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Gmp Quality Control Jobs (NOW HIRING)

Cayman Chemical Company

QC Chemist, GMP

Ann Arbor, MI · On-site

Currently, we are looking to add a GMP QC Chemist to the team: Responsibilities and Duties: * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...

Cayman

QC Chemist, GMP

Ann Arbor, MI · On-site

Currently, we are looking to add a GMP QC Chemist to the team: Responsibilities and Duties: * Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in ...

Kellton Tech

QC Analyst III

Portsmouth, NH · On-site

$33/hr

GMP QC lab experience required. * Strong communication and problem-solving skills. * Experience with TrackWise, LIMS, and Microsoft Office Suite a plus.

IntelliPro Group Inc.

NC · On-site

$40/hr

GMP Quality Assurance Duration: 06/29/2026--- 04/04/2027 with possible extension Office: Research ... Provide timely support of Learning Management System, Change Control, Deviation Management Systems ...

Novartis

QC Chemist

Indianapolis, IN

$97K - $146K/yr

On-time and GMP-compliant release of dosage forms * Support Quality Control and AS&T as a valued business partner, with a culture of safety, quality, * delivery to patients, cost, compliance, and ...

Connexion Systems & Engineering, Inc.

Be Seen First

Sr. Specialist, GMP Quality

Boston, MA · Remote

$60 - $75/hr

Hands-on experience with analytical or QC work * Additional familiarity with stability and quality review activities, including: * GMP data review support for stability protocols , stability testing ...

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

QA Contractor, GMP Quality Assurance Location: Onsite at Research Triangle Park, NC Duration: 9 ... Provide timely support of Learning Management System, Change Control, Deviation Management Systems ...

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Gmp Quality Control information

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How much do gmp quality control jobs pay per hour?

As of Jun 22, 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.

More about Gmp Quality Control jobs
What cities are hiring for Gmp Quality Control jobs? Cities with the most Gmp Quality Control job openings:
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Gmp Quality Control jobs near you
Infographic showing various Gmp Quality Control job openings in the United States as of June 2026, with employment types broken down into 64% Full Time, 28% Part Time, 1% Temporary, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

Associate Director, Quality Assurance (GMP QC Lab Oversight)

Coherus Oncology

Camarillo, CA • On-site

Full-time

Posted 18 days ago

Job description

Title: Associate Director, Quality Assurance (GMP QC Lab Oversight)
Reports to: Head of Quality Assurance Operations
Location: Camarillo, CA (On-site)
Classification: Exempt
Overview:
The Associate Director, Quality Assurance provides strategic and operational QA oversight of GMP Quality Control laboratory activities at the Camarillo site and reports to the Head of QA Operations. This role requires a regular on-site presence to effectively support daily GMP QC laboratory operations.
Key responsibilities include ensuring compliant laboratory operations through oversight of laboratory systems, facilities, and the qualification and validation of instruments and equipment. The role is accountable for review and approval of Certificates of Analysis (CoAs) and other GMP documentation, supporting laboratory investigations and batch disposition decisions, and contributing to Quality Management Review processes. The Associate Director also serves as a key partner to QC in driving inspection readiness, continuous improvement, and sustained GMP compliance.
Responsibilities:
  • Provide QA oversight of GMP QC laboratory operations to ensure compliance with cGMP, FDA, and ICH requirements.
  • Oversee QC laboratory systems, instruments, and equipment throughout their lifecycle, ensuring they remain in a validated and inspection-ready state.
  • Review and approve QC-related GMP documentation, including analytical records, CoAs/CoTs, method qualification and validation reports, stability data, deviations, CAPAs, and change controls.
  • Lead and oversee laboratory investigations (e.g., OOS, OOT, deviations, and data integrity events), ensuring robust root cause analysis, appropriate impact assessment, and timely, compliant resolution.
  • Support batch disposition by ensuring QC data, CoAs, investigations, and associated documentation are complete, accurate, and compliant with internal procedures and regulatory expectations.
  • Partner cross-functionally with QC, Manufacturing, Regulatory, and site leadership to ensure compliant laboratory operations, drive continuous improvement, and maintain sustained inspection readiness.
  • Provide QA support and oversight for method transfer, validation, and technical transfer activities impacting QC laboratory operations.
  • Collaborate with Facilities, IT, and QC to support equipment implementation, qualification, maintenance, and resolution of operational issues impacting GMP laboratory activities.
  • Support and participate in internal audits, external audits, and regulatory inspections; contribute to inspection readiness activities and timely, effective responses.
  • Contribute to Quality Management Review processes (e.g., QMR, PQR/APQR), including analysis of QC performance metrics, identification of quality trends, and execution of continuous improvement actions.
  • Escalate significant quality risks and critical issues to the Head of Quality Assurance and senior leadership, as appropriate.
  • Drive development, enhancement, and continuous improvement of SOPs, QA processes, and QC-related quality systems.

Qualifications:
  • Bachelor's degree in a scientific discipline (or equivalent experience) with a minimum of 8 years of direct experience supporting GMP QC laboratory operations in a regulated pharmaceutical or biotechnology environment, including QA oversight.
  • Demonstrated experience in biologics/protein therapeutics, including manufacturing and testing of drug substance, drug product, and finished goods.
  • Demonstrated experience handling QC-related issues, records, and laboratory operations, including analytical documentation, deviations, and investigations, within a GMP environment; prior hands-on QC laboratory experience strongly preferred.
  • Experience reviewing and approving equipment and instrument qualification and validation documentation (e.g., IQ/OQ/PQ), with working knowledge of lifecycle management principles; experience applying risk-based approaches to computerized systems (GAMP 5) preferred.
  • Strong working knowledge of FDA cGMP regulations and ICH guidelines applicable to QC laboratory operations.
  • Experience leading and/or overseeing laboratory investigations, including OOS, OOT, deviations, CAPAs, change control, and data integrity events within a GMP environment.
  • Solid understanding of CoA/CoT generation and approval, and experience supporting batch disposition decisions in a GMP setting.
  • Demonstrated experience supporting internal audits, external audits, and regulatory inspections, including inspection readiness and response activities.
  • Strong written, verbal, and interpersonal communication skills, with the ability to effectively influence cross-functional teams.
  • Proven ability to exercise sound judgment, prioritize effectively, and operate successfully in a fast-paced, on-site GMP environment.

Additional requirements
  • On-site presence in Camarillo is required to support daily GMP QC laboratory operations.
  • Up to 20% travel may be required to support audits, external laboratories, or business needs.

The Base Salary Range for this position is $170,000 to $200,000. Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.
Coherus provides equal employment opportunities to all employees and applicants for employment and prohibits unlawful discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We also prohibit discrimination based on the perception that anyone has any of these characteristics or is associated with a person who has or is perceived as having any of these characteristics.

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