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Job Details

Manager of Regulatory Affairs – Combination Devices for USA

Company: SEC Recruitment
Location: Switzerland
Reference: BBBH111061
Closing Date: 27 Feb 18
Type: Permanent
Salary (£): 100,000+
Benefits: Amazing Flexible Benefits

Job Summary:

An innovative and leading Science based company based in Switzerland are looking for a strong manager to lead a small team. The company have a site based in Switzerland which is state of the art and you will be working with expects in their field. This project is one of the most important for the company's future and as such you will be rewarded accordingly.

Requirements:

Manager of Regulatory Affairs – Combination Devices for USA – Up to CHF 180,000 – Switzerland based

Please get in touch with me immediately if you are interested in this role -
mark.wilkins@secpharma.com +44 (0) 207 2556665

An innovative and leading Science based company based in Switzerland are looking for a strong manager to lead a small team. The company have a site based in Switzerland which is state of the art and you will be working with expects in their field. This project is one of the most important for the company’s future and as such you will be rewarded accordingly.

You will be working with products through the development phase all the way to approval and beyond. This is a management role where you will be expected to be hands on with the work required. Significant Regulatory experience is required in either Pharma, Med Device or combination products. You must have experience of working with the FDA for the full spectrum of development because this is the area you will be developing your product within. I am looking for demonstrable examples of your experience in development, assessment, production, submission & authorisation and commercialisation of products within the FDA framework. In addition it would be extremely advantageous if you have experience in QMS and GMP. I am looking for a Regulatory professional who has the A to Z of product development from Pre-clinical to Post Marketing, which also includes manufacturing and clinical experience.

If you have management experience this would be useful as you will be managing 1 or 2 people, although not an absolute pre-requisite.

Primary function:

- Coordinate all Regulatory and Scientific activities for your product
- Provide strategic implementation for product development and commercialisation for the US
- Lead submissions strategy and development process
- Lead compliance protocols and regulatory impact requirements
- Develop the team to increase regulatory expertise

I would like to speak to those living and working in Switzerland or interested in doing so. Relocation is provided, tax assessment is provided, school assistance is provided as well as a great selection of Swiss benefits.

Having visited this company several times, this is a great opportunity for someone to take their personal and professional life to another level.

Please get in touch with me immediately if you are interested in this role – mark.wilkins@secpharma.com +44 (0) 207 2556665

Apply for this job: Manager of Regulatory Affairs – Combination Devices for USA

Contact Information:

Address:  Head Office
3rd Floor, 13-15 Moorgate London.
EC2R 6AD
England
Tel:  00 44 (0) 207 255 6600
Fax:  00 44 (0) 1483 888997
Website:  Visit Our Web Site

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