Quality Supervisor (Pharmaceutical Manufacturing)

Codis; Seymour (CT); On-site; USD 90,000 - 115,000; Full time

Job summary

Codis in Seymour, Indiana is seeking an experienced Quality Supervisor to lead our Quality team on the manufacturing floor, develop staff, solve problems, and ensure products consistently meet regulatory, customer, and company requirements.

The role provides day-to-day oversight of batch review and release, inspections, laboratory activities, document control, CAPA, change control, and investigations, while partnering with Manufacturing and other functions to drive continuous improvement and

Qualifications

• Minimum of 5 years of progressive QA experience in pharmaceutical manufacturing.
• Previous supervisory or senior‑level QA experience.
• Strong knowledge of cGMPs and regulatory requirements.
• Experience with deviations, investigations, CAPA, change control, complaints, and document control.

Responsibilities

• Lead, coach, and develop Quality team members on the shop floor.
• Provide hands-on Quality support to manufacturing operations.
• Support batch review and release activities and ensure timely review.
• Oversee Quality inspection, laboratory, and release activities.
• Coordinate investigations involving deviations, nonconformances, complaints, and SCARs.
• Lead and support CAPA and change control activities.
• Track and trend CAPAs, investigations, and quality system activities.
• Identify opportunities to continuously improve site Quality systems and processes.
• Support Annual Product Review (APR) activities and quality metrics for mgmt review.
• Support regulatory inspections and audits.

Skills

Quality leadership

Root cause analysis

Problem solving

Communication skills

Documentation

cGMP knowledge

Regulatory knowledge

Education

Bachelor's degree in Applied Science, Engineering, Quality Management, or a related scientific or technical field

Job description

Quality Supervisor

Location: Seymour, Indiana

Codis is seeking an experienced Quality Supervisor to join our Quality team at our Seymour, Indiana manufacturing facility. This is a hands-on leadership opportunity for a Quality professional who enjoys being close to manufacturing operations, developing employees, solving problems, and ensuring products consistently meet regulatory, customer, and company requirements.

The Quality Supervisor provides day-to-day leadership and oversight for Quality activities at the Seymour site, including floor support, batch review and release, Quality inspections, laboratory activities, document control, investigations, CAPA, change control, and other Quality systems.

This position works closely with Manufacturing and other departments and serves as an important link between the Quality team, site leadership, and the Quality Director.

What You'll Do

• Lead, coach, and develop Quality team members, including Quality Assurance Technicians, Auditors, Document Control Specialists, and Laboratory Technicians.
• Provide hands-on Quality support to manufacturing operations and serve as a visible Quality presence on the production floor.
• Support batch review and release activities and ensure raw materials and finished products are reviewed and released within established timelines.
• Oversee Quality inspection, laboratory, and release activities.
• Coordinate investigations involving deviations, nonconformances, customer complaints, Supplier Corrective Action Reports (SCARs), and other Quality-related issues.
• Lead and support root cause analysis and the development of effective corrective and preventive actions (CAPAs).
• Track and trend investigations, CAPAs, change controls, complaints, and other Quality system activities.
• Identify opportunities to continuously improve site Quality systems and processes.
• Support Annual Product Review (APR) activities and ensure assigned activities are completed according to schedule.
• Monitor Quality metrics and prepare information for management review.
• Support regulatory inspections, customer audits, supplier/vendor audits, and contract manufacturer audits.
• Ensure Quality documents and records are properly controlled and retained.
• Review and improve site procedures to maintain compliance and operational effectiveness.
• Partner with Manufacturing and other departments to resolve Quality issues while maintaining appropriate cGMP and Quality standards.
• Provide ongoing coaching, performance feedback, and development opportunities for Quality team members.

What We're Looking For

• Bachelor's degree in Applied Science, Engineering, Quality Management, or a related scientific or technical field.
• Minimum of 5 years of progressive Quality Assurance experience within pharmaceutical manufacturing or another highly regulated manufacturing environment.
• Previous supervisory, leadership, or senior‑level Quality Assurance experience.
• Strong knowledge of current Good Manufacturing Practices (cGMPs) and applicable regulatory requirements.
• Experience with Quality systems such as deviations, investigations, CAPA, change control, complaints, supplier quality, document control, and material/product release.
• Strong root cause analysis, risk assessment, and problem‑solving skills.
• Excellent written and verbal communication skills.
• Strong technical writing and documentation skills.
• Ability to manage multiple priorities in a fast‑paced manufacturing environment while maintaining accuracy and attention to detail.
• Pharmaceutical solid‑dose manufacturing experience is preferred.

The Right Fit

We're looking for someone who can be both a Quality leader and a collaborative business partner. You'll need to be comfortable making sound Quality decisions, coaching employees, working directly with Manufacturing, and stepping onto the production floor when an issue needs attention.

The ideal candidate understands that a strong Quality organization isn't simply about identifying problems. It's about preventing them, solving them effectively when they occur, developing strong systems, and helping teams consistently do things the right way.

If you have a strong Quality background, enjoy leading people, and want an opportunity to make a meaningful impact within a growing manufacturing organization, we'd like to hear from you.