QC Senior Associate


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https://www.teamhorizon.ie/job-search/1154-qc-senior-associate/quality/dublin/job2024-02-08 12:47:041970-01-01Team Horizon
Job TypeContractor
LocationDublin
AreaDublin, IrelandDublinIrelandDublin
SectorQualityLaboratory/Scientific
Start Date
AdvertiserDarcy Ainscough-Denton
Telephone01 574 6266
Job Ref1003162
Job Views221
Description
Team Horizon is seeking a QC Senior Associate (initial 12-month contract) for our client who is a global leader in the biopharmaceutical industry. The successful candidate will have a strong background with testing, troubleshooting, and HPLC.

This is a 24/7 shift role, with a shift premium included.

 

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.


  • There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.


  • Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.


 

What you will be doing:


  • Testing of in process, stability and finished product samples. eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management.


  • Review and authorisation of Lab Data.


  • Support Analytical Technical Transfer activity testing reports and documentation.


  • Document review/updates when required.


  • Equipment Calibration, Maintenance and Trouble Shooting.


  • Method Validation/Verification.


  • Training of QC Chemistry Laboratory colleagues.


  • Laboratory Investigation support.


  • Laboratory Housekeeping and maintaining GMP standards.


  • Assisting in regulatory audits.


  • Would be great to see if the candidate has significant HPLC experience coupled with Empower Software.


  • Would be advantageous if they have a bit of protein concentration testing experience.


  • GMP lab environment experience.


  • Want to be able to see that the candidates can troubleshoot.


  • In the past, when talked to previous candidate haven’t been able to come up with many examples of where they’ve had to troubleshoot or encountered issues that must be resolved and demonstrate what they did to resolve those problems.


  • We would want someone with a strong background because when they’re on night shifts, management aren’t there at night so do want the candidates to be able to make decision under these sorts of circumstances.


  • Any other duties as assigned.


 

What you need to apply:


  • Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject.


  • Have at least 5 years relevant experience in a pharmaceutical/healthcare environment.


  • Be very proficient in the use of Microsoft Word, Excel etc.


  • Have strong technical writing skills.


  • Be detail oriented, self-motivated with good troubleshooting and problem-solving abilities.


  • Be a self-starter and capable of working on own initiative.


  • Strong teamwork skills.


  • Proven track record of meeting deadlines.


  • Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous.


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Darcy Ainscough-Denton
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