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Senior QC Associate - HPLC

Reference:SMC028586
Location: Dublin
Qualification:Degree
Experience:See description
Job Type:Fixed Term Contract
Salary:Not Disclosed
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May be suitable for: Nurse Associate, QC Analyst

Summary

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

Duties
• With a high degree of technical flexibility, work across diverse areas within the lab
• Plan and perform routine analyses with 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.
• 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 and operational excellence improvement on a continuous basis.
• Approve lab results
• May participate in lab investigations.
• May provide technical guidance.
• May train others.
• May contribute to regulatory filings.
• May represent the department/organization on various teams
• May interact with outside resources.

Education & Experience
• Bachelor’s degree in a science discipline.
• Experience in a wide variety of analytical techniques including but not limited to HPLC, Gels or
Capillary Electrophoresis.
• Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning
• 3+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
• Experience with regulatory compliance in GMP manufacturing and testing of pharmaceutical products.


If you would like further Information you can contact the recruiter directly:

Sean McCarthy | Tel: +353 (0) 87 798 8480



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