LSC have a great contract opportunity for a QC Analyst to join a leading pharmaceutical company based in Cork.
If you have 1+ years' experience in Quality Control or similar function in the medical device, pharmaceutical or related industry and are ready for your next challenge, this could be the perfect project for you!
POSITION SUMMARY:
This position is responsible for carrying out tasks and projects related to raw material, utility, in process, release and stability testing of biotechnology products as required by Good Manufacturing Practice (GMP).
GENERAL SCOPE OF RESPONSIBILITIES:
- Achieves a high level of competency in laboratory methods and procedures to support raw material, utility, in process, release and stability testing of biotechnology products.
- Performs routine and non-routine Microbiological and/or Biochemical/Chemical testing activities as required.
- Ensures that all testing is completed, reviewed and approved within agreed turnaround times.
- Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
- Trains other QC analysts and Manufacturing personnel in laboratory methods and procedures when required.
- Writes/updates and reviews TMs, SOPs and WIs as required.
- Writes and reviews invalid assays, non-conformances and deviations as required.
QUALIFICATIONS AND EXPERIENCE:
- BSc (Honors) in a scientific/technical discipline.
- A minimum of 1 year experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry.
- Demonstrated knowledge and testing experience in an FDA/HPRA approved QC laboratory.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Sarina Abdulha on 021 4777 329 if you have any more questions about this opportunity!
