Deputy Head of Quality/ Responsible Person
Location: NetherlandsSIRE 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 Noord-Brabant Netherlands.
This role is located within the affiliate of a well-know pharmaceutical company. The company has a large portfolio of medicines in many therapeutic areas including animal health products.
This position is a perfect combination between a family working mentality and the reputation and budget allocation of a big pharmaceutical company.
ROLE DESCRIPTION
The Deputy Head of Quality/ Responsible Person will be responsible for the maintenance and correct implementation of improvements in the Quality Management System.
As a Responsible Person, he/she will ensure the compliance of GDP guidelines in order to avoid potential hazards from poor distribution practices.
The Deputy Head of Quality/RP for the Benelux will ultimately back up the Head of Quality and take the responsibility when needed.
Additional information:
- Type of contract: temporary via payroll or freelance (ZZP)
- Duration: 1.5 years (end 2018 +potential extensions)
- Full-time
- Start date: 1st of August (negotiable)
RESPONSIBILITIES
- Ensure a correct maintenance of the QMS
- Process owner for change control, CAPA management and deviations
- Introduction of improvements
- Batch record review
- Take leadership on document management and accuracy of Quality records
- Correct respond to product recalls
- Deal with customer complaints
- Ensure compliance of GDP regulations
- Perform regular audits and internal inspections
- Point of contact for Authorities (Benelux )
REQUIREMENTS
- Master in Pharmacy
- Absolute minimum of 3 years of experience in Quality (preferably in distribution and production)
- Strong knowledge of GMP/ GDP guidelines
- Valid registration as Responsible Person (Benelux)
- Ability to work without much supervision
- Proficient level in English and Dutch, French is appreciated
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
