Quality Engineer Temp (6-12 months)
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional organisation, based in Oost-Vlaanderen Belgium.
You participate to design review meetings & act as quality expert
You write and/or approve changes & CAPA’s.
You own and maintain the product risk management file
You handle and follow-up product complaints from end users, affiliates, distributors and partners
You optimize, validate and implement QC methods and procedures
You discuss complaints which could have consequences on public health and liaise with the Risk Assessment Committee
You provide support to the QC department
Project management experience
3 years quality experience in pharmaceutical or diagnostic environment
Insight in customer & market requirements
Fluent in both English and Dutch
Good written and oral communication skills
Positive, pro-active and flexible attitude
Team player: open minded, cooperative, takes initiative
Good problem solving - problem analysis
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven
The Company
The company has over 50 years of experience in developing and manufacturing pharmaceutical products world wide.Role Description
In this temporary you will be working within the quality team.Responsibilities
You review and approve technical documentation generated during the development process & improvement projectsYou participate to design review meetings & act as quality expert
You write and/or approve changes & CAPA’s.
You own and maintain the product risk management file
You handle and follow-up product complaints from end users, affiliates, distributors and partners
You optimize, validate and implement QC methods and procedures
You discuss complaints which could have consequences on public health and liaise with the Risk Assessment Committee
You provide support to the QC department
Requirements
Master degree in bio-environmentProject management experience
3 years quality experience in pharmaceutical or diagnostic environment
Insight in customer & market requirements
Fluent in both English and Dutch
Good written and oral communication skills
Positive, pro-active and flexible attitude
Team player: open minded, cooperative, takes initiative
Good problem solving - problem analysis
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven
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