Job Description
An amazing opportunity for a QC Analyst with minimum 1 year's experience within a GMP lab to join a leading biopharmaceutical company in north Dublin on a short term contract until December 2024 with the potential for extension into 2025. 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 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. Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative. BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES. Skills: HPLC GMP Quality Control Biopharmaceuticals