Pharma Process Engineer: Scale-Up & Tech Transfer

Teva Pharmaceuticals; Whitchurch-Stouffville; On-site; CAD 74,000 - 93,000; Full time

Benefits offered by this job

Health plan

Dental plan

Retirement savings

Employee Stock Purchase Plan

Education assistance

Paid time off

Job summary

Teva Canada is seeking a Process Engineering Specialist to join the MS&T team. You will design and optimize pharmaceutical processes, lead tech transfer, and support validation activities across the product lifecycle.

The role requires a strong foundation in GMP, regulatory knowledge, and cross-functional collaboration with QA, Regulatory, Manufacturing, and Supply Chain teams. On-site with rotating shift required; 5+ years in product development or process validation.

Qualifications

• Bachelor's degree in Pharmacy, Chemical Engineering, or related scientific field; Master's preferred.
• 5+ years of experience in pharmaceutical product development, formulation development, technology transfer, and/or manufacturing support.
• Experience with solid oral dosage forms and controlled-release products.
• Strong GMP, regulatory knowledge and quality standards.

Responsibilities

• Design, develop, and optimize pharmaceutical processes and formulations.
• Lead scale-up, site transfer, and technology transfer activities.
• Participate in equipment qualification and process validation (IQ/OQ/PQ).
• Ensure compliance with GMP and regulatory requirements.
• Collaborate with Quality Assurance, Regulatory Affairs, Manufacturing, Validation, and Supply Chain.

Skills

Problem solving

Regulatory knowledge

GMP knowledge

Project management

Stakeholder management

Technical reports

Communication skills

Leadership

On-site rotation

Education

Bachelor's degree in Pharmacy or Chemical Engineering

Master's degree preferred

Job description

Teva Canada is seeking a Process Engineering Specialist to join the MS&T team. You will design and optimize pharmaceutical processes, lead tech transfer, and support validation activities across the product lifecycle.

The role requires a strong foundation in GMP, regulatory knowledge, and cross-functional collaboration with QA, Regulatory, Manufacturing, and Supply Chain teams. On-site with rotating shift required; 5+ years in product development or process validation.