Senior Medical Device Toxicologist: Biocompatibility

Boston Scientific Gruppe

Galway

On-site

EUR 90,000 - 140,000

Full time

14 days+
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Job summary

Boston Scientific Galway is seeking a Senior Medical Device Toxicologist on a permanent basis to join our global toxicology and biocompatibility team. The role provides technical leadership in ISO 10993 biology evaluation for new product development and regulatory submissions.

You will author Biocompatibility Assessments, test plans, and risk assessments, mentor junior staff, and collaborate with cross-functional teams to ensure patient safety and product quality under GMP/GLP guidelines.

Qualifications

  • Bachelor degree in Toxicology or related discipline.
  • MS or PhD in Toxicology or related field preferred.
  • Experience with regulatory standards (ISO 10993) and GLP/Risk assessment.

Responsibilities

  • Provide technical support for biocompatibility and toxicology processes per Global Preclinical objectives.
  • Author Biocompatibility Assessments, test plans, and reports; review data for regulatory submissions.
  • Mentor junior staff on test plan development and data interpretation; advise on biocompatibility strategies.
  • Maintain internal communications with stakeholders on biocompatibility and toxicology issues; support problem solving.
  • Contribute to regulatory submissions and adherence to GMP/GLP guidelines.

Skills

Toxicology
Biocompatibility
Regulatory knowledge
GLP experience
Risk assessment

Education

Bachelor degree in Toxicology or related discipline
MS in Toxicology or related field
PhD in Toxicology or related field

Job description

Boston Scientific Galway is seeking a Senior Medical Device Toxicologist on a permanent basis to join our global toxicology and biocompatibility team. The role provides technical leadership in ISO 10993 biology evaluation for new product development and regulatory submissions.

You will author Biocompatibility Assessments, test plans, and risk assessments, mentor junior staff, and collaborate with cross-functional teams to ensure patient safety and product quality under GMP/GLP guidelines.

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