QA Specialist
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 Biotechnology and Pharmaceutical organization, based in Noord-Brabant Netherlands.
The company is a multinational with a a cosmopolitan atmosphere and you'll be working in an international team of ambitious people.
ROLE DESCRIPTION
In this role you will be responsible for the support of the complaint system by running investigations on product complaints and performing data analysis on collected complaint information. You will signal errors and defects and make an action plan in order to solve these problems in an effective way.
RESPONSIBILITIES
- Update the complaint database as soon as information is available and make a report of closed investigations
- Review investigations to make sure they are science based and performed in the correct manner
- You will write reports on the investigations in a way that it is understandable for non-techincal reviewers
REQUIREMENTS
- Project management skills: able to set priorities and time management
- Excellent writing and and verbal skills: able to work cross functional
- Analytical and problem solving
- Able to work in a GMP environment
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Kimberley Rijnbeek.
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 and Pharmaceutical organization, based in Noord-Brabant Netherlands.
The company is a multinational with a a cosmopolitan atmosphere and you'll be working in an international team of ambitious people.
ROLE DESCRIPTION
In this role you will be responsible for the support of the complaint system by running investigations on product complaints and performing data analysis on collected complaint information. You will signal errors and defects and make an action plan in order to solve these problems in an effective way.
RESPONSIBILITIES
- Update the complaint database as soon as information is available and make a report of closed investigations
- Review investigations to make sure they are science based and performed in the correct manner
- You will write reports on the investigations in a way that it is understandable for non-techincal reviewers
REQUIREMENTS
- Project management skills: able to set priorities and time management
- Excellent writing and and verbal skills: able to work cross functional
- Analytical and problem solving
- Able to work in a GMP environment
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Kimberley Rijnbeek.
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
