Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Division/Site Specific Information:
Our Mississauga facility covers all phases of drug product development from early-phase formulation development to clinical trial material to commercial supply in the same plant using scalable equipment for non-GMP and GMP work.
Discover Impactful Work:
Support the Technical Operations department in generation of protocols, master batch record review, batch analysis, Quality Investigation Report/Quality Deviation Report (QIR/QDR) follow-up, process execution and equipment procurement.
Generate technical documents (protocols, reports, proposals, gap/risk assessment, batch records, URS, etc).
Post-secondary diploma in Chemistry, Engineering, Science or related field.
BSc in Chemistry or Engineering is an asset.
Minimum 3 years of experience within Pharmaceutical Manufacturing or Quality Assurance departments
Minimum 2 years of combined hands on pharmaceutical experience in Production and Development (scale up and technology transfer of solids and liquids).
Minimum 1-year experience in Master Batch Record/Protocol/Report preparation within the Pharmaceutical Industry, including proven abilities in report writing and batch record preparation required
Previous experience in statistical analysis and data compilation an asset.
Previous experience with SAP enterprise software to source information and navigate business operations an asset.
Equivalent combinations of education, training, and relevant work experience may be considered.
Knowledge, Skills and Abilities:
Knowledge of processing/packaging equipment. Knowledge of current Good Manufacturing Practices and ability to follow Standard Operating Procedures. Strong written and oral skills. Detail oriented and organized, with a high degree of accuracy and thoroughness. Excellent interpersonal skills and communication skills. Ability to multi-task, meeting tight deadlines in a fast paced environment. Proven problem solving abilities. Demonstrated computer proficiency with Microsoft Office programs. Proficiency with the English Language.
Light physical effort and fatigue. Walks, sits or stands for limited periods. May require occasional equipment operation including keyboard equipment. Lifts light items for limited duration. Typically located in a comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as dust, fumes or odours, temperature extremes, loud noise, strong drafts, or bright lights. Use of Personal Protective equipment may be required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator on occasionally.
Excellent Benefits
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Benefits & Total Rewards | Thermo Fisher Scientific
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Medical, Dental, & Vision benefits-effective Day 1
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Paid Time Off & Designated Paid Holidays
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Retirement Savings Plan
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Tuition Reimbursement
OTHER
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Relocation assistance is NOT provided
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Must be legally authorized to work in Canada now or in the future, without sponsorship.
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Must be able to pass a comprehensive background check
Compensation
The estimated annualized pay range for this position in Ontario is $56,400.00–$84,600.00.
