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Senior Quality Control Jobs (NOW HIRING)

We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP environments, from R&D through commercial manufacturing. You'd lead a team of QC Analysts and Specialists ...

Senior QC Engineer

Austin, TX · On-site

$103K - $142K/yr

ECI has an immediate opening for a Senior QC Engineer in Austin, TX. The successful candidate will act as the department quality control engineer for all Substation and Relay & Control Design ...

Senior QC Attorney

Washington, DC · On-site

$80 - $90/hr

Paid time off Integres LLC is seeking to fill the Senior QC Attorney position. We strive to provide the next generation of cutting-edge technologies. Our growth means exciting career opportunities ...

Job Title: Sr Quality Control Technician Location : This position is based in our Campbell, California offices. This position is on site and full time. Why Imperative Care? Do you want to make a real ...

The Senior QA/QC Inspector plays a critical role in maintaining quality standards, supporting project execution, and fostering strong client relationships. Explore your tasks and responsibilities The ...

We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP environments, from R&D through commercial manufacturing. You'd lead a team of QC Analysts and Specialists ...

... Sr QC Technician - Lebanon- Night Shift As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing ...

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Senior Quality Control information

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How much do senior quality control jobs pay per hour?

As of Jul 8, 2026, the average hourly pay for senior quality control in the United States is $28.68, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $30.77 per hour, depending on experience, location, and employer.
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What are the most commonly searched types of Quality Control jobs? The most popular types of Quality Control jobs are:
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Senior Quality Control Manager

Senior Quality Control Manager

Antheia

Menlo Park, CA • On-site

$160K - $195K/yr

Other

Re-posted 2 days ago


Job description

We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP environments, from R&D through commercial manufacturing. You'd lead a team of QC Analysts and Specialists, serve as the primary interface with our CDMO and contract lab partners, and build the systems and processes that scale with us as we grow.

What You'll Own

Team & Operations

  • Lead and develop a team of QC Analysts and Specialists: hiring, mentoring, performance, day-to-day priorities
  • Build and improve lab operations infrastructure (scheduling, resource planning, data review workflows)
  • Ensure compliance with GMP, ICH, USP/EP, and FDA/EMA standards across all applicable testing

External Partnerships

  • Serve as the primary QC point of contact for CDMOs, CROs, and contract testing labs
  • Review and approve analytical packages, protocols, and reports from third parties for regulatory compliance and data integrity
  • Drive resolution when external partners hit analytical issues or timeline delays

Technical Leadership

  • Lead method development, transfer, and validation aligned with ICH Q2(R2) and Q14
  • Own complex investigations (OOS, OOT) through root cause analysis and CAPA, with a bias toward speed and continuous improvement
  • Ensure data integrity across workflows (ALCOA+ principles, LIMS, Empower, ELNs)

Strategy

    • Develop QC strategies that align with product lifecycle and multi-site growth
    • Contribute to vendor selection, lab qualification, and capital planning
    • Support regulatory filings with accurate, complete analytical documentation

Qualifications

  • Bachelor's or Master's degree in Chemistry, Biology, or related field. 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 laboratories, supervising analytical staff, and coordinating external testing activities.
  • Deep knowledge of chromatographic (HPLC, GC), spectroscopic (UV/Vis, FTIR), and wet chemistry techniques; bioanalytical familiarity is a plus.
  • Strong background in method development, validation, and lifecycle management (ICH Q2, Q14).
  • Solid experience in OOS/OOT investigations, deviation handling, and CAPA implementation.
  • In-depth understanding of FDA, EMA, and ICH regulatory expectations; prior audit experience highly desirable.
  • Familiarity with laboratory systems such as LIMS, Empower, and ELNs.
  • Excellent written and verbal communication skills with ability to lead cross-functional teams and interface with regulatory agencies and partners.

Additional Information:   

  • Base salary: $160,000 - $195,000 + annual bonus + equity in a high-growth company

[1] This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.

Please note that Antheia doesn't discriminate based on age, race, ethnicity, national origin, religion, gender, sexual orientation, disability, medical history, and other non-merit characteristics.