QC Project Analyst - Norway - Initial 6-Month Contract - Life Sciences We are partnering with a rapidly expanding Contract Development and Manufacturing Organisation (CDMO) based in Norway, recognised for delivering innovative pharmaceutical manufacturing solutions. As part of their continued growth, they are seeking an experienced QC Project Analyst with strong expertise to support their current project.
What you’ll deliver:
- Lead and support analytical method development, validation and method transfer activities
- Execute and oversee stability studies within a GMP pharmaceutical environment
- Perform analytical testing using HPLC, UPLC, GC and other laboratory instrumentation
- Prepare and review protocols, reports and technical documentation
- Support customer projects, project meetings and cross functional scientific activities
Key requirements include:
- Proven GMP pharmaceutical industry experience
- Strong hands on experience with HPLC, UPLC and GC
- Experience with analytical method development, validation and transfer
- Stability study experience and strong technical documentation skills
- Ability to work independently and engage with both internal and customer stakeholders
If this role is of interest, please apply now!#LI-EA1