Description
Global Validation Project Manager - Permanent - Based in the UK or EuropeA Global pharmaceutical/biopharmaceutical organisation requires a Global Validation Project Lead. The purpose of the position will be to lead and coordinate major project initiatives across the division with representatives from multiple sites. The role will suit an experienced project manager who has experience of managing multiple validation projects.
The Role:
*Participate and coordinate cross-functional teams responsible for the execution of major and minor Validation projects across the organisation
*Manage and lead various best practice projects, including implementing new standards across all sites to provide consistent and improved Validation executions.
*Develop Validation Standard Documents associated with Validation Master Plans, Cleaning Validation Master plans and other identified areas
*Drive and share Validation best practices associated with Validation across sites
*Manage interfaces with key site stakeholders and functional heads to deliver Validation initiatives in accordance with Quality and Regulatory expectations.
*Prepare monthly in-depth project status reports, documenting decisions, risks etc
*Support complex product transfers across all the manufacturing sites
*Contribute to IQP (Innovation, Quality & Productivity) productivity targets at sites
*Oversee site inspection responses and ensure they are followed up on, tracked, and system improvements are delivered across the network.
Experience:
*Degree in Chemical/Process/Mechanical Engineering, or a BA/BS degree in a science related field
*Minimum of 10 years experience leading Validation project teams, applying and implementing FDA / MHRA cGMP regulations is essential
*Expert knowledge in validation with a diverse compliance background in cGMP manufacturing
*Expertise in a broad range of vaccine and biotech processes
*Background in Pharmaceutical / Biological industry is essential
*Trained in six sigma / Lean Manufacturing
*Project management skills, including creating / managing project budgets, resources (internal and external) and schedules.
*International Experience working in cross cultural and cross functional teams
*Please note that this position can be based in the UK or Europe at one of the manufacturing sites
*A willingness and ability to travel both nationally and internationally is essential
*Please note: This position can be based in the UK or Europe.
An outstanding salary and benefits package is on offer alongside an exceptional opportunity to join a major pharmaceutical/biopharmaceutical organisation.
Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this opportunity.