Senior Pharmaceutical Validation Specialist

Elevate your career with LAPORTE as a Senior Pharmaceutical Validation Specialist in Greater Calgary. This role demands over five years of validation experience and focuses on compliance in the dynamic pharmaceutical sector.

As a vital member of LAPORTE, you'll manage all validation aspects, draft essential documentation, and execute qualification protocols. Working closely with clients' QA teams, you'll address deviations and oversee client account management while driving adherence to Good Manufacturing Practices to ensure project success.

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

Bring your validation expertise to LAPORTE, engaging in impactful projects in Calgary's pharmaceutical landscape.
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