3528
QC Chemistry Analyst
Waterford, Ireland
Life Science
Fix Term Contract
3528
Posted on:
October 7, 2024
The Highlights:
- Work with a global biopharmaceutical company
- Gain experience in all essential areas of Micro Department
- Approachable management and positive work culture
The Role:
Elusav Recruitment have an excellent opportunity with a leading global Pharma and Biopharma company who is seeking a QC Chemistry Analyst to bring value to their state-of-the-art facility in Waterford.
This is an excellent opportunity to work with a global and progressive leader, with modern labs, with a lot of change and growth in their Waterford site. This role allows opportunity to become highly skilled within the team and gain experience in all areas essential to the running of a chemistry department.
Job Responsibilities:
- Provide analytical chemistry services and support to Site.
- Effective interaction with other departments on matters related to raw materials, intermediates and finished batch releases. In particular, close contact maintained with Quality Assurance Production, Engineering and Planners.
- Maintain, update and issue chemical methods, specifications and SOP’s in compliance to pharmacopeial and regulatory requirements.
- Assist with training of the analysts in areas of expertise and knowledge and in new methods, SOP’s and updates.
- Trend such results, record on COA’s where required and complete OOS’s investigations on a timely basis.
- Update the QC Team Leader on potential problems and highlight improvements where possible by use of the normal communication means.
- Ensure all quality documentation and records are complete and current Ensure QC laboratories meet current Good Laboratory Practice (cGLP) requirements.
- Ensure relevant procedures are correctly defined and followed.
- Ensure that critical chemical testing and related equipment meets current validation requirements (IQ, OQ, PQ) where required.
- Audit and review chemistry test results on a daily basis and ensure compliance with cGLP.
- Checking/auditing laboratory notebooks and analytical reports.
- Ensure compliance to cGMP at all times.
Job Requirements:
- Degree in Science (Chemistry or Biochemistry preferred).
- 2+ years experience working in a manufacturing environment preferred.
If you would like to learn more about the vacancy, apply now, or contact Stephen O'Brien on stephen@elusav.com or +3536959993.
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QC Chemistry Analyst
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