Freelance Pharmaceutical Specialist
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-Holland Netherlands.
They are an international organization who focus on healthcare. A company that delivers their part in a healthier world. In over 140 counties they help people and animals with medicals, vaccines etcetera in an innovative way.
ROLE DESCRIPTION
Currently we are looking for a talented and ambitious interim pharmaceutical specialist. You will be responsible for the initiation and execution of the quality policy and focus on regulatory. You will be in contact with several departments that have to do with all integrated processes and other related items. You will practice the quality assurance and give advice on technical pharmaceutical issues. The solutions for problems you will report to the QA director. The end date of this project is not yet known, expected 6-8 months.
RESPONSIBILITIES
You will focus on coordinating and processing the quality policy. You have the ability to evaluate the external guidelines.
- Lead audits
- Participate on behalf of QA in projects
- Deliver and review quality agreements
- Lead reports and complex quality defects
- Work together with quality specialists
- Work with GMP system
REQUIREMENTS
- MSc. in Pharmaceutical, technical processing or chemical background
- 3-5 years of experience as a Pharmaceutical specialist
- Experience with GMP, registration medicals, packaging technology and validation studies
- Fluent in English and Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
