Johnson & Johnson

Preclinical Operations Supervisor

Johnson & Johnson$109K — $174K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a related domain
  • Minimum of 3 years of relevant scientific experience in preclinical, medical, or clinical research
  • Knowledge of GLP requirements
  • Strong leadership and project management skills
  • Excellent oral and written communication skills with attention to detail
  • Experience with IACUC regulations and protocol development
  • Familiarity with 510(k) documentation and processes

Responsibilities

  • Supervise and coordinate RAD Preclinical Operations activities
  • Organize and manage surgical laboratory research studies
  • Manage surgical laboratory supplies, tools, and inventory
  • Oversee lab operations staff and plan team meetings
  • Manage relationships with vendors for lab needs
  • Ensure compliance with environmental health and safety regulations
  • Document and maintain records according to regulatory requirements

Benefits

  • Participation in the Company's retirement plan and 401(k)
  • Long-term incentive program eligibility
  • Vacation time of 120 hours per year
  • Sick time, varying based on location
  • 13 holidays per calendar year including floating holidays
  • Parental leave of 480 hours
  • Caregiver leave and bereavement leave available
  • Volunteer leave of 32 hours per year
Full Job Description
Job Function:
R&D Operations

Job Sub Function:
Laboratory Operations

Job Category:
People Leader

All Job Posting Locations:
Cincinnati, Ohio, United States of America

Job Description:

About Surgery

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

Johnson and Johnson's 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.

Purpose:

Robotics & Digital Solutions is part of J&J MedTech, a global leader in surgery with products and solutions found in almost every operating room around the world. J&J MedTech has made significant contributions to surgery for more than 100 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through J&J MedTech's surgical technologies and solutions including robotics, digital solutions, sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact.

This is a hands-on role within the Preclinical team and represents an outstanding opportunity to work cross functionally with various groups that utilize the Preclinical Labs. Supervision, assistance, and support in this space will be essential to the development of J&Js highly innovative Ottava robotic and digital surgery platform. This position will also support the development of technical documents for Preclinical studies that inform J&Js regulatory submissions and evidence-generation strategies.

You will be responsible for:

Key Operations
  • 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 SOP's 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


Key Technical Writing Skills
  • 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.


Qualifications / Requirements:

Required:
  • Bachelor's degree in a 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


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.

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off 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 period10 days
  • Volunteer Leave - 32 hours per calendar year
  • Military Spouse Time-Off - 80 hours per calendar year


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.

#LI-Onsite

Required Skills:

Preferred Skills:
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

Additional Description for Pay Transparency:

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Our team at Johnson & Johnson thrives on collaboration and diversity. You will work alongside over 130,000 employees globally who are committed to making a lasting impact. With a culture that values diversity training and leadership, you are supported in both personal and professional growth.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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