Chemical Analyst (Quality Control)
Location: NetherlandsSIRE 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 Noord-Brabant Netherlands.
They are a global leader in the development and production of animal vaccines.
ROLE DESCRIPTION
You play an important role in the team as you ensure that all experiments are properly executed and that all processes meet the scheduled demand. Your job will be to guarantee all work is done according to GMP-, GGO- and SHE-standards. You will be flexible, continuously improving yourself, and thinking in terms of solutions, not problems.
This function will be for a project of 12 months.
RESPONSIBILITIES
You and your team will be responsible for all quality control in the lab:
- Ensure GMP-, GGO, and SHE-practices are followed;
- Signal and report possible errors and deviances in the procedures;
- Enter test data in the processing systems;
- Analyse tests, results and the release of data.
REQUIREMENTS
An MLO-degree in (bio-) chemistry or a related field
- Experience with QC;
- Familiarity with GMP, GGO and SHE;
- Knowledge and experience with SAP would be an asset.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
Opis stanowiska
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 Noord-Brabant Netherlands.
They are a global leader in the development and production of animal vaccines.
ROLE DESCRIPTION
You play an important role in the team as you ensure that all experiments are properly executed and that all processes meet the scheduled demand. Your job will be to guarantee all work is done according to GMP-, GGO- and SHE-standards. You will be flexible, continuously improving yourself, and thinking in terms of solutions, not problems.
This function will be for a project of 12 months.
RESPONSIBILITIES
You and your team will be responsible for all quality control in the lab:
- Ensure GMP-, GGO, and SHE-practices are followed;
- Signal and report possible errors and deviances in the procedures;
- Enter test data in the processing systems;
- Analyse tests, results and the release of data.
REQUIREMENTS
An MLO-degree in (bio-) chemistry or a related field
- Experience with QC;
- Familiarity with GMP, GGO and SHE;
- Knowledge and experience with SAP would be an asset.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Kontrola jakości / Audyt produkcji
