GMP Fill/Finish Manufacturing Supervisor

Pyramid Pharma Services, Inc.; Costa Mesa (CA); Presencial; USD 90.000 - 130.000; Jornada completa

Descripción de la vacante

Pyramid Pharma Services, Inc. is seeking a Manufacturing Supervisor to lead GMP-compliant fill/finish manufacturing, including formulation, aseptic processing, and equipment setup.

You will supervise staff, plan production, and ensure strict batch record integrity while coordinating with QA, Engineering, and Supply Chain. The role requires a Bachelor's degree in a related field and 2–6+ years in a regulated pharma environment, with strong leadership and documentation skills to drive safe,

Formación

• Hands-on experience with fill/finish manufacturing lines (vials, prefilled syringes, cartridges).
• Experience in a regulated pharmaceutical, biotech, or medical device environment.
• Demonstrated leadership with 1–2+ years of supervisory experience preferred.
• Ability to interpret batch records, SOPs, and quality systems.

Responsabilidades

• Lead day-to-day GMP fill/finish operations and direct manufacturing personnel.
• Plan, assign, and escalate issues to maintain schedules and quality.
• Ensure batch records and logs are accurate, complete, and compliant.
• Oversee equipment setup, line clearance, and aseptic processing activities.
• Collaborate with QA, Engineering, Supply Chain, and other departments.
• Identify deviations, implement corrective actions, and support validations.
• Monitor safety, training, and adherence to GDP and cGMP requirements.
• Support production planning and ensure resource availability for projects.

Conocimientos

GMP knowledge

Staff supervision

Production planning

Documentation control

Cross-functional collaboration

Educación

Bachelor's degree in Chemistry, Pharmacy, Engineering, Life Sciences

Herramientas

NetSuite ERP

HMI systems

MS Excel

MS Office

Descripción del empleo

Pyramid Pharma Services, Inc. is seeking a Manufacturing Supervisor to lead GMP-compliant fill/finish manufacturing, including formulation, aseptic processing, and equipment setup.

You will supervise staff, plan production, and ensure strict batch record integrity while coordinating with QA, Engineering, and Supply Chain. The role requires a Bachelor's degree in a related field and 2–6+ years in a regulated pharma environment, with strong leadership and documentation skills to drive safe,