Director CMC Quality Compliance (Hybrid)

Posted 2 Days Ago
Be an Early Applicant
Boston, MA, USA
Hybrid
185K-277K Annually
Expert/Leader
Biotech • Pharmaceutical
The Role
Lead inspection readiness and compliance across internal and external GMP sites (CMOs and manufacturing/testing). Provide technical and strategic oversight of inspection management, risk-based controls, quality governance and culture, integrate new modalities, advise cross-functional teams, and manage and develop staff.
Summary Generated by Built In

Job Description

General Summary:

The CMC Quality Compliance Director is responsible for inspection readiness and compliance of internal and external sites including evaluating, improving, and monitoring commercial level quality compliance and quality culture.  This position provides technical and strategic leadership for inspection readiness and compliance including processes and associated governance across all GMP areas.  This position focuses not just on the “what” but the “how”, ensuring phase appropriate and risk-based compliance.

Key Duties and Responsibilities:

  • Accountable for inspection readiness, inspection management, and compliance programs across all GMP areas including external CMOs and internal manufacturing/testing sites. 
  • Monitor and interpret cGMP regulatory guidelines and trends in the regulatory space and incorporate into phase appropriate control strategies
  • Responsible for overseeing internal and external sites, working with cross-functional teams to identify areas of compliance risk, and implementing action plans to improve the overall compliance and quality culture of the sites. 
  • Monitors health of the inspection readiness and management system, ensures appropriate escalations, and reports to leadership through established governance structure. 
  • Works across quality and functional areas to ensure inspection program is scalable and flexible including integration of new modalities into the quality systems as Vertex expands its scope of operations
  • Provides technical and strategic support to all areas including other quality groups for compliance and inspection related decisions. 
  • As a people manager within the organization, provides leadership, development and coaching to staff.  Provides enterprise-level thinking and strategy direction to staff and acts as a change agent for improvements.

Knowledge and Skills:

  • Expert knowledge of global GMP requirements and experience across multiple GxP areas

  • Highly collaborative and effective at building strong enterprise and cross-functional relationships; a strategic change leader who delivers results through influence, partnership, and leadership.

  • Ability to evaluate quality matters and make decisions utilizing risk-based approach

  • Strong technical knowledge including but not limited to: GMP regulations, inspection management, risk management, and quality governance

  • Solid quality culture knowledge and understanding of how to influence and improve overall compliance

  • Superb facilitation, Communication, and Coaching/influencing skills with proven ability to lead teams

Education and Experience:

  • Bachelor's degree in a scientific or allied health field (or equivalent degree)
  • Typically requires 10 years of work experience and 3 years of management experience, or the equivalent combination of education and experience

Other:

  • 5-10% Travel may be required

#LI-hybrid #LI-JS1

Pay Range:

$184,600 - $277,000

Disclosure Statement:

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.  From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as: 
1.    Hybrid: work remotely up to two days per week; or select
2.    On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time. 

#LI-Hybrid
 

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [email protected]

Skills Required

  • Bachelor's degree in a scientific or allied health field (or equivalent)
  • Typically requires 10 years of work experience
  • Typically requires 3 years of management experience
  • Expert knowledge of global GMP requirements and experience across multiple GxP areas
  • Experience with inspection readiness, inspection management, and compliance programs across all GMP areas including external CMOs and internal sites
  • Strong technical knowledge of GMP regulations, inspection management, risk management, and quality governance
  • Ability to evaluate quality matters and make risk-based decisions
  • Proven leadership, coaching, facilitation, communication, and influencing skills to lead cross-functional teams and drive change

Vertex Pharmaceuticals Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Vertex Pharmaceuticals and has not been reviewed or approved by Vertex Pharmaceuticals.

  • Parental & Family Support Policies provide 12 weeks of 100% paid bonding leave for all U.S. parents with additional fully paid time for birth parents. Family-forming supports include adoption and surrogacy assistance, fertility options like IVF and egg cryopreservation, breast‑milk shipping, subsidized childcare, backup care, and a DCFSA match.
  • Leave & Time Off Breadth Time off includes roughly four weeks of vacation, 13 holidays, sick time, and two companywide shutdowns (summer and year‑end). Some roles also include flexible or unlimited time off and paid volunteer time.
  • Retirement Support Programs include a 401(k) plan with employer contributions and an employee stock purchase plan. Filings describe employer contributions occurring in company stock, supporting long‑term ownership.

Vertex Pharmaceuticals Insights

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The Company
HQ: Boston, MA
5,000 Employees
Year Founded: 1989

What We Do

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases. We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases. Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development. Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

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