CSW Therapeutics AB
Biomedical Research Associate Preclinical Development
Om jobbet
Design and support data acquisition protocols for preclinical studies involving soundwave therapy.
Analyze and interpret biophysical and histological data related to angiogenesis, tissue regeneration, and cardiovascular function.
Assist in the development and refinement of preclinical endpoints, with a focus on translational relevance.
Contribute to the development of V&V protocols, and help document processes in line with ISO 13485 and FDA standards.
Collaborate with cross-functional teams (electronics, biology, regulatory) to ensure scientific rigor and clarity in experimental design.
Prepare documentation and materials to support grant applications, scientific publications, patent applications and regulatory submissions.
Help compile and organize a design history file (DHF) and assist in creating documentation for design for manufacturing (DFM).
Qualifications
Master's degree in Biophysics, Biomedical Engineering, Physics, or a related field (PhD is a plus).
Experience in preclinical research, preferably involving cardiovascular models or regenerative medicine.
Understanding of histological methods, immunohistochemistry, or biomarker identification (not mandatory but helpful).
Familiarity with medical device testing, scientific documentation, and basic regulatory concepts (e.g., IEC 60601, FDA QSR).
Demonstrated ability to work interdisciplinarily, interpret biological findings from physical or analytical perspectives, and communicate clearly.
Self-driven, organized, and eager to contribute in a fast-paced startup setting.
What You'll Get
A central role in shaping translational research at an early-stage MedTech company.
Mentorship from experienced scientists and clinicians.
Flexibility in work setup and responsibilities as the company grows.
Opportunity to impact patients with a non-invasive, potentially life-changing therapy.
Analyze and interpret biophysical and histological data related to angiogenesis, tissue regeneration, and cardiovascular function.
Assist in the development and refinement of preclinical endpoints, with a focus on translational relevance.
Contribute to the development of V&V protocols, and help document processes in line with ISO 13485 and FDA standards.
Collaborate with cross-functional teams (electronics, biology, regulatory) to ensure scientific rigor and clarity in experimental design.
Prepare documentation and materials to support grant applications, scientific publications, patent applications and regulatory submissions.
Help compile and organize a design history file (DHF) and assist in creating documentation for design for manufacturing (DFM).
Qualifications
Master's degree in Biophysics, Biomedical Engineering, Physics, or a related field (PhD is a plus).
Experience in preclinical research, preferably involving cardiovascular models or regenerative medicine.
Understanding of histological methods, immunohistochemistry, or biomarker identification (not mandatory but helpful).
Familiarity with medical device testing, scientific documentation, and basic regulatory concepts (e.g., IEC 60601, FDA QSR).
Demonstrated ability to work interdisciplinarily, interpret biological findings from physical or analytical perspectives, and communicate clearly.
Self-driven, organized, and eager to contribute in a fast-paced startup setting.
What You'll Get
A central role in shaping translational research at an early-stage MedTech company.
Mentorship from experienced scientists and clinicians.
Flexibility in work setup and responsibilities as the company grows.
Opportunity to impact patients with a non-invasive, potentially life-changing therapy.
CSW Therapeutics AB
FöretagCSW Therapeutics AB