Pharma MQA Supervisor: Lead Quality & Batch Release

SCA Pharma

Windsor (CT)

On-site

USD 90,000 - 130,000

Full time

4 days ago
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Job summary

SCA Pharmaceuticals is seeking a Manufacturing Quality Assurance (MQA) Supervisor to lead a team of QA Specialists responsible for oversight of compounding, inspection, labeling and testing activities on site in Windsor, CT. The role focuses on timely batch review, release, and continuous improvement of MQA processes, with emphasis on cGMP compliance and regulatory readiness.

The ideal candidate will have a Bachelor’s degree in a life sciences or engineering field, at least 3 years of

Qualifications

  • Bachelor's degree in life sciences, engineering, or related discipline.
  • 3 years of supervisory experience.
  • 5 years working experience in pharmaceutical, medical device or other related industries.

Responsibilities

  • Direct a team of QA Specialists in Manufacturing Quality Assurance.
  • Coordinate batch review and release activities and issue resolution.
  • Support process-improvement and insure regulatory compliance.
  • Maintain a strong communication network within the MQA team and across the organization.
  • Train, mentor, and develop direct reports.
  • Perform final QA review of validation protocols, investigations, change controls, CAPAs and SOPs.
  • Proactively identify change opportunities and drive efficient batch release.
  • Track batch record corrections, report metrics, and reduce errors to improve right-first-time release.

Skills

Cross-functional
Investigations
Urgency
Regulatory exposure

Education

Bachelor's degree in life sciences/engineering

Tools

Microsoft Office

Job description

SCA Pharmaceuticals is seeking a Manufacturing Quality Assurance (MQA) Supervisor to lead a team of QA Specialists responsible for oversight of compounding, inspection, labeling and testing activities on site in Windsor, CT. The role focuses on timely batch review, release, and continuous improvement of MQA processes, with emphasis on cGMP compliance and regulatory readiness.

The ideal candidate will have a Bachelor’s degree in a life sciences or engineering field, at least 3 years of

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