- Global Regulatory Affairs Labeling Specialist
I am looking for the individual looking to take the next step up in their career! This role offers career development, a great challenge and the opportunity to work with a vastly expanding, high reputable Global Pharmaceutical Company!
- Regulatory Affairs Specialist/Senior Regulatory Affairs Specialist - EMEA-122360
PPD is recruiting for Regulatory Affairs Specialists.
In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services. You will also act as liaison with internal and external clients in the provision and marketing of regulatory affairs services. ...
- Regulatory affairs specialist, 2 roles in Brussels
My client, an international company recognised in the world of food supplement and cosmetics is currently reorganizing his global regulatory affairs team. For that reason, they are creating two regulatory roles in Belgium. One will be focus on Benelux market and the second one on Germany, Austria and Switzerland market. ...
- Regulatory Affairs Specialist - 12 Month Maternity Cover-120887
PPD has a new vacancy for a Regulatory Affairs Specialist. This opportunity is for 12 month maternity cover.
Position location will be in a PPD office where a regulatory team exists, and will depend upon candidate experience and business need.
In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services. ...
- Regulatory Affairs Specialist
Our Client is a CRO specialising in oncology looking to add a number of Regulatory Affairs Specialists to their team to work on an exciting client project. Located conveniently in Hertfordshire this organisation has a great reputation for training and development opportunities. Job Role: To provide regulatory and quality support to select clinical research projects involving investigational or marketed drugs, devices, biologics, or new medical procedures. ...
- Regulatory Affairs “Tracking Specialist” Contract Role - Global Pharma Company – Excellent Rate - Brussels, Belgium
You will be working on a large variety or projects in different stages of development, for different projects across all therapy areas and the hourly rate is very good and will be based on experience, expertise and ability to work independently as well as within a Global team. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 -
- PW 6335 Global Submission Specialist / Regulatory Submissions Project Manager
Opportunity for a Submissions Manager to join this Top 20 Pharma on a fixed term contract as our Client’s Global Regulatory Submissions Specialist. The role is office based in the South East, focuses on compliant submissions, Ectd standardisation and sits within a cross functional global team. Contract length is 6 months and strong likelihood to extend further.
- Senior Regulatory Affairs Specialist-Full time-Competitive Salary
Our client is a well-established medical device company, based in Scotland with more than 1000 employees. The company is focused on future development in the area of diabetes and is looking for an experienced Regulatory Affairs Specialist to work full-time.
- Regulatory Affairs Specialist-Exciting FDA Project-Devices-CH
Our client, a world leading medical device company are offering a regulatory affairs specialist the excellent prospects of working on exciting FDA projects. You will be one of the key experts on site who will manage the 510K and PMA process; providing for a great opportunity to develop your skills on a global level.
- Regulatory Affairs Specialist - Medical Devices
A global leading medical device technology firm specialising in integrated solutions are currently looking to bring on multiple contractors in the Regulatory Affairs team