PhD in life sciences, engineering or related discipline and a minimum of 17 years of relevant ... Comprehensive knowledge of global GMP regulations and Quality systems * Advanced leadership ...
PhD in life sciences, engineering or related discipline and a minimum of 17 years of relevant ... Comprehensive knowledge of global GMP regulations and Quality systems * Advanced leadership ...
Director, GMP Quality
Somerville, MA · On-site
Director, Gmp Quality Generate:Biomedicines is a new kind of therapeutics company existing at the ... engineering, and medicine pioneering Generative Biology to create breakthrough medicines where ...
Director, GMP Quality
Somerville, MA · On-site
Director, Gmp Quality Generate:Biomedicines is a new kind of therapeutics company existing at the ... engineering, and medicine pioneering Generative Biology to create breakthrough medicines where ...
PhD in life sciences, engineering or related discipline and a minimum of 17 years of relevant ... Comprehensive knowledge of global GMP regulations and Quality systems * Advanced leadership ...
PhD in life sciences, engineering or related discipline and a minimum of 17 years of relevant ... Comprehensive knowledge of global GMP regulations and Quality systems * Advanced leadership ...
PhD in life sciences, engineering or related discipline and a minimum of 17 years of relevant ... Comprehensive knowledge of global GMP regulations and Quality systems * Advanced leadership ...
PhD in life sciences, engineering or related discipline and a minimum of 17 years of relevant ... Comprehensive knowledge of global GMP regulations and Quality systems * Advanced leadership ...
Provide GMP QA oversight for manufacturing operations, validation, analytical laboratories, and engineering activities. * Review and support Change Controls, Validation Protocols, Risk Assessments ...
Quick apply
Provide GMP QA oversight for manufacturing operations, validation, analytical laboratories, and engineering activities. * Review and support Change Controls, Validation Protocols, Risk Assessments ...
Vice President, Quality Assurance - GMP
Alameda, CA · On-site
$250/hr
... engineering or related discipline and a minimum of 21 years of relevant experience; or, MS/MA ... Comprehensive knowledge of global GMP regulations and Quality systems Advanced leadership ...
Vice President, Quality Assurance - GMP
Alameda, CA · On-site
$250/hr
... engineering or related discipline and a minimum of 21 years of relevant experience; or, MS/MA ... Comprehensive knowledge of global GMP regulations and Quality systems Advanced leadership ...
The Executive Director, GMP Quality Assurance leads Artiva Biotherapeutics' internal GMP quality ... Bachelor's degree in life sciences, chemistry, engineering, or a related field required; advanced ...
The Executive Director, GMP Quality Assurance leads Artiva Biotherapeutics' internal GMP quality ... Bachelor's degree in life sciences, chemistry, engineering, or a related field required; advanced ...
Associate Director, GMP Quality
$161K - $202K/yr
Bachelor's degree in scientific discipline (e.g., Chemistry, Biology, Engineering, Pharmaceutical Sciences) * Minimum of 10 years' experience in pharmaceutical GMP Quality Assurance, with specific ...
Associate Director, GMP Quality
$161K - $202K/yr
Bachelor's degree in scientific discipline (e.g., Chemistry, Biology, Engineering, Pharmaceutical Sciences) * Minimum of 10 years' experience in pharmaceutical GMP Quality Assurance, with specific ...
Executive Director, GMP Quality Assurance
San Diego, CA · On-site
$270K - $290K/yr
The Executive Director, GMP Quality Assurance leads Artiva Biotherapeutics' internal GMP quality ... Bachelor's degree in life sciences, chemistry, engineering, or a related field required; advanced ...
Executive Director, GMP Quality Assurance
San Diego, CA · On-site
$270K - $290K/yr
The Executive Director, GMP Quality Assurance leads Artiva Biotherapeutics' internal GMP quality ... Bachelor's degree in life sciences, chemistry, engineering, or a related field required; advanced ...
Executive Director, GMP Quality Assurance
San Diego, CA · On-site
$250/hr
This role owns the quality systems governing internal GMP manufacturing, batch disposition ... Bachelor's degree in life sciences, chemistry, engineering, or a related field required; advanced ...
Executive Director, GMP Quality Assurance
San Diego, CA · On-site
$250/hr
This role owns the quality systems governing internal GMP manufacturing, batch disposition ... Bachelor's degree in life sciences, chemistry, engineering, or a related field required; advanced ...
The Office of Regulatory Affairs & Quality (ORAQ) is looking for a GMP, Quality Assurance Associate ... You will work with a wide range of partners across manufacturing, engineering, validation, and ...
The Office of Regulatory Affairs & Quality (ORAQ) is looking for a GMP, Quality Assurance Associate ... You will work with a wide range of partners across manufacturing, engineering, validation, and ...
Sr Supplier Qual Engineer
Grand Rapids, MI · On-site
Ensure suppliers meet GMP, quality system, and regulatory requirements. * Support supplier ... Collaborate with Engineering, Operations, Quality, and suppliers. * Develop supplier audit ...
Quick apply
Sr Supplier Qual Engineer
Grand Rapids, MI · On-site
Ensure suppliers meet GMP, quality system, and regulatory requirements. * Support supplier ... Collaborate with Engineering, Operations, Quality, and suppliers. * Develop supplier audit ...
The Office of Regulatory Affairs & Quality (ORAQ) is looking for a GMP, Quality Assurance Associate ... You will work with a wide range of partners across manufacturing, engineering, validation, and ...
The Office of Regulatory Affairs & Quality (ORAQ) is looking for a GMP, Quality Assurance Associate ... You will work with a wide range of partners across manufacturing, engineering, validation, and ...
Quality Engineer - GMP Operations
Frederick, MD · On-site
$60 - $80/hr
Quality Engineer - GMP Operations Frederick, United States | Posted on 06/26/2026 Our client, a worldleader in biotechnology and gene therapy, is looking for a "Quality Engineer - GMP Operations ...
Quality Engineer - GMP Operations
Frederick, MD · On-site
$60 - $80/hr
Quality Engineer - GMP Operations Frederick, United States | Posted on 06/26/2026 Our client, a worldleader in biotechnology and gene therapy, is looking for a "Quality Engineer - GMP Operations ...
Remote GMP Quality Mgr
Atlanta, GA · Remote
Remote GMP Quality Mgr needs 8+ years of experience required, with relevant experience in biotech ... Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering, pharmacy) or ...
Quick apply
Remote GMP Quality Mgr
Atlanta, GA · Remote
Remote GMP Quality Mgr needs 8+ years of experience required, with relevant experience in biotech ... Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering, pharmacy) or ...
Associate Director, GMP Quality
Boston, MA · On-site
$161K - $202K/yr
Bachelor's degree in scientific discipline (e.g., Chemistry, Biology, Engineering, Pharmaceutical Sciences) * Minimum of 10 years' experience in pharmaceutical GMP Quality Assurance, with specific ...
Associate Director, GMP Quality
Boston, MA · On-site
$161K - $202K/yr
Bachelor's degree in scientific discipline (e.g., Chemistry, Biology, Engineering, Pharmaceutical Sciences) * Minimum of 10 years' experience in pharmaceutical GMP Quality Assurance, with specific ...
6437 - Senior Quality Engineer / Senior Quality GxP Auditor
Boston, MA · On-site
$96K - $130K/yr
Senior Quality Engineer Responsibilities ... Quality Oversight & GMP Operations * Provide Quality Assurance oversight for GMP manufacturing ...
6437 - Senior Quality Engineer / Senior Quality GxP Auditor
Boston, MA · On-site
$96K - $130K/yr
Senior Quality Engineer Responsibilities ... Quality Oversight & GMP Operations * Provide Quality Assurance oversight for GMP manufacturing ...
Quality Engineer III
Saint Louis, MO · On-site
$70K - $90K/yr
As a Quality Engineer III within the Product Quality organization, you will play a key role in ... Review and approve GMP documentation, including batch records, deviations, change controls, CAPAs ...
Quality Engineer III
Saint Louis, MO · On-site
$70K - $90K/yr
As a Quality Engineer III within the Product Quality organization, you will play a key role in ... Review and approve GMP documentation, including batch records, deviations, change controls, CAPAs ...
Quality Engineer III
$67K - $87K/yr
As a Quality Engineer III within the Product Quality organization, you will play a key role in ... Review and approve GMP documentation, including batch records, deviations, change controls, CAPAs ...
Quality Engineer III
$67K - $87K/yr
As a Quality Engineer III within the Product Quality organization, you will play a key role in ... Review and approve GMP documentation, including batch records, deviations, change controls, CAPAs ...
Senior Manager, GMP QA Operations
Waltham, MA · On-site
The Senior Manager, GMP QA Operations oversees quality activities associated with contract ... Bachelor's degree in Engineering, Science, or relevant discipline; or Master's Degree preferred ...
Senior Manager, GMP QA Operations
Waltham, MA · On-site
The Senior Manager, GMP QA Operations oversees quality activities associated with contract ... Bachelor's degree in Engineering, Science, or relevant discipline; or Master's Degree preferred ...
Gmp Quality Engineer information
See salary details
$45K - $51.7K
1% of jobs
$51.7K - $58.5K
3% of jobs
$58.5K - $65.2K
7% of jobs
$65.2K - $71.9K
13% of jobs
$72.2K is the 25th percentile. Wages below this are outliers.
$71.9K - $78.6K
18% of jobs
The median wage is $81.4K / yr.
$78.6K - $85.4K
19% of jobs
$90.9K is the 75th percentile. Wages above this are outliers.
$85.4K - $92.1K
17% of jobs
$92.1K - $98.8K
9% of jobs
$98.8K - $105.5K
6% of jobs
$105.5K - $112.3K
4% of jobs
$112.3K - $119K
2% of jobs
$45K
$84K
$119K
How much do gmp quality engineer jobs pay per year?
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For Gmp Quality Engineer jobs, the most frequently searched job titles are:
Vice President, Quality Assurance - GMP
Alameda, CA
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 8 days ago
Job description
SUMMARY/JOB PURPOSE
The Vice President, Quality Assurance - GMP is accountable for leading the enterprise GMP Quality Assurance strategy and ensuring GMP QA activities are aligned with the enterprise Quality system across clinical and commercial operations.
This role serves as the final decision authority for product disposition while ensuring compliance with global regulatory requirements.
As a member of the PSC leadership team, the Vice President, Quality Assurance - GMP partners with clinical and commercial manufacturing, supply chain, logistics, third-party contractors, GCP QA and Quality Systems to ensure GMP requirements are supported, governed and escalated effectively.
ESSENTIAL DUTIES/RESPONSIBILITIES
Lead and oversee the GMP Quality Assurance department
Drive compliant execution across all GMP QA responsibilities in alignment with the enterprise GMP Quality Assurance strategy
Lead organizational readiness for GMP inspections at Exelixis and third-party vendors, including regulatory inspections by the FDA and other agencies and audits or inspections by collaboration partners
Lead Quality input into GMP quality agreements to ensure they support operational needs, compliance expectations and appropriate Quality oversight
Oversee final review and disposition of clinical and commercial materials and products in compliance with global regulatory standards to ensure reliability, quality, efficacy and compliance
Lead GMP Operations QA, Labeling QA, Audit and Inspection Readiness and associated Quality functions to ensure QA GMP operates at the highest standards
Partner with the Head of Quality Systems to ensure GMP QA requirements are reflected in Quality systems, governance processes, and continuous improvement activities
Oversee labeling governance for clinical and commercial products to support regulatory compliance and consistency
Partner with PSC functions to establish effective GMP supplier quality and vendor audit programs
Ensure independent Quality oversight of manufacturing, testing, distribution and external partners
Ensure effective execution of investigations, root cause analysis, risk assessments, change controls and CAPAs at Exelixis and third-party contractors
Ensure performance metrics for GMP QA are established, appropriate and regularly assessed
Identify, evaluate and escalate product quality risks to senior leadership
Represent GMP Quality in cross-functional governance forums and regulatory interactions
Lead and develop organizational capability, including talent strategy and succession planning
Performs other duties as assigned
Complies with all policies and standards
SUPERVISORY RESPONSIBILITIES
Provide executive leadership for GMP Quality Assurance, including GMP Operations QA, audit, inspection readiness and associated Quality functions
Develop organizational structure, recruit talent and manage performance of direct and indirect reports
Set organizational priorities and align resources to meet business objectives
Partner across functions to achieve organizational goals and ensure compliance
Serve on the enterprise Quality leadership team. providing independent oversight, cross-functional governance, and escalation of Quality-related risks and decisions in partnership with GCP/GVP QA and Quality Systems and Process functions
EDUCATION/EXPERIENCE/KNOWLEDGE/SKILLS & ABILITIES
Education
BS/BA degree in life sciences, engineering or related discipline and a minimum of 21 years of relevant experience; or,
MS/MA degree in life sciences, engineering or related discipline and a minimum of 19 years of relevant experience; or,
PhD in life sciences, engineering or related discipline and a minimum of 17 years of relevant experience; or,
Equivalent combination of education and experience
Advanced degree preferred
Experience
Extensive experience in biotechnology, pharmaceutical or regulated industry
Significant leadership experience in GMP Quality Assurance
Experience with regulatory inspections and global GMP audit programs
Experience overseeing external manufacturing and supply networks
Experience leading Quality organizations through commercialization, expansion or organizational change preferred
Knowledge, Skills and Abilities
Required:
Comprehensive knowledge of global GMP regulations and Quality systems
Advanced leadership, analytical and problem-solving skills
Strong executive communication skills with the ability to translate technical concepts for diverse audiences
Ability to work with ambiguity and make risk-based decisions
Ability to align Quality strategies across functions and GxP domains
Demonstrated ability to lead organizational transformation and change
Experience interacting with global regulatory agencies and executive governance bodies
Ability to influence enterprise strategy and organizational decision-making
#LI-HG1
Our compensation reflects the cost of labor across severalU.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this positionis $315,500 - $366,500 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.If you have a disability and need an accommodation in relation to the recruiting process, please email us at: ApplicantAccommodations@exelixis.com.
WORKING CONDITIONS:
Our office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.
DISCLAIMER:
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.
About Exelixis
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
501 - 1,000 Employees
Headquarters location
Alameda, CA, US
Year founded
1994