Specialist Quality Assurance Clinical
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 Pharmaceutical organization, based in Noord-Brabant Netherlands.
Do you want to work at a company who really serves their patients? A company who encourage our team members to have fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities? Then this company will suit you perfectly.
ROLE DESCRIPTION
Do you want a great opportunity to be part of growing company, while working on your own development whilst making sure their medicines find their way to the patients? Is it your goal to ensure the quality of the medicine? Then this is the job for you! This role is offered for 6 months and can be extended to a year.
RESPONSIBILITIES
In this passion you will be the quality assurance contact for all activities related to new clinical products introductions, including change control review and approval. You will provide guidance and direction to Quality, Clinical Supply Chain Management, Production and Warehouse/ Distribution with regards to compliance with quality policies, standards and procedures. Additionally, this involves:
- contact for Non-conformances and CAPA’s
- participation in audits (internal, external, corporate, etc.) and in the implementation of audit commitments
- writing, reviewing and approving procedures and/or job aids in compliance with corporate, site and regulatory requirements
- product Disposition (Investigational Medicinal Product)
REQUIREMENTS
- Bsc or Msc degree in the pharmaceutical industry
- Minimum 3+ years of experience in pharmaceutical industry
- You have had experience as a QP or alternatively you have a few years of experience in Quality Assurance and have the potential to become a QP
- You are able to maintain oversight on different projects and provide Quality guidance to other functions
- Knowing how to work in teams and communicating effectively with all kind of stakeholders is crucial in this role
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
