Quality Control Analyst
Sligo, County Sligo, Ireland · À temps plein
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- Salaire
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- Ouvertures
- 1
- Publié
- il y a 2 heures
- Mode de travail
- Au bureau
- Éducation
- 3rd level qualification in Science
- CV
- Candidature requise
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Description de l'emploi
About AbbVie
AbbVie focuses on developing and delivering innovative medicines targeting serious health conditions. Their work spans multiple key therapeutic sectors such as immunology, oncology, neuroscience, and includes products within the Allergan Aesthetics portfolio.
Job Overview
The Quality Control Analyst role is based in Sligo, Ireland, supporting a dynamic team on a fixed 12-month contract. The position involves shift work with rotating 12-hour day and night shifts.
Key Responsibilities
- Ensure adherence to laboratory documentation standards and computerized system data integrity.
- Understand and comply with regulatory and business protocols for maintaining data integrity in the lab.
- Perform laboratory housekeeping tasks diligently.
- Complete chemical testing of raw materials promptly as per schedule.
- Operate and maintain test equipment correctly to ensure accuracy.
- Manage change requests and data verifications when assigned.
- Complete all in-process sampling and testing efficiently and on time.
- Keep accurate, complete, and updated records for every test conducted.
- Follow current Good Manufacturing Practice (cGMP) and Good Laboratory Practice (GLP) standards strictly.
- Assist in identifying and resolving quality issues as needed.
- Contribute to the development and revision of internal laboratory processes.
- Help train new analysts joining the team.
- Support new product transfers within the lab environment.
- Adhere to and promote Environmental, Health, Safety, and Ergonomics policies and standards.
Qualifications & Experience
- Possession of a third level qualification in a relevant scientific field is mandatory.
- At least six months’ experience with High Performance Liquid Chromatography (HPLC) or Gas Chromatography (GC).
- Proven ability to work under cGMP standards with various laboratory instruments.
- Experience within pharmaceutical manufacturing is advantageous but not strictly required.
Additional Details
- The work schedule involves 12-hour shifts rotating between day and night.
- AbbVie promotes equal opportunity employment and is committed to integrity, innovation, community service, and inclusion.