Top 105 Director of quality Jobs in Woburn, Ma

Associate Director, Global Inspection Management
Ultragenyx Pharmaceutical —Bedford, MA
- $179,600 - $221,900 a year
- Hybrid work
- 11+ years
- Bachelor's degree
- Children
- Gym membership
5d
Senior Quality Director
Nova Biomedical —Waltham, MA
- $220,000 - $300,000 a year
- Full-time
- Hybrid work
- Ability to lift 50 pounds
- In-person
- Senior level
- Paid holidays
- Health insurance
Quick Apply
Sr. Director of Quality
Teledyne Technologies Inc. —Billerica, MA
- $188,000 - $250,700 a year
- Full-time
- Product management
- Mentoring
- Organizational skills
Director, Quality Assurance
Textron Systems —Wilmington, MA
- $165,700 - $254,900 a year
- Full-time
- 5 years
- Word processing
- Analysis skills
- Health savings account
- Disability insurance
Director of Quality Resident Services
Benchmark Senior Living —Waltham, MA
- $100,000 - $120,000 a year
- Full-time
- Nursing
- Word processing
- Computer literacy
- Paid holidays
- Health insurance
Quick Apply
Director, Quality
Electric Hydrogen —Devens, MA
- $192,270 - $226,200 a year
- Engineering
- Senior level
- Leadership
- Disability insurance
- Health insurance
Head of Quality Control
Takeda Pharmaceutical —Lexington, MA
- $177,000 - $278,080 a year
- Weekends as needed
- Bachelor's degree
- Travel
- Mentoring
- Paid holidays
- Disability insurance
5d
Quality Director
University of Massachusetts Medical School —Westborough, MA
- $130,000 - $145,000 a year
- Full-time
- Hybrid work
- 3 years
- Bachelor's degree
- Senior level
Director of Quality Assurance & Control
Eckert & Ziegler Radiopharma Inc —Wilmington, MA
- $170,000 - $200,000 a year
- Full-time
- Bachelor's degree
- In-person
- Senior level
- Paid holidays
- Disability insurance
Quick Apply
Sr. Director, Quality Assurance for Quality Control
Vaxcyte —Boston, MA
- $229,000 - $268,000 a year
- Remote
- 11+ years
- Bachelor's degree
- Senior level
6d
Director of Clinical Quality and Resident Care (RN license required)
Rogerson Communities —Boston, MA
- $135,000 - $150,000 a year
- Full-time
- Nursing
- 7 years
- RN License
Quick Apply
14d
RA/QA Director
NeuroSync Inc. —Holliston, MA
- $160,000 - $180,000 a year
- Full-time
- Master's degree
- In-person
- Senior level
- Health insurance
- Dental insurance
Quick Apply
5d
Senior Director, Quality Control
EPM Scientific —Boston, MA
- Contract
- Bachelor's degree
- Mentoring
- US work authorization
Quick Apply
6d
Director, Head of Quality Operations
Takeda Pharmaceutical —Boston, MA
- $177,000 - $278,080 a year
- Full-time
- English
- Senior level
- Business
- Paid holidays
- Disability insurance
5d
Director, Supplier Quality Engineering
Zoll Medical Corporation —Chelmsford, MA
- $190,000 - $210,000 a year
- Engineering
- Master's degree
- Mentoring
14d
Director, Clinical Quality Assurance
Oruka Therapeutics —Waltham, MA
- $213,000 - $240,000 a year
- Remote
- Nursing
- Bachelor's degree
- Travel
Senior Director, Corporate Quality – PV
Sarepta Therapeutics —Bedford, MA
- $222,400 - $278,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Project management
Director of QMS & Compliance
Enjet Aero, LLC —Malden, MA
- Full-time
- Engineering
- Analysis skills
- Travel
- Profit sharing
- Paid holidays
Quick Apply
Senior Director, Head of Clinical Program Quality & Excellence (TAU)
Takeda Pharmaceutical —Cambridge, MA
- $212,000 - $333,190 a year
- Full-time
- 11+ years
- Office
- Master's degree
- Paid holidays
- Disability insurance
Senior Director, Quality
Repligen Corporation —Waltham, MA
- $191,250 - $260,000 a year
- Full-time
- Engineering
- 11+ years
- Product management
- Dental insurance
- Flexible spending account

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Associate Director, Global Inspection Management

Ultragenyx Pharmaceutical -
Bedford, MA

Apply Now

Job Details

$179,600 - $221,900 a year
5 days ago

Benefits

Gym membership

Qualifications

Biotechnology
Drug regulation
GMP
Project management experience in manufacturing
Bachelor's degree
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Biomedical regulatory compliance
Supply chain experience within healthcare industry
Manufacturing
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

Why Join Us?

Be a hero for our rare disease patients

At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won't go – challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life-changing treatments. We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in ways that are most meaningful for them.

Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth – so employees can thrive in all areas of their lives, in and outside of work. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work.

If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team.

Position Summary:

ultracurious – Apply your biggest ideas in courageous ways

We are seeking a dynamic and experienced Associate Director of GMP Inspection Management to execute a global inspection readiness and management program. The role is accountable for the successful execution of all inspection management and readiness activities across the Ultragenyx network. This role will be responsible for ensuring consistent, proactive, and risk-based inspection readiness across internal manufacturing and testing operations, as well as external Contract Manufacturing Organizations (CMOs). The ideal candidate will bring strong expertise in GMP compliance, regulatory inspections, and cross-functional collaboration to drive a culture of continuous improvement and inspection excellence.

Work Model:

Flex: This role will typically require onsite work 2-3 days each week, or more depending on business needs. In many locations, the business will set certain days each week that Flex employees are required to be onsite.

Responsibilities:

Global Inspection Strategy & Readiness

Support the implementation of a comprehensive global GMP inspection management framework and governance

Support inspection readiness initiatives across internal and external manufacturing and testing sites

Develop and maintain inspection storyboards/playbooks, mock inspection protocols, and response templates

Monitor and report inspection management and readiness performance metrics

Inspection Execution & Management

Support regulatory GMP inspections (FDA, EMA, PMDA, etc.), including coordination, and response management as needed

Oversee inspection logistics, real-time support, and post-inspection follow-up activities

External Manufacturing Oversight

Partner with Quality, Manufacturing, and Supply Chain teams to ensure CMO sites are inspection ready

Participate in inspection readiness assessments and support CMOs during regulatory inspections

Training & Continuous Improvement

Deliver inspection training programs for SMEs and inspection teams

Analyze inspection trends and regulatory intelligence to inform risk mitigation strategies

Drive continuous improvement in inspection readiness processes and tools.

Leadership & Collaboration

Participate in cross-functional inspection readiness teams and governance forums.

Collaborate with Global Quality, Regulatory Affairs, and Compliance teams to align on inspection strategy.

Requirements:

Bachelor's degree in Life Sciences or related field

12+ years of experience in GMP compliance, quality assurance, or regulatory affairs within the biopharmaceutical industry

Proven track record of leading global regulatory inspections and readiness programs

Strong knowledge of global GMP regulations and inspection practices

Experience with both internal operations and external manufacturing oversight

Excellent communication and project management skills

Ability to influence across levels and functions in a matrixed organization

Experience with biologics or gene therapy manufacturing

Prior experience working with global CMOs and managing complex supply chains

Familiarity with digital tools for inspection management and quality systems

Up to 25% travel may be required (Domestic and International)

#LI-KJ1 #LI-Hybrid

Full Time employees across the globe enjoy a range of benefits, including, but not limited to:

Generous vacation time and public holidays observed by the company

Volunteer days

Long term incentive and Employee stock purchase plans or equivalent offerings

Employee wellbeing benefits

Fitness reimbursement

Tuition sponsoring

Professional development plans

Benefits vary by region and country

Ultragenyx Pharmaceutical is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at [email protected].

See our CCPA Employee and Applicant Privacy Notice.

See our Privacy Policy.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Note to External Recruiters: All candidate activity and open positions are managed strictly through our Human Resources Department. Our Human Resources Department kindly requests that recruiters not contact employees/hiring managers directly in an attempt to solicit business and present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organization. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation. Inquiries on developing a recruiting relationship with us, may be directed to: [email protected].

Apply Now

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director of quality jobs in woburn, ma

Associate Director, Global Inspection Management

Senior Quality Director

Sr. Director of Quality

Director, Quality Assurance

Director of Quality Resident Services

Director, Quality

Head of Quality Control

Quality Director

Director of Quality Assurance & Control

Sr. Director, Quality Assurance for Quality Control

Director of Clinical Quality and Resident Care (RN license required)

RA/QA Director

Senior Director, Quality Control

Director, Head of Quality Operations

Director, Supplier Quality Engineering

Director, Clinical Quality Assurance

Senior Director, Corporate Quality – PV

Director of QMS & Compliance

Senior Director, Head of Clinical Program Quality & Excellence (TAU)

Senior Director, Quality

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