Aseptic Manufacturing Operator — GMP Focus

Piramal Pharma Ltd

Lexington (KY)

Presencial

USD 42.000 - 54.000

Jornada completa

14 días+
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Descripción de la vacante

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO) located in Lexington. The Manufacturing Operator performs production related activities including component preparation, filling, capping, autoclaving, terminal sterilization, compounding, and lyophilization.

The role reports to the Production Supervisor and requires working days shifts. Responsibilities include line clearances, equipment operation, material verification, and adherence to GMP and SOPs while

Formación

  • High School education or equivalent.
  • 2+ years' working within an industrial or manufacturing environment.
  • Pharmaceutical manufacturing and/or aseptic manufacturing environment preferred.
  • Mechanical aptitude and ability to operate processing equipment.
  • Ability to read, interpret, and follow written instructions.
  • Knowledge of cGMP, OSHA, FDA regulations is a plus.

Responsabilidades

  • Perform production activities including component preparation, filling, capping, autoclaving, sterilization, compounding and lyophilization.
  • Operate and maintain production related equipment.
  • Weigh, measure and verify raw materials for correct batches.
  • Read and follow SOPs and participate in process improvements.
  • Maintain clean and compliant work area and record-keeping.

Conocimientos

Mechanical aptitude
Equipment operation
Regulatory literacy
Team collaboration
Attention to detail

Educación

High School education or equivalent

Descripción del empleo

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO) located in Lexington. The Manufacturing Operator performs production related activities including component preparation, filling, capping, autoclaving, terminal sterilization, compounding, and lyophilization.

The role reports to the Production Supervisor and requires working days shifts. Responsibilities include line clearances, equipment operation, material verification, and adherence to GMP and SOPs while

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