Team Lead Biotech Associate – Downstream Manufacturing

RECRUITERS; Dunboyne; On-site; EUR 70,000 - 90,000; Full time

Job summary

RECRUITERS is seeking an experienced Biotech Associate Team Lead for downstream manufacturing in Dunboyne on an 11-month, fully onsite contract. You will lead a team of 9 associates, oversee batch progression and ensure GMP/EHS compliance in a high-speed 24/7 shift.

The role requires a Level 8 Bachelor's in a technical field and at least 5 years in biopharma, with downstream experience in filtration/purification and exposure to paperless manufacturing and single-use equipment.

Job description

Team Lead Biotech Associate – Downstream Manufacturing | Dunboyne

• 11 months contract
• Dunboyne | Fully onsite
• Shift-based role | 3-2-2 initially, moving to 4-on/4-off

An exciting 11-month contract opportunity for an experienced Biotech Associate to join a leading biopharmaceutical manufacturing site in Dunboyne. This is a hands‑on team lead role, leading a team of 9 Biotech Associates within downstream manufacturing and supporting safe, compliant and efficient batch progression.

Key Responsibilities

• Lead and support a team of 9 Biotech Associates within downstream manufacturing operations.
• Act as the technical point of contact for the shift team and key liaison with the Manufacturing Shift Lead.
• Oversee batch progression and support the production of biologic drug substance through filtration and purification processes.
• Progress automated recipes using paperless manufacturing technology and operate single‑use equipment between runs.
• Troubleshoot operational issues and lead problem‑solving activities to maintain safe and compliant production.
• Coach and mentor team members, supporting training, development and consistent application of GMP and EHS standards.
• Lead or support continuous improvement projects, process optimisation and emergency response activities.

Requirements

• Bachelor’s Degree (Level 8) in a technical, engineering or science-based discipline, or equivalent.
• Minimum 5 years’ experience within the biopharmaceutical industry.
• Previous experience in downstream manufacturing, ideally including chromatography, filtration or purification.
• Demonstrated team leadership experience and ability to coach and develop colleagues.
• Strong knowledge of cGMP, regulated manufacturing environments and biologics operations.
• Experience with electronic manufacturing systems such as SAP, Delta or equivalent.
• Strong problem‑solving skills, attention to detail and ability to work proactively under pressure in a 24/7 shift environment.