Validation Engineer, Equip. & Utility Qualificatio
Date Posted
1/6/21
Location
Princeton, NJ 08540
Position Id
1117
Degree Required
Job Type
FullTimeRegular
Job Description
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.