Document Reviewer
Thermo Fisher Scientific
10d ago

Summary :

Responsible for reviewing all data, lab notebooks, and completed Certificates of Analysis (C of A) generated in the Quality Control (QC) and Microbiology laboratories.

Shift : Monday-Friday Afternoon (13 : 30 - 22 : 00 hours)

Essential Functions :

  • Reviews all data notebooks and C of A generated in the QC and Microbiology laboratories; ensures the accuracy of calculations, and that testing methods and standard operating procedures have been followed during the performance of the analytical analysis;
  • and verifies the integrity and traceability of all data generated and reported

  • Consults with the department supervisor / manager regarding omissions, incomplete testing results or other irregularities
  • Updates Standard Operating Procedures (SOPs) when necessary
  • May be essential to perform alternating or rotating shift work (as required)
  • Other duties as required
  • Requirements :

  • B.Sc. in a related science
  • 3 years experience in a pharmaceutical / Chemistry or Microbiology laboratory
  • Knowledge of and experience with High Performance Liquid Chromatography (HPLC); assay and impurity analysis, some method development and validation; and dissolution.
  • Proficient in Microsoft Office Suite (Word, Excel, and PowerPoint).
  • Excellent written and verbal communication skills.
  • Well organized and detail oriented.
  • Ability to work with little supervision.
  • Ability to prioritize multiple tasks.
  • Familiarity with Good Manufacturing Practices.
  • Proficient with the English language.
  • Shift : Monday-Friday Afternoon (13 : 30 - 22 : 00 hours)
  • Thermo Fisher Scientific is an equal opportunity employer andis committed to the principle of diversity and is particularly interested in receiving applications from a broad spectrum of people.

    Accommodations for job applicants with disabilities are available upon request.

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