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Production Technician

Job in Toronto, Ontario, C6A, Canada
Listing for: Apotex Inc.
Full Time position
Listed on 2026-09-17
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production Associate / Production Line
Salary/Wage Range or Industry Benchmark: 40000 - 48000 CAD Yearly CAD 40000.00 48000.00 YEAR
Job Description & How to Apply Below

About Apotex Inc.

Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.

About

Apotex Inc.

Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.

For more information visit:  .

Job Summary

Manufactures product as per customer and company requirements while working within a team environment. Is responsible for sanitation, set-up and operation of all production equipment. Follows all GMP’s, SOD’s and company policies/ regulations and remains aligned to the Apotex Strategic Objectives.

Job Responsibilities Compliance
  • Perform all duties according to the SOD’s, GMP’s and all other established safety standards and company policies
  • Correctly complete all documentation as per SOD’s, GDP and GMP requirements, i.e., observations, test results, batch record information, etc.
  • Access Apotex intranet for the purpose of locating and utilizing relevant SOD’s, MSDS’s, company policies and procedures
  • Notify Supervisor / Admin in the event of a departure from procedure, product defect, safety incident or other serious problem
  • Execute line clearance and cleaning verification activities as per SODs and established standard work
  • Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies
Productivity and Equipment
  • Dismantle, clean, sanitize, move (where required), install, and align parts to assemble manufacturing equipment as part of equipment set-up activities according to established SODs to ensure GMP compliance and meet department changeover targets in support of department and productivity goals.
  • Perform equipment inspection and safely operate all required industry standard equipment and machinery including those used to manufacture, store, clean and transport production related assets, goods to support operational tasks. This also includes safe handling of work tools.
  • Ensure proper selection, care and use of parts, equipment, tools while performing all job related duties.
  • Operate equipment with computerized control panel / Human Machine Interface (HMI) to monitor the manufacturing process.
  • Monitor and control start up and shut down activities of an equipment and a process.
  • Execute and document in-process testing required during manufacturing of a product.
  • Execute applicable SAP, LIMS, APO-OEE, POMSnet (where applicable) transactions accurately and in a timely manner.
  • Effectively process batches within established specifications to meet department batch execution targets by ensuring optimal run rates in support of schedule adherence.
  • Complete master batch records and associated production documentation accurately, timely following SODs, GDP, GMP requirement and batch right the first time (BRFT) approach.
  • Understa…
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