Technical Leader, Medical Devices

3 weeks ago

Keighley, United Kingdom Russell Taylor Full time

Technical Leader, Medical Devices

**Location**: Skipton, hybrid role - 2 days remote. Occasional travel to other UK sites.

**Type**: upto 9-12 month fixed term contract (has the potential to go permanent)

**Salary**: £42,000

**Additional**: Upto 10% bonus, Pension - EE 3%, ER 6% or EE 4%, ER 8%, 4x annual salary life assurance

ContBUPA private medical care, canteen, gym etc

**Hours**: Monday - Thursday (8.30 - 16:30), Friday (8:30 - 13:30)
- Russell Taylor Group is working exclusively with a Global Medical Devices company and looking to appoint a Technical Leader, a new role for the company and one that has the potential to go permanent. _

**The Role**:

- Deliver technical solutions to the business for manufacturing processes in problem solving, innovation and improvement; provide line support to resolve issues to meet service level and revenue commitments.
- Develop and validate processes and equipment (where appropriate) for new and existing products and technology transfer projects.
- Develop and validate test methods and laboratory equipment (where appropriate as required to support projects.
- Identify, manage, execute and implement the technical aspects of raw material changes and Supplier Change Notifications to meet service level and revenue commitments.
- Lead and or support projects, including capital, NPI, product stability and COGS savings.
- Technically lead complex projects, multiple project work streams or several smaller projects simultaneously to completion within agreed time constraints, quality, customer and regulatory requirements.
- Take responsibility for managing the workload providing an appropriate level of support.
- Generate strategies, protocols, reports and rationales for; development trials, process validations, stability studies, test method development and validation, product design control, material changes. Execute and or co-ordinate such activities as appropriate.
- Perform or manage process development and performance qualifications.
- Lead Technical investigations as required including NCR, CAPA, p-FMEA.
- Prepare and maintain project documentation and files to ensure compliance with internal and external Quality Systems.
- Gain a sound knowledge and understanding of the products and processes associated with assigned projects.
- Awareness of change control, product stability, design control, medical device regulation, biological safety and material compliance (REACH, Prop 65, EU MDR etc).
- Provide technical information and rationales as appropriate to all functions within the business. Present reports and results in a clear, concise and accurate manner. Ability to communicate results to all levels of the business.
- Manage customer communication on technical issues and respond to customer enquiries.
- Provide technical input to material, product and process specifications.
- Collaborate with finance to establish project costings if required.
- Deputise for the Technical Manager(s) if required.

**The Person**:

- Will hold a Degree in a relevant/ Scientific discipline
- Experience in people management/ Project Scientist level.
- Experience in project management, technical assessment, process validation etc.
- WILL HAVE WORKED IN MEDICAL DEVICES/ ISO 13485

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