Overview
An excellent opportunity for a QC Analyst with 1 - 2 years analytical testing experience within a cGMP regulated pharmaceutical lab. Significant experience performing HPLC, KF, FTIR required. Experience working with raw materials within a pharmaceutical company is preferred.
12 month contract located in North Dublin.
Responsibilities
* Performing QC testing (TOC, pH, Conductivity) of water samples. Performing analysis of Raw Materials including HPLC, KF, UV, IR and wet chemistry techniques. Completion in a timely and accurate manner of laboratory documentation as directed by the QC Manager.
* 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.
* Sample management activities - ensuring chain of custody is maintained using CIMS and LIMS.
* Assisting with qualification of laboratory instruments.
* Data review based on demonstrated proficiency on assays.
Qualifications and Experience
* Previous experience performing QC testing within a regulated pharmaceutical or biopharmaceutical laboratory is required.
* Experience performing HPLC, KF, FTIR, wet chemistry tests within the pharmaceutical industry.
* Proficient user of Empower software.
* BSc. in Science/Chemistry/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.
Seniority level
* Associate
Employment type
* Contract
Job function
* Science
Industries
* Pharmaceutical Manufacturing
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