Pharmaceutical Validation Specialist

Position: Pharmaceutical Validation Specialist LAPORTE
Join LAPORTE as a Pharmaceutical Validation Specialist in Greater Calgary with over 5 years of validation experience. Oversee crucial operations in the pharmaceutical sector and ensure robust compliance with industry regulations.

This senior role focuses on managing all aspects of validation, including drafting essential documents and executing necessary qualification protocols. You will also work closely with clients' QA teams to address deviations and oversee client account management. Your commitment to Good Manufacturing Practices will drive success in this role.

Key Responsibilities:

• Draft and manage critical validation documents

• Execute equipment/system qualification protocols

• Ensure adherence to Good Manufacturing Practices

• Collaborate with QA/Compliance on change controls

• Maintain client accounts and foster relationships

Requirements:

• Degree in science, engineering, or related fields

• Minimum of 5 years of pharmaceutical industry experience

• Expertise in Good Manufacturing Practices

• Familiarity with pharmaceutical manufacturing processes

• Willingness to travel for client engagement

Leverage your validation expertise with LAPORTE, engaging in impactful projects in Calgary's pharmaceutical landscape.
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