QC Analyst

  • Nationwide
  • Temporary 11 months
  • JO-1701-62117_1484311170

Summary

QC Analysts
11 month contract

Role Description:
Maintain regulatory compliance through established programs for laboratory testing, maintenance, training, SOP's, validation and system administration within QC.
Skills Required:

  • Perform analysis, method transfer, validation and qualification as per relevant test procedures
  • Analytical procedures include raw material, in-process and finished product testing
  • Analytical methodologies including methods such as ELISA, HPLC, Western Blot, Bioassay/Cell Culture & PCR. Experience in one of above testing methodologies essential
  • Supporting Tech Transfer and of analytical test methods
  • Laboratory support testing including consumable control and qualification
  • Inventory control and maintenance of laboratory consumables
  • Responsible for calibration, use and administration of laboratory instrumentation
  • Perform and assist in additional duties as directed by the QC Supervisor
  • Complete documentation in a timely manner
  • Report and document any non-conformances to the QC Supervisor
  • Preparation and review of area documentation (e.g. SOP's, Reports, Protocols)
  • Assist in the training of other analysts
  • Ensure training compliance within the assigned work area and QC
  • Adhere to safety systems within the laboratories and on site
  • Prepared to work laboratory shift patterns

Education/Experience

  • B.Sc. degree in biology, chemistry, or other related technical degree
  • Min 2 years working experience in a pharmaceutical manufacturing environment, preferably in a quality control role
  • Previous QC/QA and/or pharmaceutical experience in a GMP or GLP facility.
  • Excellent communication and interpersonal skills
  • An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment



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