Senior Manager Global Facility Management & Automation

PolyPeptide Group

Malmö, Sweden
On-site
7+ years maintenance leadership in pharma
Cgmp regulated environment experience
Total productive maintenance (tpm) methodology
PolyPeptide Group is seeking a Senior Manager for Global Facility Management & Automation to lead maintenance and facility operations across its six international sites. The ideal candidate should have extensive experience in maintenance leadership within the pharmaceutical or biotech sectors, particularly in GMP-regulated environments

Job Summary

  • This role is accountable for driving global effective and aligned standards and procedures for Facility Management and Maintenance across six manufacturing sites.
  • You will lead the global roll-out of the Total Productive Maintenance (TPM) methodology to embed maintenance excellence and operational reliability throughout the organization.
  • The position offers a dynamic workplace where employees can grow alongside the company's mission to support patients through novel drug therapies.

Matching Summary

Match Score: 85

PolyPeptide Group is seeking a Senior Manager for Global Facility Management & Automation to lead maintenance and facility operations across its six international sites. The ideal candidate should have extensive experience in maintenance leadership within the pharmaceutical or biotech sectors, particularly in GMP-regulated environments.

Skills & Requirements

Must-have

  • 7+ years maintenance leadership in pharma
  • cGMP regulated environment experience
  • Total Productive Maintenance (TPM) methodology
  • CMMS governance and data model management
  • Multi-site facility management alignment
  • Asset lifecycle management and reliability
  • Risk assessment methodologies FMECA RCA

Nice-to-have

  • Strong change management capabilities
  • Cross-functional collaboration skills
  • Fluent English communication
  • International travel readiness
  • Solution-oriented thinking
  • Innovation and excellence mindset

Key Requirements

  • Bachelor's degree in Engineering required
  • Advanced degree preferred
  • Experience in pharmaceutical or biotech CDMO environments
  • Knowledge of ISPE guidance and FDA expectations

Work Rights

Not specified

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