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Manager, Operational Quality - VCGT

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Vertex Pharmaceuticals LLC
Contract position
Listed on 2026-10-30
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Data Analyst
Salary/Wage Range or Industry Benchmark: 65 - 75 USD Hourly USD 65.00 75.00 HOUR
Job Description & How to Apply Below
Job Description

The Operational Quality Manager provides QA oversight for GMP manufacturing and testing operations. The role reviews batch records, deviations, in-process and environmental monitoring data, QC release and stability testing, and related quality documentation to support product disposition.

Key Responsibilities
  • Review master batch records and approve quality tasks for manufactured products.
  • Review in-process, environmental monitoring, and QC data, including certificates of analysis, and provide required quality approvals.
  • Perform final review of executed batch records and critical systems documentation, including certificates of analysis and conformance, in accordance with procedures.
  • Confirm all required documentation is complete and acceptable before product or system release.
  • Support investigations, deviations, and change controls within manufacturing operations.
  • Support day-to-day management of the batch release process.
  • Communicate proactively with internal and external partners and management.
  • Maintain and archive records so documents are readily available and retrievable.
  • Prepare metrics and data for program reporting.
  • Escalate critical and major findings to Quality management.
  • Collaborate with external vendors to review GMP documentation supporting product disposition.
Qualifications
  • Bachelor’s degree in a scientific or allied health field and 5–7 years of relevant experience, or an equivalent combination of education and experience.
  • Knowledge of current Good Manufacturing Practices (cGMP) in a pharmaceutical environment.
  • Experience providing QA oversight for GMP manufacturing and testing operations.
  • Experience reviewing GMP documentation from external vendors.
  • Experience leading investigations, deviations, and change controls.
  • Experience with systems such as Veeva, LIMS and Oracle.
  • Strong attention to detail and effective written and verbal communication skills.
  • Ability to manage competing priorities and timelines in a fast-paced environment.

Contract Length: 12 months

Pay Range

$65/hr.

-$75/hr.

Shift/Hours

Monday–Friday, onsite.

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

No C2C or Third-Party Vendors

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