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Qc Stability Jobs (NOW HIRING)

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

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 ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

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 ...

Abzena Inc.

QC Manager

San Diego, CA · On-site

$120K - $150K/yr

We are seeking a highly experienced Quality Control (QC) Manager to lead cGMP QC operations ... Stability studies (ICH-compliant programs) * Testing associated with Qualification/Validation of ...

Careers at RK Pharma Inc.

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc. * Performs ... Train other QC chemists in a timely manner on all the general Laboratory SOPs and test methods.

Grifols

QC Lead

Emeryville, CA · On-site

Method Validation, Antigen Release and Stability, QC Raw Materials (QCRM), QC Microbial (including seedstock) and QC Equipment/eSystems programs. The lead will independently perform the daily ...

Stand-By Personnel

Quality Control

Catoosa, OK

$24/hr

Quality Control Inspector Pay: $24+/hour Shift: Night Shift Position: Temp-to-Hire Location ... and stability. Additional Benefits: * $50 Advance: Available after your first day of work.

Stand-By Personnel

Quality Control

Catoosa, OK

$24/hr

Quality Control Inspector Pay: $24+/hour Shift: Night Shift Position: Temp-to-Hire Location ... and stability. Additional Benefits: * $50 Advance: Available after your first day of work.

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All JobsQc Stability Jobs

Qc Stability information

See salary details

$30.5K

$81.3K

$129.5K

How much do qc stability jobs pay per year?

As of Jul 12, 2026, the average yearly pay for qc stability in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What are the typical day-to-day responsibilities of a QC Stability professional?

A QC Stability professional is responsible for managing stability studies on pharmaceutical products, which includes preparing stability samples, testing products at specified intervals, analyzing and documenting results, and ensuring data integrity. This role often involves working closely with cross-functional teams such as quality assurance, production, and research and development to address any findings or deviations. You can expect to spend time in the laboratory conducting tests, as well as at your desk compiling reports and supporting regulatory submissions. The position requires meticulous organization and the ability to handle multiple studies simultaneously, making time management a valuable asset.

What are the key skills and qualifications needed to thrive in the Qc Stability position, and why are they important?

To thrive as a QC Stability professional, you need a solid background in chemistry, analytical testing, and good documentation practices, typically supported by a degree in life sciences or related field. Familiarity with laboratory information management systems (LIMS), chromatography software (such as HPLC or GC), and regulatory guidelines like GMP and ICH is essential. Strong attention to detail, problem-solving abilities, and effective communication skills are key soft skills in this role. These competencies ensure accurate data analysis, regulatory compliance, and efficient teamwork in maintaining product quality over time.

What is a QC Stability job?

A QC Stability job focuses on monitoring and evaluating the stability of pharmaceutical products over time to ensure they maintain their quality, safety, and efficacy. Responsibilities typically include designing stability studies, analyzing samples at different time points, and documenting results in compliance with regulatory guidelines (e.g., ICH, FDA). QC Stability professionals work closely with quality control and regulatory teams to ensure data integrity and provide critical information for product shelf-life determination.

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Qc Stability jobs near you
QC Chemist

QC Chemist

System One

Cranbury, NJ • On-site

$36 - $40/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 25 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

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