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SIRE Life Sciences®

RA/QA Officer

Netherlands, zagranica Pełny etat

SIRE Life Sciences®

RA/QA Officer

Location: Netherlands

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 Healthcare and Pharmaceutical organization, based in Utrecht Netherlands.

The company is global healthcare company focussing on life saving medicines.

ROLE DESCRIPTION

As a regulatory affairs & quality assurance officer you will be reporting to the RA/QA Director Benelux.

RESPONSIBILITIES

Regulatory Affairs:
- Advice clients on pharmaceutical and medical issues
- Preparations of submissions and variations
- Follow-up of drug and biocides legislation
- Ensure compliance of with laws and regulations
- Labeling activities

Quality Assurance:
- Assist in QA related activities such as product quality complaints, CAPAs and exception reporting
- Back-up responsible person

REQUIREMENTS

- Pharmacist or Master degree in a life science discipline
- Several years of experience with regulatory affairs
- Excellent communication skills in English and Dutch (French is also preferred)
- Knowledge of Dutch regulations and authorities is a plus
- Attention to detail
- Ability to coordinate and plan activities and meet deadlines
- Pro-active and hands-on mentality

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

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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 Healthcare and Pharmaceutical organization, based in Utrecht Netherlands.

The company is global healthcare company focussing on life saving medicines.

ROLE DESCRIPTION

As a regulatory affairs & quality assurance officer you will be reporting to the RA/QA Director Benelux.

RESPONSIBILITIES

Regulatory Affairs:
- Advice clients on pharmaceutical and medical issues
- Preparations of submissions and variations
- Follow-up of drug and biocides legislation
- Ensure compliance of with laws and regulations
- Labeling activities

Quality Assurance:
- Assist in QA related activities such as product quality complaints, CAPAs and exception reporting
- Back-up responsible person

REQUIREMENTS

- Pharmacist or Master degree in a life science discipline
- Several years of experience with regulatory affairs
- Excellent communication skills in English and Dutch (French is also preferred)
- Knowledge of Dutch regulations and authorities is a plus
- Attention to detail
- Ability to coordinate and plan activities and meet deadlines
- Pro-active and hands-on mentality

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

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 Badania / Rozwój