Our Engineer in Validation and Specification leads and coordinates validation activities across the site, initiating and implementing improvements in cost, quality and customer service. They work closely with the Site Validation, Engineering and Technical Managers to have full working knowledge of the Capex Plan and Site Validation Master Plan.
Responsibilities
* Lead and coordinate engineering validation activities across the site, providing clear evidence of status and equipment performance, focusing on delivering efficiency, cost, and service improvements.
* Manage projects within budgets and deadlines to ensure implementation of supply validation strategy.
* Work closely with the Site Validation, Engineering, and Technical Managers to have full working knowledge of the Capex Plan and Site Validation Master Plan.
* Support the Global Pharmaceutical Manufacturing facilities providing Validation support as required, working with the Regional Supply Heads to support global manufacturing, technical and engineering strategies.
* Lead audit inspections with respect to equipment, cleaning and facilities validation and ensure the site is audit ready in all markets at all times.
* Have in-depth knowledge and experience of engineering validation.
* Are familiar with UK, EU and FDA standards and legislation.
* Have a good understanding of material properties and processing technology.
* Ability to work with and influence cross functional teams.
* Have strong communication skills.
* Can break down problems in several ways, identifying less obvious and more relationships.
Qualifications and Skills
* Supply Chain Management
* Business Partnership
* Collaboration
* Partnership building
* Relationship management
* Business acumen
* Productivity management
* Improve business processes
* Advanced analytics
* Data analytics
* Manufacturing excellence
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