Qa manager / QP
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 Pharmaceutical organization, based in West-Vlaanderen Belgium.
My client is a world-leading specialist in generic medication, and European wide import specialist to distribute generic medicines throughout Europe.
ROLE DESCRIPTION
You will head a QC & QA Team of 15 to 20 specialists, to maintain a high QA standard in accordance to GDP. You're responsible to ensure GDP from a QC Belgium standpoint, and in close collaboration with your counterparts in other European countries. In this role you will report to the VP Quality.
RESPONSIBILITIES
Responsible for goal setting, review, and career development of QA/QC Specialists
Competence development of staff
Administrate department workload to assure all activities and timelines are met
Supervise that all work is completed in a safe and efficient manner, while meeting the standards of quality
GDP and service levels of the company are taken into account, and insure company standards are met
Lead internal and external audit programs/inspections by QA/QC team
Ensure internal quality audits are performed and reported as scheduled
Audit suppliers and customers
Investigate and resolve supplier quality issues
Coordinate and possible recall operations
Investigate product quality complaints
Research complaint documentations
Pre-approval of all printed packaging material - including PIL
CAPA responsibility
Define SOPs
Ensure maintenance and continuous improvement of QMS
Supervise product release
Create a inspirational and top performance culture in the QC/QA teams
REQUIREMENTS
MSc. Pharmacist
Fluent in Dutch, English & French
5 to 7 years experience in pharmaceutical industry
5 to 7 years experience in an ISO/GxP or comparable environment
Strong people manager
experience in KPI driven organization
Proven trackrecord managing QMS / ISO / SOPs
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.
