Biopharma Process Engineer — Sterile Operations (Contract)

Wallace Myers International

Waterford

On-site

EUR 60,000 - 90,000

Full time

3 days ago
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Job summary

Wallace Myers International is recruiting Multiple Process Engineers on contract to work at our Global Biopharma client's site in Waterford. Experience in sterile processes preferred. Some shift work may be required. Immediate EU work authorization is required for these contracts.

Role involves leading operations improvements, process development, scale-up, and transfer, with a focus on aseptic manufacturing and quality compliance in a regulated biopharma environment.

Qualifications

  • Degree in Chemical, Industrial or equivalent Engineering discipline.
  • Advanced degree in Pharmaceutics, Pharmacy or related science considered an advantage.

Responsibilities

  • Provide leadership and support to operations teams to ensure standards are met.
  • Develop and implement improvement initiatives in manufacturing and development operations.
  • Lead technical problem resolution and RCA for manufacturing operations with cross-functional teams.
  • Implement and monitor performance metrics and cycle time reduction initiatives.
  • Act as SME for new product introductions, process development, scale-up and tech transfer.
  • Ensure cGMP compliance and maintain quality documents.

Skills

Aseptic manufacturing knowledge
Design of Experiment
Statistical techniques
Project management
Structured problem solving
Verbal communication
Report writing
Laboratory and pilot plant skills

Education

Chemical/Industrial Engineering degree

Job description

Wallace Myers International is recruiting Multiple Process Engineers on contract to work at our Global Biopharma client's site in Waterford. Experience in sterile processes preferred. Some shift work may be required. Immediate EU work authorization is required for these contracts.

Role involves leading operations improvements, process development, scale-up, and transfer, with a focus on aseptic manufacturing and quality compliance in a regulated biopharma environment.

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