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Details

Lead OSD Process Engineer


Reference:SMC02994 Location: Westmeath
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Process Engineer

Lead Process Engineer | Oral Solid Dosage | Athlone
We're currently recruiting for an exciting opportunity with a leading multinational pharmaceutical manufacturer based in Athlone, supporting a significant investment in oral solid dosage manufacturing capabilities.

The successful candidate will act as a Process and Equipment SME, supporting the design, introduction, qualification and start-up of new OSD manufacturing processes and equipment.

This is an excellent opportunity for an experienced pharmaceutical Process Engineer to take technical ownership across a major capital programme, from early-stage design through to GMP manufacturing readiness.

Duties

  • Act as Process and Equipment SME for assigned oral solid dosage manufacturing processes.
  • Support engineering activities from Basis of Design through construction, commissioning, qualification and handover.
  • Provide technical leadership during the introduction of new manufacturing equipment and processes.
  • Support OSD unit operations including dispensing, blending, granulation, tableting and cleaning.
  • Participate in FAT, SAT, equipment qualification and process validation activities.
  • Ensure equipment and process designs meet GMP, quality, safety and operational requirements.
  • Support technology transfer, operational readiness and GMP manufacturing start-up.
  • Collaborate with engineering partners, equipment vendors and cross-functional manufacturing teams.
  • Develop and review engineering, process and operational documentation

Education & Experience

  • Degree in Engineering or a relevant Science discipline.
  • Minimum 5–7 years' experience in pharmaceutical manufacturing, process engineering or equipment qualification.
  • Strong knowledge of oral solid dosage manufacturing processes and equipment is highly desirable.
  • Experience supporting capital projects, equipment introduction or technology transfer.
  • Good understanding of GMP, process validation and Good Engineering Practice.
  • Strong technical problem-solving, communication and stakeholder management skills.
  • Availability to work on-site in Athlone five days per week, with occasional supplier-site travel if required.

If interested, contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.