Pharma Quality Control Officer – Clonmel
Als Life Sciences
Clonmel, Tipperary
About the Position. ALS are in the final stages of fitting out a new Pharmaceutical Chemistry building in Clonmel to add to the current Pharmaceutical Microbiology offering in Clonmel. This role is a genuine career opportunity for someone looking to enhance their career prospects and to join a market-leading company with highly ambitious growth plans in Ireland. Reporting to the Laboratory Management team on site, you will support them to manage and monitor all laboratory aspects of Quality Control within the Chemistry and Microbiology departments on a day to day basis at the ALS Pharmaceutical Laboratories located in Clonmel, Co. Tipperary. This position is a permanent position and will be based at Clonmel following an initial training period at the ALS Pharma laboratories in Ely, England. Responsibilities. Support Laboratory Management in the completion of corrective/preventive actions arising from anomalies, complaints, OOS investigations, internal and external audits (including INAB, HPRA and clients) within agreed timelines as per ALS Group procedures. Support the Laboratory Team in management of equipment and equipment records ensuring that all items of equipment are correctly recorded, labelled and are calibrated at the appropriate frequency in accordance with the site calibration/service schedule. Ensure that all methods and procedures held by the laboratories are current and that there is evidence that all relevant staff are trained accordingly in current and revised procedures upon re-issue as per the group document control process. Regularly update trending systems for Right First Time (RFT) data generated by the laboratory. Support the Laboratory Team to ensure that training records are maintained in line with ALS Group procedures. Support the Laboratory Team in approval of daily checks for balances, pipettes, pH meters, incubators, waterbaths, fridges and freezers. Support the Laboratory Team in management of External and Internal Quality Control samples including maintenance of the in-house IQC reference material. Assist the Laboratory Team during customer and regulatory visits/audits. Archiving of laboratory records in accordance with ALS Group procedures. Support the Laboratory Team to ensure that all relevant Health and Safety information is included on Client provided methods. Work closely to support Laboratory Management to ensure all Quality requirements are met and delivered on time and reviewing procedures and systems regularly for continuous improvement. To provide the Laboratory Team with updates and reports upon request. About you. To be successful in this role you will have: A scientific background (degree level) where analytical skills can be used for problem solving. An understanding of Quality Management Systems, INAB/UKAS and GMP requirements. Minimum of 2 years working in a GMP environment. The ability to work on your own and manage projects to tight deadlines. Excellent communication and interpersonal skills. Understanding of the Pharmaceutical Industry and clients’ needs. Good computer literacy skills. High level of reporting and writing skills. Excellent organisational skills and the ability to multi-task. High attention to detail and a methodical approach. This is an excellent opportunity for a motivated and skilled person looking to develop their career in an international company. Attractive remuneration and benefits can be available dependant on performance . This job originally appeared on RecruitIreland.com.
2005 days ago