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Pharmaceutical Quality System Manager Jobs (NOW HIRING)

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and ... Experience with Empower, LIMS, or similar systems * Strong documentation, data integrity (ALCOA ...

Manage the current Kapton Films Quality Management System, which is currently certified under ISO 9001:2015. Maintain effectiveness of the QMS and drive improvements and rigor with the operations ...

Quality System Specialist

Newark, CA · On-site

$78K - $88K/yr

Senior Quality Assurance Engineering Manager Job Summary: The Quality System Specialist is responsible for developing, implementing, maintaining, and continually improving the organization ...

Pharmaceutical QC Chemist

Elgin, IL · On-site

$25 - $30/hr

We are seeking a dedicated and detail-oriented Pharmaceutical QC Chemist to join our team. The QC ... Copy machine * HPLC systems * UV/VIS spectrophotometer * IR spectrophotometer * Dissolution ...

New

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and ... Experience with Empower, LIMS, or similar systems * Strong documentation, data integrity (ALCOA ...

Quality Systems Manager

Schaumburg, IL · On-site

$110K - $129K/yr

This is a hands-on management role with responsibility for quality system processes, QA functions ... Experience in a medical device, pharmaceutical, or regulated manufacturing environment. * Internal ...

Coordinates with Quality System Program Manager on the generation of standard reports for QDA ... pharmaceutical industry, OR a Master's degree with 0 prior experience required. Nice to Have ...

Support the administration and maintenance of a harmonized Quality Management System (QMS) across multiple manufacturing sites. * Coordinate quality system processes including document control ...

New

Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... Provide mentorship, oversight and development for the Quality Assurance, Quality System, Quality ...

Showing results 21-40

Pharmaceutical Quality System Manager information

See salary details

$54K

$98.6K

$154K

How much do pharmaceutical quality system manager jobs pay per year?

As of Aug 10, 2026, the average yearly pay for pharmaceutical quality system manager in the United States is $98,613.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $122,500.00 per year, depending on experience, location, and employer.
Infographic showing various Pharmaceutical Quality System Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $98,613 per year, or $47.4 per hour.

QC Chemist

System One

Cranbury, NJ • On-site

$36 - $40/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 23 days ago


Job description

Job Title: QC Chemist (cGMP / HPLC / Solid Dose) Location: Cranbury, NJ (Onsite) Type: Contract-to-Hire Schedule: 40 hrs/week Shift: M-F 8am-5pm Pay: $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a cGMP pharmaceutical manufacturing environment. Ideal candidates will have strong experience with solid oral dosage forms (tablets/capsules) and hands-on HPLC/UPLC analysis. Key Responsibilities

  • Perform batch release and stability testing for pharmaceutical products
  • Conduct assay, dissolution, impurity, and related substances testing
  • Operate, calibrate, and troubleshoot HPLC / UPLC systems
  • Maintain GMP documentation and ensure audit readiness (ALCOA+)
  • Investigate OOS / OOT results and support CAPA activities
  • Manage stability programs, sample pulls, and trending analysis
  • Collaborate with QA and Manufacturing to meet production timelines

Requirements

  • 6–8+ years of pharmaceutical QC experience (cGMP REQUIRED)
  • Strong background in solid oral dosage (tablets, capsules)
  • Recent hands-on experience with HPLC / UPLC (REQUIRED)
  • Experience with assay, dissolution, impurities, and stability testing
  • Working knowledge of FDA, GMP, ICH guidelines
  • Experience with Empower, LIMS, or similar systems
  • Strong documentation, data integrity (ALCOA+), and troubleshooting skills
  • Ability to work independently and in a fast-paced manufacturing setting

Keyskills QC Chemist, Quality Control Analyst, cGMP, GMP, Pharmaceutical, Solid Dose, Solid Oral Dosage, Tablets, Capsules, HPLC, UPLC, Dissolution, Assay, Impurities, Stability Testing, Batch Release, OOS, OOT, CAPA, FDA, ICH, Empower, LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One) Medical, Dental, Vision, 401(k), Life Insurance, and additional voluntary benefits System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M3- #LI- Ref: #558-Scientific