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Chemistry Lab Associate The Chemistry Lab Associate at Scientech Laboratories is responsible for independently executing established analytical methods, processes, and procedures for the preparation and analysis of samples from OTC drug, Pharmaceutical, and Cosmetic industry clients. Reports to: Laboratory Manager Collaborates with: Laboratory and Quality Assurance colleagues ROLES & RESPONSIBILITIES • Independently run validated methods for a variety of analytical chemical analyses on laboratory instruments (LC, GC, IR, UV, dissolution, viscosity, melting point, and others)., • Prepare samples of OTC drug, prescription pharmaceutical, cosmetic, dietary supplement, and botanical products for analysis in the above methods., • Process data from instruments (LC, GC, and others) to produce results ready for data review and QA., • Document experiments, analyses, and results accurately in lab notebooks or software systems in an FDA cGMP compliant manner. Ensure that all laboratory work complies with regulatory standards (e.g., FDA, DEA, ISO)., • Help maintain equipment, chemicals, reagents, and disposables supplies., • Follow safety protocols to handle chemicals, equipment, and waste properly. REQUIREMENTS • Bachelors degree in Chemistry with 1-2 years relevant laboratory work experience in Industry., • Experienced with following laboratory SOPs to prepare samples for analysis, run experiments, collect data, and report results., • Experience with HPLC and/or GC methods and instrumentation., • Experience working in an FDA-regulated environment, preferably cGMP., • Independently manages own day-to-day activities to support lab objectives., • Organized and able to plan work efficiently and effectively., • Independent, yet a great team player., • Ability to consistently deliver on-time results for clients., • This is a 100% onsite position.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: Product Managers (PM) lead a cross-functional role for existing and new products. PMs are involved with all product management aspects associated with product definition, product development, forecasting, pricing, market introduction, sales tools, sales training and promotion plans. Serving as the primary marketing resource for supporting catalog product overall strategy and revenue goals in US. This ideal candidate will have a blend of skills including technical knowledge, stakeholder management, excellent project management, and strong communication. Please note that this position is based onsite in Piscataway, NJ. The estimated salary range is $80,000 - $100,000, based on experience. Responsibilities: • Promote product portfolio in North America and international regions, while working across product lines and workflows., • Coordinate promotional activities with product line managers and the sales teams., • General promotional assets, including landing pages, flyers, brochures, etc., • Execute promotional activities including sampling programs, advertisement, conference/tradeshow booking and/or attendance, product demonstrations, and customer presentations., • Demonstrate product expertise when attending conferences or tradeshows, • Categorize customer types and analyze effectiveness of territory performances based on client category, promotional activities and help execute improvement plan., • Analyze each portfolio in different territories, market needs and gather market information through surveys and client discussions to identify potential areas of growth or improvement., • Provide trainings, guidance and recommendations to Sales, Product Line Managers, R&D, and Production groups based on recognizing customers' current and future needs during continued business relationship., • Organize and provide training for customers, sales, and external distributors by delivering presentations or/and demos., • Collaborate with internal teams/departments to achieve sustainable growth, • Minimum bachelor degree in relevant life science disciplines, such as biology, protein chemistry, biochemistry, cell biology, immunology, molecular biology, biotechnology, etc., • Marketing experience highly preferred., • Exceptional verbal and written communication and presentation skills, • Must be customer-centered and proactive/action-oriented, • Excellent analytical skills & problem-solving skills, able to grasp new concepts quickly, • Strong organization skills with great attention to detail, • Enjoy working in a fast-paced and team-oriented environment, • Quick learner and well organized with good time managements and multitasking skills., • Solid business sense is a plus, • Must have basic computer skills in Microsoft Office #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Overview: This role leads the strategic sourcing and procurement of direct materials and consumables for production, ensuring alignment with cost, quality, and regulatory requirements. Responsibilities include developing alternative vendors to ensure supply continuity, conducting category management for cost savings, and leveraging negotiation and analytical skills for cost reduction. The role involves executing vendor management, including performance reviews, contract negotiations, and master supply agreements. Close collaboration with production teams and cross-functional departments is essential to address procurement needs, while maintaining communication with vendors to manage risks and opportunities. The role also includes managing compliance, audits, and providing necessary documentation. Location: Piscataway, NJ The estimated salary range is $75,000 - $85,000, based on experience. Job Responsibilities: • Responsible for managing the end-to-end Source-to-Pay (S2P) procurement process, including identifying business needs, sourcing and negotiating with suppliers, converting purchase requisitions (PR) to purchase orders (PO), handling PO-related communication and problem solving, and resolving payment-related issues., • Lead the strategic sourcing and manage procurement process for direct materials and consumables used in production, ensuring alignment with cost objectives, quality standards and regulatory requirements., • Responsible for developing alternative vendors for critical materials and components to ensure uninterrupted supply continuity and mitigate supply risks., • Conduct category management to identify opportunities for cost savings by consolidating vendors and exploring the use of alternative materials and components., • Leverage negotiation, analytical, and market research skills to drive value through cost reduction. Track and report on KPIs related to cost savings, cost avoidance, OTD (on time delivery) and efficiency improvements., • Execute vendor management by building supplier profiles, conducting regular vendor business reviews to monitor performance, and accomplish short- and long-term pricing contracts and MSAs (master supply agreements), • Serve as primary contact for negotiating and executing contracts or agreement in consultation with legal support team., • Work closely with the production team and planning to provide efficient and effective procurement support by gaining a deep understanding of production processes, changes in material consumption, and maintaining a sense of urgency to proactively address critical issues, • Maintain active communication with vendors for critical materials to stay informed about supplier market conditions, ensure timely delivery, and identify potential opportunities and risks., • Collaborate with cross-functional teams including quality and finance to ensure the compliance procurement processes., • Take responsibility for addressing challenges from internal and external audits by providing the required procurement documentation and justifications. Qualifications: • Bachelor's degree or higher in Business, Supply Chain Management, Biology and Chemistry, or other related fields., • 3-5 years of experience in procurement and strategic sourcing responsibilities, preferably in the biotech or pharmaceutical industries., • Strong negotiation, analytical, and communication skill., • Good knowledge of materials used in biotech/pharma production, including raw materials, consumables and packing materials., • Ability to effectively communicate complex situations and demonstrate agility in identifying opportunities for cost reduction and problem-solving., • Proficiency in ERP systems of SAP and S2P is a plus #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job Description LABORATORY MANAGER 1.0 Corporate Job Title Laboratory Manager 2.0 Reporting Relationships Branch Manager for day-to-day laboratory responsibilities and Laboratory Director for quality systems responsibilities. 3.0 Position Summary Manages and coordinates laboratory functions for the branch. Provides guidance, leadership and training to laboratory staff on routine matters. Responsible for taking the necessary steps to ensure that all laboratory functions and resources are run safely, accurately and efficiently. 4.0 Minimum Requirements • Requires a B.S. (preferable Chemistry degree) with a minimum of five years general laboratory experience or three years experience in a petroleum laboratory., • Must possess managerial and inter-personal skills., • Must be able to distinguish color., • Must pass pulmonary test for respirator use. 5.0 Responsibilities • Acts as the liaison between Laboratory Coordinator and general laboratory staff with respective Branch Manager, Operations Department and Laboratory Director., • Works closely with Operations Department to obtain day-to-day analytical testing requirements based upon nominations received from clients in order to provide accurate, reliable results on a timely basis. Works directly with customers for laboratory submitted samples if required., • Ensures that laboratory staff and visitors follow all documented safety requirements as defined by the company safety program., • Uses judgment and discretion in directing, coordinating and scheduling the work activities of laboratory staff consistent with accepted operating practices and procedures, including periods during non-working hours, weekends and holidays., • Receives, compiles, and verifies the data resulting from laboratory analyses and ensures accurate and complete preparation of applicable reports as per standard procedures., • Works in conjunction with the Laboratory Director to maintain internal quality control / quality assurance program to ensure the use of standard laboratory practices., • Works with laboratory staff to analyze and compile round robin and quality control sample results to ensure operating efficiency of process and/or testing equipment., • Ensures the laboratory has the equipment and supplies necessary to meet customer demands and established quality program. Manages equipment and supply inventory, including scheduled preventive maintenance requirements of the equipment. Coordinates the replacement or repair of faulty equipment or supplies as needed., • Responsible for the maintenance and control of the sample retain area, including standard cradle-to-grave sample requirements and waste disposal., • Ensures that laboratory staff is qualified to perform necessary testing and meets the training / refresher training requirements of the quality system. Ensures Test Method Assessments, • (TMA’s) are conducted as per the required procedure and schedule., • Using advanced knowledge gained in the laboratory, identifies the root causes of quality system problems (customer, specifications or Camin Cargo system) in respective areas of responsibility and uses good judgment to independently troubleshoot, initiate, recommend, and/or implement timely solutions to the problems. 6.0 Fitness for Duty – Physical Demands Workday may consist of 8-12 hours however this can vary day to day and shift to shift. Some of the retain work is performed outdoors, wearing full Personal Protective Equipment (PPE), and could include possible exposure to high and low temperatures for a prolonged duration of time. Laboratory work is normally performed indoors under climate-controlled conditions. All times listed in the table below are approximate. • Maximum Lift-Floor to knee; Knuckle to waist; Waist to shoulder Weight Up to 45 lbs.- Duration/Day Up to 1 hours. • Walking Weight Up to 45 lbs. -Duration/Day Up to 10 hours • Pushing-Pulling Weight Variable-Duration/Day Up to 1 hour • Carrying Weight Up to 45 lbs.- Duration/Day Up to 2 hours • Ascend/Descend Ladder/Stair Weight Up to 45 lbs.- Duration/Day Up to 1 hour • Extended Reach Weight Up to 45 lbs.- Duration/Day Up to 1 hour • Standing Weight Up to 45 lbs.- Duration/Day Up to 12 hours • Crouch/Squat/Knee Weight Up to 45 lbs.- Duration/Day Up to 1 hour • Tool use Weight 5-8 lbs.- Duration/Day Up to 1 hour • Sitting Weight 5-8 lbs. -Duration/Day Up to 6 hours • Driving Weight N/A- Duration/Day Up to 6 hours All are required to perform this position This document contains Confidential and Proprietary information which is the property of Camin Cargo Control. None of the information contained herein may be disclosed, reproduced, distributed or used without prior written consent from Camin. All rights reserved.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA. Group's key figures are approx. 6.95 billion Euros turnover, over 950 laboratories across 63 countries and about 63,000 staff. Job Description Come Join the leader in Environment Testing. Eurofins Environment Testing has a fulltime entry level opportunity with full benefits. The Laboratory Technician I, using general laboratory methods, techniques, equipment, and instrumentation in compliance with Eurofins Environment Testing America’s Quality Assurance programs and standard operating procedures, supports laboratory operations through general maintenance of laboratory and supply storage areas, equipment, instruments, and supplies. Shift & Hours: Position is full time, Monday-Friday 7:00am-4:00pm Compensation (DOE) - $16.50/hourly Plus Full Benefits Essential Duties and Responsibilities • Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include:, • Preparation of samples using standard techniques, • Performing chemical analysis using standard techniques, • Calculating data, • Recording and reporting data and any unusual test occurrences to the supervisor, • Performing routine instrument maintenance, • Responsible for performing job functions in compliance with EHS and QA standards, • Responsible for general housekeeping in his/her work area, • Works under close supervision using routine and standard methods, • Aliquots and weighs samples, • Washes glasswareQualifications To perform this job successfully, an 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. Requirements • Education: High school Chemistry coursework a must, basic laboratory experience, • Analytical and/or General Science  Scientific methods and method compliance, • Strong Mathematics background, • Knowledge of Standard Operating Procedures, • Knowledge of laboratory procedures, • General knowledge of chemistry and/or general science, • Basic mathematical skills, • Production work, • Good organizational skills, • Good communication skills, • Problem solving skills, • Ability to muti-task, • Quick learner, • Work independently, • Use calculator/mathematical formulas and concepts, • Complete work within time and quality constraints, • Work independently following written or verbal instructions, • Cooperate and coordinate both orally and in writing, • Follow and learn appropriate protocols in one or more of the following disciplines:, • Organic preparation, • Metals preparation and analysis, • Gas Chromatography, • Gas Chromatography/Mass Spectrometry, • Radio Chemistry, • Wet Chemistry, • High Resolution preparation and analysis, • Lifting and Carrying: Lifting up to 50 pounds and carrying up to 30 pounds when moving samples and disposing of waste, • Pushing and Pulling: Pushing and pulling up to 200 pounds when moving sample carts and gas tanks, • Body Positions: Approximately 60% of time standing when analyzing samples, 10% walking when moving about laboratory, and 30% sitting when working at computer, doing paper work, or analyzing samples. These percentages vary significantly Page 4- Analyst I depending upon duties being performed. Must be able to sit, stand, or stoop for long periods of time., • Body Movements: Stooping, kneeling, crouching, and reaching when getting samples and performing analyses, • Smelling: For unusual odors, leakage, contamination, • Hand Use: Handling samples, operating instruments, data entry, • Hearing: Conversational hearing ability, • Vision: Performing analyses, viewing computer screen, doing paperwork Additional Information We do not offer Visa Sponsorship for this role. Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionTitle: Analytical Chemist Location: Piscataway, NJ Type: Long Term Contract Pay rate: $28/hr. to $31/hr. Job Description: Analyze samples of finished products using chromatographic, spectroscopic, wet chemistry, and other analytical techniques. Process analytical data and prepare reports to communicate results and findings to key stakeholders. Qualifications: Bachelor's degree in chemistry; 2+ years of experience in analytical chemistry. Experience in the cosmetics/consumer goods industry; good communication skills. About Us: Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU. IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at . Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility. Powered by JazzHR ud7FdN0Y0F

Job DescriptionSalary: DOE - Provide desired salary QA Specialist Opening in Edison, NJ! We have an opening for a Quality Assurance Specialist in Edison, NJ; at a renowned skincare manufacturer.As a Quality Assurance Specialist, you will play a pivotal role in upholding superior quality and efficacy. You will be responsible for implementing and maintaining robust quality assurance processes in accordance with Good Manufacturing Practices (GMP) standards, ensuring that the skincare products meet the highest regulatory and quality standards. Key Responsibilities: • Quality Control Oversight: Conduct comprehensive inspections and audits of all stages of the manufacturing process to ensure adherence to GMP standards and internal quality control protocols., • Document Management: Maintain accurate and up-to-date documentation related to quality assurance activities, including batch records, test results, and compliance documentation., • Product Testing and Analysis: Coordinate and perform routine and ad-hoc testing of raw materials, intermediates, and finished products to assess quality attributes and compliance with specifications., • Supplier and Vendor Management: Collaborate with project development and supply chain teams to evaluate and qualify suppliers and vendors, ensuring that raw materials and components meet quality requirements., • Non-Conformance Management: Investigate and address deviations, non-conformances, and quality incidents, implementing corrective and preventive actions to mitigate risks and prevent reoccurrence., • Continuous Improvement Initiatives: Identify opportunities for process optimization and quality enhancement, driving continuous improvement initiatives across manufacturing and quality assurance functions., • Regulatory Compliance: Stay abreast of relevant regulatory requirements and industry standards, ensuring that quality assurance practices align with current regulations and best practices., • Cross-Functional Collaboration: Collaborate closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and quality control, to support new product development and ensure seamless integration of quality processes. Qualifications: • Bachelor's Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field. Advanced degree or relevant certifications preferred., • Minimum of 2 years of experience in quality assurance roles within the skincare, cosmetics, or pharmaceutical industries, with a strong understanding of GMP principles and regulations., • Proven experience in conducting quality audits, performing analytical testing, and managing quality documentation., • Strong knowledge of skincare product formulation, raw materials, and manufacturing processes., • Excellent attention to detail, analytical skills, and problem-solving abilities., • Effective communication skills with the ability to collaborate across multidisciplinary teams., • Ability to thrive in a fast-paced environment and adapt to changing priorities. Hours Monday-Thursday 8:30AM-5PM, Fridays 8AM-4:30PM Pay Rate Depending on experience. Please include salary requirements when you submit your resume. Call us for more information orstop by our office! Staffing Alternatives 187 Smith Street, Perth Amboy, NJ or call us at 732-638-4000. Submit your resume to .

Job DescriptionCompany Description Eurofins Environment Testing operates out of more than 50 laboratories and over 40 service centers across the US. The network can provide full-service Environment Testing capabilities in all US states, either via direct local laboratory participation, or via the extensive logistics network. Through our sustained investment in people, technology, instrumentation, and infrastructure, Eurofins Environment Testing laboratories are positioned to support public and private sectors, DoD, DOE and Municipalities. Services include but are not limited to testing of the following matrices, compound/elemental/wet chemistry suites: Air & Vapor, Drinking/Potable Water, Dioxins/Furans and PCB Congeners, SVOC, VOC and Hydrocarbon, Groundwater, Surface & Non-Potable Water, Metals and Metal Speciation, PFAS, Radiochemistry, Sediment & Tissue, Treatability & Aquatic Toxicology, Soil & Hazardous Waste, Nutrients, Inorganic Non-Metallics, Oil, Fuel & Grease. Job Description Eurofins Environmental Testing Southwest is searching for a Laboratory Technician I in Edison, NJ This position is Tues Saturday 7:00am-4:00pm Training is Mon-Fri 9:00am-5:00pm for a couple of weeks. Compensation is $16-17/ hour plus full benefits. Great entry level opportunity for growth. The Sample Preparation Laboratory Technician I is responsible for utilizing general laboratory methods, techniques, equipment, and instrumentation in compliance with Eurofins Quality Assurance programs and SOP’s, to weigh, digest and prepare soil and water samples for GC and GCMS analysis. Laboratory Technician I responsibilities include, but are not limited to, the following: • Sample preparation duties may include, but are not limited to the following responsibilities:, • Evaluate backlog and prioritize daily workload based on required due dates and holding times., • Retrieve samples from sample storage for preparation., • Weigh and measure sample alliquots for preparation, • Document required sample preparation details and observations, • Prepare reagents and standards for daily use, • Maintain laboratory equipment in acordance with the laboratory quality asurance program, • Perform daily duties while adhering to the environmental health and safety policies, • Wash laboratory glassware as needed, • Maintain a clean, safe, and organized working environment., • Active communication with department manager, analytical team and project managers about job status, rush ETA, sample matrix issues, holding time etc., • Assist other areas of the laboratory as needed, • Perform all tasks in a safe, responsible, and efficient manner., • Perform other duties as assigned.Qualifications Basic Minimum Qualifications: • High school diploma or equivalent, • High school Chemistry coursework, basic laboratory experience, • Authorization to work in the United States indefinitely without restriction or sponsorship, • General knowledge of chemistry and/or general science, • Basic mathematical skills, • Strong problem solving skills, • Ability to learn quickly and multi-task, • Work independently, • Work within time constraints, • Strong computer, scientific, and organizational skills, • Excellent communication (oral and written) and attention to detail, • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Additional Information We do not offer Visa Sponsorship for this role. Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description 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., • 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, • 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

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Summary: We are seeking a detail-oriented and proactive Analytical Associate Scientist or Scientist to join our US Protein Department. This role involves performing analytical testing and characterization of protein products to support research, development, and production activities. The ideal candidate will have a strong background in analytical chemistry, biochemistry, or biotechnology, with practical laboratory experience and familiarity with regulatory standards. Key Responsibilities: • Perform routine and non-routine analytical testing on protein samples using techniques such as HPLC, SDS-PAGE, ELISA, UV-Vis spectroscopy, and others as required., • Prepare reagents, standards, and samples according to established protocols., • Record, analyze, and interpret data with accuracy and integrity; prepare detailed reports and documentation., • Maintain and calibrate laboratory instruments and ensure compliance with quality standards and safety regulations., • Assist in method development, validation, and troubleshooting of analytical procedures., • Collaborate with cross-functional teams to support project timelines and deliverables., • Participate in the review and update of SOPs, batch records, and other quality documentation., • BS/MS in analytical chemistry, biochemistry, biotechnology, or related with 2+ years of relevant experience in protein purification/characterization., • Hands-on experience with analytical instruments such as HPLC, SDS-PAGE, ELISA, UV-Vis, or similar is preferred., • Strong attention to detail, organizational skills, and commitment to data integrity., • Ability to work independently and collaboratively in a fast-paced team environment., • Good communication skills and the ability to clearly document and present data., • Experience working in a CRO or CDMO setting is an advantage. #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA. Group's key figures are approx. 6.95 billion Euros turnover, over 950 laboratories across 63 countries and about 63,000 staff. Job Description Eurofins Environment Testing is hiring for a Project Manager on location in Edison, New Jersey. Candidates should live within a commutable distance to the lab. Do you have 5 years of Project Management experience working in Environment? Apply today for a rewarding opportunity with the leader in Environment Testing. This position is full-time, Monday - Friday, 1st shift on site in Edison, NJ Compensation (DOE) - salary mid $50-$65k Plus Full Benefits The Project Manager I (PM I) is accountable for coordinating and managing clients’ projects through all phases of laboratory operations, including project set-up and maintenance, login review, communication of analytical issues, client account maintenance, reporting, invoicing, bottle orders, client pickups, and identification of work share facilities. The PM I role fosters and develops client relationships in support of the laboratory mission. Essential Duties and Responsibilities: Project Set-up • Project review in LIMS, • Sets up project, • Adds any project notes (special reporting and invoicing instructions, etc.), • Reviews project documentation, • Adds any project documentation to central repository, • Sets up client for Total Access, • Manages purchase orders, task orders, contracts, and change order requests, • Verified that lab compound lists and limits meet project requirements for new projects not quoted, • Add any project specific limits/lists to LIMS, • Deliverable assignment and delivery route, • For new projects not quoted, confirms that EDD format is available (deliverable assignment and delivery route). Submits a helpdesk ticket for any new formats needed., • Communicates project details to operations, • Initiates project kick off call with client and pertinent staff, if needed, • Engages work share labs, service centers, and non-Eurofins locations as needed for new projects not quoted, • Works with operations to ensure adequate capacity for incoming work (forecasting), • Provides updates to operations on upcoming work, • Familiarity with state and national program requirements as it pertains to work mix, • Create bottle orders, • Schedules courier and field sampler, if needed, • Confirms non-Eurofins subcontract labs area on the approved list and set-up as vendors for new work, • Confirms non-Eurofins subcontract labs are on the approved list and set-up as vendors for existing work, • Initiates approval process for any subcontract labs not on the approved list, • Generates subcontract paperwork, • Generates accounting software requisition when sending subcontract samples, • Verifies that lab certification meets project requirements, • Verifiers that lab compound lists and limits meet project requirements for new quotes, • For new quotes confirms that EDD format is available (delivery assignment and delivery route). If new format is needed, submits a helpdesk ticket, • Engages work share labs, service centers, and non-TA locations as needed for new quotes, • Communicates any issues to clients for duration of project, • Manages incoming work for rush and short holds, • Reviews log-in, • Resolves log-in issues with client, • Informs client of any log-in discrepancies, • Sets samples to “available” after review, • Sends client sample receipt confirmation, • Reviews draft invoice, • Client specific report requirements, • Reviews job list daily and manages due dates, • Communicates any expected delays to clients before the job due date, • Confirms any data anomalies (filtered>dissolved, deviations from historicals, etc) with operations before submitting to client, • Reviews reports and EDDS before issuing to the client, • Confirms correct report format and EDD format is used, • Creates and issues final report by client due date, • Issues final data packages, • State reporting forms and submission, • DMR forms, • EDD checkers, • Data upload, • Sets up delivery route, • Reviews final invoice before issuing to client, • Generates credit/debit memos as needed, • Submits credit/debit memos for approval, • Submits approved credit/debit memos to client, if needed, • Submits revised invoices, • Initiates follow up calls to confirm correct invoicing, • Works with collections on A/R follow up, • Work with CSM to communicate lab capabilities to the client, • Requests new client review, • Confirms sales assignments with Business Development Manager, • Takes new quote requests from clients, • Reviews client contract requirements/coordinates review, • Reviews purchase orders, • Submits purchase orders for approval and returns approved orders to client, • Follow up calls and visits with clients, • Provides technical support as needed, • Uses company resources to follow up on client requests, • Familiarity with company capabilities and key contacts, • Forward opportunities and leads to sales, • Forecasts upcoming work, • Asks for the next opportunity, • Area of responsibility (air, regulations, etc), • Submits client complaints and participates in correction action/follow up as needed, • Communicates client issues/complaints to sales, • Follow up on client requests, • Initiates project QAPP review with operations, QA, and subcontract labs as needed, • Initiates technical support from operations as needed (special requests, method development, technical review, etc), • Quote generation and approvals, • Reviews client quote requests for capabilities, certifications, scope, • Confirms client contracts (if applicable) and pricing, • Determines lab placement for the work, • Confirms that lab certification meets project requirements, • Confirms the lab compound lists and limits meet project requirements, • Creates quotes, • Submits quotes for approval, • Sends quotes to client, • Forecasts quotes, • Provides QAPP/SOW information to the client as needed, • Updates status in LIMSQualifications To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. • BS/BA in Chemistry/Sciences or related field (four years related experience may substitute for a degree, • 6-12 months of client relationship/customer service experience, • Prefer some bench chemist or field experience, • Requires additional lab training in methods and QA across multiple departments, • Working knowledge of environmental regulations, • Basic knowledge of the LIMS, • Strong interpersonal, communication and problem solving skills, • Effective time management, • Strong organizational skills, • Leadership skills, • Multi-tasking, • Adaptability and flexibility, • Ability to ensure requirements for On-Time Delivery are met, • Authorization to work in the United States indefinitely without restriction or sponsorship, • Must be able to pass a pre-employment background check and drug screen, • Attention to clients: demonstrates a desire to understand customer needs; listens to what customers are saying and asks questions as appropriate; demonstrates awareness of client goals. Follows up with clients during projects and following project completion; keeps clients up to date about decisions that affect them; seeks the comments, criticisms and involvement of clients; adjusts services based on client feedback, • Technical familiarity: seeks information from a variety of sources in a variety of ways to respond to client’s technical questions about the project and to effectively communicate project status., • Customer service orientation: strives to meet customer expectations and takes responsibility to resolve client complaints. Provides prompt, efficient and personalized assistance to meet the requirements, requests, and concerns of customers; provides thorough, accurate information to answer customers’ questions and inform them of commitment times or performance guarantees; actively looks for ways to help customers by identifying and proposing appropriate solutions and/or services; establishes boundaries as appropriate for unreasonable customer demands., • Is pleasant, courteous and professional when dealing with internal or external customers; displays a good-natured, cooperative attitude; is calm and empathetic when dealing with hostile customers., • Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Additional Information We do not offer Visa Sponsorship for this role. Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionDescription: length of assignment: 6 months Work hours per day: 8 hours (Monday through Friday; 40 hours/week) Interview Process: Teams (other arrangements possible as needed) Job Responsibilities: • Perform analysis of samples and raw materials using chromatographic, spectroscopic, wet chemistry, physical testing and other analytical techniques. Techniques utilized include specific gravity, viscosity, potentiometric titrations, Karl Fisher, TLC, pH, liquid chromatography, gas chromatography, FTIR, others., • Apply existing test methods and procedures to complete the required analytical testing., • Collects, process and interpret accurately results, derive conclusions based on sound science, and prepare reports to effectively communicate results and findings to key stakeholders (audience with and without scientific backgrounds)., • Perform root cause analyses for non-conformance events related to laboratory testing., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and practices to ensure good quality, compliance, and safety., • Ability to quickly adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and laboratory practices to ensure good quality and compliance., • Adhere to site and department’s health and safety guidelines and maintain personal and shared workspace., • Adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones. Qualifications: • Bachelor’s degree in Chemistry, or related field, with 1-3 years of professional experience, • Working knowledge of pH, TLC, Auto-titrators, FT-IR, Karl Fisher, Viscosity, and along with other wet chemistry analysis., • HPLC experience (preferred) and GC experience, • Strong written and verbal communication skills required., • Demonstrate ability to work in a diverse environment to manage multiple projects simultaneously and meet timelines., • Capability of working independently as well as working in a fast paced team driven environment, • Excellent bench skills and organization while maintaining a safe work environment., • Experience with Empower, ELN and LIMS software preferred Interview Process: Teams (other arrangements possible as needed) Job Responsibilities: • Perform analysis of samples and raw materials using chromatographic, spectroscopic, wet chemistry, physical testing and other analytical techniques. Techniques utilized include specific gravity, viscosity, potentiometric titrations, Karl Fisher, TLC, pH, liquid chromatography, gas chromatography, FTIR, others., • Apply existing test methods and procedures to complete the required analytical testing., • Collects, process and interpret accurately results, derive conclusions based on sound science, and prepare reports to effectively communicate results and findings to key stakeholders (audience with and without scientific backgrounds)., • Perform root cause analyses for non-conformance events related to laboratory testing., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and practices to ensure good quality, compliance, and safety., • Ability to quickly adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and laboratory practices to ensure good quality and compliance., • Adhere to site and department’s health and safety guidelines and maintain personal and shared workspace., • Adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones. Qualifications: • Bachelor’s degree in Chemistry, or related field, with 1-3 years of professional experience, • Working knowledge of pH, TLC, Auto-titrators, FT-IR, Karl Fisher, Viscosity, and along with other wet chemistry analysis., • HPLC experience (preferred) and GC experience, • Strong written and verbal communication skills required., • Demonstrate ability to work in a diverse environment to manage multiple projects simultaneously and meet timelines., • Capability of working independently as well as working in a fast paced team driven environment, • Excellent bench skills and organization while maintaining a safe work environment., • Experience with Empower, ELN and LIMS software preferred, • Basic knowledge of the Microsoft Office Suite

The Future Talent Program features internships that last up to 12 weeks and will include one or more opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals.

Job Description The Future Talent Program features internships that last up to 12 weeks and will include one or more opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our companys Research Labs Discovery and Process Research Departments across multiple geographies are seeking summer interns with a passion for scientific research strong academic performance communication skills and the ability to work on cross-functional teams. We offer opportunities in our state-of-the-artscience laboratories to solve fundamental synthetic or biological problems relevant to drug discovery and development while functioning as fully integrated members of the company project teams. 2026 Process Research Chemical Biotechnologies Internships (Rahway NJ) The Chemical Biotechnologies (CBT) group within the Process Research & Development (PRD) Enabling Technologies (ET) Department at our company is seeking motivated candidates to contribute to the invention development and innovative implementation of biocatalysts and other biomolecules to advance our companys pipeline and its impact on the scientific community. The candidates will work alongside company scientists in a laboratory environment to impact our drug discovery development and manufacture in the three key areas of CBT: Biocatalysis Protein Engineering and Microfluidics. The role will involve the development of novel approaches novel proteins and enzyme-catalyzed reactions to enable access to biologically active compounds and chemical reactions relevant to the synthesis of drug-like molecules (e. g. small molecule peptide and bioconjugate therapeutic candidates). Day-to-day research for the intern will focus on solving key challenges in: (a) biocatalysis which is the development of novel enzymatic transformations and expansion of biocatalytic toolbox to solve complex chemistry problems (b) protein engineering which is the design and engineering of proteins with novel functions and (c) microfluidics screening and platform development including laboratory automation data science modeling and informatics and more! Candidates will leverage their chemistry biology engineering and/or analytical expertise to solve complex technical problems while working in both chemistry and biology laboratory spaces. The internship will provide an opportunity to gain firsthand knowledge on how our Research & Development division develops and uses technologies to progress medicines and vaccines. The interns will participate in departmental and project team meetings to provide a broad perspective on the drug discovery or development process in the pharmaceutical industry. Interns will also gain skillsets via exposure to practical aspects and day-to-day problems of pharmaceutical research. Interns will be responsible for and trained in methods for accurate electronic notebook recording and safe laboratory addition they will have an opportunity to present their research results in both oral and written formats. **Please note when applying for this positionif the candidateis selected for an interview the applicant must be prepared to submit letters of recommendation and a brief research statement and a copy of transcripts. Required Education & Experience: * Candidates must be currently enrolled as a sophomore junior or senior students pursuing a Bachelors degree in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science;ORa currently enrolled graduate student pursuing a Masters or Ph. D. in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science. * Candidates must have completed at least two years of study toward a bachelors degree by June 2026. * Candidatesmust be available to work full-time for 11-12 weeks between May 2026 - August 2026. Preferred Experience & Skills: * Candidates should have a significant interest in organic chemistry enzymology protein design directed evolution chemical engineering or bioengineering and/or high throughput screening. molecular biology synthetic biology and materials science and engineering are also relevant disciplines. * Candidates should have basic laboratory skills and research experiences such as the use of lab notebook recording and safe lab practices. * Candidates should have experience and/or exposure to chemistry laboratory set-up techniques for multiple unit operations including but not limited to reactions workups (including liquid-liquid extraction) use of vacuum evaporation devices and multiple purification techniques such as thin-layer chromatography flash chromatography crystallization and precipitation. * Candidates should have experience and/or exposure to the use of analytical techniques and data interpretation such as high-performance liquid chromatography (HPLC) nuclear magnetic resonance (NMR) spectroscopy mass spectrometry (MS) and spectrophotometric techniques. * Candidates should have experience and/or exposure to polymerase chain reaction (PCR) techniques biochemical assays and data analysis. * Candidates should have experience and/or exposure to programming languages including Python or MATLAB and (structural) data visualization tools. * Candidates should have a GPA of 3.0 or higher Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PRD Current Employees apply ___ Current Employees apply Job Description The Future Talent Program features internships that last up to 12 weeks and will include one or more opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our companys Research Labs Discovery and Process Research Departments across multiple geographies are seeking summer interns with a passion for scientific research strong academic performance communication skills and the ability to work on cross-functional teams. We offer opportunities in our state-of-the-artscience laboratories to solve fundamental synthetic or biological problems relevant to drug discovery and development while functioning as fully integrated members of the company project teams. 2026 Process Research Chemical Biotechnologies Internships (Rahway NJ) The Chemical Biotechnologies (CBT) group within the Process Research & Development (PRD) Enabling Technologies (ET) Department at our company is seeking motivated candidates to contribute to the invention development and innovative implementation of biocatalysts and other biomolecules to advance our companys pipeline and its impact on the scientific community. The candidates will work alongside company scientists in a laboratory environment to impact our drug discovery development and manufacture in the three key areas of CBT: Biocatalysis Protein Engineering and Microfluidics. The role will involve the development of novel approaches novel proteins and enzyme-catalyzed reactions to enable access to biologically active compounds and chemical reactions relevant to the synthesis of drug-like molecules (e. g. small molecule peptide and bioconjugate therapeutic candidates). Day-to-day research for the intern will focus on solving key challenges in: (a) biocatalysis which is the development of novel enzymatic transformations and expansion of biocatalytic toolbox to solve complex chemistry problems (b) protein engineering which is the design and engineering of proteins with novel functions and (c) microfluidics screening and platform development including laboratory automation data science modeling and informatics and more! Candidates will leverage their chemistry biology engineering and/or analytical expertise to solve complex technical problems while working in both chemistry and biology laboratory spaces. The internship will provide an opportunity to gain firsthand knowledge on how our Research & Development division develops and uses technologies to progress medicines and vaccines. The interns will participate in departmental and project team meetings to provide a broad perspective on the drug discovery or development process in the pharmaceutical industry. Interns will also gain skillsets via exposure to practical aspects and day-to-day problems of pharmaceutical research. Interns will be responsible for and trained in methods for accurate electronic notebook recording and safe laboratory addition they will have an opportunity to present their research results in both oral and written formats. **Please note when applying for this positionif the candidateis selected for an interview the applicant must be prepared to submit letters of recommendation and a brief research statement and a copy of transcripts. Required Education & Experience: * Candidates must be currently enrolled as a sophomore junior or senior students pursuing a Bachelors degree in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science;ORa currently enrolled graduate student pursuing a Masters or Ph. D. in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science. * Candidates must have completed at least two years of study toward a bachelors degree by June 2026. * Candidatesmust be available to work full-time for 11-12 weeks between May 2026 - August 2026. Preferred Experience & Skills: * Candidates should have a significant interest in organic chemistry enzymology protein design directed evolution chemical engineering or bioengineering and/or high throughput screening. molecular biology synthetic biology and materials science and engineering are also relevant disciplines. * Candidates should have basic laboratory skills and research experiences such as the use of lab notebook recording and safe lab practices. * Candidates should have experience and/or exposure to chemistry laboratory set-up techniques for multiple unit operations including but not limited to reactions workups (including liquid-liquid extraction) use of vacuum evaporation devices and multiple purification techniques such as thin-layer chromatography flash chromatography crystallization and precipitation. * Candidates should have experience and/or exposure to the use of analytical techniques and data interpretation such as high-performance liquid chromatography (HPLC) nuclear magnetic resonance (NMR) spectroscopy mass spectrometry (MS) and spectrophotometric techniques. * Candidates should have experience and/or exposure to polymerase chain reaction (PCR) techniques biochemical assays and data analysis. * Candidates should have experience and/or exposure to programming languages including Python or MATLAB and (structural) data visualization tools. * Candidates should have a GPA of 3.0 or higher Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PRD Current Employees apply Job Description The Future Talent Program features internships that last up to 12 weeks and will include one or more opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our companys Research Labs Discovery and Process Research Departments across multiple geographies are seeking summer interns with a passion for scientific research strong academic performance communication skills and the ability to work on cross-functional teams. We offer opportunities in our state-of-the-artscience laboratories to solve fundamental synthetic or biological problems relevant to drug discovery and development while functioning as fully integrated members of the company project teams. 2026 Process Research Chemical Biotechnologies Internships (Rahway NJ) The Chemical Biotechnologies (CBT) group within the Process Research & Development (PRD) Enabling Technologies (ET) Department at our company is seeking motivated candidates to contribute to the invention development and innovative implementation of biocatalysts and other biomolecules to advance our companys pipeline and its impact on the scientific community. The candidates will work alongside company scientists in a laboratory environment to impact our drug discovery development and manufacture in the three key areas of CBT: Biocatalysis Protein Engineering and Microfluidics. The role will involve the development of novel approaches novel proteins and enzyme-catalyzed reactions to enable access to biologically active compounds and chemical reactions relevant to the synthesis of drug-like molecules (e. g. small molecule peptide and bioconjugate therapeutic candidates). Day-to-day research for the intern will focus on solving key challenges in: (a) biocatalysis which is the development of novel enzymatic transformations and expansion of biocatalytic toolbox to solve complex chemistry problems (b) protein engineering which is the design and engineering of proteins with novel functions and (c) microfluidics screening and platform development including laboratory automation data science modeling and informatics and more! Candidates will leverage their chemistry biology engineering and/or analytical expertise to solve complex technical problems while working in both chemistry and biology laboratory spaces. The internship will provide an opportunity to gain firsthand knowledge on how our Research & Development division develops and uses technologies to progress medicines and vaccines. The interns will participate in departmental and project team meetings to provide a broad perspective on the drug discovery or development process in the pharmaceutical industry. Interns will also gain skillsets via exposure to practical aspects and day-to-day problems of pharmaceutical research. Interns will be responsible for and trained in methods for accurate electronic notebook recording and safe laboratory addition they will have an opportunity to present their research results in both oral and written formats. **Please note when applying for this positionif the candidateis selected for an interview the applicant must be prepared to submit letters of recommendation and a brief research statement and a copy of transcripts. Required Education & Experience: * Candidates must be currently enrolled as a sophomore junior or senior students pursuing a Bachelors degree in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science;ORa currently enrolled graduate student pursuing a Masters or Ph. D. in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science. * Candidates must have completed at least two years of study toward a bachelors degree by June 2026. * Candidatesmust be available to work full-time for 11-12 weeks between May 2026 - August 2026. Preferred Experience & Skills: * Candidates should have a significant interest in organic chemistry enzymology protein design directed evolution chemical engineering or bioengineering and/or high throughput screening. molecular biology synthetic biology and materials science and engineering are also relevant disciplines. * Candidates should have basic laboratory skills and research experiences such as the use of lab notebook recording and safe lab practices. * Candidates should have experience and/or exposure to chemistry laboratory set-up techniques for multiple unit operations including but not limited to reactions workups (including liquid-liquid extraction) use of vacuum evaporation devices and multiple purification techniques such as thin-layer chromatography flash chromatography crystallization and precipitation. * Candidates should have experience and/or exposure to the use of analytical techniques and data interpretation such as high-performance liquid chromatography (HPLC) nuclear magnetic resonance (NMR) spectroscopy mass spectrometry (MS) and spectrophotometric techniques. * Candidates should have experience and/or exposure to polymerase chain reaction (PCR) techniques biochemical assays and data analysis. * Candidates should have experience and/or exposure to programming languages including Python or MATLAB and (structural) data visualization tools. * Candidates should have a GPA of 3.0 or higher Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PRD Current Employees apply

Job Description The Future Talent Program features cooperative (co-op) education that last up to 6-months and will include one or more projects. These opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our Company is a global health care leader with a diversified portfolio of prescription medicines vaccines and consumer health products as well as animal health products. Today we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity knowledge imagination skill diversity and teamwork of people like you. To this end we strive to create an environment of mutual respect encouragement and teamwork. As part of our global team youll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Our Research Labs Pharmaceutical Sciences & Clinical Supplies (PSCS) organization is responsible for translating a therapeutic agent into a functional drug product optimized for patients. The Global Clinical Supply organization within PSCS located in Rahway (NJ) and West Point (PA) are seeking co-ops who will work collaboratively in a team environment to help solve key challenges in clinical supply chain. Global Clinical Supplies (GCS) is accountable for managing the end-to-end integrated clinical supply chain across our companys portfolio to enable the execution of any clinical trial using our companys asset (location: Rahway NJ and West Point PA. Example co-op projects include: * Network Integrations Support integration activities including knowledge transfer of clinical supply chain between entities. * Regional clinical supply chain support for US/Ex-US Clinical supply chain initiatives. * Logistics & Trades support for implementation of logistics digitization project. * Clinical Supply Chain Operational Excellence project support * Supply & Master Planning project support. * External Partners and Resource Management projects. * Clinical Supply Planning projects. We are seeking co-op candidates at all levels with strong academic performance communication skills teamwork and the ability to work in a multi- functional environment. The co-ops will participate in departmental and project team meetings to provide a broad perspective on clinical supply chain in the pharmaceutical addition the co-op student will have an opportunity to present their project results in both oral and written formats. During your co-op appointment you will work closely with experienced pharmaceutical industry clinical supply chain experts on a variety project within the GCS Organization. Locations: Rahway NJ; West Point PA This is a full-time co-op position (4-6 months) Required Education and Experience: * Candidates must be a currently enrolled undergraduate sophomore junior or senior student pursuing a Bachelors degree OR a currently enrolled graduate student pursuing a Masters or PhD in Pharmaceutics Pharmaceutical Sciences Chemistry Analytical Chemistry Engineering or Supply Chain Management. * Candidates must be available to work full-time 4-6 months from June - November 2026. * Candidates must have completed at least (2) years of study toward a bachelors degree by June 2026. Preferred Experience and Skills: * Candidates should have significant interest in Pharmaceutical Sciences & Clinical Supplies. * Candidates should have a GPA of 3.0 or higher. Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PSCS2026 Current Employees apply ___ Current Employees apply Job Description The Future Talent Program features cooperative (co-op) education that last up to 6-months and will include one or more projects. These opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our Company is a global health care leader with a diversified portfolio of prescription medicines vaccines and consumer health products as well as animal health products. Today we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity knowledge imagination skill diversity and teamwork of people like you. To this end we strive to create an environment of mutual respect encouragement and teamwork. As part of our global team youll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Our Research Labs Pharmaceutical Sciences & Clinical Supplies (PSCS) organization is responsible for translating a therapeutic agent into a functional drug product optimized for patients. The Global Clinical Supply organization within PSCS located in Rahway (NJ) and West Point (PA) are seeking co-ops who will work collaboratively in a team environment to help solve key challenges in clinical supply chain. Global Clinical Supplies (GCS) is accountable for managing the end-to-end integrated clinical supply chain across our companys portfolio to enable the execution of any clinical trial using our companys asset (location: Rahway NJ and West Point PA. Example co-op projects include: * Network Integrations Support integration activities including knowledge transfer of clinical supply chain between entities. * Regional clinical supply chain support for US/Ex-US Clinical supply chain initiatives. * Logistics & Trades support for implementation of logistics digitization project. * Clinical Supply Chain Operational Excellence project support * Supply & Master Planning project support. * External Partners and Resource Management projects. * Clinical Supply Planning projects. We are seeking co-op candidates at all levels with strong academic performance communication skills teamwork and the ability to work in a multi- functional environment. The co-ops will participate in departmental and project team meetings to provide a broad perspective on clinical supply chain in the pharmaceutical addition the co-op student will have an opportunity to present their project results in both oral and written formats. During your co-op appointment you will work closely with experienced pharmaceutical industry clinical supply chain experts on a variety project within the GCS Organization. Locations: Rahway NJ; West Point PA This is a full-time co-op position (4-6 months) Required Education and Experience: * Candidates must be a currently enrolled undergraduate sophomore junior or senior student pursuing a Bachelors degree OR a currently enrolled graduate student pursuing a Masters or PhD in Pharmaceutics Pharmaceutical Sciences Chemistry Analytical Chemistry Engineering or Supply Chain Management. * Candidates must be available to work full-time 4-6 months from June - November 2026. * Candidates must have completed at least (2) years of study toward a bachelors degree by June 2026. Preferred Experience and Skills: * Candidates should have significant interest in Pharmaceutical Sciences & Clinical Supplies. * Candidates should have a GPA of 3.0 or higher. Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PSCS2026 Current Employees apply Job Description The Future Talent Program features cooperative (co-op) education that last up to 6-months and will include one or more projects. These opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our Company is a global health care leader with a diversified portfolio of prescription medicines vaccines and consumer health products as well as animal health products. Today we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity knowledge imagination skill diversity and teamwork of people like you. To this end we strive to create an environment of mutual respect encouragement and teamwork. As part of our global team youll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Our Research Labs Pharmaceutical Sciences & Clinical Supplies (PSCS) organization is responsible for translating a therapeutic agent into a functional drug product optimized for patients. The Global Clinical Supply organization within PSCS located in Rahway (NJ) and West Point (PA) are seeking co-ops who will work collaboratively in a team environment to help solve key challenges in clinical supply chain. Global Clinical Supplies (GCS) is accountable for managing the end-to-end integrated clinical supply chain across our companys portfolio to enable the execution of any clinical trial using our companys asset (location: Rahway NJ and West Point PA. Example co-op projects include: * Network Integrations Support integration activities including knowledge transfer of clinical supply chain between entities. * Regional clinical supply chain support for US/Ex-US Clinical supply chain initiatives. * Logistics & Trades support for implementation of logistics digitization project. * Clinical Supply Chain Operational Excellence project support * Supply & Master Planning project support. * External Partners and Resource Management projects. * Clinical Supply Planning projects. We are seeking co-op candidates at all levels with strong academic performance communication skills teamwork and the ability to work in a multi- functional environment. The co-ops will participate in departmental and project team meetings to provide a broad perspective on clinical supply chain in the pharmaceutical addition the co-op student will have an opportunity to present their project results in both oral and written formats. During your co-op appointment you will work closely with experienced pharmaceutical industry clinical supply chain experts on a variety project within the GCS Organization. Locations: Rahway NJ; West Point PA This is a full-time co-op position (4-6 months) Required Education and Experience: * Candidates must be a currently enrolled undergraduate sophomore junior or senior student pursuing a Bachelors degree OR a currently enrolled graduate student pursuing a Masters or PhD in Pharmaceutics Pharmaceutical Sciences Chemistry Analytical Chemistry Engineering or Supply Chain Management. * Candidates must be available to work full-time 4-6 months from June - November 2026. * Candidates must have completed at least (2) years of study toward a bachelors degree by June 2026. Preferred Experience and Skills: * Candidates should have significant interest in Pharmaceutical Sciences & Clinical Supplies. * Candidates should have a GPA of 3.0 or higher. Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PSCS2026 Current Employees apply

Job Description The Future Talent Program features cooperative (co-op) education that last up to 6 months and will include one or more opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our companys Research Labs Discovery and Process Research Departments across multiple geographies are currently enrolled students with a passion for scientific research strong academic performance communication skills and the ability to work on cross-functional teams. We offer opportunities in our state-of-the-artscience laboratories to solve fundamental synthetic or biological problems relevant to drug discovery and development while functioning as fully integrated members of the company project teams. 2026 Process Research Chemical Biotechnologies Co-Op (Rahway NJ) The Chemical Biotechnologies (CBT) group within the Process Research & Development (PRD) Enabling Technologies (ET) Department at our company is seeking motivated candidates to contribute to the invention development and innovative implementation of biocatalysts and other biomolecules to advance our Companys pipeline and our Companys impact on the scientific community. The candidates will work alongside company scientists in a laboratory environment to impact our drug discovery development and manufacture in the three key areas of CBT: Biocatalysis Protein Engineering and Microfluidics. The role will involve the development of novel approaches novel proteins and enzyme-catalyzed reactions to enable access to biologically active compounds and chemical reactions relevant to the synthesis of drug-like molecules (e. g. small molecule peptide and bioconjugate therapeutic candidates). Day-to-day research for the co-op will focus on solving key challenges in: (a) biocatalysis which is the development of novel enzymatic transformations and expansion of biocatalytic toolbox to solve complex chemistry problems (b) protein engineering which is the design and engineering of proteins with novel functions and/or (c) microfluidics screening and platform development including laboratory automation data science modeling and informatics and more! Candidates will leverage their chemistry biology engineering and/or analytical expertise to solve complex technical problems while working in both chemistry and biology laboratory spaces. The co-op will provide an opportunity to gain firsthand knowledge on how our Research & Development Division develops and uses technologies to progress medicines and vaccines. The co-ops will participate in departmental and project team meetings to provide a broad perspective on the drug discovery or development process in the pharmaceutical -ops will also gain skillsets via exposure to practical aspects and day-to-day problems of pharmaceutical -ops will be responsible for and trained in methods for accurate electronic notebook recording and safe laboratory addition they will have an opportunity to present their research results in both oral and written formats. **Please note when applying for this positionif the candidateis selected for an interview the applicant must be prepared to submit letters of recommendation and a brief research statement and a copy of transcripts. Required Education & Experience: * Candidates must be a currently enrolled sophomore junior or senior student pursuing a Bachelors degree in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science;ORa currently enrolled graduate student pursuing a Masters or Ph.D. in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science. * Candidates must have completed at least two years of study toward a bachelors degree by June 2026. * Candidatesmust be available to work full-time for 4-6 months beginning in May 2026. Preferred Experience & Skills: * Candidates should have a significant interest in organic chemistry enzymology protein design directed evolution chemical engineering or bioengineering and/or high throughput screening. molecular biology synthetic biology and materials science and engineering are also relevant disciplines. * Candidates should have basic laboratory skills and research experiences such as the use of lab notebook recording and safe lab practices. * Candidates should have experience and/or exposure to chemistry laboratory set-up techniques for multiple unit operations including but not limited to reactions workups (including liquid-liquid extraction) use of vacuum evaporation devices and multiple purification techniques such as thin-layer chromatography flash chromatography crystallization and precipitation. * Candidates should have experience and/or exposure to the use of analytical techniques and data interpretation such as high-performance liquid chromatography (HPLC) nuclear magnetic resonance (NMR) spectroscopy mass spectrometry (MS) and spectrophotometric techniques. * Candidates should have experience and/or exposure to polymerase chain reaction (PCR) techniques biochemical assays and data analysis. * Candidates should have experience and/or exposure to programming languages including Python or MATLAB and (structural) data visualization tools. * Candidates should have a GPA of 3.0 or higher Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PRD Current Employees apply ___ Current Employees apply Job Description The Future Talent Program features cooperative (co-op) education that last up to 6 months and will include one or more opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our companys Research Labs Discovery and Process Research Departments across multiple geographies are currently enrolled students with a passion for scientific research strong academic performance communication skills and the ability to work on cross-functional teams. We offer opportunities in our state-of-the-artscience laboratories to solve fundamental synthetic or biological problems relevant to drug discovery and development while functioning as fully integrated members of the company project teams. 2026 Process Research Chemical Biotechnologies Co-Op (Rahway NJ) The Chemical Biotechnologies (CBT) group within the Process Research & Development (PRD) Enabling Technologies (ET) Department at our company is seeking motivated candidates to contribute to the invention development and innovative implementation of biocatalysts and other biomolecules to advance our Companys pipeline and our Companys impact on the scientific community. The candidates will work alongside company scientists in a laboratory environment to impact our drug discovery development and manufacture in the three key areas of CBT: Biocatalysis Protein Engineering and Microfluidics. The role will involve the development of novel approaches novel proteins and enzyme-catalyzed reactions to enable access to biologically active compounds and chemical reactions relevant to the synthesis of drug-like molecules (e. g. small molecule peptide and bioconjugate therapeutic candidates). Day-to-day research for the co-op will focus on solving key challenges in: (a) biocatalysis which is the development of novel enzymatic transformations and expansion of biocatalytic toolbox to solve complex chemistry problems (b) protein engineering which is the design and engineering of proteins with novel functions and/or (c) microfluidics screening and platform development including laboratory automation data science modeling and informatics and more! Candidates will leverage their chemistry biology engineering and/or analytical expertise to solve complex technical problems while working in both chemistry and biology laboratory spaces. The co-op will provide an opportunity to gain firsthand knowledge on how our Research & Development Division develops and uses technologies to progress medicines and vaccines. The co-ops will participate in departmental and project team meetings to provide a broad perspective on the drug discovery or development process in the pharmaceutical -ops will also gain skillsets via exposure to practical aspects and day-to-day problems of pharmaceutical -ops will be responsible for and trained in methods for accurate electronic notebook recording and safe laboratory addition they will have an opportunity to present their research results in both oral and written formats. **Please note when applying for this positionif the candidateis selected for an interview the applicant must be prepared to submit letters of recommendation and a brief research statement and a copy of transcripts. Required Education & Experience: * Candidates must be a currently enrolled sophomore junior or senior student pursuing a Bachelors degree in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science;ORa currently enrolled graduate student pursuing a Masters or Ph.D. in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science. * Candidates must have completed at least two years of study toward a bachelors degree by June 2026. * Candidatesmust be available to work full-time for 4-6 months beginning in May 2026. Preferred Experience & Skills: * Candidates should have a significant interest in organic chemistry enzymology protein design directed evolution chemical engineering or bioengineering and/or high throughput screening. molecular biology synthetic biology and materials science and engineering are also relevant disciplines. * Candidates should have basic laboratory skills and research experiences such as the use of lab notebook recording and safe lab practices. * Candidates should have experience and/or exposure to chemistry laboratory set-up techniques for multiple unit operations including but not limited to reactions workups (including liquid-liquid extraction) use of vacuum evaporation devices and multiple purification techniques such as thin-layer chromatography flash chromatography crystallization and precipitation. * Candidates should have experience and/or exposure to the use of analytical techniques and data interpretation such as high-performance liquid chromatography (HPLC) nuclear magnetic resonance (NMR) spectroscopy mass spectrometry (MS) and spectrophotometric techniques. * Candidates should have experience and/or exposure to polymerase chain reaction (PCR) techniques biochemical assays and data analysis. * Candidates should have experience and/or exposure to programming languages including Python or MATLAB and (structural) data visualization tools. * Candidates should have a GPA of 3.0 or higher Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PRD Current Employees apply Job Description The Future Talent Program features cooperative (co-op) education that last up to 6 months and will include one or more opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our companys Research Labs Discovery and Process Research Departments across multiple geographies are currently enrolled students with a passion for scientific research strong academic performance communication skills and the ability to work on cross-functional teams. We offer opportunities in our state-of-the-artscience laboratories to solve fundamental synthetic or biological problems relevant to drug discovery and development while functioning as fully integrated members of the company project teams. 2026 Process Research Chemical Biotechnologies Co-Op (Rahway NJ) The Chemical Biotechnologies (CBT) group within the Process Research & Development (PRD) Enabling Technologies (ET) Department at our company is seeking motivated candidates to contribute to the invention development and innovative implementation of biocatalysts and other biomolecules to advance our Companys pipeline and our Companys impact on the scientific community. The candidates will work alongside company scientists in a laboratory environment to impact our drug discovery development and manufacture in the three key areas of CBT: Biocatalysis Protein Engineering and Microfluidics. The role will involve the development of novel approaches novel proteins and enzyme-catalyzed reactions to enable access to biologically active compounds and chemical reactions relevant to the synthesis of drug-like molecules (e. g. small molecule peptide and bioconjugate therapeutic candidates). Day-to-day research for the co-op will focus on solving key challenges in: (a) biocatalysis which is the development of novel enzymatic transformations and expansion of biocatalytic toolbox to solve complex chemistry problems (b) protein engineering which is the design and engineering of proteins with novel functions and/or (c) microfluidics screening and platform development including laboratory automation data science modeling and informatics and more! Candidates will leverage their chemistry biology engineering and/or analytical expertise to solve complex technical problems while working in both chemistry and biology laboratory spaces. The co-op will provide an opportunity to gain firsthand knowledge on how our Research & Development Division develops and uses technologies to progress medicines and vaccines. The co-ops will participate in departmental and project team meetings to provide a broad perspective on the drug discovery or development process in the pharmaceutical -ops will also gain skillsets via exposure to practical aspects and day-to-day problems of pharmaceutical -ops will be responsible for and trained in methods for accurate electronic notebook recording and safe laboratory addition they will have an opportunity to present their research results in both oral and written formats. **Please note when applying for this positionif the candidateis selected for an interview the applicant must be prepared to submit letters of recommendation and a brief research statement and a copy of transcripts. Required Education & Experience: * Candidates must be a currently enrolled sophomore junior or senior student pursuing a Bachelors degree in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science;ORa currently enrolled graduate student pursuing a Masters or Ph.D. in Chemistry Biochemistry Biological Sciences Chemical Engineering Bioengineering or Material Science. * Candidates must have completed at least two years of study toward a bachelors degree by June 2026. * Candidatesmust be available to work full-time for 4-6 months beginning in May 2026. Preferred Experience & Skills: * Candidates should have a significant interest in organic chemistry enzymology protein design directed evolution chemical engineering or bioengineering and/or high throughput screening. molecular biology synthetic biology and materials science and engineering are also relevant disciplines. * Candidates should have basic laboratory skills and research experiences such as the use of lab notebook recording and safe lab practices. * Candidates should have experience and/or exposure to chemistry laboratory set-up techniques for multiple unit operations including but not limited to reactions workups (including liquid-liquid extraction) use of vacuum evaporation devices and multiple purification techniques such as thin-layer chromatography flash chromatography crystallization and precipitation. * Candidates should have experience and/or exposure to the use of analytical techniques and data interpretation such as high-performance liquid chromatography (HPLC) nuclear magnetic resonance (NMR) spectroscopy mass spectrometry (MS) and spectrophotometric techniques. * Candidates should have experience and/or exposure to polymerase chain reaction (PCR) techniques biochemical assays and data analysis. * Candidates should have experience and/or exposure to programming languages including Python or MATLAB and (structural) data visualization tools. * Candidates should have a GPA of 3.0 or higher Please note that this position may be closed before the posted end date or may remain open longer at the discretion of the company. Salary range: The salary range for this role is $39600.00-$105500.00 USD FTP2026 RL2026 PRD Current Employees apply

The Chemistry Lab Associate at Scientech Laboratories is responsible for independently executing established analytical methods, processes, and procedures for the preparation and analysis of samples from OTC drug, Pharmaceutical, and Cosmetic industry clients. Bachelors degree in Chemistry with 1-2

Technical Leadership Position In Supply Analytical Sciences.Our company is seeking an exceptional individual for a technical leadership position within the Supply Analytical Sciences (SAS) - Analytical Chemistry in Development and Supply (ACDS) organization located in the US.The successful candidate

BS/BA in Chemistry or related field from an accredited university.

Internship Opportunity In Discovery Sample Management.The Future Talent Program features internships that last up to 12 weeks and will include one or more projects.These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the ri

Job Title: Technician – Module Lab Location: South Plainfield, NJ Work Model: Onsite – Contract to Hire Hours: Monday–Friday, 8AM to 430PM Pay: $20–$22/hour TECHNICIAN – MODULE LAB This is a training-based, cleanroom-friendly role ideal for candidates looking to break into high-tech manufa

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Scientist – Biopharma Services.Title Level Commensurate with Experience (Senior Associate Scientist II or Scientist I).Location: South Plainfield, NJ.We are open to hiring at either the.Title and responsibilities will align with your education, experience, and demonstrated capabilities.Admera Heal

Job Title: Technician – Module Lab Location: South Plainfield, NJ Work Model: Onsite – Contract to Hire Hours: Monday–Friday, 8AM to 430PM Pay: $20–$22/hour TECHNICIAN – MODULE LAB This is a training-based, cleanroom-friendly role ideal for candidates looking to break into high-tech manufa

Title Level Commensurate with Experience (Senior Associate Scientist II or Scientist I).Location: South Plainfield, NJ.We are open to hiring at either the.Title and responsibilities will align with your education, experience, and demonstrated capabilities.Admera Health Entering the ADvanced Molecul

Excellent analytical and problem-solving skills and ability to think creatively. Excellent analytical and problem-solving skills and ability to think creatively.

Contribute to the overall operations of the lab and to the achievement of departmental goals and objectives.Perform laboratory support functions such as:.Clean, sterilize, and put away glassware, lab equipment and instruments.Maintain inventory management and equipment calibration.Prepare and weigh

Associate Vice President of Research Computing.Prominent statewide educational institution.The Company is in search of an Associate Vice President for its Office of Advanced Research Computing.This leadership role is pivotal in overseeing a dedicated team that provides high-performance computing and

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Independently designing and conducting experiments using relevant operational parameters and analytical inputs. Collaborate with upstream process development, Biologics Analytical R&D, and other cross-functional teams in both Research and Manufacturing to advance biologics pipeline.

Post-Graduate/Post-Doctoral Research Scientist, Sterile Product Development Onsite Role.Work Schedule: Mon - Fri, Business Hours.We are seeking a highly motivated post-graduate student or postdoctoral level scientist to join the Sterile Product Development organization at Client's New Brunswick, NJ

Weston has been a premier provider of environmental services for 65 years.We work with our clients in both the public and private sectors to help identify, solve, mitigate, and manage critical environmental issues to help clients achieve a more sustainable future.Weston is seeking an Associate Scien

To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing a diverse and inclusive environment for all. PhD with 0+ years of relevant experience (or expected PhD graduation within 6 months from

The role will involve the development, qualification, and implementation of analytical separation methods. The successful candidate should be self-motivated, have excellent communication skills, be a team player, and have strong knowledge and experience in bioanalytical separation sciences.