Manufacturing QA Supervisor: Lead Batch Release & Compliance

SCA Pharma; Rainbow (CT); On-site; USD 95,000 - 125,000; Full time

Job summary

SCA Pharmaceuticals is seeking a Manufacturing Quality Assurance (MQA) Supervisor to lead a team of QA Specialists responsible for batch review, release, and compliance with cGMP across manufacturing operations in Connecticut.

The role coordinates MQA activities, drives timely batch record review, and supports process improvements while ensuring quality and regulatory adherence throughout the facility.

Qualifications

• Bachelor’s degree in life sciences, engineering, or related discipline.
• 3 years of supervisory experience required.
• 5 years working experience in pharmaceutical, medical device or related industries.
• Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook).
• Thorough knowledge and understanding of cGMP.
• Experience in pharmaceutical quality unit and aseptic processing preferred.
• Demonstrated skills/abilities in conducting and documenting investigations.
• Is goal and task oriented, has strong sense of urgency.
• Some exposure to regulatory agency inspections (FDA, etc.).
• Familiarity with regulatory requirements for 503(b) sterile compound outsourcing facilities preferred.

Responsibilities

• Direct a QA Specialists team and oversee MQA activities.
• Coordinate batch record review and timely batch release.
• Support process improvements and maintain regulatory compliance.
• Train, mentor, and develop direct reports.
• Maintain communication within MQA and across the organization.

Skills

Supervisory leadership

Microsoft Office

cGMP knowledge

Investigations

Cross‑functional collaboration

Education

Bachelor’s degree in life sciences / engineering

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

SCA Pharmaceuticals is seeking a Manufacturing Quality Assurance (MQA) Supervisor to lead a team of QA Specialists responsible for batch review, release, and compliance with cGMP across manufacturing operations in Connecticut.

The role coordinates MQA activities, drives timely batch record review, and supports process improvements while ensuring quality and regulatory adherence throughout the facility.