WHO ARE WE?

Atypical partner of pharmaceutical companies providing expertise in QP/RP/RA & RIP matters

WHAT IS OUR AMBITION?

Provide the best service to our customers (expertise, pro-activity & communication)
100% satisfied clients

Juggle between different QP/RP projects on a daily/weekly basis.
Provide an impeccable service to the clients entrusted to you.
Endorse all the QP & RP responsibilities in the context of clients‘ activities (audit, batch certification, implementing and maintaining QMS, assessment of Product Quality Reviews, Quality Agreements, inspection, supplier qualification…)
Become the go-to expert for all Quality Assurance (Good Manufacturing Practices/Good Distribution Practices) related questions/problems
Share your experience and learn from your amazing colleagues

QP certification by FAMHP
Professional with experience in Quality Assurance, as Qualified Person or Responsible Person
(Willing to acquire an) in-depth knowledge of all aspects of GMP/GDP Quality Management System.
(Willing to acquire and maintain an) in-depth thorough knowledge of the legislation and guidelines (e.g. Eudralex volume 4, Belgian Law of 25 March 1964, RD 14 December 2006, Good Distribution Practices)
Being able to cope with a broad range of projects and changing priorities
High level of independence
Excellent communication skills
Demonstrated proficiency in MS Office
Experience in Regulatory Affairs, Pharmacovigilance and/or as Responsible Person for Information and Publicity is an asset
Preferably FR/ENG/NL

A role with a lot of responsibilities within a broad variety of projects and the chance to work self-organised in a dynamic & positive environment
Being able to develop yourself (training, coaching)
Attractive salary package, including bonus system
You can work in our beautiful office, at client’s site or work home-based without losing connectivity with the team