QC Analyst

Bedrijfsnaam: -
Plaatsingsdatum: 02/07/2019
Standplaats: -


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 and Chemicals organisation, based in Oost-Vlaanderen Belgium.The CompanyOur client is one of the leading CDMOs in Europe providing high-quality, customized drug development solutions for specialty and biopharma clients. Their focus is to support clients on the earliest phases of their development pathway (from API to the clinical packaging).

Its Belgian subsidiary is based in Ghent, offering a complete drug development package for new drug entities (biological and chemical) up to early clinical phases to third parties to help them in speeding up the development and manufacturing of their drugs. To support our ambitious growth plan, we are today looking for a QC Analyst for our site in Ghent, Belgium.

Role DescriptionThe Belgian subsidiary wishes to enforce its team with a QC Analyst. We are looking for a person that reports to the QC Manager.

ResponsibilitiesYou perform Quality Control activities according to instructions, procedures and protocols in compliance with the GMP principles and the Quality Management System.
• You perform Quality Control analyses.
• You perform ICH compliant stability studies.
• You validate analytical methods to support the quality control and release of drug products for use in clinical trials.
• You support preparation of the applicable protocols and reports.
• You accurately report, document and review the analytical test results.
• You support the maintenance, calibration and qualification of the analytical equipment.

RequirementsProfessional Bachelor degree in biomedical laboratory technology, chemistry or pharmaceutical sciences with a minimum of 5 years relevant professional experience.

• Experience in a regulated Quality Control laboratory and experience with core pharmaceutical analytical techniques (HPLC/UPLC, Dissolution) is a must.
• Experience with Empower processing software is a must.
• Experience with KF, Particle sizing, UV spectroscopy, etc. are real assets.
• You are punctual and are able to work independently after a training in matters entrusted to you.
• You are flexible, problem solving and quality minded.
• You are fluent in Dutch and English (written and spoken).

Other informationWe offer you
• A position with responsibility within a dynamic company
• Personal development through learning on the job and additional external trainings
• A market oriented compensation

Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Rutger Koning




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
3 - 5 jaar
Contactgegevens :