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Scientist – Bioscience Process and Validation – Biodevices

Scientist – Bioscience Process and Validation – Biodevices

CompanyZoetis
LocationDurham, NC, USA
Salary$Not Provided – $Not Provided
TypeFull-Time
DegreesBachelor’s, Master’s
Experience LevelSenior

Requirements

  • BS or MS in a relevant scientific field, or equivalent training/experience
  • Minimum of 5 years in animal research or relevant laboratory science
  • Practical and relevant laboratory experience
  • Demonstrated hands-on interactions integrating mechanical devices and biological processes

Responsibilities

  • Lead product development initiatives for innovative biodevice offerings, ensuring a thorough understanding of biological impacts and device safety.
  • Collaborate with engineering, Technical Service, and Field Service teams to refine design requirements, specifications, and product testing.
  • Design, develop, execute, and analyze experiments and testing protocols for product characterization and validation, applying bioscience development and statistical analysis methodologies.
  • Conduct evaluations both in-house and at customer test sites, including field-testing and assay execution, while overseeing trial-related activities such as onsite visits, data collection, and reporting, ensuring meticulous and compliant records of experimental data.
  • Communicate effectively with internal teams, trial sites, sponsors, and external collaborators to foster collaboration and ensure project success.
  • Adapt to both fast-paced and slower-paced environments, demonstrating enthusiasm, initiative, and self-motivation as needed.
  • Work efficiently in both independent and team settings, fostering collaboration and shared success.
  • Train and mentor junior staff on research activities and protocols, fostering professional growth within the team.
  • Collaborate with study team members to support project execution and ensure alignment with objectives.
  • Uphold the team values of respect, integrity, and open communication, creating an environment where all members feel valued and empowered to contribute.

Preferred Qualifications

  • Medical device development exposure is a plus.
  • Experience with GLP/GCP compliance is a plus.