Project and Validation Ingenieur / Pharma / region Antwerp / GxP / GMP & CAPA

Bedrijfsnaam: -
Plaatsingsdatum: 24/02/2019
Standplaats: -

Functieomschrijving

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 Antwerpen Belgium.The CompanyOur client is a pharmaceutical contract manufacturer for a wide range of international companies, specialized in the mixing and packaging of powders and liquids.
They are looking for a motivated and dynamic Project and Validation Engineer.

Read more to find out if you are one...

Role DescriptionThe function has a varied range of branches that you take with great autonomy and where you can learn every day. You report to the operations manager and work closely with the QA department.

Interesting for those who want's to grow and expand their knowledge!

ResponsibilitiesAs Project and Validation Engineer your function exists of the following responsibilities:

- You will use your GxP and technical expertise at, among others, preparation of risk assessments, change proposals (changes control) and quality reviews.
- You will manage your improvement projects, monitor the implementation of CAPA actions and make proposals for continuous improvement of processes, machines
and procedures.
- You are responsible for qualification activities in production.
- You will comply with the maintenance and calibration planning.

Handy to know; our client is a small company with 50 employees, you will get a varied package of duties!

RequirementsOur client is looking for someone who...:
- ...has had a relevant scientific-technical education, with a pre-engineer (Bio) engineer.
- ...has relevant experience in a GMP environment (required), preferably two years or more.
- ...has a good knowledge of Dutch and English, both spoken and written.
- ...works well in a team and independent
- ...doesn't shy away from administration
- ...has strong organization skills, has an eye for details and oversees the big picture.
- ...has proven experience as a project leader is a plupunt.

Our customer offers you the possibility to organize your time independently or flexibly. You have an interactive role with other departments and customers. Our client has an open company culture with direct communication, where transparency is central

Other informationThe ideal candidate has 'all above' + experience with non-sterile products / powder; for such products as utilities; experience with automation.

The job is for 40 hours a week including meal checks and other fringe benefits. And for those who want's to expand knowledge there is the possibility of further (external) training.

OW! And our client is located in region Antwerp, just past Berchem! Handy to know if you're considering it because of the traffic, just saying...

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.

 

Aanbod/arbeidsvoorwaarden
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Samenvatting

Plaatsingsdatum :
24/02/2019
Referentienummer :
97513
Standplaats :
-
Adres :
-
Postcode :
9723 HK
Opleidingsniveau :
HBO
Uren :
Nader te bepalen
Dienstverband :
Vast
Werkervaring :
3 - 5 jaar
Contactgegevens :
bekijk