QC BioAnalytical

https://www.teamhorizon.ie/job-search/414-qc-bioanalytical/laboratory/scientific/dublin/job2022-02-08 14:13:532052-03-28Team Horizon
Job TypeContractor
AreaDublin, IrelandDublinIreland
SectorLaboratory/Scientific
Start Date
AdvertiserMary King
Job Ref2351
Job Views1572
Description
If you have experience in cell-based potency bioassays, cell culture, GMP/GDP Elisawe may have the job for you. We are seeking applications for an experienced QC BioAnalytical Sciences for our client, who are a leading biopharmaceutical company based in Dublin.You will act as a senior associate on the manufacturing site, responsible for leading, coordinating, facilitating, and undertaking activities pertaining to lab operations and compliance, with minimal supervision. And as a role model for other lab colleagues.

 

Why you should apply:



  • This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.


  • Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.


What you will be doing:



  • Planning and delivering complex routine/ non-routine methods and procedures and a large variety of assays.


  • Taking part in the peer review of analytical data.


  • Giving technical guidance while applying expertise and critical thinking to help to resolve technical issues.


  • Leading the training of staff on technical aspects


  • Creating, updating and implementing procedures that comply with appropriate regulatory requirements.


  • Qualification of analytical equipment and related testing functions.


  • Taking part in analytical method transfers


  • Following standard operating procedures and registered specifications.


  • Making sure the laboratory is operated in a safe manner


  • Ensuring ongoing compliance to cGLP and cGMP.


  • Completing laboratory investigation reports and deviations.


  • Taking part in various report and documentation updates and equipment qualifications.


  • Participating in regulatory agency inspections as required.


  • Planning and implement procedures and systems to maximise operating efficiency.


 
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