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SIRE Life Sciences®

QA Associate II

Qu?n 3, Vietnam, zagranica Pełny etat

SIRE Life Sciences®

QA Associate II

Location: Qu?n 3, Vietnam
Quality Assurance Specialist 


Location: Hoofddorp
Duration: 1 year  (extension is possible)
Language: English
Industry: Pharma
Start date: 1-10-2022 

The company

Our client is a biopharmaceutical company engaged in the development of cancer immunotherapies with the aim to provide long term response and eliminate this chronic disease.

About the role
As a Quality Assurance Specialist you will be responsible for ensuring the accuracy and completeness of the QA issued documents.

Responsibilities
- Control the issuance of batch document and label packages including the final product labels per cGMP
- Identify and escalate compliance gaps across the controlled issuance process

-Support Audits (internal, external)
- Execute strategic initiatives to improve the controlled issuance process
- Controlled the issuance of logbooks

Requirements
- 2+ years’ experience on document management in a regulated environment
- Advanced level of English communication
- Ability to effectively communicate with peers.


Ready for the next step in your QA career? Reach out to me by applying to this vacancy. 
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

Opis stanowiska

Quality Assurance Specialist 


Location: Hoofddorp
Duration: 1 year  (extension is possible)
Language: English
Industry: Pharma
Start date: 1-10-2022 

The company

Our client is a biopharmaceutical company engaged in the development of cancer immunotherapies with the aim to provide long term response and eliminate this chronic disease.

About the role
As a Quality Assurance Specialist you will be responsible for ensuring the accuracy and completeness of the QA issued documents.

Responsibilities
- Control the issuance of batch document and label packages including the final product labels per cGMP
- Identify and escalate compliance gaps across the controlled issuance process

-Support Audits (internal, external)
- Execute strategic initiatives to improve the controlled issuance process
- Controlled the issuance of logbooks

Requirements
- 2+ years’ experience on document management in a regulated environment
- Advanced level of English communication
- Ability to effectively communicate with peers.


Ready for the next step in your QA career? Reach out to me by applying to this vacancy. 

Dodatkowe informacje

Ostatnia aktualizacja
Wymiar etatu
Pełny etat
Rodzaj umowy
Na czas nieokreślony
Liczba wakatów
1
Min. doświadczenie
1 rok
Min. wykształcenie
Średnie ogólnokształcące
Branża / kategoria
Praca Automatyka / Robotyka