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Senior Scientist

Posted on Jan. 29, 2026

  • Turku, Finland
  • 0 - 0 USD (yearly)
  • Full Time

Senior Scientist job opportunity

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Job Purpose

As a Senior Scientist in our LBA/Immunoassay group, you will serve as the technical Study Lead (“Responsible Scientist”) for a portfolio of ligand-binding and cell-based immunoassays, together with a more experienced colleague when necessary. You will design and execute method development, validation, and routine sample analysis; manage small cross-functional teams; interact directly with clients; and ensure on-time, on-budget delivery of bioanalytical data in full compliance with GLP, GCP, GMP (GxP) requirements.


Main Areas of Responsibility

  • Act as a study lead for ligand-binding (e.g. ELISA, MSD, DELFIA™) and functional immunoassays (e.g. cell-based reporter assays).
  • Lead study specific laboratory staff and ensure compliance with GxP and latest guidelines as well as standard operating procedures (SOPs).
  • Manage development, validation and application of bioanalytical, immunological and cell-based assays for pre-clinical, clinical studies, and drug batch characterization.
  • Create and maintain method validation and study plans, reports, method documentation and SOPs.
  • Serve as primary technical contact for study discussions, troubleshooting and data interpretation both internally and in client communication.
  • Stay updated on bioanalysis trends, continuous GxP-related training, implementation of EMA/FDA guidelines and White papers.
  • Provide training and support to staff.

Qualifications & Experience

Required:

  • Master’s degree in a natural science or 4-5 years of relevant experience.
  • Strong knowledge of analytical techniques (e.g. LC/MS, flow cytometry, immunoassays).
  • Proficiency on one or more platforms (e.g. MSD (ECL), Epoch, flow cytometers, PCR systems).
  • Good written and verbal communication skills (English and Finnish) as well as strong collaboration and negotiation skills.
  • Willingness to learn GxP quality standards
  • Willingness to continuous training.

Desired:

  • Knowledge of GxP regulations (GLP, GCP, GMP, GCLP) and ICH bioanalytical guidance and experience of working in a regulated laboratory.
  • Willingness to travel as needed.

Please submit your application and CV/resume in Finnish or English.


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