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QC Analyst

RandoxCrumlin, AntrimFull-timePermanent
Randox Laboratories continues to develop disruptive innovations in Diagnostics and Healthcare globally. We are proud to have been named the Number 1 company in Northern Ireland for the second consecutive year in the Belfast Telegraph Top 100 Companies List for 2024. Our staff are at the heart of everything we do and achieve. We have exciting new career opportunities for QC Analyst within our QC Immunology team.


What does the QC Immunology team do?

Accurate, fast, simple to use and trusted globally all sum up the world class ELISA range that has been developed and manufactured by Randox for over 30 years. These include an extensive array of drug residue ELISAs specifically designed for the global food industry, plus ELISAs used for the rapid detection of drugs in various biological specimens. We have an exciting opportunity to join our QC Immunology team who are responsible for assessing product quality and, if necessary, improving it. We’d love to hear from anyone who feels they could make a positive contribution to this team. The successful Analyst will be involved in the day-to-day ELISA testing to support the manufacture and release of these product lines.


Location: Randox Site 4, 34 Diamond Road, Crumlin, BT29 4QX.

Contract Offered: Full-time, Permanent.

Working Hours / Shifts: 40 hours per week following a pattern of either 4 days from 07.30 to 18.10, or Monday to Friday from 08.40 to 17.20 (subject to change).


What does the QC Analyst role involve?

The core function of the position is to conduct routine and non-routine analysis of in-process materials, raw materials, finished goods, or stability samples. This is a varied role that will require you to develop an equally varied skill set including:
  • Interpret test results, comparing them to established specifications and control limits, and make recommendations on appropriateness of data for release.
  • Perform visual inspections of finished products.
  • Compile laboratory test data and perform appropriate analyses.
  • Complete documentation needed to support testing procedures, including data capture forms, equipment logbooks, or inventory forms.
  • Calibrate, validate, or maintain laboratory equipment. Identify and troubleshoot issues.
  • Participate in out-of-specification and failure investigations and recommend corrective actions.
  • Investigate or report questionable test results.
  • Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines.
  • Ensure that lab cleanliness and safety standards are maintained.
  • Identify quality problems and recommend solutions.
  • Train other analysts to perform laboratory procedures and assays.
  • Participate in internal assessments and audits, as required.

Full on the job training will be provided on our processes.


Who can apply?
Essential criteria:​​​​​​​
  • Qualified to degree standard in Biomedical Science and a Diploma in Professional Practive, Immunology, or a Life Science Degree.
  • Possess excellent written and verbal communication skills.

Desirable:
  • Previous experience with ELISA test procedures.
  • Working knowledge of quality systems.
  • Working knowledge of Health and Safety, including CoSHH.

This advert may be open for as long as 30 days although we may close the advert early if we receive sufficient applicants to fill the roles.

The closing date for applications is Wednesday the 14th of August 2024

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