Production Manager
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| Job Type | Permanent |
| Area | Mayo, Ireland |
| Sector | ManagementOperations & Manufacturing |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1002728 |
| Job Views | 351 |
- Description
- Team Horizon is seeking a Production Manager (Technical Shift Lead) for our client based in Mayo. In this role you will lead and facilitate the safe operations of the Biologics manufacturing team in a bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements.
As part of your new and exciting role you will ensure the long-term effectiveness of the team: deliver high levels of customer service, ensure the quality of products and services, comply with all regulatory requirements, achieve desired financial performance, including cost reductions, and build 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 a key point of the technical contact for aseptic fill-finish activities.
Supervision and execution of compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and support processing activities in the biologics fill-finish facility to meet clearly stated operating objectives.
You will lead, coach & mentor your manufacturing team to maximize the effectiveness through clear and effective communication of task details and goals to their team members, to allow the biologics technicians to work effectively.
As part of this diverse and inclusive team, you will conduct on the floor promotion of a culture of contamination control and compliance with aseptic best practices.
Communicate the departmental goals to provide cost-effective quality compliant products in a safe, effective manner.
We believe in collaboration, so in this role, you will liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing.
Resolve operations/project issues with team members, project customers, and others as appropriate.
Responsible for driving operations excellence and key operations targets, including OEE where applicable.
Provide direct interface as a subject matter expert with the QA department to interact with HPRA, FDA and applicable health authority and internal audits.
And any other duties as assigned
What you need to apply:
Minimum of 5 years experience in batch processing, automation, commissioning, and validation in an FDA/HHPRA-regulated industry.
Bachelor’s degree in chemistry, pharmacy, engineering or related scientific field is required; an advanced degree is preferred.
Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
Comprehensive understanding of contamination control principles and regulatory expectations for aseptic processing.
Has a technical background in pharmaceutical, biologics, or similar industries
A minimum of 1-year direct supervisory experience in a team environment
Possess strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors.
Exercises judgment and advises management as to the appropriate actions
