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Senior Scientist

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Job Description - Senior Scientist

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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