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Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

Senior QC Associate NPI


Reference:RK4845 Location: Dublin
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QC Analyst

Senior QC Associate NPI
RK4845
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 support QC and manufacturing operations, as such some extended hours and weekend work flexibility may be necessary as required.



Duties:

  • QC Representative for NPI activities and routine Product meetings
  • Assist with activities related to QC projects and/or QC tasks within Site projects
  • Plan and perform non-core testing related to NPI activities
  • Manage all sample management activities related to NPI activities throughout the site
  • Create/own and approve protocols, sample plans, SOP and documentation related to NPI
  • QC Representative responsible for Method Validation and Transfers co-ordination and readiness
  • Sample shipments and temperature monitoring activities for NPI activities
  • LIMS data coordination of non-core (NPI) activities.
  • Plan and perform analyses with great efficiency and accuracy.
  • Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
  • Report, evaluate, back-up/archive, trend and approve analytical data.
  • Troubleshoot, solve problems and communicate with stakeholders.
  • Initiate and/or implement changes in controlled documents.
  • May train others as necessary
  • Participate in audits, initiatives and projects that may be departmental or organizational in scope.
  • Write protocols and perform assay validation and equipment qualification/ verification.
  • Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
  • Evaluate lab practices for compliance on a continuous basis.
  • Approve lab results



Educational and Experience
  • Bachelors degree in a science discipline
  • 2-3 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
  • Strong background in Chemistry, Analytical testing and NPI experience is required.
  • Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.



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