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Details
QC Chemistry Analyst (Shift)
Reference: | RK20683 | Location: |
Carlow |
Qualification: | Degree | Experience: | 2-3 Years |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
QC Analyst
QC Chemistry Analyst (Shift)
RK20683
11 Months
Carlow
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties:
- Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP.
- Required to drive compliance with Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions
- Participate in QC Tier 1 daily meetings and ensure effective communication of testing progress, deviations etc
- Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same
- Operate as part of the QC team performing the allocated testing and laboratory-based duties
- Perform various analytical techniques including but not limited to HPLC, (HIC, CE, IEX, HP-SEC), Capillary Electrophoresis and other compendial test methods in compliance with GMP requirements
- Peer review testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved
- Participate in the laboratory aspects of OOS investigations
- Provide support with audit/inspection requirements to ensure department compliance/readiness.
- Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility.
- Drive continuous improvement, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues e.g., FMEA, Fishbone diagrams, 5 why's etc,
Education and Experience :
- Bachelors Degree or higher preferred; ideally in Analytical Chemistry/ Biochemistry or a closely related discipline
- 2-3 years of experience in a pharmaceutical laboratory
- A good working knowledge of HPLC systems and software is desirable
- A good knowledge of cGMP, GLP, Quality Management Systems
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
Valid XHTML - CSS