Experis Life Sciences is your partner in your research for professional opportunities.
Our expertise and our large client portfolio in the pharmaceutical, chemical and food industries allows us to make the good connections between your experience, your expectations and the needs of the market.
You will have the opportunity to enter various departments (R&D, Production, Supply Chain,
QA, QC, RA, ...) according to your interests.
Interested by Laboratory work ? You want to work in an innovative and international pharmaceutical industry?
This position is for you.
This team's primary responsibility is to develop and validate analytical methods for release, stability testing and in-process control of our biological drug substances and products, according to the required GMP and regulatory standards from early clinical phases to life-cycle management of the product. The team is also involved in method transfers and preparation of regulatory submissions with internal or external business partners.
Scope of the mission:
The primary goal of the mission is to develop and validate the methods used for the release and stability testing as appropriate, according to the agreed quality standards and timelines. The incumbent will work in a team environment, collaborating with various scientists and technicians in cross-functional project teams.
The main techniques used are HPLC/UPLC, ICP-MS, qPCR, gel/capillary electrophoresis, immunoassays.
The main activities of this position will be:
All these activities will be performed in compliance with the GMP/HSE rules and with the regulatory requirements for each development phase of the product.
Our offer :