Quality Control Supervisor, Manufacturing

1 month ago

Toronto, Ontario, Canada Sun Pharmaceutical Industries, Inc. Full time

Position:
Quality Control Supervisor, Manufacturing

Sun Pharmaceutical Industries, Inc. is a global leader in the pharmaceutical sector, dedicated to enhancing the quality of life through innovative healthcare solutions.

Our commitment lies in fulfilling the needs of our clients and the broader community by innovating, developing, producing, and marketing top-tier healthcare products.

With a rich history, our state-of-the-art manufacturing facility employs a diverse team of professionals dedicated to excellence.

Our specialization in dermatological products has positioned us as a prominent manufacturer and supplier of a wide range of topical formulations, including creams, ointments, liquids, and gels.

Supported by our parent company, we strive to create a healthy, safe, and rewarding workplace for all employees. Our comprehensive benefits packages are tailored to meet the diverse needs of our workforce and their families.

We offer numerous opportunities for professional growth and development, including:

  • Benefit programs designed to support employees and their families, featuring a comprehensive health and dental benefits package, group retirement savings matching program, direct access to healthcare and wellness initiatives, and paid time off.
  • Employee training and development programs, including tuition reimbursement, internal mobility opportunities, and recognition initiatives.

Key Responsibilities:

The primary role of this position is to lead and mentor team members, establish and uphold quality control systems and processes for evaluating and qualifying alternative suppliers for materials (Active Pharmaceutical Ingredients, Raw Materials, and Packaging Components) in compliance with regulatory standards.

This role will generate comprehensive quality control reports (Vendor Assessments concerning analytical specifications, analytical validations, and product evaluations related to Residual Solvent Requirements, Elemental Analysis Requirements, and Nitrosamines) to facilitate the qualification of new suppliers in a compliant manner.

This position promotes a culture of quality assurance, ensuring thoroughness and timeliness in lab investigations.

Additional Responsibilities Include:

  • Supervising, guiding, and mentoring staff through ongoing coaching, performance evaluations, and routine meetings.
  • Planning, scheduling, organizing, and monitoring workloads to ensure all operations are executed within required turnaround times and adherence to established schedules.
  • Authoring risk assessments and reports for evaluations related to Nitrosamines, Elemental Analysis, and Residual Solvents.
  • Providing troubleshooting support for testing methods and equipment issues.
  • Identifying and implementing key process improvements to enhance systems and elevate compliance standards.
  • Participating in Internal, Customer, and Regulatory Audits.
  • Collaborating with relevant departments to integrate quality into processes and systems.
  • Conducting monthly Health and Safety Audits and safety training.
  • Managing other responsibilities and special projects as required.

Qualifications:

A Bachelor's Degree in a Science-related field is required, along with strong supervisory experience being an asset.

Sun Pharmaceutical Industries, Inc. values diversity in the workplace and is committed to achieving employment equity. We will provide accommodations throughout the recruitment and selection process to applicants with disabilities.

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