QC Analyst

  • Nationwide
  • Temporary
  • JO-1705-62526_1495526214


QC Analyst
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 on finished drug product, in process materials and stability samples - UV, HPLC, wet chemistry.
  • Responsible for calibration and use of laboratory instrumentation.
  • Complete documentation associated with analytical results in a timely manner.
  • Report and document any non-conformances to the QC Supervisor.
  • Assist in the preparation and review of area documentation e.g. SOP's, Reports, Protocols.
  • Assist in the training of other analysts.
  • Ensure training compliance within assigned work area and QC.
  • Perform and assist in additional duties as directed by the QC Supervisor.
  • Ensure relevant assays are performed on samples in support of release test and stability test programs
  • Support any validation and qualification of test methods and processes
  • Facilitate laboratory investigations and support associated product investigation
  • Support Laboratory inspection and audits
  • Troubleshoot laboratory methods and instrument problems.
  • Establish and monitor trend analysis program.
  • Contribute to the operations of the Quality Control Laboratories.
  • Liaise with all customers both internal and external
  • Record and review laboratory testing documentation to cGMP standard.
  • Implement and adhere to appropriate levels of cGMP within the laboratory.
  • Promote safety awareness and the established culture of IIF within the assigned work area
  • Ensure that sample analysis is conducted to meet batch disposition requirements.


  • 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

Fastnet has a strict confidentiality policy - please be assured that your details will never be forwarded to any third party without your consent.

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