We are looking for a Senior Associate Scientist to join the Quality Control department of a modern pharmaceutical market leader in cell therapy. This role supports the development and oversight of analytical methods used for advanced therapeutic products. You will be part of a team focused on scientific support, technological improvements, and quality‑related activities within a fast‑paced and innovative environment.
Job Description
As a Senior Associate Scientist, you will contribute to the introduction of new analytical technologies, the improvement of existing test methods, and the scientific support of QC operations. You will work closely with various teams to ensure new methods are properly validated and integrated into routine testing. The role includes reviewing documentation, assessing potential impacts on laboratory activities, resolving method‑related issues, and supporting compliance activities. You will help maintain high quality standards by trending data, contributing to investigations, and supporting the lifecycle management of analytical methods.
Responsibilities
- Coordinate with global teams on the introduction of new analytical methods and technologies.
- Lead method implementation and technology transfer projects within QC.
- Prepare and update validation protocols, analytical specifications, and related documentation.
- Participate in method validation and support automation initiatives.
- Troubleshoot analytical methods and contribute to CAPA activities.
- Review proposed changes to analytical processes and support regulatory documentation to ensure ongoing compliance.
- Lead investigations related to out‑of‑specification results and analytical deviations.
- Trend analytical and stability data and contribute to continuous improvement efforts.
Requirements
- Master's degree in Chemistry, Biology, or related field with 8+ years of relevant industry experience, or a PhD with 5+ years.
- Strong technical knowledge of analytical methods such as flow cytometry, ELISA, PCR, and cell‑based assays.
- Familiarity with cGMP and GLP environments.
- Ability to manage projects is an advantage.
- Strong communication and interpersonal skills, comfortable collaborating with diverse teams.
- Skilled in Excel and JMP.
- Able to work independently, manage time effectively, and maintain a positive, adaptable attitude.
Benefits
- Contract: one year trough Oxford Global Resources, possibility for extension
- Full time position, 40 hours per week
- Salary range: €5500,- to €6000,- gross per month, plus other benefits (holiday pay, travel allowance)
- Opportunity to work in an innovative environment centered on advanced therapies.
- Collaboration with experienced multidisciplinary teams.
- Location: Hoofddorp
- Vacancy number: 27084
