Production Team Lead – Pharmaceutical Sector – €32 per hour – Co. Meath

This role will be part of the Manufacturing Self-Directed Work Team/Hub at our client’s multi-product biotech facility. The Team Lead is responsible for overseeing all procedures and processes associated with the manufacture of Drug Substance, ensuring the highest standards of Safety, Quality, and Compliance are upheld.

Location:
Dunboyne

Pay Rate:
€32 per hour

Key Responsibilities:

• Lead the team in completing COMMIT cards to promote continuous improvement and foster a strong COMMIT culture within the SDWT’s, Hubs, and across the site.
• Supervise and ensure that all manufacturing documentation and tasks are completed in accordance with Good Manufacturing Practices (GMP).
• Manage and coordinate a dedicated process team, driving flexibility, teamwork, and accountability to meet production goals.
• Review, approve, and generate Standard Operating Procedures (SOPs) and Work Instructions (WIs) to ensure compliance with regulatory and operational standards.
• Collaborate with cross-functional teams to ensure the effective planning and scheduling of tasks, aligning with the overall manufacturing process and site schedule.
• Act as a point of contact for escalation within the team, providing guidance and support to ensure smooth operations and problem resolution.
• Serve as an Emergency Response Team (ERT) leader in emergency situations if trained, ensuring the team is prepared and well-coordinated.

The Team Lead will play a critical role in mentoring and guiding team members, ensuring the smooth operation of the production process, and driving continuous improvement across the site

Requirements:

• Level 7 qualification in a science or engineering discipline, or a Level 6 qualification with a minimum of 3 – 5 years’ experience in a GMP Manufacturing environment.
• Proven leadership skills with demonstrated successes in leading teams within a project or work-related activities, preferably in a high-performance environment.
• Strong understanding of Drug Substance Manufacturing Operations, including key processes and technical knowledge.
• In-depth understanding of GMP requirements in a Biopharmaceutical Facility, with a track record of maintaining high standards of quality and compliance.
• Exceptional communication skills with the ability to lead and motivate cross-functional teams and collaborate effectively across departments.
• Must be eligible to work full-time hours and flexible shifts as required by the production schedule.
• Proven ability to manage change and drive continuous improvement initiatives within the team.