(Junior)QA Manager / region Gent / Permanent / GMP / ISO13485

Bedrijfsnaam: -
Plaatsingsdatum: 02/02/2019
Standplaats: -


SIRE® 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 Pharmaceutical and Biotechnology organisation, based in Oost-Vlaanderen Belgium.The CompanyOur client offers innovative brands & products, they create new or alternative ways to make life better and healthier. By focussing on fundamental research & development, They're not only innovative in formula and design, but also in marketing. They match scientific progress with consumer insights.

Their goal? To improve not only our lives, but also those of the next generation.

Role DescriptionYou will be working in the Quality team with 2 other colleagues, reporting to the Head of Quality.

ResponsibilitiesWant to get experienced? This is the job to boost your career.

- Support the Design Transfer of new products to Operations
- Daily contacts/follow-up of suppliers (subcontractors): Compiling all documentation, necessary for production and QC of final products, approval of master batch records, deviation handling, follow-up process validation
- Release of Final Products to the customer
- Follow-up of stability studies
- Customer Complaint Handling (Investigation, Report, Follow-up)
- Initiate and follow-up CAPA reports

RequirementsEverything has his requirements, but if you match, you are the one!

- Knowledge of GMP and/or ISO13485 standard
- Minimum 2 years of experience in a similar role in a Pharmaceutical Company
- You have a Master’s degree (Pharma, Sciences, Bio..)
- Experience in a Production Environment is a plus
- You are fluent in Dutch and English
- You have a mature personality. You are assertive and like challenges. You are passionate and have strong organizational and analytical skills.

Other informationOW! You need to have a proactively mindset and be solution-oriented. And last but nor least, you are a team player. Through your excellent communication skills, you ensure optimal cooperation within the company with the other departments!

So do you have what it takes? Apply!

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
3 - 5 jaar
Contactgegevens :