ACTIVE DEVICES MEDICAL DEVICE PRODUCT EXPERT - EMEA

Posted 4 days ago by Bosch Global Associates Ltd

ACTIVE DEVICES MEDICAL DEVICE PRODUCT EXPERT - EUROPE

Industry: Medical Devices & Healthcare

Job Title: Scheme Manager - Technical Specialist - Medical Device Expert - Certification Manager - Project Manager - Design Control Manager - CE Marking - Certification -Project Manager - R&D.

Location: UK OR FRANCE.

Salary: 45-65k or 55-85k Eur.

Bonus: 10%.

Type: Permanent.

Organisation: a Notified Body for the Medical Device Industry.

Typical:

Today you are working from home reviewing fatigue test data on a new active device product design and technology of one of your customers. Tomorrow you audit the manufacturing facilities of a large manufacturer of Active devices in Germany. Next week you present at a medical device regulatory conference in Sweden. As A Technical Lead, Scheme manager, Product expert and part of one of our global technology teams, you appreciate the dynamic of working in a mix of regulatory affairs, quality auditing and medical technology innovations. You enjoy an international working environment in a growing team of medical device experts, working with small start-up and large multi-national clients, a bit of travelling and reviewing the latest technologies.

Requirement: Currently recruiting Medical Device Technical Experts for the following device categories:

  • Implantable devices in the orthopaedic, dental, ophthalmic, IVD, Dialysis, Active devices, soft tissue implants, wound care and cardiovascular fields.
  • Sterility Aseptic Sterile Manufacturing
  • Electro-medical devices for diagnostic or therapeutic purposes.

Function of the position:

  • As a technical expert assessing the manufacturer's technical files and design dossiers;
  • As a member of a team auditing a device manufacturer's quality system;
  • As a regulatory expert and scheme manager, managing a portfolio of clients with respect to services provides to them.

Team members have overall client management responsibilities and will be competent to review critical design data (including risk analysis, labeling, clinical investigation data and post market surveillance information) and to prepare recommendations for CE certification.

Qualifications and Experience:

Candidates will have medical device experience within an industrial, academic or clinical background.

Their qualifications will reflect a thorough understanding of the technological considerations and manufacturing processes relevant to the field in which they have worked.

Successful candidates will be motivated to perform detailed investigation of complex technical issues, have a desire to learn new disciplines, are strong communicators, and have strong analytical and organizational skills, and have the presence to make and explain difficult decisions if necessary.

Neurostimulators, electronics design, validation, verification, active implantable medical device prototypes, implantable stimulator, bioelectricity, bioelectrodes, design and analysis of experiments, biomedical signal processing, biocompatibility, senior engineer, development engineer, product development, design, ABBOTT / SANOFI / FRESENIUS / KABI / GAMBRO / BAXTER / DRUG DELIVERY / CAREFUSION / SIEMENS / PHILIPS / TUV / SGS / BBRAUN / SORIN / GE HEALTHCARE / SMITHS MEDICAL / VARIAN / SUPERSONIC / CLINICAL RESEARCH / 60601 / 60602 / ACTIVE DEVICES / ELECTRICAL / ELECTRONICS / ELECTRO-MECHANICAL / ELECTROMECHANICAL / ELECTRO MECHANICAL / QA / QUALITY ASSURANCE / ISO13485 / AUDITING / AUDITORS / REGULATORY AFFAIRS / R&D / MEDICAL DEVICES / RESEARCH / DEVELOPMENT / MANUFACTURING / ENGINEERING / OPHTHALMICS / ACTIVE IMPLANTABLES / DEVELOPMENT ENGINEER / R&D ENGINEER / FDA / MHRA / ELECTRO SURGICAL / VASCULAR / CERTIFICATION / QMS / RESEARCH / PRODUCT DEVELOPMENT / NPD / NPI / MANUFACTURING / HEALTHCARE / CLASS 1 / CLASS 2 / CLASS 3 / CLASS 3A / CLASS 3B / CLASS I / CLASS II / CLASS III / PROCESS ENGINEER / PRODUCTION / NPD / PHARMA / PHARMACEUTICALS / R&D MANAGER / RESEARCH MANAGER / DEVELOPMENT MANAGER / HEAD OF R&D / RESEARCH / DEVELOPMENT / MEDICAL DEVICES / STERILES / SURGICAL / ELECTRO MEDICAL / ELECTRO-MECHANICAL / ORTHOPEADIC / DENTAL / OPHTHALMIC / SOFT TISSUE / VASCULAR / IMPLANTS / IMPLANTABLES / WOUND CARE / WOUNDCARE / CARDIOVASCUALR / MEDICAL DEVICES / ELECTRO SURGICAL / SURGICAL DEVICES / GERMANY / EUROPE / BELGIUM / SWITZERLAND / RADITATION/ BENELUX / "GERMAN","FRANKFURT","POLAND, BELGIUM, SWITZERLAND, FRANCE, GERMAN, LEVERKUSEN, MAINZ / FREIBURG / WOLFSBURG / HOFFENHEIM / AUGSBURG / ENGLAND / UK / EUROPE / IVD / ABBOTT / SANOFI / FRESENIUS / KABI / GAMBRO / BAXTER / DRUG DELIVERY / CAREFUSION / SIEMENS / TUV / SGS / BBRAUN / SORIN / GE HEALTHCARE / SMITHS MEDICAL / VARIAN / SUPERSONIC / RELOCATE / SWEDEN / AUSTRIA / BELGIUM / FRANCE / PARISOLYMPUS / BESPAK / DIAGNOSTICS / NIKKISO / TERUMO / OLYMPUS / BESPAK / DIAGNOSTICS / NIKKISO / TERUMO / PARIS / FRANCE / LYON / CLERMONT / SWEDEN / MARSEILE / TOULOUSE / BORDEAUX / NANTES / RENNES / BREST / LE HARVE / BOURGES / LE MANS / NANCY / BRUSSELS / STRASBOURG / GENEVE / DIJON / GRENOBLE / DIALYSIS / PHYSICIST / MEDICAL / UK / UNITED KINGDOM / LONDON / SOUTH / SOUTH EAST / NORTH WEST / ENGLAND / RELOCATE / MIDLANDS / OXFORD / HOME COUNTIES / MILTON KEYNES / SOUTH WEST / CONTRACEPTIVES/SSL/MOLYNCKE/SCHOLL/CONDOMS/P&G /

Required skills

  • Design Development
  • Global R&D
  • Medical Devices
  • Product Design
  • 60601

Application question

Do you have at least 5 years R&D or product development expertise in medical devices?

Reference: 30479741

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