ZipRecruiter

Log In

1

Gmp Quality Control Jobs (NOW HIRING)

Codexis Inc

Sr. Scientist, Quality Control

Plano, TX · On-site

$160K - $175K/yr

... QC laboratory in a GMP manufacturing facility. This is an on-site position initially be based in ... Redwood City, CA, with the potential to transition to our Hayward location in the future or operate ...

Alnylam Pharmaceuticals

Quality Site Head

Cambridge, MA · On-site

$276K - $373K/yr

Lead all GMP Quality functions for the Norton Manufacturing Facility, including Quality Assurance, Quality Control, Site Quality Systems, compliance, validation oversight, and inspection readiness.

Alnylam Pharmaceuticals

Quality Site Head

Norton, MA · On-site

$276K - $373K/yr

Lead all GMP Quality functions for the Norton Manufacturing Facility, including Quality Assurance, Quality Control, Site Quality Systems, compliance, validation oversight, and inspection readiness.

Abzena Inc.

QC Associate I/II - Contract

San Diego, CA · On-site

$40 - $60/hr

The Quality Control (QC) Associate I / II is responsible for performing analytical testing and ... Ensure all activities comply with GMP, ALCOA+ principles, and data integrity regulations (FDA, EMA ...

TekWissen LLC

Quality Control Specialist

Vacaville, CA · On-site

$20 - $26/hr

Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ... Ensure GMP compliance throughout operations. * Participate in project teamwork, process ...

next page

Showing results 1-20

All JobsGmp Quality Control Jobs

Gmp Quality Control information

See salary details

$11

$21

$33

How much do gmp quality control jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for gmp quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Gmp Quality Control vs Gmp Quality Assurance?

AspectGmp Quality ControlGmp Quality Assurance
Primary FocusTesting and inspecting products to ensure compliance with standardsDeveloping and maintaining quality systems and processes
ResponsibilitiesSampling, testing, and documenting product qualityAuditing, process validation, and quality system oversight
CertificationsGMP training, laboratory skillsGMP knowledge, quality management system training
Work EnvironmentLaboratories, manufacturing sitesQuality departments, compliance offices

Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.

Which pays more, QA or QC?

In the context of GMP Quality Control, QA (Quality Assurance) roles typically pay more than QC (Quality Control) positions because QA involves broader responsibilities such as process audits and compliance oversight. QC roles focus on testing and inspection of products, often with more routine tasks. Salary differences can vary based on experience, certifications, and industry, but generally QA positions offer higher compensation.

Is QC a high paying job?

Quality Control (QC) roles in industries like pharmaceuticals and manufacturing can offer competitive salaries, especially with experience and relevant certifications. However, pay varies based on location, company size, and level of expertise, and QC positions are generally considered mid-range in terms of salary compared to other technical roles.

Is quality control part of GMP?

Yes, quality control is an essential component of Good Manufacturing Practice (GMP) standards. GMP requires quality control processes, including testing and validation, to ensure products meet safety and quality specifications. Quality control professionals in GMP environments perform inspections, sampling, and testing to maintain compliance and product integrity.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Quality or Director of Quality Control typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of Good Manufacturing Practices (GMP) and regulatory compliance.
More about Gmp Quality Control jobs
What cities are hiring for Gmp Quality Control jobs? Cities with the most Gmp Quality Control job openings:
What states have the most Gmp Quality Control jobs? States with the most job openings for Gmp Quality Control jobs include:
What job categories do people searching Gmp Quality Control jobs look for? The top searched job categories for Gmp Quality Control jobs are:
Gmp Quality Control jobs near you
Infographic showing various Gmp Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.
Sr. Scientist, Quality Control

Sr. Scientist, Quality Control

Codexis Inc

Plano, TX • On-site

$160K - $175K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Job description

Sr. Scientist, Quality Control
Department: 64 - Quality Control
Employment Type: Full Time
Location: Redwood City, CA
Compensation: $160,000 - $175,000 / year
Description
The Sr. Scientist in Quality Control will be leading analytical method transfer and validation for oligonucleotide therapeutic and enzyme products. This role serves as a subject matter expert for analytical methods and instrumentation within Quality and will help leading the design and implementation of the QC laboratory in a GMP manufacturing facility. This is an on-site position initially be based in Redwood City, CA, with the potential to transition to our Hayward location in the future or operate in a hybrid capacity across both sites.
We would love to meet candidates who bring:
• Strong scientific judgment and analytical problem-solving skills
• GMP quality mindset with a focus on compliance and execution
• Adaptability and leadership in a fast-paced environment
• Clear communication and cross-functional collaboration
Key Responsibilities
  • Lead analytical method transfers and method validation activities, including protocol design, execution and reporting.
  • Author transfer/validation protocols, technical reports, SOPs and relevant regulatory filing sections.
  • Manage the lifecycle of analytical methods and laboratory instruments, including qualification, maintenance, change control to support GMP readiness.
  • Perform advanced analytical testing for raw materials, in-process and finished products.
  • Provide technical oversight for QC analytical methods and instrumentation, including troubleshoot, root cause analysis, deviations and OOS/OOT investigations.
  • Design, execute, and oversee stability programs, including protocol development, study execution, data review, trend evaluation, and technical reporting.
  • Support QC systems, documentation, laboratory practices, and analytical controls across both the ISO 9001 quality site and the transition to GMP-compliant operations.

Additional experience that would be valuable for this role includes:
  • Experience with microbiological testing and environmental monitoring, or related GMP laboratory controls.
  • Experience supporting the buildout, expansion, or operational readiness of analytical laboratories.

Skills, Knowledge & Expertise
  • Ph.D. in life sciences, chemistry, biochemistry, or a related field with 4+ years of relevant industry experience in regulated environment; or M.S./B.S. with 10+ years of relevant experience.
  • Working knowledge of cGMP and ICH guidelines.
  • Proven experience in developing analytical method validation strategies and execution.
  • Deep technical knowledge and working experience in LC-MS, IP-RP-HPLC and AEX chromatography for oligonucleotide analysis.
  • Strong scientific background in analytical techniques for biological products, including ELISA, qPCR, UV-Vis, CE-SDS, HPLC, and GC.

Job Benefits
  • Medical, Dental and Vision Insurance
  • Basic Life, AD&D, Short- and Long-Term Disability Insurance
  • 401k with Company Match up to 4%
  • Company Equity
  • Generous Paid Time Off including 18 Company Holidays (with a summer and winter shutdown), Vacation, and Wellness Time
  • Annual Lifestyle Account for reimbursement of fitness programs, equipment and more
  • Employee Stock Purchase Program (ESPP)
  • Flexible Spending Accounts (Commuter/Parking, Dependent Care & Healthcare)
  • Student Debt Program (Company Contribution to Loans)
  • Mental Health Wellness Program
  • Subsidized onsite lunch program
  • Onsite Gym Facilities
  • Paid Parental Leave

And More!

Apply