Lead Biotech Manufacturing Associate - 24/7 Shift

PSC Biotech® Corporation

Dunboyne

On-site

EUR 90,000 - 120,000

Full time

24 hours ago
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Job summary

PSC Biotech Corporation Ireland seeks a Lead Manufacturing Biotech Associate to oversee a shift-based production team producing biologic drug substances. You will act as a technical point of contact, coach team members, and ensure smooth progression of batches across a 24/7 operating schedule.

The role requires 5+ years in biopharma, strong cGMP/EHS knowledge, and proven leadership in a regulated environment.

Qualifications

  • Bachelor degree in technical/engineering/science (Level 8).
  • Minimum 5 years in biopharma.
  • Proven leadership in regulated environments.
  • Strong GMP/EHS knowledge.

Responsibilities

  • The production of biologic drug substance on their designated shift and act as a coach and a technical point of contact for others on the shift team.
  • Trouble shooting and problem solving with the ability to lead self-directed work teams.
  • Progression of an automated recipe using paperless technology to generate drug substance through filtration and purification.
  • Setting up single-use equipment between runs and ensuring world class GMP and EHS principles are applied.
  • Deliver on safety, quality, and schedule; focus on right first time and continuous improvement.
  • Coach or mentor peers on unit operations to support the value stream.
  • Lead and sponsor approved projects aligned with site strategy and continuous improvement.
  • Act as primary delegate for the manufacturing shift lead during emergencies.

Skills

Leadership
cGMP knowledge
Teamwork
Problem solving

Education

Bachelor's Degree (Level 8)

Job description

PSC Biotech Corporation Ireland seeks a Lead Manufacturing Biotech Associate to oversee a shift-based production team producing biologic drug substances. You will act as a technical point of contact, coach team members, and ensure smooth progression of batches across a 24/7 operating schedule.

The role requires 5+ years in biopharma, strong cGMP/EHS knowledge, and proven leadership in a regulated environment.

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