Process and Validation Engineer at LAPORTE in King of Prussia, Pennsylvania

Posted in Other 3 days ago.

Type: full-time





Job Description:

Process & Validation Engineer - King of Prussia, PA

Laporte is looking for a Process & Validation Engineer with 3 to 5 years of experience in CQV in Pharmaceutical Process Engineering to join our team in King of Prussia, PA.

The Validation Process Engineer will be responsible to support commissioning, qualification, and validation at client sites.

Responsibilities:
  • Write and execute commissioning, qualification, & validation protocols for facilities, utilities, and process equipment.
  • Oversee and review design and construction work related to cGMP manufacturing facility.
  • Review submittals, IOM, control sequences, and start up procedures.
  • Perform Walk Downs of As-Built P&IDs and Redlining P&IDs as required.
  • Document and manage all punch lists and deviations.
  • Write and review deviations, CAPAs, Change Controls, etc.
  • Perform basic revisions as needed to accurately reflect current procedures.
  • Must be able to wear appropriate cleanroom attire and all Personal Protective Equipment (PPE) i.e., scrubs, gowning coverall, masks, gloves, etc.
  • Work in both an office and a manufacturing lab setting.
  • Work in a lab setting with various chemical/biochemical exposures, including latex and bleach.
  • Work in a cleanroom with biohazards, human blood components, and chemicals.
  • Support project management initiatives to ensure efficient and timely progress.
  • Additional relevant duties as needed.

Qualifications:
  • Degree in Chemical, Mechanical, or Biochemical Engineering.
  • Minimum of 3 years of experience writing and executing CQV in the Pharmaceutical Industry.
  • Able to read and understand system drawings, diagrams, and specifications.
  • Experience collaborating with other design disciplines such as automation, facility design, and mechanical design groups.
  • Experience working closely with CQV and operations teams is essential.
  • Meticulous attention to detail and commitment to follow-through.
  • Experience in working in cleanrooms and familiar with gowning requirements.
  • Capable of standing and/or walking for 90% (and sitting for 10%) of a 10-hour day, which may involve climbing ladders or steps.
  • Must have near vision acuity for viewing samples at close range.
  • Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, and analytical skills.
  • Must be able to manage multiple priorities simultaneously and have the ability to meet deadlines.

Come join a company that is currently expanding across multiple geographic areas in North America - both Canada and the US. Laporte offers a competitive salary, compensatory PTO for hours worked above forty per week, extensive benefits, and an environment that promotes work-life balance and professional growth.

Job Type: Full-time

Travel required: 10-20%
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