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Pharmaceutical Quality Control Manager Jobs (NOW HIRING)

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

Job Title: QC Manager Department: Quality Control - Analytical GENERAL DESCRIPTION: * QC Manger is ... Advanced experience with QC testing in pharmaceutical or biopharmaceutical laboratories

Antheia

Senior Quality Control Manager

Menlo Park, CA · On-site

$160K - $195K/yr

Antheia is the advanced biosynthesis company transforming pharmaceutical manufacturing and ... We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP ...

Astrix Inc

QC Analyst II (Chemistry)

Rensselaer, NY · On-site

$30 - $47/hr

Candidates with strong analytical chemistry, chromatography, and pharmaceutical QC laboratory ... Review analytical data and provide summaries and documentation support to QC management * Assist ...

Antheia

Senior Quality Control Manager

Menlo Park, CA

$160K - $195K/yr

Advanced degree preferred. * 10+ years of progressive experience in pharmaceutical QC under GMP regulations, with 5+ years in a leadership or managerial role. * Demonstrated experience managing QC ...

Semiserve

Quality Control Manager

Lemoore, CA · On-site

Job: QC Manager Location: Lemoore, CA (93245) Schedule: Monday-Friday Pay: $130,000 - $135,000 Duration: Direct Hire Overview I'm working with a well-established, family-owned national Design-Build ...

PL Developments

Quality Control Manager

Miami, FL · On-site

... OTC) pharmaceutical products and consumer healthcare goods SUMMARY: The Quality Control (QC) ... Manage the development, implementation, and continuous improvement of QC goals, objectives ...

Raya Workforce

Quality Control Manager

Fort Belvoir, VA · On-site

Quality Control Manager Location: Fort Belvoir, VA Employment Type: Full-Time | On-site The candidate will be performing all facets of safety and quality control management, submittal tracking, daily ...

MEB

Quality Control Manager

Great Falls, MT · On-site

Job Brief. We are seeking an experienced Quality Control Manager to lead the quality program for a complex federal fueling infrastructure project at Great Falls Air National Guard Base (Near ...

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ · On-site

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

ECC

Quality Control Manager

Tamuning, GU

$110K - $135K/yr

Must have been the QC Manager on a vertical construction project of at least $75 million. The Quality Control Manager must manage the Contractor Quality Control program and organization for the ...

Apache Fabricators LLC

QC Manager

Houston, TX

Quality Control (QC) Manager Apache Fabricators LLC Location: Houston, TX / Shop Environment Industry: Fabrication, Oil amp; Gas, Subsea, Structural amp; Modular Equipment Position Summary Apache ...

Garonit Pharmaceutical

QC Supervisor

Fairfield, NJ

Bachelor's degree in Chemistry or a related scientific field. * 2+ years in a supervisory or management role in a pharmaceutical QC lab. * Strong experience with Empower 3, HPLC, GC, and wet ...

Apache Workforce LLC

Quality Control Manager

Houston, TX · On-site

$95K - $115K/yr

Quality Control Manager Apache Fabricators - Houston, TX Pay: $95,000 - $115,000 per year DOE Schedule: Monday - Saturday | First Shift FABRICATION SHOP EXPERIENCE REQUIRED Apache Fabricators is ...

Tandym Tech

Quality Control Manager

Frederick, MD · On-site

A recognized services company is currently seeking a new Quality Control Manager to support complex infrastructure projects in secure environments across North Washington, DC, and Frederick, MD. This ...

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Pharmaceutical Quality Control Manager information

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$30.5K

$81.3K

$129.5K

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

As of Jul 7, 2026, the average yearly pay for pharmaceutical quality control manager 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 does a Pharmaceutical Quality Control Manager do?

A Pharmaceutical Quality Control Manager oversees the testing and quality assurance processes involved in manufacturing pharmaceutical products. They ensure that all products meet regulatory standards and company specifications for safety, efficacy, and quality. This role includes supervising laboratory staff, developing and implementing quality control procedures, and maintaining compliance with government regulations such as Good Manufacturing Practices (GMP). They also analyze data, investigate quality issues, and work closely with other departments to resolve any problems. The ultimate goal is to ensure that patients receive safe and effective medications.

What is the difference between Pharmaceutical Quality Control Manager vs Pharmaceutical Quality Assurance Specialist?

AspectPharmaceutical Quality Control ManagerPharmaceutical Quality Assurance Specialist
CredentialsTypically requires a degree in pharmacy, chemistry, or related field; certifications like CQE or GMP training are commonSimilar credentials; often holds degrees in life sciences and certifications in GMP and QA practices
Work EnvironmentOversees laboratory testing, quality control labs, and production environmentsFocuses on developing, implementing, and auditing quality assurance systems across production
Employer & Industry UsageUsed in pharmaceutical manufacturing, biotech, and related industriesCommonly employed in pharmaceutical companies, ensuring compliance and process quality

While both roles require similar educational backgrounds and certifications, the Pharmaceutical Quality Control Manager primarily manages laboratory testing and quality control processes, whereas the Pharmaceutical Quality Assurance Specialist focuses on establishing and maintaining quality systems and compliance. Both are essential for ensuring product safety and efficacy in the pharmaceutical industry.

What are some common challenges faced by Pharmaceutical Quality Control Managers in ensuring compliance with regulatory standards?

Pharmaceutical Quality Control Managers often face the challenge of staying current with evolving regulatory requirements from agencies such as the FDA or EMA. They must ensure all laboratory processes, documentation, and product testing meet strict guidelines, which can be complicated by new technologies or changing manufacturing practices. Another challenge is managing cross-functional communication between production, R&D, and regulatory affairs to promptly address quality issues. Successfully navigating these challenges requires a keen eye for detail, strong leadership, and ongoing professional development.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Quality Control Manager, and why are they important?

To thrive as a Pharmaceutical Quality Control Manager, you need a strong background in pharmaceutical sciences, chemistry, or a related field, often supported by a relevant degree and experience in quality assurance. Familiarity with analytical instruments (e.g., HPLC, GC), quality management systems, and regulatory standards like GMP or FDA guidelines is typically required. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring compliance. These skills ensure product safety, regulatory adherence, and efficient team operations in a highly regulated industry.
More about Pharmaceutical Quality Control Manager jobs
What cities are hiring for Pharmaceutical Quality Control Manager jobs? Cities with the most Pharmaceutical Quality Control Manager job openings:
What are the most commonly searched types of Pharmaceutical Quality Control jobs? The most popular types of Pharmaceutical Quality Control jobs are:
What states have the most Pharmaceutical Quality Control Manager jobs? States with the most job openings for Pharmaceutical Quality Control Manager jobs include:
What job categories do people searching Pharmaceutical Quality Control Manager jobs look for? The top searched job categories for Pharmaceutical Quality Control Manager jobs are:
Pharmaceutical Quality Control Manager jobs near you
Infographic showing various Pharmaceutical Quality Control Manager 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 $81,324 per year, or $39.1 per hour.
Manager, Quality - QC Analytical

Manager, Quality - QC Analytical

Glaukos

San Clemente, CA • On-site

Full-time

Re-posted 8 days ago

Job description


How You'll Make an Impact:
The Quality Control Manager in San Clemente, CA oversees all QC laboratory operations and testing activities. This role supervises QC staff, ensures compliant and efficient lab execution, maintains cGMP compliance and data integrity, and provides technical leadership while keeping the laboratory inspection-ready and supporting project teams as needed.
What You'll Do:
General laboratory Management
  • Oversees and assigns raw material, in-process, finished product, and stability testing across multiple pharmaceutical products to ensure timely batch release and stability commitments
  • Manages cGMP stability programs for clinical and commercial products and performs trend analysis to identify risks or emerging issues
  • Oversees the internal reference standard qualification, lifecycle management, and documentation program
  • Oversees method validations, verifications, transfers, and feasibility studies to support product development and commercialization
  • Oversees audit trail review process and 21 CFR Part 11 compliance
  • Evaluates internal versus external testing strategies and recommends improvements to optimize efficiency, cost, and compliance
  • Recommends laboratory equipment, instrumentation upgrades, and new technologies to support future QC capability needs
  • Oversees qualification and calibration of analytical equipment and approves vendor qualification documentation, may include URS development, IQ/OQ/PQ approval authority, equipment lifecycle planning, obsolescence strategy
  • Monitors contract testing laboratories, reviews external analytical data, and ensures CRO/CMO compliance with quality standards
  • Identifies and resolves technical challenges impacting method transfer, assay implementation, and laboratory operations
  • Responsbile for laboratory budget management such as headcount forecasting, consumables planning, and alignment on capital expenditure planning

Documentation & Compliance
  • Reviews and approves analytical data, laboratory documentation, and Certificates of Analysis to ensure accuracy, completeness, and data integrity
  • Oversight of audit trail review process
  • Authors and/or reviews laboratory investigations (OOS, OOT, deviations) and ensures appropriate root cause analysis, impact assessment, and corrective actions
  • Authors, reviews, and approves analytical methods, validation protocols, qualification reports, and stability reports to ensure regulatory compliance
  • Provides annual product quality review analytical input
  • Ensures QC documentation, laboratory systems, and practices comply with ICH, USP, Pharm. Eur., JP, and applicable global regulatory guidelines
  • Supports regulatory submissions by preparing or reviewing technical summaries
  • Contributes to SOP development, process improvements, and continuous improvement initiatives within the laboratory

Inspection Readiness & Regulatory Activities
  • Ensures QC maintains inspection readiness, compliance, and a culture of data integrity
  • Serves as the primary technical lead for QC investigations and escalates significant quality risks appropriately
  • Analyzes and interprets complex analytical data and provides scientifically sound conclusions to support quality and regulatory decisions
  • Participates in regulatory inspections and supports responses to regulatory agencies as required
  • Owns QC laboratory performance metrics and drives continuous improvement initiatives to improve efficiency and compliance

Team Leadership & Cross-Functional Support
  • Supervises QC chemists, sets priorities, and ensures compliant execution of laboratory activities in accordance with cGMP requirements
  • Responsible for QC chemist training matrix updates in coordination with training team
  • Provides technical leadership, mentorship, development, and performance management for QC chemists
  • Participates in cross-functional development and manufacturing meetings as QC representative
  • Communicates QC priorities, timelines, and risks to stakeholders and leadership
  • Collaborates with R&D to assess and implement specialized analytical approaches, when applicable
  • Ownership of QC lab related change control or technical impact assessments and CAPA approval authority
  • Employing technical knowledge to assist with Quality risk management (FMEA) and risk management during Quality investigations

Digital and Automation Strategy
  • Oversee implementation of LIMS / electronic notebooks
  • Improve digital data analytics

How You'll GetThere:
  • 8+ years of experience in analytical chemistry within Pharmaceutical QC environment.
  • Minimum of 1 year of previous management experience in Pharmaceutical QC laboratory, including supervision of QC chemists.
  • Demonstrated leadership skills with the ability to prioritize workload, mentor staff, and ensure inspection readiness and cGMP compliance.
  • Experience managing and overseeing external contract testing laboratories (CROs/CMOs) is preferred.
  • Understanding of analytical platforms including HPLC, FTIR, UV/Vis, and Drug Release.
  • Experience overseeing analytical method validation, verification, method transfer activities, and management of cGMP stability programs.
  • Working knowledge of ICH guidelines, major pharmacopoeias (USP, Ph. Eur., JP), CTD structure, and global regulatory expectations.
  • Strong analytical skills (interpret data, summarize data, present data).
  • Strong written and verbal communication skills. •
  • Motivated and able to work independently, as well as within a team. Exhibits personal integrity, credibility, and responsibility. •
  • Excellent organizational skills and ability to work on multiple projects/tasks. •
  • Meets milestones and schedules.
  • Bachelor's degree in a scientific discipline is required

#GKOSUS
About Us
Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.
Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.
Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.
Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.

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