CMC Regulatory Manager - 's-Hertogenbosch

Vacancy information

Publication date:May 26 2020
Employment type:Permanent
Sector:Pharmaceutical
Function Group:Quality/RA

Function Group: Quality/RA / RA Manager

Organization

For the office in the Netherlands based in Den Bosch, we are looking for a CMC Regulatory Manager with several years of experience. Operating around in Benelux with offices in Den Bosch, this topnotch regulatory consultancy firm provides clients with a wide variety of global support. This consultancy firm is in the top three most promising privately owned regulatory consultancy companies in the Netherlands. The office based in Den Bosch with 30 colleagues, is serving its clients with an initial clinical study to post-approval compliance. They are working especially for chemical and biological medicinal products and medical devices. Since they are working together with the local people, they are very successful in deeply rooted relationships with clients by providing leading industry knowledge, experience, and proven processes. This mid-size company has close to 30 clients worldwide, 35+ colleagues from RA managers to CMC experts, and is supporting her clients in whole Benelux.

Function

Are you interested in an independent, responsible and consulting role in a small consultancy firm with possibilities to (further) develop yourself as a CMC Regulatory Manager? This could be something for you! You will work for several clients on projects with a duration between six months and three years. Because the work-life balance is really important for the employees of this company, everybody will take care that you will work on a project that you like and are close to home. You will be working for state of the art pharma companies till little local start-up. You will help those companies with a very wide variety of services, such as review reports on pharmaceutical product and process development, prepare and coordinate regulatory submissions and marketing authorization procedures and “translate” scientific lab results into regulatory supportive dossier documents. In this role, it is important that you are able to have effective communications with clients and that you can work autonomously on projects. It goes with saying that you have over twenty-five colleagues that will have your back and support you. Because when you are working at a client, the client actually hires the knowledge of over a twenty-five international consultants.

Requirements

The ideal candidate has:

  • a MSc/PhD in Pharmacy, Chemistry, Life Sciences
  • Scientific and technical writing/editing skills (English)
  • Knowledge of/affinity with analytical procedures, specifications, validation methods, stability testing, process controls etc.
  • Minimum three years of CMC RA experience
  • The eagerness to learn, develop and excel
  • The ability to handle stringent deadlines
  • The ability to communicate in a convincing way

Offer

In exchange for your talent, time and energy we offer:

  • Salary midpoint around €60,000 depending on experience
  • Pension scheme
  • Holiday allowance
  • Work in an international environment of pharmaceutical industry
  • Interesting projects which will stimulate you to keep learning
  • Company car

Application

If you are interested in this job, or in similar ones, please feel free to contact me directly.

Yvo Selderbeek
Sr Associate – Biotech & Pharma

+31(0)6-12576648
+31(0)23-7548660
y.selderbeek@qtcrecruitment.com

Apply

Contact

To find out what QTC Recruitment can do for you, please contact us. 
Contact us
1
Hello, how can I help you? I will answer you as soon as possible during working hours.

Press the WhatsApp button again...
Powered by