QA Operations Supervisor

About the role

We are seeking a Quality Assurance Operations Supervisor to lead Quality oversight activities and foster an empowered culture of quality across manufacturing processes supporting biologics production, including cell culture, fermentation, harvest, purification, and bulk drug substance. This role provides direct supervision of quality personnel, serves as a primary point of contact for on-the-floor escalations, supports quality records and document review and approvals, and partners with cross-functional teams to achieve production objectives.

Responsibilities

• Lead hands-on QA collaboration and oversight to staff, ensuring compliance with good documentation practices (GDP), data integrity compliance, site inspection readiness SOPs, and relevant Good Regulated Practice (GxP) requirements.
• Supervise work on the floor during production and assess decisions to ensure compliance with manufacturing procedures and regulations when departures occur.
• Lead batch record review on the floor at time of execution for buffer/media/upstream and downstream manufacturing batch records.
• Lead disposition of buffer/media solutions manufactured at Abzena.
• Supervise performance of regular area walkthroughs of the manufacturing, warehouse, and Quality Control areas.
• Author/Approve minor and major manufacturing deviations and perform thorough root cause analysis to drive remediation efforts and process improvements.
• Review and approve manufacturing deviations (minor/major), risk assessments, CAPAs, change controls, and Standard Operating Procedures (SOPs).
• Review and approve master buffer/media/process batch records and client batch records.
• Support client and internal audits as required.
• Support other departments to fulfill business needs.
• Comply with Abzena's policies and procedures.
• Communicate effectively with clients, colleagues, and staff.
• Adhere to quality standards set by regulations and Abzena policies, procedures, and mission.

Team Leadership & Development

• Supervise, coach, mentor, and develop quality assurance associates.
• Conduct performance evaluations and establish development plans for team members.
• Facilitate onboarding and qualification of new employees.
• Promote a culture of safety, teamwork, accountability, and continuous improvement.
• Lead daily shift meetings and attend daily tier meetings as required.

Safety & Operational Excellence

• Champion Environmental Health and Safety (EHS) compliance.
• Ensure safe handling of biological materials, chemicals, and manufacturing equipment.
• Lead risk assessments and support implementation of corrective actions.
• Drive Lean Manufacturing and continuous improvement initiatives.
• Monitor and improve key performance indicators (KPIs) including safety, right-first-time execution, batch success rate, and schedule adherence.

Cross-Functional Collaboration

• Partner with Manufacturing, Quality Control, Validation, Facilities, Engineering, Supply Chain, and Program Management teams.
• Support customer visits and client-facing manufacturing discussions as required.

Requirements

• Bachelor’s degree in Life Sciences or related scientific discipline.
• Minimum of 4 years of experience in biopharmaceutical manufacturing within a GMP-regulated environment.
• Minimum of 3 years of experience in a Quality Assurance related function.
• Minimum of 2 years of leadership or supervisory experience.
• Hands-on experience with biologics operations in either a Quality or Production role.

Qualifications (Preferred)

• Experience in CDMO manufacturing environments.
• Lean Six Sigma certification or continuous improvement experience.
• Knowledge of monoclonal antibody and recombinant protein manufacturing processes.

Pay

$100,000 - $120,000 a year