Job Description

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science -- bringing creative ideas, products and services to advance the health and well-being of people. Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to profoundly change the trajectory of health for humanity.

At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale and experience to reimagine the way healthcare is delivered and help people live longer, healthier lives.
In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, vision and interventional solutions with the big ideas of others to design and deliver physician and patient-centric products and solutions.
As pioneers in medical devices, we continually focus on elevating the standard of care-working to expand patient access, improve outcomes, reduce health system costs and drive value. We create smart, people-centered healthcare to help the patients we serve recover faster and live longer and more vibrantly.

Ethicon , part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 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 Ethicon\'s surgical technologies and solutions including 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. For more information, visit www.ethicon.com .

Overall Responsibilities

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

Key Responsibilities:

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

• Carries out 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.
• Ensure all laboratory commitments are met.
• Ability to create and manage Change Orders.
• Assist with stability reports.
• Execute computer system validation (CSV.)
• Ability to run database queries.
• Maintain individual training completion in a compliant state.
• Support continuous efforts for improvements and suggest ideas for process 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:

• High school diploma with a minimum (6) years of related work experience in a laboratory environment.

Required Skills & Experience:

• 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.)
• Proficient in statistical analysis software (preferably Minitab.)
• Proficient in database administration of LIMS (preferably LabWare.)

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 ($54,500) to ($87,500).

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

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

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