QC Pharma Lab Manager
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| Job Type | Permanent |
| Area | Mayo, Ireland |
| Sector | Laboratory/Scientific |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1003109 |
| Job Views | 247 |
- Description
- Team Horizon is seeking a QC Pharma Lab Manager for our client based in Mayo.
As the new Quality Laboratory Manager, you will be responsible for the planning, supervision and control of the testing schedule for all manufactured products and all product included in the global stability program. Testing is to be performed in line with WWQA standards and FDA, HPRA and other MOH regulatory requirements. This schedule compliance will be achieved by having a continued “on the floor” presence within the laboratory actively engaging with, challenging and motivating team members. You will also be responsible for promoting and ensuring safety within the workplace.
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.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Lead, motivate and mentor your team to maximize their effectiveness by clearly communicating task details and goals to your team members, allowing them to work effectively.
Hold performance meetings according to the company policy.
Ensure that all aspects of the area of responsibility are fully staffed and that constraints are managed appropriately.
Ensure all activities are completed in line with regulatory (QA and EHS) and corporate requirements.
Work directly with other laboratory supervisors to ensure that all testing is complete as per schedule.
Facilitate movement of personnel among testing teams in order to ensure that the collective testing schedules are achieved.
Provide required date per testing timelines to support product release and the global stability program.
Provide team KPI data and attend departmental and Tier meetings, Safety Gemba.
Take an active role in the recruitment of team members.
Update T&A and take appropriate action where an individual’s attendance/timekeeping is below the expected standard.
What you need to apply:
BS degree in Science or equivalent + 7 years of relevant experience.
Experienced and demonstrate high level of technical knowledge of analytical laboratory equipment, laboratory operations and good understanding of related business processes.
Experience working within a GMP regulated environment.
Proven track record in direct people management.
Excellent conflict handling skills.
Good interpersonal and communication skills essential for working across multi-functional teams.
