Process Operations Chemist

Apotex Inc.; Brantford; On-site; CAD 70,000 - 90,000; Full time

Job summary

A leading pharmaceutical company in Brantford seeks a Chemist for process operations. The role involves ensuring safe implementation and scale-up of manufacturing processes while complying with GMP guidelines. Key responsibilities include preparing documentation, coordinating with teams, troubleshooting issues, and evaluating process performance. The ideal candidate has a Bachelor’s degree in Chemistry or chemical engineering and at least 3 years of experience in a cGMP API facility. Join us to be part of a valued team committed to innovative healthcare.

Qualifications

• 3+ years of experience as process chemist in a cGMP API facility.
• Proven leadership skills and ability to work independently.
• Self-motivated and results-oriented team player.

Responsibilities

• Ensure safe and effective implementation of process technologies.
• Prepare GMP documentation including Master Batch Records.
• Conduct on-the-floor monitoring of production in progress.
• Troubleshoot problems during new process piloting.

Skills

Problem solving

Troubleshooting

Teamwork

Oral communication

Written communication

Education

Bachelor degree in Chemistry or chemical engineering

Tools

Microsoft Office suite

Job description

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: www.apotex.com .

Job Summary

The Chemist, Process Operations PO7 ensures the safe and effective implementation and scale‑up of process technologies complying with GMP and drug regulatory guidelines at Apotex Pharmachem Inc. The areas of responsibility include process characterisation and mapping, process implementation, process costing, root cause analysis and CAPA determination, process technology optimisation and scale‑up.

Job Responsibilities

• Accountable for the safe and effective implementation, scale‑up and operational optimisation of process technologies at Apotex Pharmachem Inc.
• Accountable for GMP and drug regulatory guideline compliance within the Process Operations Group throughout the implementation and commercialization of process technologies.
• Independently develops safe and effective implementation and scale‑up plans of API manufacturing processes to achieve optimal process fit to pilot/production facility through detailed process mapping. Coordinate efforts of process implementation programs with R&D and RA/QA.
• Responsible for the timely preparation of GMP documentation as required. This includes (but is not limited to) Change Control Requests, Master Batch Records, supplemental batch instructions, deviation reports, validation documentation, annual product reviews, standard operating procedures, DMF supporting documentation.
• Prepares associated process documentation and provides to Production and Materials Management staff for batch execution. Ensure completion of process documentation as required for GMP compliance, in coordination with Quality Assurance.
• Ensures the completion the Process Operations component of HAZOP reports and coordinates with R&D and Engineering on the overall completion of HAZOP reports for new and existing processes.
• Responsible for real time completion of batch summary tables and process trending for pilot and commercial processes.
• Completes Corrective Actions and Preventative Actions investigations and ensures that the identified root cause and follow‑up actions are appropriate and effective.
• Complete campaign summaries and evaluate campaign success with respect to campaign goals. Complete up‑to‑date costing analyses of assigned processes and critically evaluate production costs; identifies methods for cost reduction.
• Coordinates with Operations management, Production staff, Quality Control and Quality Assurance on scheduling priorities to meet production targets.
• Conducts on‑the‑floor monitoring of production in progress and provides guidance to production staff in the execution of pilot and commercial manufacturing processes. Conducts in‑process testing as required.
• Troubleshoot problems encountered during new process piloting or routine production, and design experiments with R&D as necessary to investigate and resolve process related challenges.
• Systematically evaluate process performance data from batch records concurrently with batch production, develop and implement procedures to ensure consistent performance and identifies opportunities for improvement while complying with GMP and drug regulatory guidelines.
• Participate as required in the transfer of process technologies to contract manufacturing sites for assigned processes.
• Works in a safe manner collaborating as a team member to achieve all outcomes.
• Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
• 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.
• All other relevant duties as assigned.

Job Requirements

• Education
  • Bachelor degree in Chemistry or chemical engineering from a recognized academic institution
• Knowledge, Skills and Abilities
  • Proven computer literacy, particularly with the Microsoft Office suite of programs
  • Proven problem solving and troubleshooting skills
  • Ability to work independently and as a team member with demonstrated leadership skills.
  • Excellent oral and written communication skills.
  • Self‑motivated, driven individual who is a results‑oriented team player with effective interpersonal skills
• Experience
  • Minimum 3 years’ experience as process chemist in a cGMP Active Pharmaceutical Ingredient (API) facility

At Apotex, we are committed to fostering a welcoming and accessible work environment, where everyone feels valued, respected, and supported to succeed.

We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.