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Quality Control Chemist

Job in North Brunswick Township, Middlesex County, New Jersey, USA
Listing for: On Target Executive Search, A Division Of On Target Staffing LLC
Full Time position
Listed on 2026-02-21
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector
  • Manufacturing / Production
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: North Brunswick Township

Schedule: Monday – Friday, 8:00 AM – 4:30 PM (On-site)

Location: New Brunswick, NJ 08901

Company: Nutraceutical Manufacturer

Our client is a growing nutraceutical manufacturer committed to producing high-quality dietary supplements that meet the highest standards of safety, efficacy, and regulatory compliance. We are seeking a detail-oriented and motivated QC Chemist to join our Quality Control team.

Position Summary

The QC Chemist is responsible for performing analytical testing and quality evaluations of raw materials, in-process materials, and finished products to ensure compliance with GMP standards and internal specifications. This role plays a key part in maintaining product quality and regulatory compliance within a nutraceutical manufacturing environment.

Knowledge, Skills, and Abilities
  • Bachelor’s degree in Chemistry, Biology, or related scientific discipline
  • Minimum of 3 years of experience in a GMP-regulated laboratory environment
  • Experience with in a nutraceutical or dietary supplement manufacturing environment preferred
  • Hands-on experience with analytical instrumentation (HPLC, GC, titrations, spectroscopy)
  • Strong understanding of GMP documentation practices
  • Excellent organizational skills and strong attention to detail
  • Ability to manage multiple priorities in a fast-paced manufacturing setting
Essential Functions
  • Send samples to third-party laboratories and manage independent verification testing programs
  • Support the setup, qualification, and validation of new laboratory instruments (e.g., HPLC, HPTLC)
  • Review raw materials, in-process materials, and finished products and make disposition decisions (approve/reject)
  • Prepare, review, and approve Certificates of Analysis (COAs)
  • Review finished product data packages and make final quality disposition decisions
  • Investigate Out-of-Specification (OOS) results and deviations; initiate and document CAPA activities
  • Develop, validate, and maintain analytical methods and material specifications
  • Maintain laboratory equipment, including calibration, troubleshooting, and preventive maintenance
  • Write, revise, and maintain SOPs related to analytical testing and laboratory operations
  • Collaborate with R&D, Product Development, Purchasing, and Quality teams to ensure material and product compliance
What Our Client Offers
  • Opportunity to grow within an established nutraceutical manufacturer
  • Collaborative and quality-focused work environment
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