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ROLE RESPONSIBILITIES

  • Perform all physical and chemical tests for in-process, finished product and related tasks in a timely manner.
  • Perform all physical and chemical tests for stability studies of finished products and related tasks in a timely manner.
  • Participate in testing of method validation for new or old products to be submitted to regulatory authorities.
  • Analysis stability testing samples as per effective stability plan with COA documentation.
  • Trained on  Standard Operating Procedures (SOPs) related to department.
  • Implementing the PQS requirements regarding the chemical laboratory
  • Perform and execute analytical method validation protocols.
  • Back-up for Incoming Materials (PM/RM) activities (Sampling and testing of PM only).

 

Qualifications

 

BASIC QUALIFICATIONS

  • Basic scientific degree.
  • 1-2 years’ experience in similar position.
  • Ability to read English and interpret documents such as cGMP/ FDA regulations, standard operating procedures, and Pfizer corporate policy manuals.
  • Ability to report results clearly and concisely.  Sound reasoning and ability to quickly analyze and solve complex problems.
  • Excellent attention to detail and time management skills.
  •  Ability to work independently and with other teams.
  • PC literate with the following applications:  MS Excel, Word, PowerPoint.

 

 

PREFERRED QUALIFICATIONS

  • Basic scientific degree.
  • 2 years’ experience in similar position

PHYSICAL/MENTAL REQUIREMENTS

  • Good command of English both written and spoken.
  • Knowledgeable with interpersonal learning.
  • Communication and team work.
  • Logic way of thinking.
  • Management and decision-making skills.
  • High analytical skills.
  • Professional in reports writing.

PC literate with the following applications:  MS Excel, Word, PowerPoint.

Work Location Assignment: On Premise

Tagged as: Pharmaceuticals

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