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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 https://www.jnj.com

Job Function:

R&D Operations

Job Sub** **Function:

Laboratory Operations

Job Category:

Business Enablement/Support

All Job Posting Locations:

Raritan, New Jersey, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent to join our Stability and Inventory Team as a Technician 4, R&D Engineering, Inventory, located in Raritan, NJ.

Purpose: Provide laboratory support and expertise to the stability laboratories ensuring GMP compliance and accuracy and timeliness of specified stability processes.

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

+ Provides supervision in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

+ Supervise and execute day-to-day laboratory activities for the Stability laboratory, ensuring GMP compliance and accuracy and timeliness of specified stability processes.

+ Oversees duties in compliance with all local, state, federal and international regulations and guidelines (including FDA, EPA, OSHA, DEA, etc.) as well as all company and site policies and procedures.

+ Responsible for the efficient and effective functioning of the stability laboratory.

+ Ensure all laboratory commitments are met.

+ Complete and submit laboratory testing and/or data analysis per protocol or procedure requirements into LIMS.

+ Assures calibrations and preventive maintenance of laboratory equipment is completed in a timely manner per procedure.

+ Responsible for maintaining organized, legible laboratory notebook.

+ Responsible for proper labeling of samples and equipment per procedure.

+ Supervise and coordinate the receipt, storage and chamber pulls for Stability samples per procedure.

+ Supervise and respond to temperature and humidity control of stability chambers and take appropriate action per procedure.

+ Supervise and document chamber maintenance, repairs and excursions in logbooks per procedure.

+ Review and ensure accurate inventory and chain of custody records for all products are maintained.

+ Oversees provision of samples to the laboratories on a scheduled and as-needed basis per procedure.

+ Maintain individual and ensure team training completion in a compliant state.

+ Identify efforts for continuous improvements.

+ Maintain a clean and safe work environment in compliance with all applicable environmental, health, and safety regulations.

+ Uphold our Credo values including creating a positive work environment.

+ Responsible for communicating business related issues or opportunities to next management level

+ For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.

+ Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.

+ Performs other duties assigned as needed.

Education and Required Experience:

+ Bachelor’s Degree or a minimum of (6) years of related work experience in a laboratory environment.

+ Work in a team-oriented environment that embraces change, risk, and flexibility.

+ Excellent verbal and written communication skills.

+ Willing to solve problems using analytical technologies.

+ Good interpersonal relationship and people skills.

+ Creativity regarding basic problem solving and troubleshooting in laboratory tasks.

+ Possess the capability to develop improvement ideas and independently implement associated solutions.

+ Ability to function with limited management guidance/direction.

+ Prior experience in stability program management.

+ Prior experience in an analytical or chemical laboratory setting.

+ Detailed knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify/remediate gaps in processes or systems.

+ Ability to manage multiple priorities daily while being flexible and responsive to frequently shifting priorities.

+ Ability to read and interpret documents such as SOPs, work instructions, test methods and protocols.

+ Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) and LIMS (preferably LabWare.)

+ Proficient in document management systems (preferably ADAPTIV.)

+ Proficient in environmental monitoring systems (preferably EMS and Amegaview.)

Other:

+ This position is based in Raritan, NJ and requires up to 10% (International/Domestic) travel.

The anticipated base pay range for this position is [$70,500] to [$109,000]

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.

Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, pension plan, disability plan, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans. Additional information can be found through the link below.

Eligible for benefits to include medical, dental, vision and time off as well as any others as provided for in the applicable Collective Bargaining Agreement.

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

\#LI-BD1

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_**