Technical Shift Supervisor
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| Job Type | ContractorFixed Term |
| Area | Mayo, Ireland |
| Sector | Operations & Manufacturing |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1002727 |
| Job Views | 1143 |
- Description
- Team Horizon is seeking a Technical Shift Supervisor for our client based in Mayo on a fixed term contract. In this role you will lead and facilitate the safe operations of the Eye Care manufacturing, filling & printing teams in our bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements. Assuring the long-term effectiveness of the team: delivering high levels of customer service, ensuring quality of product and services, complying with all regulatory requirements, achieving desired financial performance including cost reductions, and building a culture of high performance for the team.
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:
Act as key point of technical contact for aseptic compound transfer, fill finish and printing activities.
On the floor Supervision and execution of compounding transfer, filling, Tampoprinting , equipment, preparation and support processing activities in the Eye Care facility to meet clearly stated operating objectives.
Team leadership, motivation and direction to maximize the effectiveness of your manufacturing team, clearly communicating task details and goals to your team members, to allow them to work effectively.
On the floor promotion of a culture of contamination control and compliance with aseptic best practice.
Daily reporting on the status of all operations and support activities.
Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner.
Liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and clinical manufacturing/filling.
Resolve operations/project issues by working with team members, project customers, and others as appropriate.
Drive operations excellences and Key operations targets including OEE where applicable.
Provides direct interface as a subject matter expert with QA department to interact with HPRA, FDA, applicable health authority and internal audits.
Develop direct reports by securing appropriate training, assigning progressively · challenging tasks and managing mid-year and annual reviews.
And any other duties as assigned
What you need to apply:
You will have a Bachelor’s degree or equivalent required in an engineering or Science related field
Minimum of 5 years’ experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry
A working knowledge of safety, quality systems, and current Good Manufacturing Practices as applied to equipment and process steps in area of responsibility is required.
Familiarity with pertinent regulatory filings.
Proficiency with tech transfer process and familiarity with equipment and facilities validation
Must be flexible to handle multiple tasks including ability to handle pressure in a professional manner.
Effectively work in a team environment. Maintain high level of energy and professionalism on the job.
Build effective working relationships with customers, co-workers, cross-functioned groups, and management.
A minimum of 1 year direct supervisory experience in a team environment
Intermediate to High computer and MS Office skills.
