Base Career helps you apply smarter for this job.
Key skills for this role
Thermo Fisher Scientific offers industry-leading pharma services through our Patheon™ brand, providing an integrated global network of scientific, technical, regulatory, and quality experts committed to helping deliver medicines to patients faster. The Mississauga site supports all phases of drug product development — from early-phase formulation development to clinical trial material to commercial supply — within the same facility using scalable equipment. The site supports non-GMP and GMP work for highly potent and low-potent compounds, complex formulations, pediatric dosage forms, patent-extension strategies, and conventional oral solid dosage forms.
Supports/Leads processing, packaging, and client equipment projects from initial design to operations usage.
Identifies new equipment, develops user requirement specifications, arranges capital funding and implements into Good Manufacturing Practice commercial production.
Schedules and hosts regular project meeting with internal teams, vendors and clients.
Creates and manages project plans using Project Management tools/applications, to ensure timely delivery of project milestones.
Leads all project planning activities and cross-functional project assessments, including assessments by IT groups.
Monitors capital expenditures for equipment projects.
Leads the Project Management for implementation of complex processing, packaging, PDS, and/or client equipment.
Provide leadership to Junior Project Managers by supporting problem solving and solution generation on projects, training/mentoring, and supporting project progression.
Supports improvements, training, troubleshooting and complaint investigation of equipment.
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
Allentown, USA
Los Angeles, USA
Grand Island, USA
Allentown, USA
West Point, USA
Los Angeles, USA
Cincinnati, USA
Grand Island, USA
, GBR
, USA
Louisville, USA
Creates or provides technical input into protocols / reports for equipment commissioning and qualification.
Executes/Provides Technical Support to equipment assessments, validation execution, and/or engineering trials, as required.
Supports equipment Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT), as required.
Liaises with functional areas (including clients and vendors) to meet project objectives.
Ensure a safe working environment and potential hazards are identified, assessed and escalated during project execution.
Maintain a continuous improvement mindset and actively participate in and initiate practical process improvement initiatives.
Monitors and benchmark new developments in pharmaceutical industry related to their area of expertise and/or project to look for opportunities to put Patheon in the forefront of pharmaceutical technology.
Ability to travel (as required)
Performs alternating or rotating shift work (as required)
College/Technical School diploma in relevant technical field.
University degree in relevant technical field, Engineering Degree is an asset.
Experience:
Minimum 3 years of previous related experience and general knowledge of drug processing, packaging validation and production.
Minimum 2 years Project Management experience.
Experience in technical writing and oral presentation.
Experience organizing complex work.
Experience in technical/scientific discussions with clients.
Equivalent combinations of education, training, and relevant work experience may be considered.
Relocation assistance is NOT provided
Must be legally authorized to work in Canada
Must be able to pass a comprehensive background check
Compensation
The world leader in serving science.
Visit company websiteJobs and hiring trendsCAD 69400-104050 yearly / year
Full-time
Mid · 3+ years experience
Onsite
Apply faster on company sites with our extension.