XDES is specialist in recruitment van technisch personeel.

Job Description

In this function you are responsible to develop and validate analytical methods to obtain reliable and robust release testing procedures. Furthermore, you're involved in non-routine analyses to support investigations as well as the support of submission –related activities for new product introductions into the production department. Taking into account the experience with complex product testing it is considered that you may act as key-expert in trouble-shooting analytical challenges with this type of products.

Key activities:

Perform complex testing
Development, validation, verification and/or remediation of analytical methods
Writing of protocols and reports
Maintain adherence to corporate policies and appropriate regulations through actions and decisions
Active participation in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test results discussions
First-line Troubleshooting of laboratory equipment
Active participation in changes or act as change owner as part of continuous improvement.

Job Requirements

Bachelor degree in analytical chemistry/pharmacy or equivalent experience
Knowledge and familiarity with the use of Pharmacopoeia methods
A strong analytical oriented mindset.
Experience with working in a pharmaceutical environment
Experience with development/validation or verification of analytical methods for complex drug products like liposomal or protein coated drugs
Experience with UPLC, CD, PSD, FFF is a preference
Good knowledge of Pharmaceutical quality systems and production processes
Team player
Strong can-do mentality

Salary and Benefits

A great job opportunity at a big pharmaceutical company.

Contact Us

Contactpersoon voor deze functie is Joost Storms, bereikbaar op telefoonnummer 023 55 78 529 of via e-mail: joost@xdes.nl Kenmerk: 10005.

QC Analyst II Method Implementation&Transfer