Senior Operator
Location: NetherlandsSIRE® 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 Pharmaceutical and Biotechnology organisation, based in Noord-Holland Netherlands.
Leading in deviation investigation and follow up
Process Excellence activities to continuously improve the work as well as personal skills.
Accurately completion of documentation such as batch records, logbooks, etc.
Working precisely and meticulously and to detect and communicate possible abnormalities.
Taking part in / coordinate all activities related to the production of cGMP clinical batches of Biopharmaceuticals produced on mammalian cell lines. This includes processes such as cell and virus culture, purification processes, formulation & fill and in-process testing.
Coordinate setting up documentation to ensure successful production runs.
- Experience in Pharmaceutical or Biotech industry
- cGMP knowledge and experience
- Certified Lean belt
- Real Team player
- Team leading skills
- English (required), Dutch (plus)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Asanka Boxma.
The Company
This Multinational is specialised in biotechnology vaccines and biopharmaceutical technologies.Role Description
As a Senior Operator you will work in the Drugs Substance Operations Department in a team of approximately 30 people. The team works on the manufacturing of clinical batches to support the development of new vaccines.Responsibilities
You will be responsible for:Leading in deviation investigation and follow up
Process Excellence activities to continuously improve the work as well as personal skills.
Accurately completion of documentation such as batch records, logbooks, etc.
Working precisely and meticulously and to detect and communicate possible abnormalities.
Taking part in / coordinate all activities related to the production of cGMP clinical batches of Biopharmaceuticals produced on mammalian cell lines. This includes processes such as cell and virus culture, purification processes, formulation & fill and in-process testing.
Coordinate setting up documentation to ensure successful production runs.
Requirements
- BSC in life sciences related study- Experience in Pharmaceutical or Biotech industry
- cGMP knowledge and experience
- Certified Lean belt
- Real Team player
- Team leading skills
- English (required), Dutch (plus)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Asanka Boxma.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Opis stanowiska
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 Pharmaceutical and Biotechnology organisation, based in Noord-Holland Netherlands.
Leading in deviation investigation and follow up
Process Excellence activities to continuously improve the work as well as personal skills.
Accurately completion of documentation such as batch records, logbooks, etc.
Working precisely and meticulously and to detect and communicate possible abnormalities.
Taking part in / coordinate all activities related to the production of cGMP clinical batches of Biopharmaceuticals produced on mammalian cell lines. This includes processes such as cell and virus culture, purification processes, formulation & fill and in-process testing.
Coordinate setting up documentation to ensure successful production runs.
- Experience in Pharmaceutical or Biotech industry
- cGMP knowledge and experience
- Certified Lean belt
- Real Team player
- Team leading skills
- English (required), Dutch (plus)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Asanka Boxma.
The Company
This Multinational is specialised in biotechnology vaccines and biopharmaceutical technologies.Role Description
As a Senior Operator you will work in the Drugs Substance Operations Department in a team of approximately 30 people. The team works on the manufacturing of clinical batches to support the development of new vaccines.Responsibilities
You will be responsible for:Leading in deviation investigation and follow up
Process Excellence activities to continuously improve the work as well as personal skills.
Accurately completion of documentation such as batch records, logbooks, etc.
Working precisely and meticulously and to detect and communicate possible abnormalities.
Taking part in / coordinate all activities related to the production of cGMP clinical batches of Biopharmaceuticals produced on mammalian cell lines. This includes processes such as cell and virus culture, purification processes, formulation & fill and in-process testing.
Coordinate setting up documentation to ensure successful production runs.
Requirements
- BSC in life sciences related study- Experience in Pharmaceutical or Biotech industry
- cGMP knowledge and experience
- Certified Lean belt
- Real Team player
- Team leading skills
- English (required), Dutch (plus)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Asanka Boxma.
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 Obsługa klienta