SIRE Life Sciences®

QA Freelancer

Location: Germany

SIRE 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 Baden-Württemberg Germany.

Our client is an International Pharma company near Mannheim.

ROLE DESCRIPTION

In this role you will be responsible for GMP documents review and gap analysis.

RESPONSIBILITIES

- Review of GMP documentation
- Compliance of SOPs (packaging, batch records, analytical validation, protocols, reports)
- Review of specifications
- Supervising a small team of max 3 people
- Negotiating gaps in quality documents
- Statistical interpretation of data
- Collaborating with other departments and QA

REQUIREMENTS

- Life Science degree bachelor/master/phd
- Experience in GMP environment
- Affinity with IT systems
- Fluency in English

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.

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

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