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Vice President Biotech Quality Control Jobs (NOW HIRING)

Lumanity

Vice President, Regulatory Strategy

Acts as trusted strategic partner to pharmaceutical and biotech C-suite executives and other ... Sets and reinforces delivery quality standards across regulatory team, ensuring consistency in ...

Corpay

VP, Operations Automation

Brentwood, TN · On-site

Defining how automation will improve scale, cost-to-serve, quality, control effectiveness ... Vice President or cross-functional approval. Back-Office Automation * Identifying, sizing ...

New

Deep Origin

VP/SVP of Drug Discovery

San Francisco, CA · On-site

$200 - $300/hr

About the Role We are seeking an experienced and highly strategic VP/SVP of Drug Discovery to lead ... The role is ideal for a senior biotech leader who wants to help build a next‑generation ...

Lumanity

Acts as trusted strategic partner to pharmaceutical and biotech C-suite executives and other ... Sets and reinforces delivery quality standards across regulatory team, ensuring consistency in ...

Actalent

QA/QC Inspector

Loves Park, IL

$20/hr

QA/QC Inspector - Antibody Products Make an Impact in Biotech Quality & Innovation Join a dynamic and growing biotechnology team where your work directly supports the quality and integrity of ...

New

Legend Biotech US

VP, Medical Affairs

Bridgewater, NJ · On-site +1

Legend Biotech is seeking a VP of Medical Affairs as part of the Medical Affairs team based in ... Assure that the highest quality, ethical & professional values are demonstrated in all aspects of ...

Fives-S Group

Quality Control Manager

Beaumont, TX

The Construction Quality Control (QC) Manager will work closely with the Vice President of Engineering and Quality to supervise, train, and develop a team of Quality Control Inspector's. The ...

New

Five-S Group

Quality Control Manager

Beaumont, TX · On-site

The Construction Quality Control (QC) Manager will work closely with the Vice President of Engineering and Quality to supervise, train, and develop a team of Quality Control Inspector's. The ...

New

Five-S Group

Quality Control Manager

Scott, LA · On-site

The Construction Quality Control (QC) Manager will work closely with the Vice President of Engineering and Quality to supervise, train, and develop a team of Quality Control Inspector's. The ...

New

PerkinElmer

VP, Client Solutions

Raleigh, NC · On-site

$134K - $172K/yr

... biotech, and advanced therapy organizations. They report to the SVP, Commercial Excellence and are a key contributor to the firm's overall commercial strategy and revenue targets. Key ...

Five-S Group

Quality Control Manager

Lake Charles, LA · On-site

The Construction Quality Control (QC) Manager will work closely with the Vice President of Engineering and Quality to supervise, train, and develop a team of Quality Control Inspector's. The ...

New

Actalent

Qa/Qc Inspector

Rockford, IL

$20/hr

QA/QC Inspector - Antibody Products Make an Impact in Biotech Quality & Innovation Join a dynamic and growing biotechnology team where your work directly supports the quality and integrity of ...

New

Fives-S Group

Quality Control Manager

Scott, LA

The Construction Quality Control (QC) Manager will work closely with the Vice President of Engineering and Quality to supervise, train, and develop a team of Quality Control Inspector's. The ...

New

Five-S Group

Quality Control Manager

Baton Rouge, LA · On-site

The Construction Quality Control (QC) Manager will work closely with the Vice President of Engineering and Quality to supervise, train, and develop a team of Quality Control Inspector's. The ...

New

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All JobsVice President Biotech Quality Control Jobs

Vice President Biotech Quality Control information

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$31K

$125.6K

$213.5K

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

As of Aug 9, 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.

What cities are hiring for Vice President Biotech Quality Control jobs? Cities with the most Vice President Biotech Quality Control job openings:
What are the most commonly searched types of Biotech Quality Control jobs? The most popular types of Biotech Quality Control jobs are:
What states have the most Vice President Biotech Quality Control jobs? States with the most job openings for Vice President Biotech Quality Control jobs include:
What job categories do people searching Vice President Biotech Quality Control jobs look for? The top searched job categories for Vice President Biotech Quality Control jobs are:
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 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Vice President Drug Safety

Catalyst Pharmaceuticals, Inc.

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 3 days ago

Job description

The Vice President (VP) of Drug Safety will lead drug safety operations across Catalyst's development and commercial portfolio, overseeing PV infrastructure, case management systems, vendor oversight, budget, compliance, training, and inspection readiness. Reporting to the Chief Medical Officer, this role provides strategic and operational leadership for the design and execution of drug safety capabilities and product/program specific drug safety plans in alignment with regulations and corporate goals.
This role manages a multidisciplinary PV operations team, including internal PV specialists and external vendors/partners. The VP, Drug Safety also partners cross-functionally with Clinical Development, Regulatory Affairs, Medical Affairs, Quality, Legal, and Commercial to enable efficient and compliant safety oversight across all programs. The VP, Drug Safety is also responsible for regular periodic regulatory updates and reports, along with spontaneous reporting as necessary and indicated.
This is a remote position that will require travel to company headquarters and other locations as needed to support business operations.
Requirements
Responsibilities (including but not limited to):
  • Develop and execute a strategic vision for the drug safety function, aligning with Catalyst's corporate goals and industry best practices
  • Lead PV operations, including collection, evaluation, and analysis of safety data from clinical trials, post-marketing sources, investigator-initiated studies, and real-world evidence
  • Oversee the preparation, quality control, and timely submission of expedited and periodic safety reports (e.g., ICSRs, DSURs, PSURs/PBRERs) to health authorities
  • Lead benefit-risk assessments and signal detection activities across the lifecycle of products, ensuring proactive identification and communication of emerging safety risks
  • Design and implement risk management strategies, including Risk Evaluation and Mitigation Strategies (REMS), to ensure patient safety and regulatory compliance
  • Provide PV subject matter expertise during Health Authority interactions, including inspections, audits, regulatory responses, and scientific advice meetings
  • Oversee the development, maintenance, and compliance of PV SOPs, work instructions, and training programs to ensure adherence to regulatory requirements
  • Drive inspection readiness efforts in collaboration with Quality and Regulatory teams, ensuring timely, thorough, and compliant responses to regulatory inquiries
  • Manage a high-performing team of PV professionals, fostering a culture of excellence, collaboration, and continuous improvement
  • Provide executive oversight of safety database infrastructure, MedDRA updates, and system enhancements in partnership with IT and external vendors
  • Ensure optimal execution of PV vendor partnerships, establishing service-level agreements, KPIs, and governance frameworks to ensure quality and accountability
  • Collaborate cross-functionally with Clinical Development, Regulatory, Medical Affairs, and Commercial to align safety strategy with product development and lifecycle plans
  • Contribute to scientific communication efforts, including publications, field training materials, and stakeholder engagement related to safety profiles
  • Participate in due diligence, alliance management, and external collaborations as needed, serving as the executive PV representative
  • Additional responsibilities include executive oversight of implementation of safety technologies, contribution to benefit-risk management, and representation on external alliances

Education/Experience/Skills:
  • MD in relevant clinical/scientific field
  • Minimum 15 years of pharmacovigilance experience in the biopharmaceutical industry, including at least 10 years in a senior leadership or management role overseeing Drug Safety functions
  • Broad therapeutic experience with Rare Diseases and/or neuromuscular disease experience being additive
  • Demonstrated experience leading safety operations across clinical development and post-marketing, with a strong understanding of the end-to-end safety lifecycle
  • Proven success in managing safety surveillance, signal detection, regulatory reporting, and compliance with regulatory requirements, including FDA, EMA, ICH, and GCP
  • Deep knowledge of Good Clinical Practice (GCP) and pharmacovigilance regulations and expectations, including adverse event reporting for investigational and marketed products
  • Experience with safety databases (e.g. ARGUS) and other pharmacovigilance systems and tools
  • Strong clinical judgment with the ability to assess complex safety data and provide clear, evidence-based recommendations
  • Excellent organizational and interpersonal skills, with a high degree of leadership credibility, initiative, and the ability to mentor high-performing teams
  • Ability to operate effectively in a fast-paced, biotechnology environment, adapting to dynamic priorities and cross-functional demands
  • Willingness to travel to company headquarters and other locations as needed to support business operations

Catalyst is committed to providing competitive wages and comprehensive benefits including health, dental, and vision insurance, generous paid time off, a retirement savings plan with Company Match, and more. Further details about our benefits package can be found here: https://www.linkedin.com/company/catalystforrare/life/life-at-catalyst/?viewAsMember=true
The base salary for this position will range from $405,000 to $430,000. Candidate experience, professional licensing, and geographic location will be taken into consideration.
Employment is contingent upon successful completion of all required screening and verification processes, including for authority to work in the United States.
EEO Statement
Catalyst Pharmaceuticals is an Equal Opportunity Employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status.
Recruitment & Staffing Agencies: Catalyst Pharmaceuticals does not accept unsolicited agency resumes. Agency resumes will only be accepted if the agency is formally engaged by Catalyst Human Resources.

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