GMP & Lean Manufacturing Supervisor

Civica Rx; Petersburg (VA); On-site; USD 90,000 - 120,000; Full time

Job summary

Civica Rx is seeking a Manufacturing Support Supervisor to help drive facility start-up and the daily production of high-quality injectable products in Petersburg, VA. You will hire, coach, and lead a team through equipment qualifications and process improvements while ensuring safety, quality, and supply continuity.

The role emphasizes hands-on supervision, SOP development, and readiness for FDA/cGMP inspections, with a 6:00 AM – 6:30 PM, 2-2-3 schedule and on-site work.

Qualifications

• Bachelor's degree required with 4+ years in a cGMP/FDA/ISO regulated environment (or 6+ years with an Associate's).
• Experience operating autoclaves and parts washers is required.
• 1+ year of supervisory experience in GMP manufacturing.
• Lean manufacturing or Six Sigma Green Belt preferred.
• Strong documentation and communication skills are essential.

Responsibilities

• Lead daily manufacturing operations and staff to ensure safe, compliant production of injectable products.
• Own and improve SOPs, specs, and governing docs to meet qualification and business needs.
• Mentor staff on change management and CAPA processes to drive project completion.
• Ensure staff training, equipment qualifications, and readiness for inspections.

Skills

Supervisory experience

GMP compliance

Process improvement

Lean Six Sigma Green Belt

Analytical problem-solving

Leadership skills

Education

Bachelor's degree in a science field

Associate's degree with 6+ years GMP experience

Tools

Autoclaves

Parts Washers

Clean-in-place (CIP)

Material Transfer Isolators (MTIs)

Job description

Civica Rx is seeking a Manufacturing Support Supervisor to help drive facility start-up and the daily production of high-quality injectable products in Petersburg, VA. You will hire, coach, and lead a team through equipment qualifications and process improvements while ensuring safety, quality, and supply continuity.

The role emphasizes hands-on supervision, SOP development, and readiness for FDA/cGMP inspections, with a 6:00 AM – 6:30 PM, 2-2-3 schedule and on-site work.