Compound Logistics Scientist Full-time

Compound Logistics Scientist

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.

We are searching for the best talent for a Compound Logistics Scientist to be in La Jolla, CA.

Purpose: We are seeking a Compound Logistics and Sample Management Scientist within the Discovery Technologies and Molecular Pharmacology group.

The Compound Logistics Scientist will coordinate the inventory of research compounds and day-to-day sample management workflows to support global research initiatives. They will drive innovation by assisting team members and contributing to sample management process improvements and novel automated and manual workflows. The successful candidate demonstrates a quality-focused mindset, critical thinking, and adaptability, maintaining a dedication to professional growth within the evolving field of sample management, compound logistics, and laboratory automation.

You will be responsible for:

• Assist with coordinating and providing day-to-day operational support for Sample Logistics and Inventory Management, including registering, weighing, storing, maintaining inventory, and shipping research compounds (internal and external).
• Operate integrated, off-the-shelf automated liquid handling and sample management instruments to fulfill Compound Logistics orders.
• Ensure instruments meet quality control specifications and are properly maintained and documented.
• Manage inventory and stock lists for device and sample management consumables, ensuring availability and identifying alternatives as needed.
• Support the Controlled Substance Program Manager with compliance and audit-readiness activities to meet DEA requirements.
• Maintain accurate, compliant documentation and records in accordance with regulatory requirements and standard operating procedures.
• Support workflow analyses; troubleshoot routine automation workstation and integration issues; and provide technical input through written reports and oral presentations.
• Manage multiple initiatives concurrently and meet tight timelines.
• Partner with assay automation, assay development, and cell culture teams to identify and implement lean process improvements that enhance quality, scalability, and efficiency across sample management operations.
• Stay current on emerging trends, technologies, and best practices in laboratory automation through continuous learning and professional development.

Qualifications / Requirements:

• Minimum of a Bachelor's degree in STEM, Life Sciences, or equivalent is required.
• Minimum 1 year of industry experience in compound logistics, sample management, integrated laboratory automation, or a related field.
• Hands-on experience assisting with automated compound logistics workflows using integrated, off-the-shelf devices and task/workflow scheduling software.
• Ability to work effectively in a cross-functional environment and collaborate with multidisciplinary teams.
• Strong analytical and problem-solving skills, including the ability to analyze small data sets, troubleshoot issues, and propose solutions.
• Excellent written and verbal communication skills, with the ability to present sample management concepts and findings to diverse audiences.
• Highly organized and detail-oriented, with the ability to manage documentation and inventory and follow standard operating procedures.
• Demonstrated growth mindset and commitment to continuous learning; stays current on emerging trends and technologies in sample management, compound logistics, and laboratory automation.

Preferred:

• Hands-on experience with robotic liquid handlers (e.g., Tecan, Hamilton, Beckman, Agilent, or equivalent) and/or integration/scheduling software (e.g., HighRes Biosolutions Cellario, Thermo Scientific Momentum, or equivalent).
• Developing knowledge of laboratory automation and compound processing/tracking, including experience with Laboratory Information Management Systems (LIMS) and/or Laboratory Execution Systems (LES).
• Experience with, or participation in, a Controlled Substances Management program or similar regulatory licensing program (e.g., DSCSA, RDRC, NRC/FDA).

The anticipated base pay range for this position in the US is $76,000 to $121,900 per year.

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis.

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short and long-term disability, business accident insurance, and group legal insurance. 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)).

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 period 10 days
• Volunteer Leave – 32 hours per calendar year
• Military Spouse Time-Off – 80 hours per calendar year

For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefits

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, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.