Director Of Maintenance And Engineering

Mulgrave

Windsor, Nova Scotia, Canada
Base: $127,745.00 - $199,601.00 cad py; bonus/equi...
Onsite
Cgmp manufacturing facility management
Engineering and maintenance leadership
Pharmaceutical manufacturing equipment knowledge
BIOVECTRA, now part of Agilent, is a leader in contract development and manufacturing of active pharmaceutical ingredients specializing in clinical-to-commercial scale production

Job Summary

  • BIOVECTRA, now part of Agilent, is a leader in contract development and manufacturing of active pharmaceutical ingredients specializing in clinical-to-commercial scale production.
  • The Director of Engineering and Maintenance is responsible for ensuring equipment and systems perform reliably in a cGMP manufacturing facility while leading a high performing team focused on safety, quality, and integrity.
  • This role offers the opportunity to work with cutting-edge technologies and collaborate with dedicated professionals to improve patient care through advanced manufacturing.

Matching Summary

BIOVECTRA, now part of Agilent, is a leader in contract development and manufacturing of active pharmaceutical ingredients specializing in clinical-to-commercial scale production.

Salary

Base: $127,745.00 - $199,601.00 CAD per year; Bonus/Equity: eligibility for bonus and stock; Benefits: included

Skills & Requirements

Must-have

  • cGMP manufacturing facility management
  • engineering and maintenance leadership
  • pharmaceutical manufacturing equipment knowledge
  • maintenance management systems (CMMS)
  • regulatory compliance with Health Canada and FDA
  • capital project management
  • sterile manufacturing process maintenance

Nice-to-have

  • Lean manufacturing methodologies experience
  • team development and talent management
  • collaboration with IT for manufacturing technology
  • safety culture promotion
  • strong communication and stakeholder engagement
  • experience in biopharmaceutical equipment qualification

Key Requirements

  • Bachelor’s degree in engineering or related field
  • 8+ years engineering and facilities management experience
  • 5+ years leadership in life sciences or pharmaceutical facility
  • Professional certifications preferred (PE, CFM, CHFM, LEED AP)
  • Experience with sterile manufacturing equipment maintenance
  • Knowledge of GMP and regulatory standards
  • Experience with building systems commissioning and qualification

Work Rights

Not specified

Tailored Resume

Cover Letter