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Vice President Biotech Quality Control Jobs (NOW HIRING)

Alexza

VP Quality & Regulatory Affairs

Fremont, CA · On-site

Job Summary The VP, Quality & Regulatory Affairs is an executive leadership role responsible for ... QC experience, including at least 8 years executive level experience, in the Pharma biotechnology ...

TScan Therapeutics

Head of Quality (VP/SVP)

Waltham, MA · On-site

... Control (QC), Quality Systems, Validation, Supplier Quality, GMP Compliance, and GxP Quality ... The successful candidate will be an experienced biotechnology executive with a demonstrated ability ...

TScan Therapeutics

Head of Quality (VP/SVP)

Waltham, MA · On-site

... Control (QC), Quality Systems, Validation, Supplier Quality, GMP Compliance, and GxP Quality ... The successful candidate will be an experienced biotechnology executive with a demonstrated ability ...

SAB

Vice President Quality Assurance

Sioux Falls, SD · Remote

$275K - $310K/yr

This leader will partner closely with QC, CMC, Manufacturing, Clinical Development, Regulatory ... biotech industry. * Demonstrated success leading Quality organizations through late‑stage ...

GRIFOLS, S.A.

Vice President, Quality

Clayton, NC · On-site

The Vice President of Quality manages all quality assurance, quality control, and quality ... IND/NDA's for all biotech compounds researched at GT or any other licenser that will be ...

Grifols, S.A

Vice President, Quality

Clayton, NC · On-site

$150 - $200/hr

Summary The Vice President of Quality manages all quality assurance, quality control, and quality ... biotech compounds researched at GT or by any other licenser that will be manufactured. * Direct ...

Grifols

Vice President, Quality

Clayton, CA · On-site

The Vice President of Quality manages all quality assurance, quality control, and quality ... IND/NDA's for all biotech compounds researched at GT or any other licenser that will be ...

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Vice President Biotech Quality Control information

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How much do vice president biotech quality control jobs pay per year?

As of Aug 17, 2026, the average yearly pay for vice president biotech quality control in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What is the difference between Vice President Biotech Quality Control vs Director Biotech Quality Control?

AspectVice President Biotech Quality ControlDirector Biotech Quality Control
ResponsibilitiesStrategic oversight, department leadership, policy developmentOperational management, team supervision, project execution
Required CredentialsAdvanced degree (PhD, MS), extensive industry experience, leadership skillsBachelor's or Master's degree, relevant biotech experience
Work EnvironmentExecutive-level, cross-department collaboration, strategic planningTeam management, daily lab operations, project coordination

The Vice President Biotech Quality Control focuses on strategic leadership and high-level decision-making, while the Director Biotech Quality Control handles daily operations and team management. Both roles require strong biotech credentials, but the VP role emphasizes strategic vision and industry influence, whereas the Director role concentrates on execution and team supervision.

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What are the most commonly searched types of Biotech Quality Control jobs?

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Vice President Biotech Quality Control jobs near you
Infographic showing various Vice President Biotech Quality Control job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Vice President, Analytical Development & Quality Control

Revolution Medicines

Redwood City, CA • Hybrid

Full-time

Re-posted 16 days ago

Job description

The Opportunity:

We are seeking a strategic and execution-driven Vice President, Analytical Development & Quality Control (ADQC) to lead the vision, strategy, and execution of analytical development and QC across our growing portfolio.

Reporting to the Senior Vice President, Pharmaceutical Development & Manufacturing, this executive will build and scale a phase-appropriate, forward-looking analytical organization that enables rapid development of small molecule programs while positioning the company for late-stage development and global commercialization.

As a key member of the PDM leadership team, this role will shape analytical strategy at the enterprise level, ensuring robust control strategies, regulatory readiness, and operational excellence across internal and external networks.

Responsibilities:

Strategic & Organizational Leadership

  • Define and drive the enterprise-wide analytical development and QC strategy aligned with portfolio and corporate objectives.

  • Build, lead, and scale a high-performing ADQC organization to support a multi-asset oncology pipeline.

  • Establish a culture of scientific excellence, accountability, and collaboration aligned with RevMed values.

  • Serve as a core member of the PDM leadership team, influencing cross-functional CMC and development strategies.

Technical & Analytical Excellence

  • Design and implement phase-appropriate analytical strategies, including characterization, specification setting, and control strategies.

  • Oversee impurity profiling, degradant analysis, comparability, and lifecycle management of analytical methods.

  • Ensure alignment of analytical approaches with clinical and regulatory needs, enabling accelerated development timelines.

  • Drive innovation in analytical technologies and approaches for complex, mechanism-driven small molecules.

Quality Control & Operations

  • Establish and oversee compliant, efficient QC operations with strong data integrity and digital systems.

  • Ensure inspection readiness and adherence to global regulatory standards (FDA, EMA, ICH).

  • Implement scalable processes to support late-stage development and commercialization.

External Network & Partnerships

  • Lead the strategy and oversight of outsourced analytical development and QC activities.

  • Select, qualify, and manage CDMOs and contract laboratories to ensure high performance and compliance.

  • Oversee method transfer, validation, and lifecycle management across external partners.

  • Proactively manage risks, timelines, and quality across the external network.

Regulatory Leadership

  • Provide analytical leadership for global regulatory submissions (IND, IMPD, NDA, MAA, JNDA.

  • Represent ADQC in health authority interactions and inspections as needed.

Required Skills, Experience and Education:

  • PhD (preferred) or MSc in Analytical Chemistry, Pharmaceutical Sciences, or related field.

  • ~18+ years of industry experience with significant leadership in analytical development and QC.

  • Proven track record supporting late-stage development and global regulatory filings (IND/NDA/MAA/JNDA).

  • Demonstrated success leading and scaling teams (10+ years in leadership roles preferred).

  • Deep expertise in GMP, quality systems, and global regulatory expectations (FDA, EMA, ICH).

  • Extensive experience managing external analytical networks (CDMOs, CTLs).

  • Strong strategic thinking with the ability to make data-driven, risk-balanced decisions.

  • Excellent communication and stakeholder influence at executive levels.

Preferred Skills:

  • Experience in oncology or targeted therapies.

  • Background in accelerated or expedited development pathways.

  • Experience building analytical/QC functions in a high-growth biotech environment.

  • Ability to balance speed, quality, and risk in a dynamic setting. 

    #LI-Hybrid  #LI-GL1

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