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Jobsinlifesciences.com

GCP Auditor

Switzerland, zagranica Pełny etat

Jobsinlifesciences.com

GCP Auditor

Location: Switzerland

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 Basel-Stadt Switzerland.
Our client is a multinational Pharma company in Switzerland

ROLE DESCRIPTION
GCP Auditing in Asia Pacific
RESPONSIBILITIES
- Performed and lead audits ICH/GCP and project timelines
- Reviewed protocols, amendments, case report forms (CRFs), clinical study reports (CSRs) and other relevant data
- Responsible for writing audit reports and ratings of audits including evaluation reports concerning employees
- Ensured in compliance applicable local laws, regulatory requirements and company SOPs
- Provision of education, feedback and support to study teams

REQUIREMENTS
- Fluency in English and one Asian / Pacific Language (e.g. Korean, Japanese, Chinese)
- Degree in Life Sciences or Related
- Experience in GCP Environment
- Experience in Auditing strongly advantegeous
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.

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 Basel-Stadt Switzerland.
Our client is a multinational Pharma company in Switzerland

ROLE DESCRIPTION
GCP Auditing in Asia Pacific
RESPONSIBILITIES
- Performed and lead audits ICH/GCP and project timelines
- Reviewed protocols, amendments, case report forms (CRFs), clinical study reports (CSRs) and other relevant data
- Responsible for writing audit reports and ratings of audits including evaluation reports concerning employees
- Ensured in compliance applicable local laws, regulatory requirements and company SOPs
- Provision of education, feedback and support to study teams

REQUIREMENTS
- Fluency in English and one Asian / Pacific Language (e.g. Korean, Japanese, Chinese)
- Degree in Life Sciences or Related
- Experience in GCP Environment
- Experience in Auditing strongly advantegeous
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.

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