Quality Assurance Director
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Brabant Flamand Belgium.
A global company in biotechnology with a focus on a diabetic area. With a great focus on R&D in this area of disease.
ROLE DESCRIPTION
In this role as a Quality Assurance director you are responsible for all activities in QA in a GMP environment. You will make sure that the QA department will be GMP compliant to relevant regulations and guidelines. In communication with the Global Head of Quality you will focus on ensuring development and implementation of QMS. Furthermore you are responsible of releasing.
RESPONSIBILITIES
Building the strategy and goals for the QA department and implement them. Lead, coach and develop the employees within your department.
- Report to de Global Head of Quality
- Managing of internal and external QA resources for GMP
- Oversee distributors
- Participate in inspections like FDA
- Contact for QPs
- In lead of audits
- GMP SOPs content ensuring
- Input in QMS and in a training program for GxP’s
REQUIREMENTS
- Preferred MSc in Life Sciences
- Experience in Pharmaceutical QA GMP environment, Quality Management System, 10 years at a Biotech company
- GxP knowledge
- Experience with auditing, working with CMO’s, small molecule manufacturing
- Experience with clinical trials, packaging and labeling
- Strong in communication, team player
- Your English is fluent
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
