance with good laboratory practices and other regulatory guidelines. Interfaces with internal research groups and clinical groups and assures laboratory productivity and technical research flexibility. Helps to oversee laboratory needs to ensure appropriate inventory/maintenance. Responsibilities • With limited supervision and/or oversight; design and execute analytical experiments of moderate complexity. • Perform data analysis, summarize and report experimental results. Present data in group meetings and work collaboratively to determine next steps. • Document/review laboratory work in e-notebooks that is detailed, accurate, timely, and in compliance with Good Documentation Practices. • Ensure proper operation and perform routine maintenance of laboratory equipment as needed. • Potentially could be working with biological material--no exposure to animals. Skills/Knowledge • Required B.S. with 2 - 4 years work experience or M.S. with 0 -2 years experience in Molecular & Cellular Biology, Immunology, or related discipline. • Experience working in a regulated (GLP/GMP) environment in preferred. • Flow cytometry assay development experience is preferred. • Experience with flow cytometry platforms is preferred: Miltenyi Macsquant, BD Symphony A5 and/or Canto, Beckman Coulter Cytoflex • Experience with flow cytometry software is preferred: Flowjo, FCS Express • Assay qualification/validation experience is preferred. • Excellent organization skills and ability to handle multiple tasks • Highly motivated, willingness to acquire new skills, and ability to work with minimal supervision. • Excellent verbal and written communication skills. • Must be proficient in microsoft suite