Quality Control Associate job in Pharma sector at Ontario, Canada


Kelly Scientific Resources (KSR) is a specialty service of Kelly Services, Inc., a leader in providing workforce solutions. Since its launch in 1995, KSR has provided staffing and placement services to a broad spectrum of industries, including Biotechnology, chemical, consumer products, cosmetics, environmental, food sciences, medical/clinical, pharmaceutical, and petrochemical. Today, KSR leads the world in dedicated scientific and clinical research staffing. Visit http://www.kellyscientific.com/ to learn more and view a full listing of our opportunities.

Post  : Quality Control Associate - Biotech
Responsibilities and Duties:

  • Performs QC inspection of incoming materials for inventory according to established procedures.
  • Performs QC testing of incoming materials for receiving as necessary.
  • Performs routine and non-routine analysis of raw materials, in process and finished product testing according to standard operating procedures.
  • Completes operational requirements as per schedule: performs testing and writes/ reviews records; releases products, raw materials & packaging components; supports process validation; reviews and implements new procedures; assists in maintaining QC supply inventory and testing schedule.Maintains quality results: performs tests according to quality standards ensuring compliance to cGMP; documents results according to cGMP standards; initiates and/or assists in investigations of OOS and NCMR results.
  • Maintains QC equipment performance according to SOPs & manufacturers' guidelines
  • Writes & reviews SOPs related to QC procedures and equipment.

General Responsibilities:

  • Complies with policies and procedures for timely completion of company and department goals and objectives.
  • Adheres to quality standards set by regulations, company policy and company mission.
  • Communicates effectively with supervisors and colleagues. Is committed to team effort and is willing to assist in unrelated job areas when called upon.
  • Attempts to constructively resolve any problems that interfere with completion of position responsibilities or production time lines.


  • Diploma, or BSc. in Chemistry, Pharmacy, Life Sciences or related discipline, & ability to demonstrate required GMP knowledge
  • Ability to perform a wide range of biological testing following established procedures and using proper techniques
  • Proven performer ideally from medical device industry in a progressive QC/QA environment
  • Strong documentation skills and detail oriented
  • Computer literate. (Proficiency with MS Office specifically)

Deadline : 13.04.2011