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Project Manager - Equipment Engineering

Thermo Fisher Scientific
Mississauga, CAN
Full-time
Onsite
$69,400 to $104,050.
Discovered 3 weeks ago
Equipment project managementPharmaceutical drug processing and packagingProject planning and schedulingGood Manufacturing Practices (GMP)Equipment validation and qualificationTechnical writing

Full Job Posting

Schedule

  • Standard Monday-to-Friday work schedule.
  • Rotating or alternating shift work may be required.

Workplace and site

  • The role is based at the Mississauga site, which supports pharmaceutical development and commercial supply.
  • The description identifies office environmental conditions and notes possible exposure to manufacturing and laboratory conditions.
  • Travel may be required.

Role overview

Supports or leads processing, packaging, and client equipment projects from initial design through operational use.

The site supports non-GMP and GMP work, including complex formulations and multiple dosage forms.

Responsibilities

  • Identify equipment needs, develop user requirement specifications, arrange capital funding, and implement equipment in GMP production.
  • Plan projects, coordinate meetings and cross-functional assessments, and manage milestones and capital expenditure.
  • Lead complex processing, packaging, PDS, and client equipment implementations.
  • Mentor Junior Project Managers and support equipment improvements, training, troubleshooting, and complaint investigations.
  • Contribute to commissioning and qualification protocols and reports; support assessments, validation, engineering trials, FAT, and SAT.
  • Coordinate with clients, vendors, and internal functions; identify and escalate safety hazards.
  • Participate in process improvement and monitor pharmaceutical technology developments.

Qualifications and skills

  • College or technical school diploma in a relevant technical field; a relevant university degree is an asset, especially an engineering degree.
  • At least three years of related experience and general knowledge of drug processing, packaging validation, and production.
  • At least two years of project management experience.
  • Experience in technical writing, oral presentations, organizing complex work, and technical or scientific client discussions.
  • Knowledge of drug processes, validation and commercialization, GMP, SOPs, and FDA compliance.
  • Strong computer skills, including advanced MS Word/Excel and project management applications; general knowledge of experimental design for development equipment.
  • Proficiency in English; equivalent combinations of education, training, and relevant experience may be considered.

Compensation

  • Estimated annualized pay range in Ontario is $69,400 to $104,050.

Benefits

  • Benefits include medical, dental, and vision coverage effective on the first day, paid time off and holidays, a retirement savings plan, and tuition reimbursement.
  • Relocation assistance is not provided.

Other conditions

  • Must be legally authorized to work in Canada and pass a comprehensive background check.
  • Personal protective equipment may be required; the role may involve light physical effort and occasional equipment operation.

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