Found Description
Join LAPORTE as a Pharmaceutical Validation Specialist in Greater Calgary and contribute to maintaining high-quality standards in the pharmaceutical sector. Bring your validation experience to a supportive and innovative engineering environment.
We are inviting applications for a specialist with a minimum of five years of experience in validation and qualification processes. You will be responsible for drafting and executing critical validations, ensuring compliance with GMP, and aiding client QA teams in identifying necessary changes to uphold standards. This role emphasizes professional growth and collaboration within a vibrant workplace.
Key Responsibilities: • Draft and manage crucial validation documentation • Execute qualification protocols (IQ/OQ/PQ) for pharmaceutical systems • Oversee GMP compliance during validation processes • Assist QA teams in addressing changes and deviations • Manage and nurture client accounts
Requirements: • Bachelor’s or mas...
We are inviting applications for a specialist with a minimum of five years of experience in validation and qualification processes. You will be responsible for drafting and executing critical validations, ensuring compliance with GMP, and aiding client QA teams in identifying necessary changes to uphold standards. This role emphasizes professional growth and collaboration within a vibrant workplace.
Key Responsibilities: • Draft and manage crucial validation documentation • Execute qualification protocols (IQ/OQ/PQ) for pharmaceutical systems • Oversee GMP compliance during validation processes • Assist QA teams in addressing changes and deviations • Manage and nurture client accounts
Requirements: • Bachelor’s or mas...
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