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Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

Senior QC Associate (Bioassay)


Reference:RK4946 Location: Dublin
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Nurse Associate, QC Analyst

SeniorQCAssociate(Bioassay)
RK4946
Contract 12 months
Dublin



We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.



This role will be responsible for leading, coordinating, facilitating, and undertaking activities pertaining to lab operations and compliance. The role undertakes implementing continuous improvement projects and supporting a lean culture and Right First Time (RFT).



Duties:

  • Experience in a wide variety of analytical techniques including but not limited to cell based- Bioassays, Immunoassays, Cell Culture (use of cells to execute bioassays) and Aseptic Technique. Experience with liquid-handling robots is also preferable.
  • Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
  • Participate in the peer review of analytical data.
  • Responsible for providing technical guidance and applying expertise and critical thinking to help to resolve technical issues.
  • Lead training of staff on technical aspects of job as required.
  • Develop, revise and implement procedures that comply with appropriate regulatory requirements.
  • Qualification of analytical equipment and related testing functions.
  • Participate in Analytical Method Transfers
  • Compliance with Standard Operating Procedures and Registered specifications.
  • Ensure the laboratory is operated in a safe manner
  • Maintain quality systems within the QC laboratories to ensure ongoing compliance to cGLP and cGMP.
  • Ensure timely completion of Laboratory Investigation Reports and deviations through the Non-Conformance procedures.
  • Participate in the generation and update of SOP’s, trend data, investigations, non-conformances, validation protocols, reports, method validation/verifications and equipment qualifications.
  • Participate in regulatory agency inspections as required.


Educational and Experience

  • Bachelors degree in a science discipline
  • 2-3 years of Biochemistry experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
  • Must have Cell based- Bioassays, Immunoassays, Cell Culture (use of cells to execute bioassays), Aseptic Technique andELISA experience



If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.