QA Manager
Location: NetherlandsThe Company
For a very interesting pharmaceutical company I am looking for a qualified QA Manager.Role Description
As a QA Manager and Responsible Person you are responsible for GDP (Good Distribution Practices) requirements for the different countries in which the company carries out distribution activities for medicines.Responsibilities
- You are responsible for the follow-up and implementation of new legislation and quality standards.- You optimize the quality management system, processes and procedures with the objective of optimizing the functioning of all quality processes.
- You support both internal and external quality audits and you implement the necessary actions resulting from these audits.
- You coordinate and investigate quality issues such as non-conformities, complaints about product quality, etc. You prepare action plans and adjust where necessary.
Requirements
- Masters in Pharmaceutical Sciences, Medicine, Chemistry or similar.- You have a thorough knowledge of QA systems and GxP requirements, including regulations and standards that affect medical devices, nutritional supplements and other pharmaceutical products.
- You are analytical and think problem solving with a focus on continuous improvement.
- You have strong communication skills in Dutch/English and preferably French
Other information
Are you interested or do you want to know more about this position? Do not hesitate to call me, reply to this message or send an e-mail to j.zanting@sire-search.com !Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Zanting.
Opis stanowiska
The Company
For a very interesting pharmaceutical company I am looking for a qualified QA Manager.Role Description
As a QA Manager and Responsible Person you are responsible for GDP (Good Distribution Practices) requirements for the different countries in which the company carries out distribution activities for medicines.Responsibilities
- You are responsible for the follow-up and implementation of new legislation and quality standards.- You optimize the quality management system, processes and procedures with the objective of optimizing the functioning of all quality processes.
- You support both internal and external quality audits and you implement the necessary actions resulting from these audits.
- You coordinate and investigate quality issues such as non-conformities, complaints about product quality, etc. You prepare action plans and adjust where necessary.
Requirements
- Masters in Pharmaceutical Sciences, Medicine, Chemistry or similar.- You have a thorough knowledge of QA systems and GxP requirements, including regulations and standards that affect medical devices, nutritional supplements and other pharmaceutical products.
- You are analytical and think problem solving with a focus on continuous improvement.
- You have strong communication skills in Dutch/English and preferably French
Other information
Are you interested or do you want to know more about this position? Do not hesitate to call me, reply to this message or send an e-mail to j.zanting@sire-search.com !Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Zanting.
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