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Vp Biotech Manufacturing Jobs (NOW HIRING)

... the West Coast biotech and biopharma community. WORK LOCATION: This position is remote with ... product manufacturing, and CMC regulatory strategy * Author and provide strategic input on CMC ...

... medical device manufacturers. * Resource Management & Team Utilization: Optimize resource ... Biotech, Providers, Payers). * Proven ability to partner strategically at the enterprise level ...

... medical device manufacturers. * Resource Management amp; Team Utilization: Optimize resource ... Biotech, Providers, Payers). * Proven ability to partner strategically at the enterprise level ...

Acts as trusted strategic partner to pharmaceutical and biotech C-suite executives and other ... Partners with SVP & Practice Lead to translate regulatory landscape changes (AI/digital submissions ...

Job Title: VP, Toxicology Position Type: Full Time Company Description:   Latigo Biotherapeutics, Inc. is a private, early-stage biotechnology company focused on discovering and developing the next ...

Acts as trusted strategic partner to pharmaceutical and biotech C-suite executives and other ... Partners with SVP & Practice Lead to translate regulatory landscape changes (AI/digital submissions ...

VP, Toxicology

San Francisco, CA · On-site

$310K - $340K/yr

Latigo Biotherapeutics, Inc. is a private, early-stage biotechnology company focused on discovering ... The Vice President of Toxicology will provide strategic and scientific leadership for all aspects ...

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Vp Biotech Manufacturing information

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$185.5K

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How much do vp biotech manufacturing jobs pay per year?

As of Sep 11, 2026, the average yearly pay for vp biotech manufacturing in the United States is $185,482.00, according to ZipRecruiter salary data. Most workers in this role earn between $154,500.00 and $197,500.00 per year, depending on experience, location, and employer.

What does a VP of Biotech Manufacturing do?

A VP of Biotech Manufacturing oversees the entire manufacturing process for biotechnology products, ensuring that production is efficient, compliant with regulatory standards, and meets quality specifications. They develop and implement manufacturing strategies, manage large teams, and coordinate with departments such as R&D, quality assurance, and supply chain. This executive role is responsible for setting goals, optimizing operational performance, and driving innovation within the manufacturing operations of a biotech company.

What are the primary challenges a VP of Biotech Manufacturing faces when scaling up production for new therapies?

A VP of Biotech Manufacturing often encounters challenges such as ensuring product quality and regulatory compliance during scale-up, managing supply chain complexities, and coordinating cross-functional teams. Rapidly increasing production capacity for new therapies requires robust process optimization, effective technology transfer from R&D, and strict adherence to Good Manufacturing Practices (GMP). Successfully navigating these challenges involves proactive risk management and fostering strong communication between manufacturing, quality assurance, and regulatory teams.

What are the key skills and qualifications needed to thrive as a VP of Biotech Manufacturing, and why are they important?

To thrive as a VP of Biotech Manufacturing, you need deep expertise in bioprocess engineering, regulatory compliance, and operations management, typically supported by an advanced degree in a life science or engineering field. Familiarity with GMP regulations, quality management systems, and manufacturing execution systems (MES) is essential, along with relevant certifications like Six Sigma or Lean Manufacturing. Leadership, strategic thinking, and strong communication skills set outstanding candidates apart, enabling them to guide diverse teams and drive organizational goals. Mastery of these skills ensures efficient, compliant production and positions the company for innovation and growth in a highly regulated industry.

What are the most commonly searched types of Biotech Manufacturing jobs?

The most popular types of Biotech Manufacturing jobs are:

What are popular job titles related to Vp Biotech Manufacturing jobs?

For Vp Biotech Manufacturing jobs, the most frequently searched job titles are:

Vice President, Compliance

Cambridge, MA • On-site, Remote

Amylyx Pharmaceuticals
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees

$137K - $184K/yr

Full-time

Re-posted 3 days ago


Job description

The Opportunity

Amylyx is seeking an experienced and business-oriented compliance leader to serve as Vice President, Compliance.  Reporting to the Senior Vice President, Deputy General Counsel & Compliance Officer, this individual will help design, implement, and continuously enhance a comprehensive healthcare compliance program as the company prepares for commercial launch and rapid growth.

The Vice President, Compliance will play a critical leadership role in fostering a culture of integrity and accountability, establishing a launch-ready compliance infrastructure, and serving as a trusted advisor to business leaders across the organization. The successful candidate will combine strategic vision with operational excellence, demonstrating the ability to build programs, influence stakeholders, and execute effectively in a dynamic biotechnology environment.

We anticipate hiring the VP, Compliance in September 2026

Responsibilities

  • Build a compliance program consistent with industry standards and regulatory expectations, including policies and procedures, training and communications, auditing and monitoring, investigations, corrective actions, and ongoing risk assessment.
  • Partner with the Executive Leadership Team and Board to establish and reinforce a strong tone from the top, embedding compliance and ethical conduct into leadership communications, business operations, strategic initiatives, and organizational culture.
  • Drive the Company's Compliance Committee and compliance reporting to the Board and Audit Committee.
  • Serve as a strategic advisor to commercial, medical, and other functions to ensure launch activities are conducted in compliance with applicable legal, regulatory, and industry requirements.
  • Build compliance operations, including transparency reporting, fair market value processes, grants and sponsorship review, third-party due diligence, conflict-of-interest processes, investigations, and monitoring activities.
  • Conduct compliance investigations and ensure appropriate corrective and preventive actions are implemented.
  • Develop and lead the Company's compliance training and communications strategy, translating legal and regulatory requirements into practical, business-relevant guidance.
  • Conduct ongoing compliance risk assessments and periodically evaluate the effectiveness of the Company's compliance culture, recommending enhancements based on business needs, emerging risks, and regulatory expectations.
  • Partner with the Deputy General Counsel to execute and evolve the Company's Enterprise Risk Management program.
  • Help build and mentor a high-performing compliance organization and foster a culture of collaboration, accountability, and continuous improvement.

Required Qualifications

  • Bachelor's degree required; Juris Doctor, Masters and/or Compliance Certification (CCEP), or comparable professional qualifications strongly preferred.
  • Minimum 12 years of relevant healthcare compliance experience in the biotechnology, pharmaceutical, medical device, and/or life sciences industry, with demonstrated experience designing, implementing, and/or enhancing healthcare compliance programs.
  • Experience supporting one or more U.S. pharmaceutical product launches preferred.
  • Excellent leadership and interpersonal skills, a problem-solving mindset, and ability to thrive in a fast-paced environment.
  • Excellent project management skills with the ability to manage multiple priorities simultaneously and drive execution.
  • Strong oral and written communication and presentation skills, and professionalism to handle sensitive matters confidentially and with discretion.
  • Demonstrated commitment to ethics, integrity, and values-based leadership.
  • Ability to travel approximately 15-20% of time.

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.