Biopharma Manufacturing Operations Lead

Phibro Animal Health SA

Sligo

On-site

EUR 90,000 - 130,000

Full time

25 hours ago
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Benefits offered by this job

Flexible work culture

Job summary

Phibro Animal Health Corporation in Ireland–Sligo seeks an experienced Site Lead to direct manufacturing operations, ensuring GMP compliance, safety, and operational excellence. You will mentor a growing team and partner with QA, EHS, and functions to meet production targets and quality standards.

The role requires a strong track record in biopharma operations, plus extensive experience with audits, process improvements and leadership at scale.

Qualifications

  • Bachelor’s degree in Life Science or equivalent, with extensive relevant industry experience acceptable.
  • Minimum of 10 years in a similar biopharma manufacturing role, with 5+ years in a managerial capacity.
  • Proven track record in GMP-compliant operations, audits, and regulatory inspections.

Responsibilities

  • Oversee/manag manufacturing operations to ensure GMP and regulatory compliance.
  • Lead, mentor and develop a growing team of manufacturing professionals.
  • Implement strategies to meet targets, cost efficiency and preparedness for escalations.
  • Ensure SOPs, batch records and documentation are written/reviewed and training is current.
  • Collaborate with cross-functional teams and participate in audits and inspections.
  • Drive process improvements using lean principles and CI methodologies.
  • Monitor metrics, drive safety culture with EHS collaboration, and optimise yield/quality.
  • Support SLT/S&OP processes and assist in staffing decisions for site expansion.

Skills

Leadership
GMP knowledge
Problem solving
Strategic thinking
Communication
Team development
Lean manufacturing
Continuous improvement
Cross-functional collaboration

Education

Life Science degree

Tools

MS Excel
MS Word
MS Project

Job description

Phibro Animal Health Corporation in Ireland–Sligo seeks an experienced Site Lead to direct manufacturing operations, ensuring GMP compliance, safety, and operational excellence. You will mentor a growing team and partner with QA, EHS, and functions to meet production targets and quality standards.

The role requires a strong track record in biopharma operations, plus extensive experience with audits, process improvements and leadership at scale.

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