#

QA Manager Consultant

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

QA Manager Consultant

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 Biotechnology and Pharmaceutical organization, based in Zuid-Holland Netherlands.

They are an international organization who focus especially on services in pharmaceutical development of products that are focused on curing different diseases. A company that belong to the top in pharmaceutical in the world.

ROLE DESCRIPTION

You will manage the tracking and resolution of commitment's and CAPA in corrective and preventative actions. One of you responsibilities is to conduct and lead internal and supplier audits. You will monitor legislation, guidelines and the national regulatory environment to maintain company intelligence and awareness of compliance and best practice within the affiliate.

RESPONSIBILITIES

You are going to manage the tracking and resolution of commitment's and CAPA. Audits will be part of the function as well. You will conduct and lead them internal and for suppliers.
- To monitor legislation,
- Follow guidelines and the national regulatory environment
- Maintain company intelligence and awareness of compliance and best practice within the affiliate
- Support the Associate Director of Regulatory & Quality Compliance
- Management of the Affiliate Quality Management System.
- Authoring of SOPs and supporting process development for key procedures-
- Conducting quality and compliance reviews of new and updated procedures
- Develop training materials
- Ensure the biennial updates of all procedures
- Maintain awareness of current legislation and corporate policies

REQUIREMENTS

- MSc. or BSc in related field
- Knowledge of Quality Management principles and all relatable GxP areas
- Pharmacovigilance legislation knowledge
- GDP experience
- Experience of audits
- A professional qualification in Quality or Auditing

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

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

Czy chcesz otrzymywać oferty pracy na podobne stanowiska?

Utwórz powiadomienie e-mail
Zapisz mnie

Zapisani kandydaci otrzymują informacje jako pierwsi.

Podziel się ze znajomymi