Quality Control Laboratory Manager
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| Job Type | Permanent |
| Area | Cork |
| Sector | ManagementLaboratory/Scientific |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 2417 |
| Job Views | 402 |
- Description
- We are seeking applications for an experienced Quality Control Laboratory Manager for our client, who are a leading pharmaceutical company based in Cork. The successful applicant will reporting to the Quality Director, in this role you will lead, coach and mentor Lab Supervisors and analysts supporting the drug product manufacturing onsite. This is a great development opportunity to build your leadership expertise and be part of the extended leadership team at the site
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
What you will be doing:
Lead, coach and manage a team of Supervisors and Lab Analysts and be responsible to hire, lead and develop team members to ensure that the department has the appropriate talent and level of performance to meet business objectives.
Control the products (raw materials, intermediates, and finished products) by following procedures (general, specific, of analysis and use, and qualification of equipment)
Organise laboratory activity by coordinating the action of people management, depending on demands of planning
Preserve and improve the capacity by ensuring that preventive and repair maintenance and material qualifications are carried out, plan the needs of instruments by maintaining permanent technical and technological intelligence
Ensure QC activities are operated in compliance with in-house rules, cGMP and safety requirements.
Use internal audit to check that rules are applied, propose corrective actions and check that they are applied
Carry out external audits in collaboration with the Purchasing Department (suppliers and subcontractors)
Control, retention and archiving of all GMP related records covering QC operations
Participate in reviewing and approving of SOP's protocols and reports to meet GMP/Regulatory requirement
Improve QC operations and develop systems. Focusing on efficiencies, cost, and compliance.
Participate in technical and scientific meetings, in training days, trade fairs, conferences
Participate in drafting specifications and in technical and scientific discussions with suppliers and clients.
What you need to apply:
You will have a degree in an analytical science with a minimum 5 years’ experience in QA, QC organization in a regulated environment. Direct experience of an FDA/IMB approved site is required
Demonstrated people leadership experience
Experience with similar analytical methods (HPLC/GC etc), audits
Project management, knowledge of the group organization and procedures
