Elevate your career as a Validation Associate in Mississauga, ON, focusing on process validation, cleaning protocols, and compliance within the GMP framework. Join our dynamic environment and contribute to vital projects for operational success. This role supports the timely delivery of qualification protocols and validation projects aligned with organizational goals.

Candidates will collaborate with cross-functional teams to execute validation studies and generate comprehensive reports. You will also update Standard Operating Procedures and pioneer continuous improvement initiatives in validation processes. Key Responsibilities:

- Develop and execute validation protocols for cleaning and process
- Collaborate with various departments for validation execution




- Compile and report results from validation studies
- Update and enhance Standard Operating Procedures
- Participate in initiatives for process improvement Requirements:
- Enrolled in a science or engineering program
- Organized with strong direction-following skills
- Proficient in Microsoft Office 365
- Excellent verbal and written communication abilities
- Adaptable and quick to adapt in a changing environment Bring your validation knowledge and project management skills to support our compliance efforts effectively.

📌 Validation Associate in Mississauga
🏢 Contract Pharmaceuticals
📍 Mississauga