Preclinical Research Technologist
About The Position
The Preclinical Research Technologist supports preclinical research activities for medical device development, including product evaluations in animate, inanimate, and cadaveric models. Working under significant guidance and supervision, this role contributes to study execution, laboratory documentation, study logistics, and compliance with Good Laboratory Practices, animal welfare regulations, and internal policies. The position partners with cross-functional teams to help generate high-quality preclinical evidence that supports research, regulatory, and commercial objectives.
Requirements
- Bachelors degree preferred but not required
- Familiarity with FDA 21 CFR part 58 (GLPs)
- A minimum of 2 years of related technical experience within preclinical research or research/laboratory environment is required.
- Familiarity with preclinical processes along with a basic understanding of medical device development processes and preclinical regulations is required.
- Understanding of good documentation practices
- Familiarity with animal welfare regulations and IACUC
Nice To Haves
- Experience working in a GLP environment is preferred
Responsibilities
- Supports and assists in product evaluations involving animate, inanimate, and cadaveric models
- Supports research and development of products or procedures in minimally invasive robotic surgery
- Assisting in the investigations for medical device development and preclinical evidence generation aligned to R&D, Regulatory, and Commercial needs
- Ensure accurate documentation of laboratory data and activities under the direction of the Study Director or Study Coordinator
- Assists in study logistics; e.g. pick-lists, instrument and supply requests, device transfers, study binder creation
- Helps to ensure that the conduct of lab activities are in compliance with USDA, AAALAC, and J&J Animal use policies
- Helps ensure compliance with 21 CFR Part 58 – Good Laboratory Practices.
- Supports the generation/revision of SOPs, study documentation, and data collection documents for non-GLP and GLP study protocols.
- Supports preclinical animal studies for the assessment of safety, performance, and effectiveness.
- Demonstrate the ability to work effectively in a team-oriented environment that embraces ownership and accountability for innovation, change, risk, and flexibility.
- Build successful relationships internally and develop partnerships with key business partners.
Benefits
- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
