Quality Manager
Location: NetherlandsSIRE® 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 Netherlands.
Working closely with Operations
Communicating with local and international customers, leading customers audits and providing support on quality control and quality assurance matters.
Implementing a new Quality Management System (QMS), including improvement of quality reporting.
A minimum of a year of experience as a Qualified Person
Experience with GMP en GDP.
Demonstrable ability to communicate fluently (orally and in writing) and to present complex information
Demonstrable experience with investigating, defining and resolving complex issues.
Full professional prophecy in both Dutch and English.
Demonstrable experience with planning, scheduling and monitoring work
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
.Role Description
In this role you will be responsible you will be cooperating with several departments in order to achieve continuous improvenentResponsibilities
Collaborating with the technical team, the IT teams and project managersWorking closely with Operations
Communicating with local and international customers, leading customers audits and providing support on quality control and quality assurance matters.
Implementing a new Quality Management System (QMS), including improvement of quality reporting.
Requirements
Master in a pharmaceutical-related subject.A minimum of a year of experience as a Qualified Person
Experience with GMP en GDP.
Demonstrable ability to communicate fluently (orally and in writing) and to present complex information
Demonstrable experience with investigating, defining and resolving complex issues.
Full professional prophecy in both Dutch and English.
Demonstrable experience with planning, scheduling and monitoring work
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
