Validation Specialist Role
This is an exciting opportunity for a skilled professional to work on a major expansion project in the pharmaceutical sector.
* Develop and implement cleaning and validation plans and schedules.
* Collaborate with teams to create, review, and approve protocols, reports, and assessments for ongoing validation.
* Review and endorse SIP/CIP protocols and closure.
* Analyze the impact of issues and deviations arising through assessment generation.
Requirements:
* Proven experience in quality assurance and validation activities.
* Extensive expertise in writing and approving deviations.
* Strong technical writing skills with proficiency in white papers and site reports.
* Previous exposure to GDP or administrative roles.
Ability to work independently and effectively communicate with various departments.
Key Responsibilities:
* Manage validation schedules and ensure adherence to regulatory requirements.
* Collaborate with cross-functional teams to drive process improvements.
* Develop and maintain documentation for validation procedures.
What We Offer:
* Opportunity to work on a high-profile project.
* Chance to develop new skills and expertise.
* Collaborative and dynamic work environment.