Pharmaceutical Validation Professional
This role offers a unique opportunity to support the qualification and validation of equipment, computerised systems, facilities, and utilities in a regulated environment.
Key Responsibilities:
* Review and approve qualification and validation documentation
* Provide QA oversight during execution of qualification, requalification, and validation activities
* Develop and maintain the Site Validation Master Plan
* Generate and execute project-specific validation plans
* Coordinate with manufacturing and engineering teams
* Lead investigations into deviations or deficiencies related to qualification activities
* Prepare and review SOPs, protocols, reports, and technical drawings
* Review and approve calibration and preventive maintenance schedules
* Conduct risk assessments and technical studies
* Participate in audits and inspections
Benefits:
This dynamic and fast-paced role offers excellent career development potential and opportunities to work cross-functionally with engineering, production, and quality teams.
Requirements:
A strong working knowledge of validation lifecycle principles and experience with Site Validation Master Plan development are highly valued assets for this role.
Technical Skills:
Strong analytical and problem-solving skills, with the ability to communicate complex ideas effectively
Ability to work in a team environment and contribute to achieving business objectives