Summary The 'Manager, Quality Assurance Operations' role is responsible for providing end-to-end quality oversight of Contract Manufacturing Organizations (CMOs) to ensure compliance with cGMP ...
Summary The 'Manager, Quality Assurance Operations' role is responsible for providing end-to-end quality oversight of Contract Manufacturing Organizations (CMOs) to ensure compliance with cGMP ...
Summary The 'Manager, Quality Assurance Operations' role is responsible for providing end-to-end quality oversight of Contract Manufacturing Organizations (CMOs) to ensure compliance with cGMP ...
Summary The 'Manager, Quality Assurance Operations' role is responsible for providing end-to-end quality oversight of Contract Manufacturing Organizations (CMOs) to ensure compliance with cGMP ...
Manager - Quality Assurance (QA), Operations Position Summary: * Work Schedule: Monday - Friday, core hours 8am-5pm * 100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract ...
Manager - Quality Assurance (QA), Operations Position Summary: * Work Schedule: Monday - Friday, core hours 8am-5pm * 100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract ...
Manager, QA Operations
Jupiter, FL · On-site
The Manager, QA Operations is responsible for the implementation of policies and procedures to ensure adherence to production quality standards and oversight of the Company's electronic ISO 13485 ...
Manager, QA Operations
Jupiter, FL · On-site
The Manager, QA Operations is responsible for the implementation of policies and procedures to ensure adherence to production quality standards and oversight of the Company's electronic ISO 13485 ...
QA Operations Sr. Manager
Raleigh, NC · On-site
The QA Operations Sr. Manager provides quality leadership and oversight across site operations, including materials, manufacturing, warehouse activities, quality interfaces, and product release. This ...
QA Operations Sr. Manager
Raleigh, NC · On-site
The QA Operations Sr. Manager provides quality leadership and oversight across site operations, including materials, manufacturing, warehouse activities, quality interfaces, and product release. This ...
Director, Quality Assurance Operations Adicet Bio is seeking an experienced and motivated Director ... Collaborates with cross functional teams and champions the Quality Risk Management Program.
Director, Quality Assurance Operations Adicet Bio is seeking an experienced and motivated Director ... Collaborates with cross functional teams and champions the Quality Risk Management Program.
Quality Inspection Operations (30%) Oversees source inspector and quality assurance operations ... Directly supervises team members, including scheduling, task assignment, and performance management
Quality Inspection Operations (30%) Oversees source inspector and quality assurance operations ... Directly supervises team members, including scheduling, task assignment, and performance management
The Associate Manager, Quality Assurance Operations will provide quality oversight of external manufacturing partners to ensure compliance with cGMP requirements, regulatory commitments, and Genetix ...
The Associate Manager, Quality Assurance Operations will provide quality oversight of external manufacturing partners to ensure compliance with cGMP requirements, regulatory commitments, and Genetix ...
QA Operations Associate
Plantation, FL · On-site
The QA Operations Associate is a hands-on, on-the-floor Quality Assurance professional responsible for ensuring GMP compliance during manufacturing operations while exercising independent quality ...
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QA Operations Associate
Plantation, FL · On-site
The QA Operations Associate is a hands-on, on-the-floor Quality Assurance professional responsible for ensuring GMP compliance during manufacturing operations while exercising independent quality ...
The Executive Director builds and leads the GMP QA operations organization, sets quality policy and ... Strong knowledge of batch disposition, deviation/CAPA management, change control, and annual ...
The Executive Director builds and leads the GMP QA operations organization, sets quality policy and ... Strong knowledge of batch disposition, deviation/CAPA management, change control, and annual ...
Executive Director, GMP Quality Assurance
San Diego, CA · On-site
$270K - $290K/yr
The Executive Director builds and leads the GMP QA operations organization, sets quality policy and ... Strong knowledge of batch disposition, deviation/CAPA management, change control, and annual ...
Executive Director, GMP Quality Assurance
San Diego, CA · On-site
$270K - $290K/yr
The Executive Director builds and leads the GMP QA operations organization, sets quality policy and ... Strong knowledge of batch disposition, deviation/CAPA management, change control, and annual ...
QA Operations Supervisor
San Diego, CA · On-site
$100K - $120K/yr
The Quality Assurance Operations Supervisor is responsible for leading Quality oversight activities ... The supervisor serves as a key operational leader, managing shift resources, supporting technology ...
QA Operations Supervisor
San Diego, CA · On-site
$100K - $120K/yr
The Quality Assurance Operations Supervisor is responsible for leading Quality oversight activities ... The supervisor serves as a key operational leader, managing shift resources, supporting technology ...
Director, QA Operations
Raritan, NJ · On-site
Manage the daily quality activities for the quality operations team to ensure facility, process ... assurance, manufacturing compliance, clinical quality, or cell therapy. * Knowledge of cGMP ...
Director, QA Operations
Raritan, NJ · On-site
Manage the daily quality activities for the quality operations team to ensure facility, process ... assurance, manufacturing compliance, clinical quality, or cell therapy. * Knowledge of cGMP ...
Director, QA Operations
Raritan, NJ · On-site
Manage the daily quality activities for the quality operations team to ensure facility, process ... assurance, manufacturing compliance, clinical quality, or cell therapy. * Knowledge of cGMP ...
New
Director, QA Operations
Raritan, NJ · On-site
Manage the daily quality activities for the quality operations team to ensure facility, process ... assurance, manufacturing compliance, clinical quality, or cell therapy. * Knowledge of cGMP ...
New
The Senior Manager, Operations QA is a key role in the Quality Assurance team at the RayzeBio Indianapolis manufacturing site This is a people manager position with supervisory responsibilities for ...
The Senior Manager, Operations QA is a key role in the Quality Assurance team at the RayzeBio Indianapolis manufacturing site This is a people manager position with supervisory responsibilities for ...
The Senior Manager, Operations QA is a key role in the Quality Assurance team at the RayzeBio Indianapolis manufacturing site. This is a people manager position with supervisory responsibilities for ...
The Senior Manager, Operations QA is a key role in the Quality Assurance team at the RayzeBio Indianapolis manufacturing site. This is a people manager position with supervisory responsibilities for ...
Director QA Operations
Rensselaer, NY · On-site
... Assurance to provide the quality support and oversight for drug substance manufacturing operations ... Builds and maintains a high performing team of managers, providing effective alignment and ...
Director QA Operations
Rensselaer, NY · On-site
... Assurance to provide the quality support and oversight for drug substance manufacturing operations ... Builds and maintains a high performing team of managers, providing effective alignment and ...
Specialist I, QA Operations
Columbus, OH · On-site
We are currently seeking a Specialist I, QA Operations (AAV Manufacturing) to join the Forge ... Experience utilizing an eQMS, preferably Veeva Vault or another document management system.
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Specialist I, QA Operations
Columbus, OH · On-site
We are currently seeking a Specialist I, QA Operations (AAV Manufacturing) to join the Forge ... Experience utilizing an eQMS, preferably Veeva Vault or another document management system.
Senior Manager QA Operations Responsible For (Staff): Yes The Supervisor, QA Internal Operations is responsible for leading a team of QA Operations Associates responsible for on-the- floor support ...
Senior Manager QA Operations Responsible For (Staff): Yes The Supervisor, QA Internal Operations is responsible for leading a team of QA Operations Associates responsible for on-the- floor support ...
QA Operations Specialist II
San Diego, CA · On-site
$60K - $70K/yr
... as a QA Operations Specialist II. The QA Operations Specialist II is responsible for the ... Includes the review and approval of deviations, NCRs, CAPAs, supplier management, change controls ...
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QA Operations Specialist II
San Diego, CA · On-site
$60K - $70K/yr
... as a QA Operations Specialist II. The QA Operations Specialist II is responsible for the ... Includes the review and approval of deviations, NCRs, CAPAs, supplier management, change controls ...
Executive Quality Assurance Operations Manager information
See salary details
$38K - $50.8K
3% of jobs
$50.8K - $63.6K
6% of jobs
$63.6K - $76.5K
11% of jobs
$82K is the 25th percentile. Wages below this are outliers.
$76.5K - $89.3K
12% of jobs
$89.3K - $102.1K
11% of jobs
The median wage is $114.1K / yr.
$102.1K - $114.9K
8% of jobs
$114.9K - $127.7K
4% of jobs
$137.2K is the 75th percentile. Wages above this are outliers.
$127.7K - $140.5K
27% of jobs
$140.5K - $153.4K
1% of jobs
$153.4K - $166.2K
1% of jobs
$166.2K - $179K
16% of jobs
$38K
$118.1K
$179K
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Manager, Quality Assurance Operations
Somerville, MA • Hybrid
Full-time
Re-posted 14 days ago
Key responsibilities
Provide on-call QA support for manufacturing operations, ensuring proactive identification, escalation, and mitigation of quality events and risks.
Review and approve internal and external CMO Deviations and Change Controls, and serve as QA point-of-contact for Product Complaints.
Monitor CMO quality performance metrics, identify trends, and drive continuous improvement initiatives.
Job description
Summary
The 'Manager, Quality Assurance Operations' role is responsible for providing end-to-end quality oversight of Contract Manufacturing Organizations (CMOs) to ensure compliance with cGMP regulations, regulatory commitments, and Genetix quality standards. This role serves as a key quality partner to Manufacturing, MS&T, Quality Control, and Patient Supply. The role is expected to serve as a CMO Lead point-of-contact and primary quality interface with external partners, driving proactive risk management, and Deviation and Change Control lifecycle management. The position ensures effective quality oversight through structured governance forums, review and approval of quality systems, and continuous monitoring of performance metrics.
This is a full-time hybrid position (3 days a week) in our Somerville - Assembly Row, Massachusetts office.
Responsibilities
Provide on-call QA support for manufacturing operations, ensuring proactive identification, escalation, and mitigation of quality events and risks impacting ongoing manufacturing and product disposition
Maintain a consistent and effective external oversight model, including leading QA-to-QA forums and guiding quality discussions in joint governance meetings with CMOs.
Lead regular internal Deviation/Lab Investigation Management meetings, ensuring compliance, quality, and timeliness.
Review and Approve internal and external CMO Deviations and Change Controls
Serve as QA point-of-contact for Product Complaints, ensuring appropriate investigation, documentation, and closure.
Perform Quality Impact Assessments for Change Controls, ensuring appropriate risk evaluation and mitigation.
Represent Quality Assurance Operations in Manufacturing Tier meetings, ensuring alignment on quality risks, priorities, and escalation pathways.
Represent Quality Assurance Operations in Change Control Review Board (CCRB) meetings.
Serve as QA reviewer and approver for: process validation protocols and reports, technical reports and supporting documentation, and internal and external validation deliverables
Monitor CMO quality performance metrics, identify trends, and drive continuous improvement initiatives.
Own and manage CMO Quality Agreements, including authoring, reviewing, negotiating, and maintaining compliance with current regulatory expectations.
Author and review Annual Product Quality Reviews (APQRs) to ensure comprehensive evaluation of product and process performance.
Identify trends, risks, and opportunities for improvement across the product lifecycle.
Required Education, Experience, or Qualifications (or equivalent)
Education & Experience
Bachelor's degree in Life Sciences, Engineering, or related discipline (advanced degree preferred)
7+ years of experience in Quality Assurance within GMP-regulated biopharmaceutical or cell/gene therapy manufacturing
Strong experience supporting CMO oversight and external manufacturing environments
Technical Skills
Deep knowledge of: cGMP regulations (FDA, EMA, ICH guidelines), Deviation, CAPA, and investigation processes, Change Control systems and validation lifecycle
Knowledge of lentiviral vector process preferred
Knowledge of process validation preferred
Strong understanding of cell/gene therapy manufacturing or biologics
Leadership & Competencies
- Demonstrated ability to lead cross-functional quality governance forums
- Strong risk-based decision-making and escalation capabilities
- Excellent communication, stakeholder management, and influential skills in internal and external settings
- Ability to operate effectively in a fast-paced, matrixed CMO environment
- High attention to detail with an inspection-ready mindset
Key Success Factors
Proactive risk identification and escalation during manufacturing operations
Timely closure and high-quality management of deviations and investigations
Strong, compliant oversight of CMO operations and quality systems
Effective cross-functional collaboration and governance leadership
Continuous improvement of quality systems and performance metrics