Maintenance Team Lead
Job Type | Permanent |
Area | Sligo, Ireland |
Sector | Engineering |
Start Date | |
Advertiser | David Connolly |
Job Ref | 1003589 |
Job Views | 17 |
- Description
Maintenance Tean Lead
Team Horizon is seeking a Maintenance Tean Lead for a leading manufacturing company in Sligo.
We have an exciting opportunity for a Maintenance Tean Lead to join our engineering team in Sligo. This position reports to the Engineering Manager. The successful candidate will lead and manage a team of plant support engineers and technicians to support manufacturing continuously, efficiently, and effectively.
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:
- Ensure continuity across shifts throughout the week, including a.m. handovers.
- Complete timecard review and approval for all PSEs.
- Responsible for adherence to training schedule, delivery of toolbox talks, WO coordination, WO reviews.
- Complete weekly review/accuracy/completeness of PH sheets.
- Arrange shift cover for Annual Leave, approve Annual Leave and other requests.
- Set goal, manage performance and development activities for all direct reports.
- Input to weekly planning meeting.
- Represent Engineering shift support at Tier 1 morning meetings.
- Resolve manufacturing escalations in a timely manner.
- Coordinate resources and assign tasks and activities.
- Work closely with Technical Shift Leaders/Operation Supervisors to ensure interdepartmental activities are planned and executed safely.
- Ensure Engineering compliance with all safety, environmental and quality related BOPs.
- Document all activities in line with cGMP requirements.
- Cross train team members and train new team members.
- Maintain the overall cGMP of the pharmaceutical processing areas.
- And any other duties as assigned.
What you need to apply:
- Diploma/Trade qualification in suitable science/engineering course and/or suitable experience.
- 3+ years’ experience in a highly regulated industry performing an equivalent position.
- Detailed functional knowledge required of a wide range of manufacturing equipment is essential.
- Proven instrumentation/troubleshooting ability.
- Good knowledge of procedures, policies and guidelines required to comply with cGMP and HPRA/FDA guidelines.
- Must be flexible and support the business through working shift and adhering to the standby schedule.