1000+ Best Management Jobs in Wayne, New Jersey (June 2026)

Quality Control Chemist

22 hours ago

Fairfield

Job Description Job Title: Quality Control Chemist Job Description The Quality Control Chemist performs analytical testing on raw materials, in-process samples, and finished products to ensure they meet established quality standards and regulatory requirements. This role supports process validation and stability programs, maintains accurate laboratory records, and helps ensure timely product release in a regulated manufacturing environment. The chemist works closely with other analysts and technicians in a small, collaborative team, with strong opportunities for growth and exposure to both chemistry and microbiology. Responsibilities • Perform analytical testing on raw materials, in-process samples, and finished products using techniques such as HPLC, FTIR, wet chemistry, and other analytical methods., • Support process validation and stability programs by performing required sample analysis and documenting results accurately., • Gather samples each morning, prioritize testing activities, and complete testing and data review before close of business to support on-time product release., • Set up, calibrate, and operate laboratory instrumentation for routine testing in accordance with established procedures., • Prepare laboratory solutions, reagents, and standards following established standard operating procedures (SOPs)., • Ensure accurate, complete, and compliant recordkeeping, including analytical data, equipment logbooks, and laboratory documentation., • Oversee the storage, tracking, and qualification of reference standards and retained samples to ensure integrity and traceability., • Review and verify data generated by other QC chemists and laboratory technicians for accuracy, completeness, and compliance with procedures., • Run analyses and tests on assigned samples, review results with laboratory technicians, and resolve discrepancies as needed., • Write clear, concise analytical reports and submit results to the appropriate supervisor or designee in a timely manner., • Monitor and maintain inventory levels of chemicals, reagents, consumables, and samples to support uninterrupted laboratory operations., • Wash glassware, maintain laboratory cleanliness, and ensure that work areas, equipment, and storage areas remain organized and inspection-ready., • Check, maintain, and document the status of reference standards and ensure they are used and stored in compliance with applicable guidelines., • Follow all safety protocols, laboratory procedures, and company policies to ensure safe handling of materials, equipment, and waste., • Maintain compliance with GMP, GLP, GDP, and applicable compendial requirements such as USP and AOAC methods., • Collaborate with a small team of analysts and technicians, sharing knowledge and supporting continuous improvement of laboratory practices., • Complete additional QC laboratory tasks and responsibilities as needed to support department and organizational goals. Essential Skills • Bachelor’s degree in chemistry or biochemistry; open to other related sciences where strong analytical chemistry skills are demonstrated., • Minimum of 1 year of quality control laboratory experience; 3 years of experience is strongly preferred., • Hands-on HPLC experience, either from academic laboratory work or professional industry experience., • Experience working in a manufacturing, pharmaceutical, or nutraceutical environment., • Demonstrated experience in analytical chemistry, including wet chemistry techniques., • Experience working in a GMP laboratory environment, with practical understanding of GMP, GLP, and GDP requirements., • Knowledge of relevant compendial methods and standards, including USP and AOAC., • Ability to perform and interpret analytical testing on raw materials, in-process samples, and finished products., • Ability to follow and apply standard operating procedures (SOPs) consistently and accurately., • Strong attention to detail with a high level of accuracy in data recording, documentation, and report writing., • Ability to prioritize multiple testing assignments and meet deadlines for product release., • Effective communication skills to review results with technicians and report findings to supervisors., • Ability to work safely with chemicals and laboratory equipment while adhering to established safety protocols., • Physical ability to frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds., • Ability to stand, walk, bend, and stoop for periods of five hours or more and to read and examine objects for extended periods. Additional Skills & Qualifications • Bachelor’s degree in chemistry or biochemistry is preferred; other scientific degrees with strong chemistry focus are considered., • Experience in microbiology or interest in gaining exposure to microbiology testing within a QC environment., • Familiarity with FTIR, wet chemistry methods, and other instrumental techniques used in quality control laboratories., • Experience working with or understanding nutraceutical or dietary supplement products., • Demonstrated ability to work effectively in a small team environment and contribute to building and improving laboratory processes., • Motivation to grow professionally within an expanding organization and take on increasing responsibility over time. Work Environment This position is based in a regulated GMP laboratory environment with minimal gowning requirements. The role operates on a Monday through Friday day shift schedule, with flexible start times typically between 6:30 a.m. and 9:00 a.m., and a preferred shift of approximately 7:00 a.m. to 3:00 p.m. There are no required weekend shifts, although additional hours may be available based on business needs and individual preference. You will work closely with a small team of approximately three to four analysts in a collaborative, supportive setting where you can help build processes from the ground up rather than feeling like just a number. The laboratory uses HPLC, FTIR, and wet chemistry techniques, along with standard QC equipment, and operates under GMP, GLP, and GDP guidelines with reference to USP and AOAC standards. The environment emphasizes cleanliness, organization, and inspection readiness, with routine glassware washing, equipment maintenance, and inventory management. The role involves standing, walking, bending, and stooping for extended periods, lifting and moving up to 10 pounds frequently and up to 25 pounds occasionally, and performing detailed visual and reading tasks for several hours at a time. The culture promotes growth, cross-training in chemistry and microbiology, strong team collaboration, and offers benefits such as paid time off and holidays. Job Type & Location This is a Contract to Hire position based out of Fairfield, NJ. Pay and Benefits The pay range for this position is $25.00 - $25.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fairfield,NJ. Application Deadline This position is anticipated to close on Jul 10, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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