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Section: Engineering, Manufacturing Vacancy 205 |
| Post:Consultant (Manufacturing Process Improvement) Me
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Salary contractual |
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| Requirements and conditions |
| Age: |
Has no value
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| Gender |
Has no value
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| Education: |
no
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| Work schedule: |
Has no value
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| Work place: |
Plymouth
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| The announcement text: |
Consultant (Manufacturing Process Improvement) Medical * Healthcare Sector, Cambridgeshire
To apply your technical and commercial experience to lead challenging and often complex manufacturing process improvement projects for clients in the Medical Devices industry.
The Process Improvement Practice focuses on the provision of high quality scale up and yield improvement programmes for manufacturing industries principally concentrating on Medical Devices including:
Invasive medical devices
Diagnostic devices
Drug delivery
Our client?s consulting activities are centred primarily in the UK and Northern Europe, and the USA, and although there will be some requirement to travel, the work is primarily done in the Cambridgeshire office.
Consultants work on client assignments in multidisciplinary project teams, often on more than one project and in different team roles. You will be recruited to act as a project manager. In addition, you will be required to work as a consultant as a member of project teams, alongside consultants and analysts. Responsibilities will include:
Formulating approaches to process improvement to meet specific client requirements
Project managing process improvement projects and programmes, probably in medical devices
Delivering process improvement strategy reports to senior management
Flexibility in taking on any other assignments, due diligence and assessing manufacturing capabilities
An excellent degree in engineering, ideally mechanical. Further qualifications in manufacturing would be an advantage
A minimum of five years post graduate industrial experience working in process development and scale up in manufacture of medical devices
Excellent track record in problem solving
A working knowledge of analytical process improvement techniques such as Lean Manufacturing
Project management experience essential
Working knowledge and experience of the regulatory environment in the EU and USA
Excellent interpersonal, communication and presentation skills
Our client is committed to developing its employees? careers and has a flexible policy for individual?s capabilities and preferences. Within the line management structure there are opportunities for promotion to Group Leader with responsibility for managing one of the company?s business areas, or Consultant with recognition for exceptional technical expertise, and beyond to more senior management positions. The equivalent within our project structure is Programme Manager, a permanent post carrying responsibility for managing our client?s largest and most complex projects. Our client is a growing company and promotion is linked to merit.
Working knowledge and experience of the regulatory environment in the EU and USA
Excellent interpersonal, communication and presentation skills
Good salaries, based on merit and reviewed annually
Profit share in addition to basic salary
Flexible working hours
Free lunches and refreshments
Private medical insurance and company sickness scheme
Pension scheme including free life assurance
22 days annual holiday plus bank holidays
Assistance in relocation if applicable
Active social committee
Well equipped and pleasantly situated building
Above all, real responsibility for real business problems with good career prospects based on merit
Career development and training opportunities
Investors In People accredited
Keywords: Consultant, Clinical, Healthcare, Project Manager, Programme Manager, Drugs, Manufacturing, Process, Lean Manufacturing, Diagnostics, Medical Devices, Pharmaceuticals, Mechanical, EMEA.
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| Contact information |
| Employer: |
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| Email: |
103@nottinghamcareer.informnow.com
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| Phone: |
0870 242 4664
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Publication date: 2009-03-23 11:36:28
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