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Scientist II - Biocompatibility

Job in Jersey City, Hudson County, New Jersey, 07390, USA
Listing for: PowerToFly
Full Time position
Listed on 2026-07-03
Job specializations:
  • Engineering
    Biomedical Engineer, Medical Device Industry, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly USD 85000.00 110000.00 YEAR
Job Description & How to Apply Below

Company Description

About Abb Vie

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube.

Job Description

The Scientist II - Biocompatibility is a SME which will provide highly skilled support for biocompatibility and non‑clinical safety evaluations of medical devices, tissue products, and combination products as an part of Abb Vie Research & Development. The position will be responsible for supporting cross‑functional and cross‑site collaborations involving recommendations for biocompatibility activities with limited supervision. This individual must possess a working knowledge of ISO‑10993 and other applicable standards.

The position will be responsible for supporting cross‑functional and cross‑site teams and recommendations of biocompatibility activities. This includes establishing requirements, planning, execution, and approval of biocompatibility requirements in support of regulatory submissions, project teams, operations, with a large focus on marketed product support.

Main Responsibilities
  • Function as a representative for ISO‑10993 (biocompatibility) assessments, with minimal supervision from Biocompatibility senior team members and therapeutic area SMEs. This will include the design, execution, and interpretation of biocompatibility evaluation strategies and programs per the applicable regulatory requirements, including biological risk assessments, technical documentation, and other documents for internal and external distribution and regulatory submissions.
  • Responsible for supporting Project Plans for biocompatibility with realistic deliverables with timelines. Actively involved in the planning, execution and management of experimental studies for the safety and efficacy characterization of new and existing products.
  • Serve as dedicated biocompatibility resource for product development teams, working closely with other colleagues in Development Science. Provide skilled technical knowledge to support cross‑functional project initiatives.
  • Maintain knowledge of medical device regulations to assure compliance and conformance of programs for evaluation of medical devices and other products, including performing gap analysis relevant to changes in biocompatibility standards or guidance, inclusive of updating of internal product files for component/process changes.
  • Prepare and deliver technical presentations to internal and external stakeholders with minimal supervision. Assist the team in functional training initiatives.
  • Support global change control activities as they relate to Biocompatibility.
  • Build and maintain strong connections and relationships with Contract Research Organizations, Toxicologists and Consultants for Biological Risk Assessments as needed.
Qualifications
  • Bachelor’s Degree in Life Science/Biomedical Engineering or related field with minimum 7 years of experience in a scientific role in the medical device or pharma industry or Master’s degree in Life Science/Biomedical Engineering or related field with at least 5 years of experience.
  • Medical device, pharmaceutical or related experience or experience in a regulated environment with a proven record of success supporting patient safety studies for R&D projects is preferred.
  • Experience and working knowledge of medical device and combination product regulations.
  • Strong knowledge of ISO‑10993 Standards, FDA Guidance and Regulations, and Animal Welfare Regulations.
  • Working knowledge of ISO‑10993 Standards, FDA Guidance and Regulations, and Animal Welfare Regulations.
  • Strong technical writing and verbal communication skills.
  • Self‑motivated; ability to execute with minimal supervision and direction. Can work independently or part of a team. Understands sense of urgency with relation to priority projects.
  • Ability to…
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