Research and development technician jobs in Randolph, NJ - 240 jobs

Source One is a consulting services company and we're currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturing client in Summit, NJ . No Third-Party, No Corp to Corp, No Sponsorship Now or Future Title: Product Development Scientist - Formulation Location: Skillman NJ Hybrid Work Locations; Skillman, NJ 4 days/week then in Summit, NJ 1 day per week. Hours: 8:30am to 5:00pm (Monday through Friday). May fluctuate based on needs. Contract Duration: 10 months, with likely extension Pay Rate: $43.28 per hour (w2) *PLEASE NOTE: Apply only if you have FORMULATION Experience this is required Job Description: Consumer Products - Skin Health A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline. FORMULATION Experience is required BA Degree 2 to 4 years' experience

At Insmed, every moment and every patient counts - and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as a Great Place to Work in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we're in. Are you? About the Role: We're looking for an In vivo Associate Scientist, Biology on the Research/Biologics Team to help us expand what's possible for patients with serious and rare diseases. Reporting to the Scientist II, Research, you'll be doing rodent handling, dosing, fluid and tissue collection as part of Insmed's in vivo pharmacology team. The In vivo Associate Scientist will collaborate closely within the team and cross-functionally to plan and execute complex in vivo pharmacology studies, develop custom animal models, and generate high quality data. What You'll Do: In this role, you'll have the opportunity to support Insmed's early-stage research pipeline, turning ideas into ground breaking medicines for patients in need. You'll also: Administer therapeutic agents to rodents through a variety of routes (including intraperitoneal, intravenous, oral, retroorbital, intrathecal, intratracheal, subcutaneous, intracerebroventricular). Perform blood collection through various routes (including submandibular, saphenous vein, tail vein, cardiac puncture). Perform necropsy, tissue collections, and perfusions. Monitor animal health, record clinical observations, and maintain accurate study records. Assist in developing, optimizing, and validating rodent disease models. Collaborate closely with in vivo team members, vivarium staff, internal project leads, and ex vivo analysis teams. Author and review protocols and electronic notebook entries. Analyze and present data to project teams. Follow institutionally approved animal protocols, IACUC guidelines, and adhere to all ethical, regulatory, and safety standards in an AAALAC accredited environment. Who You Are: Minimum of Bachelor's degree in biology, animal sciences, pharmacology or related field with 5+ years of relevant industry experience or Master's degree with 2+ years of industry experience. At least 2-5 years of prior experience with hands on in vivo research including work with rodents. Expert knowledge in standard rodent in vivo techniques (dosing, handling, restraint, sample collection) Comprehensive experience in standard fluid collection techniques including tail vein and saphenous vein. At least 2 years of prior experience with and demonstrated excellence in tissue collection and animal necropsy. At least 2 years of prior experience with and demonstrated success in executing in vivo studies. At least 2 years of prior experience with and demonstrated success in assisting with developing custom animal models suitable for a variety of disease applications. Experience with breeding and maintenance of genetically modified mouse strains. Strong attention to detail, excellent record keeping (E-note booking), and the ability to follow SOP's and protocols. Entrepreneurial spirit, proactive problem-solving attitude, and strong willingness to take on new challenges. Travel Requirements Minimal travel expected Pay Range: $103 000.00 Annual Life at Insmed At Insmed, you'll find a culture as human as our mission-intentionally designed for the people behind it. You deserve a workplace that reflects the same care you bring to your work each day, with support for how you work, how you grow, and how you show up for patients, your team, and yourself. Highlights of our U.S. offerings include: Comprehensive medical, dental, and vision coverage and mental health support, annual wellbeing reimbursement, and access to our Employee Assistance Program (EAP) Generous paid time off policies, fertility and family-forming benefits, caregiver support, and flexible work schedules with purposeful in-person collaboration 401(k) plan with a competitive company match, annual equity awards, and participation in our Employee Stock Purchase Plan (ESPP), and company-paid life and disability insurance Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities Employee resource groups, service and recognition programs, and meaningful opportunities to connect, volunteer, and give back Eligibility for specific programs may vary and is subject to the terms and conditions of each plan. Current Insmed Employees: Please apply via the Jobs Hub in Workday. Insmed Incorporated is an Equal Opportunity employer. We do not discriminate in hiring on the basis of physical or mental disability, protected veteran status, or any other characteristic protected by federal, state, or local law. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Unsolicited resumes from agencies should not be forwarded to Insmed. Insmed will not be responsible for any fees arising from the use of resumes through this source. Insmed will only pay a fee to agencies if a formal agreement between Insmed and the agency has been established. The Human Resources department is responsible for all recruitment activities; please contact us directly to be considered for a formal agreement. Insmed is committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation to participate in the job application or interview process, please contact us by email at and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. Applications are accepted for 5 calendar days from the date posted or until the position is filled.

Are you an experienced Biochemist - High-Throughput Screening with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Biochemist - High-Throughput Screening to work at their company in Rahway, NJ. Primary Responsibilities/Accountabilities: The Chemical Biotechnologies Group at the client is seeking an experienced researcher to support our high-throughput capabilities. The mission of the group is to invent, develop, and implement biomolecules and biocatalytic processes to advance the client's pipeline and our impact on the scientific community. This position in our biochemistry team is responsible for lysing E. coli cell pellets to liberate enzyme in solution or generate enzyme from in vitro transcription translation (iv TT) mix, setting up reactions using this solution as a catalyst solution, quenching reactions and prep them for HPLC analysis, running the HPLC, and analyzing the data generated in support of our protein directed evolution workflow. The candidate will perform high throughput workflows with 96 or 384 well formats using various automation instruments. The candidate will have hands-on, extensive experience with instrumentation essential for monitoring substrates and products profiles for reactions, especially Agilent UPLC systems. In this position, the candidate will have the opportunity to work with a diverse group of team members to effectively coordinate efforts and operate multiple projects. The candidate ensures activities of assignments are executed such that project deliverables and timelines are met. The candidate is responsible for good housekeeping and performing work in a safe manner in the work area by applicable safety equipment and personnel protective equipment (PPE). Qualifications: Bachelor's degree in Molecular Biology, Synthetic Biology, Bioengineering, Biochemistry or related field with +5 years' of experience, or MS with +2 years of experience, or PhD. Experienced in high-throughput screening and automated liquid handling (Biomek or Tecan liquid handling systems) and various analytical methods (HPLC, LC-MS, spectrophotometry, gel electrophoresis, FPLC). Proficient in preparing chemical and biochemical reactions Experience with protein handling and biochemical, biophysical, and/or phenotypic protein characterization techniques (e.g., activity assays, SDS-PAGE, UV-Vis spectrophotometry). Understanding of experimental design and data analysis principles Strong organizational skills and attention to detail Excellent teamwork and multitasking Good documentation of experimental reports Software Skills: MS office (Word/Excel) Preferred: Experience with one or more of the following: next-generation sequencing, directed evolution, protein expression or microfluidics Experience in protein characterization and purification Experience in protein expression platforms (yeast, bacillus, mammalian) is a plus Experience with data analysis using Python, R, Excel, or similar tools Industry experience is preferred.

Job Title: Chemist Duration: 12 Months Qualifications Education Minimum Requirement: • BS/BA in chemistry or related scientific fields with 2-5 years of experience. Required Experience and Skills: • Familiar with common analytical instrumentation • Strong teamwork and interpersonal skills • Strong written and oral communication skills Preferred Experience and Skills: • Experience with analytical techniques such chromatography (HPLC) and dissolution and ability in trouble shooting these methodologies • Experience using Empower is a plus • Experiences with analytical work in the pharmaceutical industry, such as method development and validation. • Experience working in a GMP / GLP environment a plus. Responsibilities We are looking for an individual who will perform analytical testing to support drug product development. This will involve development and validation of analytical test methods, analytical testing for process development support, data processing, and summarizing/presenting results to the supervisor.

Elida Beauty is a Global Personal Care Business. We proudly support and nurture our portfolio of iconic brands globally. Our ambition is to remix classic beauty brands for a new generation, making them even bigger beauty hits than they were the first time around, to drive accelerated growth and value creation. Driven by creativity and agility, we unleash the true potential of beloved brands, ‘Re-Founding' them using a start-up mentality that always ‘finds a way'. Elida Beauty is a part of the Yellow Wood Partners portfolio of companies, a private equity company that invests exclusively in the consumer industry. Position Summary The Packaging Engineer will report to the Senior Director R&D. The candidate will support on the day-to-day development activities of innovation launches across liquids, creams and the non-woven product portfolio. They will work closely with cross-functional partners as well as the external network of suppliers to bring product ideas to life from concept to execution. This individual will have a technical competency and be responsible for the creation and upkeep of packaging specifications, coordinating package line trials with external partners, and developing package testing plans to support flawless NPDs. Primary Responsibilities Partner with Marketing, Operations, Procurement, Quality and Finance on developing new packaging through external suppliers. Ensuring that projects meet the brand's needs while meeting cost, quality, design and functional requirements. Manage the creation and upkeep of packaging component specifications in specification system. Develop testing plans for NPDs and execute with third party testing labs and component suppliers. Identify and implement cost savings initiatives. Visit on-site production startups and line trials to qualify new packaging componentry and new fillers. Maintain knowledge of external vendor capabilities. Stay current with new packaging material regulations and industry trends. Troubleshoot issues in production. Support ongoing base business to ensure stock coverage. Other support duties as needed. Required Qualifications Bachelor's degree in Packaging/Plastics/Mechanical/Industrial/Chemical Engineering, or related field. 3-5 years of proven experience in package engineering & development in consumer products, beauty, or related industry. Experience creating packaging specifications for manufacturing. A technical acumen with the ability to read and interpret technical drawings for components and assemblies. Strong carton board and paper experience. Demonstrated knowledge of various manufacturing processes including extrusion blow molding, ISBM, injection molding, printing and filling. Knowledge of various CPG packaging materials and their physical and chemical properties. Ability to partner effectively across a diverse set of business partners and customers to deliver key results in a timely manner. Entrepreneurial; Business owner mentality, willing to be hands-on and contribute as one team. Ability to tackle complex problems through critical thinking. Excellent communication skills, including spoken and written English. Ability to travel Domestic and International up to 25%. Strong PC skills: MS Office, PowerPoint, CAD software is a plus. Personal Attributes Positive and energetic individual with a strong business acumen, an abiding sense of urgency to achieve results. Consumer-centric, creative, and design-oriented. Inquisitive individual who has a history of seeking out best practices and successfully assimilating them into their organization. Invokes trust, collaboration, shared accountability, and continuous improvement with the ability to quickly develop trust and loyalty at all levels in the organization and with external partners. Knows what excellence looks like and how to get there. Ability to develop and implement strategy, with a high bias for execution and activation, comfort with getting hands dirty. Demonstrated track record of problem solving and priority setting. Diversity at Elida Beauty Diversity at Elida Beauty is about inclusion, embracing differences, creating possibilities, and growing together for better business performance. We embrace diversity in our workforce. This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.

Job Title: Formulation Scientist - Skin Health Duration: 10-Month Contract Work Hours: Monday - Friday, 8:30 AM - 5:00 PM Locations: Skillman, NJ 08558 (4 days/week) / Summit, NJ 07901(1 day/week; may fluctuate based on business needs) Experience Required: 2 to 4 years of formulation experience (mandatory) Education: Bachelor's Degree (BA/BS) required Key Responsibilities: Develop and optimize new product formulations and manufacturing processes. Perform laboratory testing, evaluations, and multiple formulation iterations (batching). Conduct stability studies to ensure technical accuracy and product performance. Maintain accurate and detailed documentation throughout the product development lifecycle. Collaborate effectively with cross-functional teams. Manage timelines efficiently while maintaining attention to detail. Apply strong analytical and problem-solving skills. Communicate findings, progress, and challenges clearly and professionally. Required Skills & Qualifications: Strong formulation experience (required) Background in Consumer Products, preferably Skin Health Excellent time management and organizational skills High attention to detail Strong analytical and communication skills Ability to work collaboratively in a team environment

Role: Formulation Scientist, on-site in Raritan, NJ- Full-time Experience Required: 8 - 20 + Years Must Have Technical/Functional Skills • Product formulation and launch experience. • Biomaterials and material development. • Medical device and combination product design and development; PMA familiarity. • Problem-solving using Analytical tools. • Design of Experiments (DOE) and applied statistics. • Protocol development, reporting, and documentation. • In-vitro/ex-vivo characterization of prototypes. • Biochemical test method development and validation. • Strong communication and collaboration across teams. • Ability to work in ambiguous environments and deliver outcomes. • Experience with self-directed teams and multitasking. • Effective prioritization and decision-making. • Travel up to 20% may be required (domestic and international)

*This will be a 12-month contract with potential extensions *5 days on site in Raritan Required Skills & Experience •BS degree in polymer science, chemistry, material science, or related science is required •A minimum one (1) year related working experience is required if BS or MS degree •Previous experience in polymer characterization including thermal analysis (DSC, DMA, TGA), rheology, and x-ray diffraction testing (XRD) is required (at least 2/3 skills) •Must be able to work independently and effectively collaborate and communicate with other team members Nice to Have Skills & Experience -Experience in a GLP/GMP environment -Experience with medical devices -Experience with test method development Job Description A large life sciences/medical device client of ours is looking for a Polymer Science to join their team for a 12+ month contract. They will focus on polymer characterization, including rheology, thermal analysis (DSC, DMA, TGA), and x-ray diffraction (XRD), in support of new product development and life-cycle management. The associate will work closely with an appointed scientist to execute test methods, analyze and report results, and develop new procedures as needed. Key responsibilities include and maintaining instruments, preparing samples, ensuring timely testing and data reporting, maintaining accurate documentation and calibration records, and adhering to GMP/GLP practices. Additional tasks may involve microscopy, wet chemistry, and training other personnel.

Primary Duties & Responsibilities Member of prototype fabrication team: Project planning, execution, tracking and reporting Develop and improve processing methods for inorganic composite materials (preform fabrication, metal casting, mold production and assembly, programming and operation of advanced furnaces, programming and operation of CNC machining centers, precision finishing/lapping of hard materials, and other associated activities) Characterization of materials properties Measurement of dimensions, both manually and via computer controlled CMMs Interface with outside entities (raw materials suppliers, equipment vendors, toll manufacturers, machine shops, and test labs) Transfer successful products to manufacturing, including documentation and training Education & Experience New AAS in Engineering or Science fields (or equivalent training and experience) Relevant certifications a strong plus, such as CAM, CAD, ISO, Lean, CMM, others Skills Familiarity with manufacturing and/or lab environment Experience with advanced equipment (materials processing, furnaces, CNC machining centers, CMMs, etc.) Knowledge of assembly operations Strong mechanical aptitude Strong computer aptitude (data summaries, programmable furnaces and machining centers, etc.) Working Conditions Position requires on-site activities for prototype fabrication. Work schedule is 5 days, 40 hrs per week, first shift. Working in lab, production and office Physical Requirements Hands-on, lab-based job environment: Required to frequently lift/push/pull a minimum of 35 lbs Must be able to sit, bend, squat and walk about facility Depending on project assignment, may be required to walk/stand for entire 8 hour day Safety Requirements All employees are required to attend scheduled training, follow the site EHS procedures and Corporate EHS standards. This includes the use of proper protective equipment (PPE) as required by the job responsibilities. Managers will ensure that all safety and environmental procedures are followed consistently. They will ensure that risk assessments are performed, proper training, work instructions, required PPE is available, and will monitor compliance. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

Requisition ID 61042 Position Type (US) Full Time Workplace Arrangement #LI-Onsite About Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role The RDA Process Scientist performs research and development work with an operations focus which bridges the gap between RD&A Taste Innovation and KERRY's commercialization process. He/she will focus on process optimizations, scale-ups, solving regulatory and other hurdles to new products and technologies introductions. He/she will collaborate with other scientists (especially Taste Innovation team), engineers, maintenance, QC, sanitation, etc. Key responsibilities * Work closely with Taste Innovation team to develop and scale up taste modulation products * Focus on solving the regulatory hurdles * Liaising with cross functional teams engineering, research, technical, QC, sanitation, maintenance, and/or production staff, regulatory, procurement, etc. * Planning, organizing, and overseeing process or production trials * Suggests improvements or modifications to current processes * Generates ideas for new products and researches feasibility in terms of profitability, resource availability and compliance with regulations. * Adheres to Standard Operating Procedures (SOPs) and Cleaning In Place (CIP) * Keeps recording data log (flow rate, pressure, temperature, etc) and analyzing data * Writes and reads technical papers, reports, reviews, and specifications. Qualifications and skills * Bachelor's or Master's in food process science, food engineering, agricultural science, engineering, material science or related science fields. * Experience in a food production environment or industrial laboratory Experience with upscaling of food manufacturing processes is a plus moving from lab scale to industrial scale. * Knowledge of good manufacturing practice * Problem-solving skills, analytical skills, and attention to detail * Strong communication and interpersonal skills, able to work effectively as part of a team. * Excellent analytical, organizational, and multi-tasking skills. The pay range for this position is $107,757 to $181,563 in Annual Salary. Kerry typically does not hire an individual at the top or near the top of the range, as we are a pay-for-performance company, and this range is set to continue to reward performance annually while in role. Compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate within the above range may be influenced by a variety of factors including skills, qualifications, experience, and internal equity. Kerry offers a competitive benefits package, including medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, Employee Share Plan, Life, disability, and accident insurance, and tuition reimbursement. This job posting is anticipated to expire on Jan 30th, 2026. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at Know Your Rights Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name. Recruiter Posting Type DNI

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Research Scientist Analytical Development Position Overview: As an Analytical Development Scientist, you will be at the forefront of designing analytical experiments to drive new product development for global markets. Your role involves developing, validating, and transferring analytical methods to manufacturing sites and CMOs, ensuring that analytical procedures meet regulatory requirements and can be implemented effectively. You will interpret results accurately, derive conclusions based on sound science, and delegate analytical lab work to in-house bench chemists or contract laboratories, performing laboratory work when necessary. You will document learnings thoroughly, share knowledge with teams, and collaborate with the Analytical Development functional community to understand the chemistry of new products. Additionally, you will prepare product specifications, plan stability studies, and prioritize work to ensure timely delivery of results and achieve critical project milestones. Your responsibilities also include following written procedures and laboratory practices to ensure quality and compliance, drafting and reviewing SOPs, OIs, and relevant documents, and presenting experimental findings effectively to colleagues with scientific and non-scientific backgrounds. YOUR TASKS AND RESPONSIBILITIES: Design analytical experiments to drive new product development for global markets; Develop, validate, and transfer analytical methods to manufacturing sites/CMOs; Create analytical procedures that meet regulatory requirements and can be implemented at manufacturing sites; Interpret results accurately and derive conclusions based on sound science; Delegate analytical lab work to in-house bench chemists or contract laboratories, and perform laboratory work when necessary; Document learnings thoroughly and share knowledge with teams; Collaborate with the Analytical Development functional community to understand the chemistry of new products; Prepare product specifications and plan stability studies; Prioritize work to ensure timely delivery of results and achieve critical project milestones; Follow written procedures and laboratory practices to ensure quality and compliance; Draft and review SOPs, OIs, and relevant documents, including validation/transfer protocols and reports; Present experimental findings effectively to colleagues with scientific and non-scientific backgrounds. WHO YOU ARE: Bayer seeks an incumbent who possesses the following: Minimum Requirements: Bachelor's Degree in Science or international equivalent, with four or more years of experience; OR a Master's degree in Science or international equivalent, with two or more years of experience; OR a Ph.D. in Science or international equivalent, with one year of experience; Experience in analytical development within the Rx, OTC, Consumer products industry or in an academic setting; Strong knowledge of relevant analytical techniques (HPLC, LC-MS, GC, UV-Vis, FT-IR, AAS); Excellent oral and written communication skills, with an emphasis on clarity and conciseness; Organizational and interpersonal skills with the ability to multitask; Self-motivated to learn and develop within the organization. Preferred Requirements: Advanced degree in analytical chemistry, pharmaceutical analysis, or a related field; Hands-on knowledge in method development and validation of pharmaceutical tests (Assay, Impurities, Dissolution); Knowledge of GMPs and LIMS. Employees can expect to be paid a salary between $99,253.06 - $148,879.60 Additional compensation may include a bonus or incentive compensation (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least January 5, 2026. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location: United States : New Jersey : Morristown Division: Consumer Health Reference Code: 858288 Contact Us Email: hrop_*************

Kenvue is currently recruiting for a: Scientist, Self Care R&D Product and Process Development What we do At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA , AVEENO , TYLENOL , LISTERINE , JOHNSON'S and BAND-AID that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information , click here . Role reports to: Manager Self Care RnD Location: North America, United States, New Jersey, Summit Work Location: Fully Onsite What you will do We are seeking a motivated and experienced Senior Scientist to join Self-Care Product and Process Development team. Reporting directly to the Associate Director, this role focuses on supporting the development and optimization of consumer health products, with an emphasis on over-the-counter (OTC) medications and supplements. The Senior Scientist will play a critical role in ensuring product efficacy, safety, and compliance with regulatory standards. The ideal candidate will have a strong background in formulation science, process development, and experience in GxP compliance. Key Responsibilities: Product and Process Development: Lead consumer centric formulation and development of consumer health products, namely OTC medications, ensuring they meet quality and efficacy standards. Determining technical objectives and evaluate criteria for obtaining resolution in consultation with manager. Identify and resolve technical challenges in product and process development, utilizing sound scientific principles and experimental data with general guidance. Support the optimization of manufacturing processes to enhance efficiency, scalability, and robustness. Project Management: Contribute to project planning, timeline management, and project milestone deliverables to ensure successful project. Collaboration: Work closely with cross-functional teams, including R&D, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals. Stay up-to-date with the latest scientific advancements and incorporate them into research projects Documentation: Prepare and maintain detailed documentation for product development processes, including experimental protocols, batch records, and technical reports. What we are looking for Required Qualifications Degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Materials Engineering, Biomedical Engineering, Biophysics, or related field with 0-4 years of relevant experience. Knowledge of formulation science, process development, and foundational understanding of regulatory requirements for OTC medications and dietary supplements. Proficiency in analytical techniques and methods used in product development and quality control. Excellent written and verbal communication skills, with the ability to present complex information clearly and concisely. Ability to work collaboratively within a multidisciplinary team and across various functions. Strong analytical and problem-solving skills Desired Qualifications Experience in product and process development within the consumer health industry. Experience in solid dose formulation and manufacturing (tablets, capsules, soft chews, gummies). Experience in formulation of liquid and semi-solids for topical and/or nasal application Demonstrated ability to manage multiple projects and work effectively in a fast-paced environment. Proficiency in project management skills, including timeline management, budget oversight, and team coordination. What's in it for you Annual base salary for new hires in this position ranges: $82,025.00 - $115,800.00 This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors. Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region *Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Mammoth Brands (formerly Harry's Inc.) is the modern CPG company behind brands Harry's, Flamingo, Lume, Mando, and Coterie. We're building a new model-and home-brands, founders, and talent looking to solve unmet needs, improve peoples' lives, and ultimately challenge the status quo. Our mission is to “Create Things People Like More.” Simply put: everything we do should be better than what already exists. If it's not, we don't do it. This guides everything we do, from developing the best product experiences, to making Mammoth Brands a great place to work, to exploring innovative ways to give back to our community. We got our start in 2013 when our co-founders created Harry's. They built the brand differently-online first, prioritizing direct relationships with customers-and in the process learned they'd created something bigger: a playbook and platform that could help other brands grow and scale to their full potential, and a vision to reimagine consumer packaged goods. Today, Mammoth Brands is a growing portfolio of brands and the largest CPG company built in the last 20 years. Even as we grow, we take extra care to maintain the small, scrappy, entrepreneurial culture that helped to get us where we are today: to create a company that people like more, that better serves its customers, employees, and community. As a company, we're also committed to making a positive impact and have donated over $20 million through our network of nonprofit partners to date. About the team Are you a product enthusiast who loves making cool stuff? R&D is at the heart of product creation for our global Harry's and Flamingo brands. Join our team of passionate engineers, scientists, researchers, technicians, program managers, and more who are on a mission to create insightful, innovative products that fulfill the unmet, sometimes unspoken, needs of our customers. Within R&D, the Hard Products team is the engine behind our shaving business, developing razors, handles, and accessories; anything made from metal or plastic, in any product category. We start the process with customer-focused concept development and take ideas through design, engineering, prototyping, technical testing, user testing, demonstration, and validation, eventually bringing products like our new Harry's Plus razor to market. About the role Are you a highly motivated and detail-oriented individual with a passion for innovation? We're seeking an R&D Technician to join our Hard Product Innovation team. In this hands-on role, you'll play a vital part in the development and testing of our next-generation products and technologies. The ideal candidate is a proactive self-starter with strong technical skills, an inquisitive mindset, and a commitment to producing high-quality results in the laboratory. What you will accomplish Laboratory Operations & Testing: Operate and maintain a variety of lab equipment to perform critical tests on materials, components, assemblies, and products. Accurately record and report test data with basic analyses. Prototyping & Assembly: Assemble and inspect prototypes. Support the design and fabrication of custom fixtures to aid in measurement, inspection, testing, and evaluation. Lab Management: Ensure a safe, clean, and organized lab environment. Manage the inventory of lab tools and supplies. Coordinate regular maintenance and calibration of equipment. Collaboration: Work closely with a multidisciplinary team to support product development and consumer testing. Logistics: Coordinate the shipping and receiving of lab materials and products. This should describe you A degree or certification in a relevant technical field (e.g., Mechanical Engineering Technology, Material Science, etc.) or equivalent practical experience. Proven experience in a laboratory or R&D setting, with a strong emphasis on adhering to safety protocols. Proficiency in operating and maintaining lab equipment. Strong mechanical aptitude and problem-solving skills. Experience with CAD software (like SolidWorks) is a plus. Exceptional attention to detail and a commitment to quality. Excellent communication and interpersonal skills, with the ability to work effectively in a team environment. Creative, analytical, dynamic, and operates with flexibility Self-starter; you own your work Drives tasks and actions to closure Are familiar with measurement and inspection equipment and tools; mechanical, fluid, thermal, and environmental testing Here's who you'll work with Reporting to the Head of the Hard Product Innovation team You'll be a team member of the Hard Product Innovation team You will work cross-functionally with Product Design Engineering and Quality. This is a role supporting brands Harry's, Flamingo, Lume, Mando Benefits and perks Medical, dental, and vision coverage 401k match Equity in Mammoth Brands Flexible time off and working hours Wellness and L&D stipends 4 weeks sabbatical after 5 years, 6 weeks after 10 years, and 8 weeks after 15 years 20 fully paid weeks off for parents who give birth, or 16 fully paid weeks off for all other paths to parenthood Fun IRL and virtual events including happy hours, team building events, and parties on our rooftop Free products from all of our brands We can't quantify all of the intangible things we think you'll love about working at Mammoth Brands, like the exciting challenges we tackle, the smart and humble team you'll get to work with, and our supportive and inclusive culture. That said, our salary ranges are based on paying competitively for our size and industry, and are one part of our total rewards package, which also includes a comprehensive set of benefits and our equity program. The base salary hiring range for this position is $111,200-$140,000, but the final compensation offer will ultimately be based on the candidate's location, skill level and experience. Mammoth Brands is committed to bringing together individuals from different backgrounds and perspectives. We strive to create an inclusive environment where everyone can thrive, feel a sense of belonging, and do great work together. Mammoth Brands is an Equal Opportunity Employer, providing equal employment and advancement opportunities to all individuals. We recruit, hire and promote into all job levels the most qualified applicants without regard to race, color, creed, national origin, religion, sex (including pregnancy, childbirth and related medical conditions), parental status, age, disability, genetic information, citizenship status, veteran status, gender identity or expression, transgender status, sexual orientation, marital, family or partnership status, political affiliation or activities, military service, domestic violence victim status, arrest/conviction record, sexual or reproductive health decisions, caregiver status, credit history immigration status, unemployment status, traits historically associated with race, including but not limited to hair texture and protective hairstyles or any other status protected under applicable federal, state and local laws. Mammoth Brands' commitment to providing equal employment opportunities extends to all aspects of employment, including job assignment, compensation, discipline and access to benefits and training. We respect the laws enforced by the EEOC and are dedicated to going above and beyond in fostering diversity across our company.

The Upstream Manufacturing Scientist is responsible for executing mammalian cell culture processes and producing recombinant proteins for a wide range of mammalian based biosimilars. The candidate will be responsible for executing cell culture batches from 50 L to 1000 L volumes engineering and clinical batches in a cGMP environment. This position requires technical expertise in bioreactor operations, cell biology and knowledge of initiating batch records, protocols, investigations and other technical documents. Work in a team environment to execute batches and can work independently with minimum supervision. Essential Duties & Responsibilities • Work with a collaborative team of manufacturing associates and engineers to execute upstream batches. • Perform cell culture and bioreactor operations at multiple scales. • Ensure that engineering and clinical batches are executed in a timely manner. • Establishes operating equipment specifications and improves manufacturing techniques. • Uses programs to collect and evaluate operating data to conduct on- line adjustments to products, instruments or equipment. • Ability to interpret and provide instructions furnished in written, oral, diagram, or schedule form. • Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health and safety policies. • Review executed manufacturing and packaging batch records, executed and associated supporting documents. • Coordinate the conduction of investigations and corrections for issues found during the batch execution process. • Performs other functions as required or assigned. • Complies with all company policies and standards. Requirements Education and Experience • Requires a Bachelor or Master' degree in chemical, biological or biochemical sciences and a minimum of 3+ years of related experience in the biopharmaceutical industry. • Expertise in independently conducting and directing the design, execution, analysis, and documentation of all states of process development. • Strong fundamental knowledge and subject matter expertise to execute engineering and clinical batches. • Previous experience working in GMP and aseptic manufacturing environment. • Experience working with single use manufacturing consumables such as bags, tube sets, columns and process manifolds. Specialized Knowledge and Skills • Ability to work with other team members and independently - good interpersonal skills. • Good communication skills: verbal and written, good computer and organization skills, detail oriented. • Basic computer skills, including knowledge of Word, Excel and spread sheet. • Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review. • Knowledgeable in cleaning verification/validation.

Job Title: R&D Formulation Scientist - Soft GelJob Description We are looking for an experienced R&D Formulation Scientist specializing in soft gels to join our innovative team. You will partner closely with sales and customers to support product requirements and technical needs, develop formulations for various products, and collaborate with sourcing and purchasing teams to ensure material availability and cost efficiency. Responsibilities * Develop formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations. * Troubleshoot technical formulation issues and provide expert problem-solving support. * Assist with analytical testing and quality assessments. * Perform hands-on work in the Product Development laboratory. * Utilize analytical instrumentation including GC, HPLC, and ICP-MS. * Evaluate laboratory capabilities and identify opportunities for future R&D expansion. * Work effectively with a predominantly Spanish-speaking laboratory team. Essential Skills * 3+ years of R&D formulation experience. * Bachelor's Degree in Food Science, Chemistry, or related field. * Expertise in soft gels. * Experience in the nutraceutical industry. * Skilled in HPLC, GC, and ICP. Additional Skills & Qualifications * Bilingual skills are a plus. * Experience with raw materials and quality control. * Knowledge of analytical chemistry and fish oils. Work Environment The position will report to the Quality Director until a future R&D Director is hired. Initially, there will be only two R&D formulators on the team until the acquisition expands the team. The work schedule is Monday to Friday, 8 AM to 5 PM, 100% on-site. The dress code is business casual. Job Type & Location This is a Permanent position based out of Clifton, NJ. Pay and Benefits The pay range for this position is $75000.00 - $90000.00/yr. 401K, holidays and vacation hours along with sick time. Will be able to have a team under them in the future for the new R&D department! Workplace Type This is a fully onsite position in Clifton,NJ. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way. Responsibilities Role Summary The Analytical Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity, dissolution, residual solvents testing, Particle size distribution of active pharmaceutical ingredients, excipients and finished dosage forms. Essential Duties and Responsibilities Perform Method Development/Method validation / stability testing, including report writing, for various dosage forms that includes Tablets, Hard Gelatin Capsules, Oral/Topical Liquids, oral suspensions, Powder for oral suspensions and Nasal products with minimum supervision Support the Product Development team in developing new products Identification and characterization of the unknown impurities in the drug products and drug substances Support or independently perform Method Development/Method validation / stability testing for various dosage forms that includes Tablets, Hard Gelatin Capsules, Oral/Topical Liquids, oral suspensions, Powder for oral suspensions and Nasal products Elemental impurity testing using ICP-MS / ICP - OES. Trouble shoot analytical issues to accomplish desired results Other duties as assigned Qualifications Education & Experience Bachelor's Degree in Chemistry, Biology, or related field, Master's Degree a plus 3-6 years of experience working as an R&D Chemist for a pharmaceutical company Operational and technical expertise in developing testing such as HPLC, GC, Dissolution, Particle size distribution, etc. Experience in pharmaceutical Method Development, Method Validation and stability testing. Capable of writing reports suitable for regulatory submission with minimum supervision. Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran status, or any other classification as required by applicable law. The anticipated annual base salary range for this position in New Jersey is $62,000 to $80,000, plus a discretionary performance bonus (based upon eligibility). The final salary offered to a successful candidate may vary and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, the type and length of experience within the industry, skillset, education, business needs, etc. Lupin is a multi-state employer, and this salary range may not reflect positions that work in other states. Physical Requirements The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally, work is performed in a manufacturing environment. Search Firm Representatives Please Read Carefully Lupin USA, and its Affiliates does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms for any current openings at our company without a valid written search agreement in place will be deemed the sole property of Lupin. No fee will be paid in the event a candidate is hired by Lupin as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, No phone calls or emails.

Job title: Product Development Scientist Contract Duration: 01/12/2026 to 10/30/2026 Hours: 8: 30am to 5: 00pm (Monday through Friday). 86 Morris Avenue Summit, NJ 07901 (1 day per week). May fluctuate based on needs. Candidates must have 2 to 4 years formulation experience Description: A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline. FORMULATION Experience is required Consumer Products - Skin Health BA Degree 2 to 4 years experience

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap - Right Talent - Right Time - Right Place - Right Price and acting as a Career Coach to our consultants. Company: One of Our Clients Job Description: Job Title: Formulation Scientist Location: Skillman, NJ 08558 Duration: 09+ Months (Extendable) Pay Rate: $40.00 - 43.28 hourly. on W2 without benefits. Description: A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline. FORMULATION Experience is required Consumer Products - Skin Health BA Degree 2 to 4 years' experience Awards and Accolades: America's Most Honored Businesses (Top 10%) Awarded by USPAAC for the Fastest Growing Business in the US 12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020) Fastest 50 by NJ Biz (2020, 2019, 2020) INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list) Top 100 by Dallas Business Journal (2020 and 2019) Proven Supplier of the Year by Workforce Logiq (2020 and 2019) 2019 Spirit of Alliance Award by Agile1 2018 Best of the Best Platinum Award by Agile1 2018 TechServe Alliance Excellence Awards Winner 2017 Best of the Best Gold Award by Agile1(Act1 Group)

Are you an experienced Scientist - Cell-Based Assays with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Scientist - Cell-Based Assays to work at their company in Rahway, NJ. Position Summary: We're seeking a hands-on scientist to execute high-throughput cell-based assays in 384-well format. You will culture and plate cells, dispense compounds using the Echo, run diverse detection readouts, and analyze dose-response data to deliver high-quality EC50 results for discovery programs. Primary Responsibilities/Accountabilities: Maintain, expand, and plate mammalian cell lines for 384-well assays Set up and execute assays with compound dispensing via Labcyte/Beckman Echo Run and optimize detection formats (e.g., luminescence, cAMP, HTRF/TR-FRET, fluorescence) Generate dose-response curves (4-parameter logistic fits) and report EC50/IC50 with QC Troubleshoot assay performance, optimize Z' factors, and document SOPs/results Collaborate with discovery teams to prioritize studies and timelines Additional responsibilities may include setting up Western blot assays and learning how to run in-cell westerns Qualifications: BS/MS/PHD in Biology, Pharmacology, Biochemistry, or related field; BS with 5+ years, Masters with 3+ years and PHD with 1+ year of industry or equivalent lab experience. Proficiency in mammalian cell culture and 384-well assay workflows Experience with plate readers and assay platforms (e.g., cAMP, HTRF, luminescent assays) Strong data analysis skills: 4PL curve fitting, EC50/IC50 determination, and curve QC (e.g., R^2, top/bottom constraints) Detail-oriented, organized, and comfortable in a fast-paced, high-throughput environment Preferred: Experience with automation/LIQ handlers, LIMS/ELN, and statistical QC (Z', CV, S/B) Familiarity with GraphPad Prism, ActivityBase, or equivalent analysis tools Hands-on experience with Echo acoustic dispensing.