
CMC RA
For one of our clients located in Ixelles, we are looking for a "CMC Regulatory Affairs". Job description International Regulatory experience for full registration Vaccines dossiers (not local...
18 hours ago - Source Stepstone.be
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For one of our clients located in Ixelles, we are looking for a "CMC Regulatory Affairs". Job description International Regulatory experience for full registration Vaccines dossiers (not local...
18 hours ago - Source Stepstone.be
For one of our clients located in Wavre, we are looking for a "Technical RA Registration Manager". Job description The Technical RA manager is responsible for the preparation, authoring and...
18 hours ago - Source Stepstone.be
For one of its client, the affiliate of an entrepreneurial international pharmaceutical group, ARSANNE Consulting is looking for a Regulatory Affairs Manager Benelux (RA, QA and Vigilance...
19 hours ago - Source Stepstone.be
Provide timely preparation high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies. Author high- quality CMC documentation for HA...
19 hours ago - Source Stepstone.be
Make your mark for patients. We’re here because we want to build the future and transform patients’ lives for the better.At UCB, our people are our experiences and achievements, our passion and...
17 hours ago - Source Neuvoo PREMIUM Europe
Support for developing and implementing the regional CMC regulatory strategy and submission plans for assigned projects/products Identify supporting documents required for regional submissions...
19 hours ago - Source Jobleads Europe
Our client is a leading OTC pharmaceutical organization that work toward the health professionals & the patient in order to help them in their daily health management. In order to sustain their...
19 hours ago - Source Stepstone.be
We are currently looking for a Regulatory Affairs Manager to join the team at our client's.Support implementation locally of new initiatives, management tools or processes in cooperation with EST-...
18 hours ago - Source Stepstone.be
Based in the European HQ in Belgium, the Regulatory Affairs Support Specialist assists and supports the CSS Regulatory Affairs Global Strategic Implementation Department in the execution of...
17 hours ago - Source Neuvoo PREMIUM Europe
Under supervision, provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.Big and known pharmaceutical...
17 hours ago - Source Neuvoo PREMIUM Europe
Help us transform patients' lives.At UCB, we put our heart, soul, and skills into making a difference for people living with severe disease. Working together to push the boundaries, we blend the best...
17 hours ago - Source Neuvoo PREMIUM Europe
For one of its client, the affiliate of an entrepreneurial international pharmaceutical group, ARSANNE Consulting is looking for a Regulatory Affairs Manager Benelux (RA, QA and Vigilance...
19 hours ago - Source Stepstone.be
For one of its client, the affiliate of an entrepreneurial international pharmaceutical group, ARSANNE Consulting is looking for a Regulatory Affairs Manager Benelux (RA, QA and Vigilance...
18 hours ago - Source Stepstone.be
Based in the European HQ in Belgium, the Regulatory Affairs Support Specialist assists and supports the CSS Regulatory Affairs Global Strategic Implementation Department in the execution of...
17 hours ago - Source Neuvoo PREMIUM Europe
Based in the European HQ in Belgium, the Regulatory Affairs Support Specialist assists and supports the CSS Regulatory Affairs Global Strategic Implementation Department in the execution of...
17 hours ago - Source Neuvoo PREMIUM Europe
The Quality and Regulatory Coordinator is supporting the business AR-PRRCs and is responsible for the implementation of the procedures under the EU Medical Devices Regulation (2017/747) for Global...
17 hours ago - Source Neuvoo PREMIUM Europe
For one of our clients located in Anderlecht, we are currently looking for a "RA Officer". Job Description As RA Officer, you will join the RA department of our clients and you will support the...
18 hours ago - Source Stepstone.be
Responsibilities of the RA CMC Officer Support for developing and implementing the regional CMC regulatory strategy and submission plans for assigned projects/products Identify supporting...
16 hours ago - Source Neuvoo BULK Europe
We are currently looking for a Regulatory Affairs Manager to join the team at our client's. Support implementation locally of new initiatives, management tools or processes in cooperation with EST-...
19 hours ago - Source Jobleads Europe
Job sector: Engineering activities and related technical consultancy Contract type: Direct hire Occupation: Job details Job descriptionSupport implementation locally of new initiatives, management...
19 hours ago - Source Jobleads Europe
Based in the European HQ in Belgium, the Regulatory Affairs Support Specialist assists and supports the CSS Regulatory Affairs Global Strategic Implementation Department in the execution of...
17 hours ago - Source Neuvoo PREMIUM Europe
Provide timely preparation high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies. Author high- quality CMC documentation for HA...
19 hours ago - Source Stepstone.be
Our client is a leading OTC pharmaceutical organization that work toward the health professionals & the patient in order to help them in their daily health management. In order to sustain their...
19 hours ago - Source Stepstone.be
Global Regulatory CMC Lead, GRL CMC, Associate Director - biologic orphan drugs, Brussels Global Regulatory CMC Lead, GRL CMC, Associate Director - biologic orphan drugs, Brussels Global Regulatory...
19 hours ago - Source Jobleads Europe
Are you someone who likes trying new things and gaining different experiences? Than life as a Brunel consultant might be your thing!As a consultancy company specialized in Life Sciences,...
18 hours ago - Source Stepstone.be
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