Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. We are currently seeking a Process Engineering Specialist to join our Manufacturing Science &T; team.

In this role, you will play a key part in pharmaceutical product development, process optimization, technology transfer, validation activities, and continuous improvement initiatives that support the manufacture of high-quality medicines. This is an exciting chance for a scientifically driven professional who thrives in a cross-functional environment and enjoys solving complex technical challenges throughout the product lifecycle. Design, develop, and optimize pharmaceutical formulations and dosage forms.

Support product lifecycle management, reformulation projects, and alternate supplier qualifications. Evaluate product performance, stability, potency, purity, content uniformity, and dissolution characteristics. Support regulatory submissions through technical documentation review and data analysis.

Develop, evaluate, and optimize manufacturing processes for pharmaceutical products. Lead and support scale-up, site transfer, commercialization, and technology transfer activities. Analyze manufacturing performance data and identify opportunities for process improvements, yield enhancement, waste reduction, and cost savings.

Quality & Compliance Ensure compliance with GMP, Health Canada, FDA, and other applicable regulatory requirements. Review and approve Change Controls, Master Batch Records, manufacturing instructions, and quality documentation. Conduct technical investigations, root cause analyses,



and CAPA activities related to product and process deviations.

Assess the impact of formulation, process, material, and equipment changes on product quality and regulatory compliance. Partner closely with Quality Assurance, Regulatory Affairs, Manufacturing, Validation, and Supply Chain teams. Participate in Technical Review Meetings and provide project updates, risk assessments, and technical recommendations.

Act as a technical resource and subject matter expert for internal stakeholders and project teams. Manage multiple projects while balancing shifting priorities and business needs. Bachelor's degree in Pharmacy, Chemical Engineering, or a related scientific discipline.

Preferred: Master's degree in Pharmacy, Chemical Engineering, or a related scientific discipline. ~5+ years of experience in pharmaceutical product development, formulation development, technology transfer, process validation, and/or manufacturing support. ~ Proven experience with solid oral dosage forms and controlled-release products. ~ Strong understanding of GMP requirements, pharmaceutical manufacturing, and product lifecycle management. ~ and international regulatory requirements and quality standards. ~ Strong scientific and technical problem-solving abilities. ~ Ability to write technical reports, protocols, and development documentation. ~ Ability to prioritize multiple projects and meet deadlines in a fast-paced environment.



~ Ability to work on-site with a rotational shift structure as required.

At Teva

Canada we provide a rewarding and collaborative work experience, with career growth and development opportunities for employees, in a safe and caring environment! The base pay offered may vary depending on job-related knowledge, skills, experience, education, and internal equity. In addition to base salary, this role may qualify for an annual bonus based on employment type.

Teva Canada’s choices Benefit Plan including Health, Dental, Disability, Life Insurance Employee Assistance Program & Virtual Health Programs Retirement Savings Programs Time for yourself or those you care about, through paid time for Vacation, Wellness days, Care/Sick days, Teva Days and Volunteer Days More exciting details on the specific total rewards offerings to be provided at the offer stage depending on the position and employment type hiring for. This position will fill a current vacancy and Teva Canada may use an artificial intelligence (AI) system to assist with the initial screening and evaluation of job applications by analyzing for relevant skills, professional experience, and education, that best match the posted job qualifications. Teva Pharmaceuticals is committed to equal opportunity in employment.

It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. #

📌 Process Engineer (Remote) (Whitchurch-Stouffville)
🏢 Tevapharm
📍 Whitchurch-Stouffville