I am currently working with one of the world’s leading Medical Device organisation with a wide variety of innovative Medical Device products and medical technologies working across multiple therapeutic areas. A true global leader within their field and they are always expanding the countries they operate in and distribute to.
Senior Development Engineer – Spinal Implants, Medical Device – Zurich – CHF 130,000
I am currently working with a leading, highly specialised Global Medical Device organisation specialising in Spinal Implants and Instruments.
They are one of the leading Medical Device organisations with a diverse product range within Spinal Implants and Instruments and specialise in providing bespoke and tailored devices to their customers.
I am working with a Diagnostics Company in the East of England, who is looking for a R&D Scientist to join their R&D Department. I am looking for an ambitious professional, who wants to gain more experience and develop professionally within Medical Devices and Diagnostics in particular!
Company:Real Life Sciences Location: Cambridgeshire Salary: 100,000+ Benefits: competitive
Als CSV Manager leiten Sie verschiedene Projekte und beraten bei neuen Validierungsprojekten. Weiterhin führen Sie CSV Schulungen durch und arbeiten mit dem Außendienst zusammen. Außerdem sind Sie für Neukundenakquise zuständig und stehen als Berater den Kunden zur Seite.
Company:Blue Heron Pharmaceutical Location: Central London Salary: 100,000+ Benefits: favourable hourly rate or pro rata salary
Closing Date: 14 Nov 14
As a member of the company’s senior management team, this is a new role providing optimal regulatory publishing & submission support and advice to ensure high quality submissions are made in line with clinical and commercial business needs. The initial contract will be full-time at a favourable hourly rate or pro rata salary, for an initial period of six months, ideally to start during October/November.
My client, part of a larger group are solely focussed on the development of biosimilars. Over the next few years they will be going through extensive growth and this position has been made from expansion.
A world renowned healthcare multinational, specialising in wound care and skin care products are seeking a Country Manager to head the Singapore team. This company is dedicated to working closely with their consumers to create innovative solutions to their needs. Due to their timeless sensibility and high demand quality they are leading the industry and continue to grow their strong global presence. ...
Product Specialist - Wound Care - Eastern Switzerland
An expanding medical device company specialising in wound care products are looking to add a Product Specialist to their growing team in order to sell and promote their latest wound care device across the Eastern region of Switzerland.
This is a great regulatory affairs opportunity within a leading medical device company to mange innovative medical devices on a global scale. If you enjoy working within the emerging markets and the exciting international platform, this is the regulatory affairs role for you. Further to this, you working life will be interesting and varied as you will work with a range of authorities on a global scale. Apply now to find out more and take the next step in your career.
A fantastic management role has come in within the canton of Bern for a regulatory affairs manager. This is a great time to be joining our client's regulatory affairs department as they are at an exciting point of growth; allowing you to be part of the future! We want to hear from you today if you have several years of experience within regulatory affairs from the medical device industry. Apply now to find out more about this great role!
Senior Biotransformation/bioanalysis position – Switzerland
Senior Biotransformation/bioanalysis position - Switzerland
Heading a number of Lab's in both Bioanalysis and Biotransformation, my client is currently looking for a new senior member of their team, to oversee and manage a large number of staff, and to provide strategic direction to a large research division, managing a large number of complex projects.
Do you have extensive knowledge of the metabolite tracking area, with an excellent publications record and experience of managing a large team handling a large number of complex projects?
Would you like the opportunity to work with one of the worlds most advanced drug discovery operations, overseeing one of the most developed early stage discovery operations feeding into an enormously successful Pharma company.
An internationally successful biopharmaceutical company are expanding their sales team and are searching for an Account Manager to work in their immunology business unit and focus on expanding sales across the Central & Eastern regions of Switzerland, especially focusing on the Zurich to Aargau territory.
An internationally successful biopharmaceutical company are expanding their sales team and are searching for an Account Manager to work with their rheumatology products and focus on expanding sales across the Western part of Switzerland.
Gain a fantastic packaging opportunity within a world leading medical device company based in the greater Zurich area. As the packaging specialist in this role will gain the opportunity to work on interesting and exciting high risk devices; leading to an interesting working life and the opportunity to gain invaluable expertise. We are looking for experienced packaging specialists within medical devices, who have worked to international standards. Apply now to find out more.
Als Director Regulatory Affairs sind Sie für die Leitung der Zulassungsabteilung für den Bereich CMC zuständig. Einerseits arbeiten Sie an der strategischen Ausrichtung der Abteilung und schauen, wie neue regulatorische Vorgaben umgesetzt werden können. Sie werden das Unternehmen nach außen repräsentieren und mit den Behörden in Kontakt stehen. Weiterhin arbeiten Sie mit den Mitarbeitern an den Zulassungen und unterstützen diese bei Bedarf.
Contract for 12 Months - Project Clinical Data Manager - Switzerland - 75 - 80CHF per hour
If you would like to apply for the position or wish to learn more about the role and company please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to email@example.com
As Risk Manager you take professional responsibility for the risk management of manufacturing facility (eFMEA) and manufacturing processes (PFMEA), which forms the basis of qualification and validation activities.
Lead Consultant / Associate Director of CMC Support Operations
We are looking for dynamic and experienced candidates with extensive project management backgrounds who bring a wealth of Regulatory Affairs experience from the pharmaceutical arena. The ideal candidates must possess excellent communication skills and be comfortable dealing with global stakeholders including the US, AsiaPac and Europe.
Clinical Regulatory Affairs Manager & Director NJ, NC & Remote
A fast growing, excellent pharmaceutical company is seeking a senior level Regulatory Affairs professional to be based in North Carolina, New Jersey or remotely. This company is conducting Phase 3 global clinical trials. They offer excellent pay, bonus, stock and benefits. ...
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