QC Team Lead

Hartley People

Waterford, Tipperary, Cork

Our client, a regulated manufacturing company are looking for a QC Team Lead to join their team. This is an opportunity to join an established company in a challenging and rewarding role. The Role: • Ensure QC team work in a compliant mannerand in accordance with Good Manufacturing and Good Laboratory Practices. • Perform duties in a compliant manner and behave in accordance with site SOP’s, Quality Management System standards and guidelines and relevant legal requirements. • Ensure Adherence to all quality standards – “Lead by Example”. • Read and understand relevant Standard Operating Procedures, Global Quality Procedures and Management Policies relevant to your job role. • Ensure existing quality risk actions are completed to schedule and that any new risks are identified and escalated to the QC manager immediately. • Ensure all quality metrics are adhered to. • Ensure all quality audit findings are thoroughly investigated and effective corrective and preventive action plans are put in place to prevent a re-occurrence. Ensure timelines are adhered to. • Be aware of the impact of your job activities on quality. • Training of QC team in accordance with GLP. • Review of completed analytical reports prior to OQ approval. • Preparation, review and approval of in-house procedures e.g. SOPs, monographs, protocols etc. • Decision-making and liaison with internal departments to disposition product in accordance with GMP. • Troubleshooting analytical problems. • Participate fully in our site’s quality initiatives and support quality continuous improvement programmes. • Communicate with the QC Manager on a regular basis on QC status. • Escalate issues to the QC Manager, OQ Manager and Quality Director as appropriate. Provide motivational and effective leadership for team members. • Ensure efficient operation of the QC team and that the highest quality and safety standards are maintained at all times within QC. • Manage training and development plans for direct reports. Monitor personnel performance, time keeping and attendance and provide regular updates to the QC Manager. • Responsible for direct supervision of the following activities : 1. Sampling and testing activities relating to raw materials, packaging components, bulk product, finished product, stability and validation ensuring lead-times are adhered to. 2. Ensure there is a balanced workload among analysts. 3. Manage holiday applications and holiday cover. • Ensure thorough understanding of HR legislation and policies. • Ability to provide key input into site management decisions. • Building capability in Team. • Drive accountability within the team. • Must have can do attitude. The Person: • Educated to a minimum of primary or higher science based degree level. • 3/4 years experience in a pharmaceutical/healthcare industry in an analyst/senior analyst/supervisory capacity. Hartley People Recruitment work to the highest ethical standards within our industry and we value the trust that you place in us when you send your CV. We can provide a full consultation in confidence and we guarantee that your CV will not be sent to any of our clients without your prior consent. For immediate consideration please call Pairic on 051-878813 or email your CV in response to this job posting. Hartley People also recruit for similar roles such as Analytical Chemist, Quality Control Manager, Quality Control Technician, Quality Assurance Manager, Quality Assurance Technician, New Product Development Manger, Quality Systems Manager, Formulation Scientist, Development Technologist.

2392 days ago