Work Schedule7 1/2 hr shift
Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Working at heights
Job DescriptionJob Description
Division/Site Specific InformationThe 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.
Discover Impactful Work:Conduct Facility and Utility projects in support of equipment/building improvements and problem-solving. Provide Facility/Utility support to the engineering team members as requested in the execution of their projects. Prepare Capital Appropriation Requests related to Facility maintenance projects and identify contractors, estimates, resources and timelines for project execution. Work closely with the Facility and Utility team in providing technical support as needed.
Day in the Life:Facility and Utility Project Management and Design- Support facility and utility projects related to building, equipment, and process improvements within a GMP oral solid dose manufacturing environment.
- Assist in project design, planning, supervision, execution, and risk mitigation to ensure projects meet safety, quality, cost, productivity, cGMP, and data integrity requirements.
- Develop CAPEX requests, project scopes, schedules, cost estimates, work breakdown structures, risk assessments, and project plans.
- Select and manage contractors, vendors, and engineering resources.
- Review engineering drawings, equipment specifications, construction methods, and facility modification requirements.
- Monitor project progress to ensure completion on time, within budget, and in compliance with safety codes and company policies.
Engineering Support and Start-Up of a Project- Support facility and utility shutdowns, contractor bid packages, vendor selection, construction activities, equipment installation, commissioning, and start-up.
- Coordinate or assist with IQ/OQ/PQ execution, change controls, CMMS work orders, and related documentation.
- Monitor contractor safety, quality, and performance, and address any deficiencies promptly.
- Ensure new or modified facilities, utilities, and equipment are installed and commissioned with minimal operational disruption and in accordance with good engineering practices.
- Provide training to building operators on facility and utility equipment.
Project Administrative Tasks- Develop or support User Requirements, equipment specifications, quotation processes, and project documentation.
- Track project costs, verify contractor work, authorize payments with Facility Management and Engineering, and communicate project status, costs, safety conditions, and risks to management.
- Represent the department in facility and utility investigations, support CAPAs and deviation reports related to project deficiencies, and participate in EHS activities as required.
Learning and Training- Participate in training, development programs, seminars, workshops, and process improvement initiatives to enhance job performance and support site and departmental goals.
Other- Maintain a safe working environment, report hazards, and support alternating or rotating shifts and maintenance shutdowns as required.
Keys to Success:Education: Minimum Engineering Technologist Diploma.
Bachelor of Applied Science in Mechanical Engineering, Chemical Engineering, or related field is an asset
Experience: Minimum 3 years of experience in a GMP manufacturing facility preferably pharma.
Plant Engineering or Project Engineering experience an asset.
Equivalency: Equivalent combinations of education, training, and relevant work experience may be considered.
Knowledge, Skills, and Abilities:Good understanding of project management and project engineering principles. Ability to work with limited supervision. Proficiency using Microsoft Office applications including MS Project. Knowledge of ACAD. Strong judgment, decision making and trouble shooting skills. Excellent organizational skills. Excellent interpersonal skills (both written and oral). Ability to work on multiple projects simultaneously. Familiarity with Good Manufacturing Practices. Proficiency with the English language.
Physical Requirements: Position requires ordinary ambulatory skills and physical coordination sufficient to move about manufacturing/office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of up to 40 pounds; arm, hand and finger dexterity; visual acuity to operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Usually in a comfortable environment but with regular exposure to factors causing moderate physical discomfort from such things as dust, loud noise, bright lights, fumes, or odour. Use of Personal Protective equipment is required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator.
Excellent Benefits- Benefits & Total Rewards | Thermo Fisher Scientific
- Medical, Dental, & Vision benefits-effective Day 1
- Paid Time Off & Designated Paid Holidays
- Retirement Savings Plan
- Tuition Reimbursement
OTHER- Relocation assistance is NOT provided
- Must be legally authorized to work in Canada
- Must be able to pass a comprehensive background check
CompensationThe estimated annualized pay range for this position in Ontario is $69,400.00-$104,050.00.
