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Qc bioanalytical analyst

Dublin
Morgan Mckinley
Analyst
€60,000 - €80,000 a year
Posted: 5h ago
Offer description

Direct message the job poster from Morgan McKinley


Principal Recruitment Consultant in Quality Control (Contract & Permanent)Biochemistry, Chemistry & Microbiology

I am looking to recruit an experienced QC Bioassay Analyst who has 2+ years’ pharmaceutical industry experience working within a QC Bioanalytical lab supporting pharmaceutical manufacturing activities. This Analyst will support analytical testing within a leading biopharmaceutical company in South Dublin.

*12 month contract with view to extend.


Top Skills

* 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.
* GMP experience
* Biochemistry experience
* Degree Science – Biochemistry or Biology (a must for the role)


Key Responsibilities

* 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.


Seniority Level

Associate


Employment Type

Contract


Job Function

Science


Industry

Pharmaceutical Manufacturing

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