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Biology Scientist

Job in Franklin Lakes, Bergen County, New Jersey, 07417, USA
Listing for: MillenniumSoft, Inc
Full Time position
Listed on 2026-03-04
Job specializations:
  • Healthcare
    Medical Science
Job Description & How to Apply Below
Roles & Responsibilities
  • Act as the local SME in the design, execution, and interpretation of preclinical safety, biocompatibility, analytical chemistry, and toxicological evaluation strategies and programs, ensuring regulatory compliance.
  • Collaborate with CPDT SMEs, project teams, regulatory affairs, R&D, and external suppliers to define product testing requirements and provide CPDT deliverables.
  • Serve as the Sponsor Representative for biocompatibility and chemistry studies, supporting medical device evaluation programs.
  • Contribute to EU MDR remediation efforts by creating biocompatibility evaluation reports and conducting required testing to ensure compliance.
  • Maintain historical databases and perform searches for relevant data when necessary.
Experience Required
  • Bachelor's, Master's, or PhD degree in toxicology or a related field, with 2-8 years of pre-clinical medical device development experience depending on the level of education.
  • Experience in a GLP preclinical environment is preferred.
  • Experience in a U.S. or EU medical device setting is advantageous.
  • Board certification in toxicology (e.g., DABT, ERT) is preferred.
Skills & Certifications
  • Broad knowledge of biology, biocompatibility, toxicology, and analytical chemistry, including familiarity with ISO 10993 and related regulatory guidance.
  • Strong interpersonal and communication skills, both verbal and written, with the ability to work effectively with internal and external teams, including international stakeholders.
  • Proficiency in Microsoft Office (Word, Excel, Access, PowerPoint, SharePoint).
  • Strong multitasking and time-management abilities in a diverse work environment.
Eligibilities & qualifications
  • Bachelor's, Master's, or PhD degree in toxicology or a related field.
  • Minimum of 2-8 years of relevant pre-clinical medical device development experience, depending on educational qualifications.
  • Ability to function independently as an SME while being team-oriented.
  • Strong customer focus with the ability to work in a dynamic, cross-functional environment.
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