SIRE Life Sciences®

QA Manager

Location: Belgium
SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical and Medical Devices organisation, based in Vlaams-Brabant Belgium.

The Company

This organisation is a well-known international brand. They focus on the manufacturing of OTC products. They are rapidly growing and extending their business, and therefore they are looking for a manufacturing manager.

Role Description

As a quality manager you will guarantee that the QMS is in line with the GMP requirements for the bulk manufacturing site. Your team will exist of 2 Quality officers who you will guide and support on a daily basis. You will be leading and guiding internal and external audits. In addition, you will make sure that all documentation and related quality activities are overviewed and completed. Furthermore, you are responsible for the training of your team and for the other departments as quality is highly valued in this organisation. You are the point of contact when issues occur related to quality.

Responsibilities

On a daily basis you will overview and support your Quality team. Further responsibilities involve:
• Improvement and maintenance of the QMS according GMP requirements
• Release of bulk products
• The execution and guidance of internal and external audits
• Taking responsibility for the Quality oversight at the NPI
• Overviewing the performance of the Quality department and making reports to the MT
• Keeping track of latest quality standards and changes, and setting up strategies to apply these to the QMS

Requirements

• Bachelor or Master in the Life Sciences or Engineering
• A minimum of three years of experience in QA in a manufacturing environment
• Experience a team coordinator or supervisor would be a plus
• Extensive knowledge and solid experience with GMP standards and related regulations
• Pro-active attitude
• Strong organisational skills

Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Ewout de Jong
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

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