Be part of the Omega Team!

Omega Laboratory Limited is committed to providing Equal Employment Opportunity for all persons. Equal opportunity extends to all aspects of the employment relationship including hiring, transfers, promotions, training, terminations, working conditions, compensation, benefits, and other terms and conditions of employment.

We thank all candidates; however, only those under consideration will be contacted.
 
 Technical Writer - posted on June 9, 2010 - closing date July 2, 2010
 

Job objectives

Drafting validation reports and analytical methods.

Primary functions

  • Extract generated raw data from the Oncology Quality Control laboratory.
  • Draft forced degradation reports.
  • Prepare validation reports for the measurement of active ingredient and secondary compounds (impurities, degradation products).
  • Any duties related to department activities.

Academic training

  • Bachelor in Science, Chemistry or Biochemistry.
  • Bilingual (French and English) spoken and written.

    • Experience requirment and aptitude

    • Experience in research & development and validation of analytical methods in the pharmaceutical Industry.
    • At least three years (or equivalent) in drafting validation reports in a GMP environment.
    • Good knowledge in ICH (International Conference on Harmonization).
    • Waters Empower Proficiency.
    • Word and Excel Proficiency.
    • Familiarity with GMPs and GLPs.
    • Ability to work in a team environment.
    • Autonomous.
    • Sense of organization.

     

     
     
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