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 timeon site position.

To be part of this exciting journey with a growing Medtech Company apply below.

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