Preclinical Operations Supervisor
6267-Auris Health Inc. Legal Entity
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Benefits offered by this job
Job summary
Johnson & Johnson in Cincinnati, OH, seeks a Preclinical/Laboratory Operations Supervisor for the RAD division, onsite. You will oversee preclinical operations and manage surgical lab studies, supplies, and regulatory compliance.
The role requires a Bachelor’s degree, 3+ years in preclinical or related fields, strong leadership, and excellent communication. You will collaborate with R&D, Regulatory Affairs, and Quality Assurance to ensure high standards.
Qualifications
- Bachelor’s degree required with 3+ years in preclinical, medical, or clinical research.
- Strong knowledge of GLP requirements and IACUC regulations.
- Excellent written and oral communication with attention to detail.
Responsibilities
- Oversee RAD Preclinical Operations activities in Cincinnati on-site.
- Organize and support surgical laboratory studies and supplies management.
- Maintain regulatory compliance and oversee lab SOP updates quarterly.
- Provide direction to lab staff and coordinate vendor relationships.
- Ensure lab documentation and safety practices meet standards.
Skills
Education
Tools
Job description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
R&D Operations
Laboratory Operations
People Leader
Cincinnati, Ohio, United States of America
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of MedTech surgery? Ready to join a team that’s reimagining how we heal? Our MedTech Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. Learn more at https://jnjmedtech.com
Robotics & Digital Solutions division (RAD) is searching for the best talent for a Preclinical/Laboratory Operations Supervisor role located in Cincinnati, OH. This is a fully on-site position.
- Overall supervision and coordination of RAD Preclinical Operations activities in Cincinnati
- Organizing, managing, and supporting various surgical laboratory research studies and research activities
- Management of surgical laboratory supplies, tools, robotic instruments, inventory and distribution in compliance with regulatory requirements and organizational procedures
- Provide oversight and direction to lab operations staff, including planning team meetings
- Management of vendor accounts and fostering relationships for ongoing surgical laboratory needs
- Management of cadaveric tissue and biohazardous waste
- Promoting environmental health and safety compliance in our labs per company policies
- Manage review and revision of relevant lab SOPs on a quarterly basis or as necessary
- Ensure lab maintenance and instrumentation cleanliness/sterility in compliance with regulatory requirements and organizational procedures
- Ensure proper documentation and record keeping in compliance with regulatory requirements and organizational procedures
- Support developing, reviewing, and finalizing a wide range of scientific and regulatory documents including, but not limited to, scientific protocols and reports, post-operative evaluations, Quality audit edits and responses, responses to regulatory agencies, and IACUC documents.
- Perform literature searches to support research activities, IACUC documentation, and publications.
- Ensure all documentation complies with current regulatory standards, industry guidelines, and internal SOPs.
- Support change management activities.
- Foster strong, collaborative relationships with cross-functional teams including R&D, Regulatory Affairs, and Quality Assurance.
- Bachelor’s degree in a related domain
- Minimum of 3 years of relevant scientific experience, with a strong background in preclinical, medical, and/or clinical research or related fields
- Knowledge of GLP requirements
- Excellent oral and written communication skills with a keen eye for detail.
- Strong leadership and project management skills, including influencing, negotiating, and problem-solving.
- Demonstrated learning agility and ability to adapt to evolving technologies and regulatory landscapes.
- Experience with IACUC regulations, scientific experimental design, and protocol development
- Familiarity with 510(k) documentation and submission processes
- Copy editing, proofreading, and data synthesis skills
- Understanding of SOPs, research ethics, and quality standards
- Understanding of human/animal anatomy and surgical methods is desired
- Proficiency with Microsoft 365 applications, including Word, Excel, PowerPoint, and Copilot is required
- Ability to work independently and as part of a project team
- Proven organizational and time management skills are essential
- Analytical Reasoning
- Data Management and Informatics
- Developing Others
- Epidemiology
- Ethical and Participant Safety Considerations
- Inclusive Leadership
- Laboratory Operations
- Laboratory Safety
- Leadership
- Mental Agility
- Molecular Diagnostics
- Motivating People
- Process Improvements
- Quality Assurance (QA)
- Regulatory Compliance
- Research and Development
- Team Management
- Toxicology
The anticipated base pay range for this position is : $109,000.00 - $174,800.00
- 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
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource. If you are under 18 years of age you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.
Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
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