Aurora Lifesciences has been retained by an excited Medical Device company who are now in search for a Head of Manufacturing.
You will be responsible for Manufacturing & Process Development Engineering staff and directing tasks associated with new product development and commercialization of their cutting edge medical device product.
Job Responsibilities:
* Provide leadership, direction, technical quality support for the production of clinical devices.
* Develop and implement strategic plans within the facilities
* Develop and Improve department procedures and policies.
* Partner with Senior departmental heads in increasing production output.
* Working with Quality and R&D Engineers to develop critical manufacturing processes.
* Process development and validation of manufacturing processes for new product introduction and continuous improvement projects.
* Root cause analysis investigation for component and device nonconformance.
* Managing key suppliers and working directly with contract manufacturers.
* Provide technical quality support for design qualifications, design transfer, activities for Regulatory submissions, product and process development and implementation of design control documents, and approval of product/process change.
* Direct all manufacturing-related aspects of the project within a team of Engineers and Technicians.
* Hire, train and manage high performing technical team
Skills and Abilities Required for This Job:
* Demonstrated experience in increasing production output
* The ability to scale operations
* Must be able to work effectively and collaborate within cross functional teams.
* Must be able to effectively articulate (verbally and in writing) results and conclusions to technical and non-technical personnel.
* Must take initiative and be able to conduct hands-on work.
* Must be able to handle multiple tasks with high attention to detail.
* Knowledgeable of Facility controls, employee Health and Safety.
About You
* 10 years of experience in medical device Manufacturing, Operations, and Engineering is required. (Highly Desirable however not Essential)
* Knowledge of Product and Process design verification in the medical device industry or other regulated industries is required.
* Knowledge of equipment qualification and design verification in the medical device industry or other regulated industries is required.
* Knowledge of supply chain development and management in early stage through product transfer and project maturity.
Benefits
* 15% Annual Bonus
* 28 Days Holiday + 8 Days Bank Holiday
* Private Healthcare
Please note this is a full time on site position.
To be part of this exciting journey with a growing Medtech Company apply below