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Regulatory Affairs Jobs at New Scientist Jobs

We currently have 12 jobs for Regulatory Affairs

New Scientist Jobs offers you your biggest job opportunity, with 2468 jobs from 320 recruiters in the global Biotechnology, Pharmaceutical and Life Sciences sectors. Look below to see the latest Regulatory Affairs jobs.

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Add Clinical Research Project Manager - Medical Devices - ISO 14155

Clinical Research Project Manager - Medical Devices - ISO 14155 - North West A growing Medical Devices company in the North West are currently looking to recruit a Clinical Research Project Manager due to the success of the company's products and the growth of the organisation. As you will be leading the Clinical T ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  North West | Salary: Negotiable | Company:  Paramount Recruitment | Published Date: Friday, November 20, 2009 3:13:20 PM

Add Head of Regulatory Affairs

An exciting opportunity has arisen in a Global Multinational Medical Device Company based in Dublin. This position will be responsible for ensuring that regulatory compliance of all medical device products placed on the market under the Irish transposition of the Medical Device Directive 93/42/EEC is achieved and m ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  Republic of Ireland | Salary: Negotiable | Company:  Life Science Recruitment | Published Date: Friday, November 20, 2009 1:13:02 PM

Add Technical QA/RA Engineer - Medical Device

Technical QA/RA Engineer - Medical Device Profile Our client is a global multinational Medical Device manufacturer and they are seeking a Technical QA/RA engineer with excellent attention to detail and technical writing ability to join the team as part of a global technical file management audit project. This is a ... Job Role:  Biomedical Engineering | Job Hours:  Full-Time | Sector:  Industry | Location:  Malaysia | Company:  Life Science Recruitment | Published Date: Friday, November 20, 2009 1:08:33 PM

Add Quality Engineeer - Medical Device

Quality Engineer REQUIREMENTS -Evaluation of Customer complaints and co-coordinating the identification of adequate CAPAs -Work closely with Operations to resolve in-house and supplier quality problems using established problem solving methodologies (Root Cause Analysis, Mistake-Proofing, etc). -Actively partici ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  Republic of Ireland | Salary: €35,000-40,000 | Company:  Life Science Recruitment | Published Date: Friday, November 20, 2009 10:52:37 AM

Add Smart metering technical specialist/consultant-London-Mangement Consultancy

SMART METERING TECHNICAL SPECIALISTS/CONSULTANTS NEEDED- UK- London Our client, a leading worldwide Management Consultancy practice is looking for an experienced Smart Metering expert/consultant to join their global utilities team in London. They are seen as leaders in the utilities sector in delivering smart meter ... Job Role:  Energy Management | Job Hours:  Full-Time | Sector:  Academic | Location:  Central London / West End | Salary: £excellent and commensurate to exp | Company:  Quanta Consulting | Published Date: Thursday, November 19, 2009 10:22:21 AM

Add Regulatory Director

The company Our Client is an acute care specialist medical device start-up who has recently acquired the worldwide rights of 2 medical device products. These products help to treat GI and urinary problems in both adults and children. These products have been approved in some areas; this role will assist the team in ... Job Role:  Biomedical Engineering | Job Hours:  Full-Time | Sector:  Industry | Location:  Republic of Ireland | Salary: Negotiable | Company:  Life Science Recruitment | Published Date: Wednesday, November 18, 2009 5:51:30 PM

Add Validation Scientist

Validation Scientist KEY RESPONSIBILITIES • Lead and structure scientific debate and assessment with peers from other technical areas to develop scientific understanding whilst continuing to link all efforts to the patient. • Determine levels of importance or risk to be assigned to elements under review – using sci ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  Republic of Ireland | Salary: Negotiable | Company:  Life Science Recruitment | Published Date: Wednesday, November 18, 2009 5:18:20 PM

Add Validation Specialist

Validation Specialist KEY RESPONSIBILITIES: Support Validation Projects / Programs • Advise on protocol content/format (where appropriate) • Perform data review including statistical analysis (where appropriate / required) • Protocol execution / reporting e.g. providing oversight on manufacture, sampling and te ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  Republic of Ireland | Salary: Negotiable | Company:  Life Science Recruitment | Published Date: Wednesday, November 18, 2009 5:01:34 PM

Add Validation Manager

Validation Manager KEY RESPONSIBILITIES: • Challenge department to deliver and present at a higher level – to lead discussion & debate, to be pro-active. • Develop scientific knowledge within the Validation group (and the departments with which it interacts) and direct its application to ensure enhanced assuranc ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  Republic of Ireland | Salary: Negotiable | Company:  Life Science Recruitment | Published Date: Wednesday, November 18, 2009 4:57:02 PM

Add Clinical Research Project Manager - Medical Devices - ISO 14155

Clinical Research Project Manager - Medical Devices - ISO 14155 - North West A growing Medical Devices company in the North West are currently looking to recruit a Clinical Research Project Manager due to the success of the company's products and the growth of the organisation. As you will be leading the Clinical T ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  North West | Salary: Negotiable | Company:  Paramount Recruitment | Published Date: Friday, November 06, 2009 11:05:50 AM

Add Senior Regulatory Affairs - North West - Medical Devices

Senior Regulatory Affairs Associate - North West - Medical Devices An exceptional opportunity has arisen for an experienced Regulatory Affairs Associate to join an established Medical Device organisation to help with the regulatory affairs of their products across the globe. This company is part of a world leader i ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  North West | Salary: Negotiable | Company:  Paramount Recruitment | Published Date: Friday, October 30, 2009 2:56:22 PM

Add Senior Quality Engineer - Medical devices - ISO 13485 - CAPA

Senior Quality Engineer - Medical devices - ISO 13485 - CAPA - Oxfordshire A leading Medical Devices company in the Oxfordshire area are looking to recruit an experienced Senior Quality Engineer with hands on engineering experience. This company has been growing for a number of years and will continue to do so in t ... Job Role:  Regulatory Affairs | Job Hours:  Full-Time | Sector:  Industry | Location:  Oxfordshire | Salary: Negotiable | Company:  Paramount Recruitment | Published Date: Thursday, October 29, 2009 9:34:49 AM


 

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