QMS Software Engineer

Bedrijfsnaam: -
Plaatsingsdatum: 12/03/2019
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 organisation, based in Noord-Brabant Netherlands.Role DescriptionAs Part of the Business Transformation program, we are developing standard Processes and IT solutions for complaint handing and Document Control. Since these are critical, and regulated processes, it is essential we validate these processes and IT solutions according applicable standards and regulations. To help/support the Team in the validation execution, we are looking for experienced (validation) engineers, who are familiar with Software Validation, writing & execution of test scripts, specifically performance qualifications / Testing against user requirements.

Responsibilities• GAMP5 / validation knowledge, experience with the type of verbiage to be used in describing test actions, expected results and actual results in scripts executions is required
• Need to have the Preciseness and authoring consistency of an experienced tester, hands on experience with good documentation practices and verbiage used in validation cycles in general
• Need to be able to learn how the business process is supported by an application
• Strong in Good Documentation Practices: Able to write /execute test scripts.

Requirements- Location/Timezone preferable NL (or CET). If NL, being able to visit Eindhoven once a week is preferred.

must have items:
- good Documentation Practices experience in medical devices, Experience in software validation, script writing and execution.

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

 

Aanbod/arbeidsvoorwaarden
-

Samenvatting

Plaatsingsdatum :
12/03/2019
Referentienummer :
97746
Standplaats :
-
Adres :
-
Postcode :
9723 HK
Opleidingsniveau :
HBO
Uren :
Nader te bepalen
Dienstverband :
Detachering
Werkervaring :
3 - 5 jaar
Contactgegevens :
bekijk