QC Pharma Laboratory Supervisor
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| Job Type | Fixed Term |
| Location | Mayo |
| Area | Mayo, Ireland |
| Sector | ManagementLaboratory/Scientific |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | 01 574 6266 |
| Job Ref | 1003146 |
| Job Views | 225 |
- Description
- Team Horizon is seeking a QC Pharma Laboratory Supervisor (12-month fixed-term contract) to join our client who are a global leader in the biopharmaceutical industry, for their site in . The Laboratory Supervisor is responsible for the planning, supervision, and control of the testing schedule for all site manufactured product and all product included in the Global Stability program. Testing is to be performed in line with Corporate 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 area actively engaging with, challenging and motivating team members.
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:
You will lead and provide motivation to the team and take appropriate corrective action on individual/team performance where required.
As part of this diverse and inclusive team, you will share your knowledge and actively participate in the training and certification of new employees.
You will hold performance meetings according to company policy.
We believe in collaboration so in this role, you will partner with TA and take an active role in the recruitment of team members.
You will update TMS and take appropriate action where an individual’s attendance / timekeeping is below the expected standard.
In this role you will ensure that all aspects of the area of responsibility are fully staffed and that any constraints are managed appropriately.
You will also ensure all activities are completed in line with regulatory (QA and EHS) and corporate requirements.
You will provide required date per testing timelines to support product release and the global stability program.
You will provide team KPI data.
You will attend Departmental and APEX meetings; Safety Gembas, Green Team Meetings.
You will hold the agreed number of Team Meetings and Andon Board meetings.
You will review and approve local and corporate documents.
Work directly with other Laboratory Testing Leads to ensure that all testing is completed as per schedule.
You will facilitate movement of personnel among testing teams in order to ensure that the collective testing schedules are achieved.
You will work in conjunction with the laboratory trainer to ensure that sufficient technicians are proficient in the necessary product assays.
Any other duties as assigned.
What you need to apply:
You will have a relevant third level qualification (Degree Level or master’s Preferable). Technical Skills and Experience.
Proven track record in direct people management.
Scientific qualification in relevant discipline.
Knowledge of laboratory GMP standards.
Ability to articulate clearly when dealing with external bodies.
Excellent conflict handling skills.
