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Job ID :
66938BR
Location :
Canada - Whitby
:
Job Description
Summary:
Performs required analysis for the Pharmaceutical Development Services (PDS) Analytical Development ensuring that all Patheon Standard Operating Procedures (SOP), current Good Manufacturing Practices, current Good Laboratory Practices (GLP) and corporate quality standards are achieved. Provides support in monitoring business process performance measures and notify management of potential quality or regulatory issues that may affect product quality of regulatory compliance.

This is a one-year contract position.

Essential Functions:
  • Performs testing and assays in accordance to approved methods and SOPs.
  • Performs all duties in strict compliance to all Patheon quality systems (SOPs, Good Manufacturing Practices).
  • Documents all experimental data in accordance with Good Manufacturing Practices and Patheon SOPs.
  • Assists in method validation as directed by AD Supervisor.
  • Recognizes and reports out of specification (OOS) results or deviations to Supervisor immediately.
  • Assists in trouble shooting and investigations as required by AD Supervisor.
  • Comples with all Environmental Health & Safety (EH&S) requirements and participate in EH&S training.
  • Other duties as required.
  • May be essential to perform alternating or rotating shift work.
Requirements:
  • B.Sc. in Chemistry, or related science, with hands-on experience in chromatographic and spectroscopic analytical instruments.
  • Two years experience in pharmaceutical analytical development.
  • Good understanding of basic chemistry, chromatography (eg High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), thin-layer chromatography (TLC) and spectroscopic technologies (e.g. Ultraviolet (UV), Infrared (IR).
  • Good problem solving skills and logical approach to solving scientific problems.
  • Interest in improving skills and knowledge in pharmaceutical development.
  • Excellent written and oral communication skills.
  • Proficiency with the English language.
  • Legibility in documentation as per Good Manufacturing Practices requirement.
  • Possesses analytical thinking skills which are applied to solving a complex scientific problem.
  • An awareness of regulatory requirements in the pharmaceutical industry.
  • Works well in a team environment and cooperates with other members of the team to find a solution.




Thermo Fisher Scientific  is an equal opportunity employer and is 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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