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QC Analyst/12 months Contract/19 Eruos an hour/Oniste/Dublin
- QC Analyst to join the QC Separations Laboratory, the function of which is to support drug product and drug substance release testing.
- The successful candidate will be involved in assisting in laboratory operations, performing
- testing of samples and performing laboratory duties in accordance with cGMP regulations.
Responsibilities will include (but not limited to):
- Performing release testing for biological products.
- Assisting in updating and issuing documentation, including SOPs, as required.
- Performing routine data analysis, assist in the investigation of OOS results, perform trending
- analysis and writing investigation reports.
- Accurately documenting laboratory work.
- Execute and assist in technical transfer and co-validation activities.
- Assisting with the qualification of laboratory instruments.
- Data review based on demonstrated proficiency on assays.
Qualifications and Experience required:
- Previous experience in a regulated biopharmaceutical laboratory is preferred. HPLC/UPLC and
- Empower experience is preferred but not essential.
- The ideal candidate should hold a minimum of a BSc. in Biochemistry or related discipline.
- The successful candidate must demonstrate an ability to work independently and recognize anomalous trends or results.
- Must demonstrate problem solving ability, as well as the ability to prioritize objectives from multiple projects and adhere to scheduled timelines. Excellent communication and the ability to work in a team based collaborative environment are required.
Key Skills
Ranked by relevance
the ability to prioritize
data analysis
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- Posted
- Feb 14, 2025
- Type
- Contract
- Level
- Associate
- Location
- Dublin
- Company
- Russell Tobin
Industries
Pharmaceutical Manufacturing
Categories
Analyst
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