GMP Operational Quality Manager (Contract) 151515

This position reports directly to the GMP Operational Quality Senior Manager.

Key Responsibilities:

• Collaborate with internal and external business partners to resolve quality issues to ensure compliant solutions.
• Provide QA support of change controls, investigations, CAPA’s, and effectiveness checks.
• Draft, review, and manage approval of quality system documentation, including but not limited to, deviations, change controls, and CAPA’s.
• Lead meetings, as necessary, and collaborate with customer groups to ensure quality systems are monitored and established metrics are met.
• Perform Batch Record Review of Health Donar and Drug Product lots
• Perform Lot Disposition of Critical Components and Drug Product lots
• Perform archival activities to support lot disposition
• Partner with External CDMOs
• Act as subject matter expert in quality related improvement activities
• Perform change control assessments and closure approvals.
• Collect data and report on metrics
• Represent Vertex Quality on cross functional working teams, applying strong communication and collaboration skills.
• Participate in continuous improvement projects, identify risks and communicate gaps for process/systems to ensure the team continues to meet expanding business needs.
• Draft, review, and manage approval SOP’s, Job Aids, and Work Instructions to support quality functions.
• Support regulatory agency inspections including inspection readiness activities and supporting regulatory and internal site inpections.
• Manage day-to-day activities for a Quality Assurance Associate(s)/Specialist(s), as applicable.

Minimum qualifications:

• Bachelor’s degree in Life Sciences, Engineering, Pharmacy, Chemistry, or a related discipline.
• Relevant experience in Quality Assurance, Quality Operations, or a related GMP-regulated function within biotechnology, pharmaceuticals, or advanced therapies.
• Demonstrated experience supporting GMP operations in a manufacturing or operational quality environment.
• Strong understanding of quality systems, including deviations, CAPA, change control, investigations, and document management.
• Knowledge of applicable regulatory requirements and industry expectations for GMP environments.
• Experience working cross-functionally and influencing teams in a complex operational setting.
• Strong problem-solving, communication, and organizational skills.
• Ability to manage multiple priorities and make sound quality decisions in a fast-paced environment.

Technical Skills Required:

• GMP / cGMP compliance
• Quality systems management

Pay Range:

Requisition Disclaimer:

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at [email protected]. Please include the job title in the subject of your email.