Validation Engineer, Equip. & Utility Qualificatio

1/6/21

Princeton, NJ 08540

1117

FullTimeRegular

Validation Engineer, Equipment & Utility Qualification

This position is responsible for duties associated with qualifying manufacturing and packaging equipment and Pharmaceutical utilities, including HVAC Systems for Clean Classified Areas, USP Purified Water, USP Water-for-Injection, Clean Compressed Air, and nitrogen consistent with cGMP requirements for clinical manufacturing, scale-up and commercial manufacture of sterile and specialty pharmaceutical products.

Major job functions include generation of qualification / validation documents, execution of qualification / validation documents, generation of reports, managing project timelines, and participating in cross functional teams.

Responsibilities:

  • Responsible for the validation studies required for qualifying Manufacturing, Packaging equipment and Pharmaceutical utilities, including HVAC Systems for Clean Classified Areas, USP Purified Water, USP Water-for-Injection, Clean Compressed Air, and nitrogen.
  • Collect and tabulate laboratory data, review laboratory data for errors and discrepancies, and transcribe results into final reports.
  • Generate, review and approve qualification/validation procedures.
  • Generate final reports, compile historical data packages, and route documents for approval.
  • Review and approve set-up and operation procedures for production and packaging equipment.
  • Generate risk assessments to discuss the approach to qualification related activities.
  • Support the rationale for the sample size selection during process equipment qualification.
  • Review and complete assigned Change Control tasks.

Qualifications:

  • Bachelor’s Degree in Engineering, Life Sciences or related discipline
  • A minimum of 2 years of relevant experience performing validation activities within pharmaceutical environment; or equivalent combination of education and experience.
  • Familiarity with current industry practices and guidelines including those required / outlined by the FDA, ISO, EU and ICH.
  • Proficiency in Microsoft Office including Word, Excel, PowerPoint, MS Project, Visio, etc.
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