Manufacturing Technician – Tech Transfers NPI (12-Hour Shifts)

About the Company:

Innopharma Technical Services on behalf of our Global Multinational Client are seeking Manufacturing Technicians to support the tech transfer of new products, enabling the clinical manufacture of both small and large molecule drug products.

Location: Co. Mayo
Contract Type: Permanent
Shifts: 12-hourrotational shifts (days, nights, weekends)
Sector: (Bio)Pharmaceutical

Are you looking to join a cutting-edge manufacturing team at the forefront of pharmaceutical innovation? Our client is seeking a Manufacturing Technician.

About the Role:

In this role, you’ll contribute across Manufacturing, Biologic Drug Product commercial support, and New Product Introduction (NPI)/Project Management. You’ll be part of a high performing, collaborative team delivering quality drug products in line with GMP standards and global timelines.

Key Responsibilities:

• Manufacture pharmaceutical products at various lifecycle stages (clinical, non-clinical,
  pre-clinical).
• Perform batch preparation (vial washing, sterilisation, area prep).
• Operate in aseptic conditions and controlled environments.
• Conduct compounding, sterile filtration, and sterile filling activities.
• Prepare components/equipment for use in Grade A environments.
• Support multi-product suite operations with efficient changeovers.
• Perform environmental monitoring and support EHS procedures.
• Collaborate with vendors to enhance single-use technologies.
• Review and contribute to protocols, reports, and manufacturing documentation.
• Engage with cross-functional teams: RCD, Engineering, Quality, Validation, Supply Chain, and Operations.
• Ensure full compliance with GMP, SOPs, and quality standards.

What We’re Looking For:

• Third-level qualification in a relevant scientific/technical discipline and/or Minimum 12–
  18 months’ experience in pharmaceutical or medical device industries
• Experience working in cleanroom environments is essential.
• Familiarity with aseptic practices and GMP regulations preferred.
• Knowledge of:
  o Autoclave sterilization, depyrogenation, and filter integrity testing
  o Lyophilization/freeze dryer operations
  o Single-use technologies
• Strong technical writing, documentation, and communication skills.
• Ability to work effectively in a team-based and project-driven environment.
• Proactive mindset with strong problem-solving capabilities.

Why Apply?

• Join a collaborative team making a real impact in global healthcare.
• Access structured career progression opportunities.
• Competitive salary, excellent benefits, and a strong focus on work-life balance

Apply Now

If you’re passionate about manufacturing excellence and eager to grow in a fast-paced, regulated environment, we want to hear from you.

Apply Now