QC Operations Manager (Night Shift) | cGMP Leadership

Vertex Pharmaceuticals Inc (US)

United States

On-site

USD 118,000 - 177,000

Full time

9 days ago
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Benefits offered by this job

Annual bonus
Annual equity awards
Medical benefits
Dental benefits
Vision benefits
Generous paid time off
Educational assistance programs
Commuting subsidy
Matching charitable donations
401(k)

Job summary

Vertex Pharmaceuticals Inc (US) is seeking a Manager, Quality Control to oversee analytical functions across the Vertex Manufacturing Center and Leiden Center, ensuring cGMP compliance and efficient operations. The role includes formal people management and a Wednesday–Saturday 10-hour night shift from 9:00pm to 9:00am.

Responsibilities include guiding lab programs, coordinating activities to meet commitments, ensuring proper training, and approving data and SOPs.

Qualifications

  • Bachelor’s degree in science or related discipline with 8+ years in pharma/biopharma.
  • Experience in QA/QC regulatory environments and inspections helpful.
  • Strong knowledge of analytical methods and GMP expectations.

Responsibilities

  • Oversee lab programs within QC department and coordinate activities to meet deadlines.
  • Lead troubleshooting of analytical methods/equipment as needed.
  • Author/review/approve data and SOPs; monitor lab metrics and records.
  • Provide guidance to reports; coach and develop staff.
  • Act as QC representative in cross-functional teams and with external vendors.

Skills

QC management
cGMP knowledge
Analytical methods (flow cytometry)
Data review & reporting
Communication skills
Training / coaching

Education

Bachelor’s degree in science or related discipline

Job description

Vertex Pharmaceuticals Inc (US) is seeking a Manager, Quality Control to oversee analytical functions across the Vertex Manufacturing Center and Leiden Center, ensuring cGMP compliance and efficient operations. The role includes formal people management and a Wednesday–Saturday 10-hour night shift from 9:00pm to 9:00am.

Responsibilities include guiding lab programs, coordinating activities to meet commitments, ensuring proper training, and approving data and SOPs.

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