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Project Manager - Pharma
Job Posted: 8 days ago
Salary: £ 47 - 56 / Annum
Job Type: Permanent
Location: Mayo County
Expire in: 20 days
Job Description
Maintenance Team 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 scheduleBefore You Apply
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