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SIRE Life Sciences®

QA Manager - Nanoparticles

Germany, zagranica Pełny etat

SIRE Life Sciences®

QA Manager - Nanoparticles

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 Biotechnology organization, based in Germany.

It is an ambitious and fast growing biotech company specialised in individualised medicine.

ROLE DESCRIPTION

In this position you will take responsibility of GMP-Standards within R&D and production of new pharmaceutical/biotechnical products.

RESPONSIBILITIES

- Taking care of GMP-guidelines
- Developing the companies QM-system
- Analytical research on products and raw materials via GC, HPLC, ...
- Working together with R&D, production and the service unit
- Writing SOPs
- Development and validation of analytical methods

REQUIREMENTS

- Finished studies in chemistry, pharmacy and pharmaceutical technology
- At leas 3-5 years experience
- Knowledge of nanoparticles and drug delivery
- Deep knowledge or GMP-guidlelines
- English and German fluent

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

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

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 Biotechnology organization, based in Germany.

It is an ambitious and fast growing biotech company specialised in individualised medicine.

ROLE DESCRIPTION

In this position you will take responsibility of GMP-Standards within R&D and production of new pharmaceutical/biotechnical products.

RESPONSIBILITIES

- Taking care of GMP-guidelines
- Developing the companies QM-system
- Analytical research on products and raw materials via GC, HPLC, ...
- Working together with R&D, production and the service unit
- Writing SOPs
- Development and validation of analytical methods

REQUIREMENTS

- Finished studies in chemistry, pharmacy and pharmaceutical technology
- At leas 3-5 years experience
- Knowledge of nanoparticles and drug delivery
- Deep knowledge or GMP-guidlelines
- English and German fluent

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

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, Praca Kadra zarządzająca / Executive