Quality Assurance Manager / Pharma / Perm / QP / GMP and GDP

Location: Netherlands

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 organisation, based in Noord-Brabant Netherlands.

The Company

Our client is a pharmaceutical CPO. They are a global company and their quality department is the core of their quality vision and mission. The company reaches millions of patients with their work in over 40 countries worldwide. It is the quality department's responsibility to make sure that our people, processes, materials and machines work together to assure patient safety.

Role Description

Our client is searching for a Quality Assurance Manager with one year (ore more) of experience as Qualified Person. As a QA Manager you'll be focusing on patient-centered quality control and quality assurance projects. It means that you will be working in multi-disciplinary teams. Think about working with partners from across the supply chain and communicating with international customers. Your English and Dutch has to be on a professional communicating level, written and spoken. This way your will be playing an integral part in the implementation of complex and innovative products that make a real difference to patients ‘lives.

Your are the person that makes it matters!

Responsibilities

What you are going to do to make it matter...

... you need to collaborate with the technical team, the IT teams and with project managers from across the company on validation projects. You are going to work closely with the operation team, designing and providing targeted quality training to team leaders.You will be communicating with local and international customers, so having experience is a plus. Leading customers audits and providing support on quality control and quality assurance is no problem for you. Another responsibilities of yours is implementing a new Quality Management System (QMS).

Requirements

What do you need and what does it takes? Found out!

First of all the client requires candidates with a MSc (or equivalent) in a pharmaceutical-related subject. A Bachelor can also be interesting, so don't give up, but you have to be able to compensate with something. Are you also in possession of a Qualified Person certificate? And do you have minimal one year of experience as a Qualified Person? Than the will adore you even more! Having knowledge and experience with GMP en GDP is also important for the client. But that is not all, you also need to be able to communicate fluently and to present complex information to both pharmaceutical and non-pharmaceutical audiences. You need to have experience with investigating, defining and resolving complex issues. Also with planning, scheduling and monitoring work to meet time and quality targets.

Other information

Our client promise they will help you become successful in your new job. Their working conditions include 39 days off, an attractive pension and a yearly salary increase depending on your performance.

What are you waiting for? Apply!

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