Pharmaceutical Validation Specialist - LAPORTE

Join LAPORTE as a Pharmaceutical Validation Specialist focusing on validations in the Greater Toronto Area. You will utilize your savvy in GMP compliance and validation protocols to drive success.

LAPORTE is seeking seasoned professionals with at least five years of pharmaceutical industry experience. This position involves overseeing the drafting and execution of essential validation documents and coordinating compliance with industry regulations. Your contributions will be vital in ensuring clients’ manufacturing processes meet the highest standards.

Key Responsibilities:

• Develop and draft validation master and execution documents

• Coordinate all qualification protocols, ensuring adherence to GMP

• Provide QA support on change notices and compliance issues

• Maintain effective management of client accounts

• Contribute to continuous improvement in validation processes

Requirements:

• Bachelor’s or master’s degree in engineering or science

• Five or more years in pharmaceutical validation

• Robust knowledge of GMP practices

• Familiarity with manufacturing operations

• Flexibility to travel as client needs arise

Expand your career potential in pharmaceutical validation with LAPORTE's innovative approach.
#J-18808-Ljbffr