Senior Technician, Product Development Testing - Entry Level - Johnson and Johnson

Ethicon, a member of Johnson & Johnson's family of companies, is recruiting for an Senior Technician, Product Development Testing located in Raritan, NJ.

At Johnson & Johnson MedTech, we're changing the trajectory of health for humanity, using robotics to enhance healthcare providers' abilities and improve patients' diagnoses, treatments, and recovery times. Johnson & Johnson Robotics was established in 2020 with the integration of Auris Health, Verb Surgical, C-SATS, and Ethicon. It comprises three key med-tech platforms: Flexible Robotics (MONARCH™), Surgical Robotics (OTTAVA™), and Digital Solutions. Join our collaborative, rapidly growing teams in the San Francisco Bay Area (Redwood City and Santa Clara), Cincinnati, and Seattle. You'll collaborate on breakthrough medical technologies that unite multiple subject areas to build a connected digital ecosystem that advances medical professionals' skills and improves patient outcomes.
Job Summary

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

Key Responsibilities:

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

• Executes day-to-day laboratory activities for the Stability laboratory, ensuring GMP compliance and accuracy and timeliness of specified stability processes.
• 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.
• Execute efficient and effective functioning of the stability laboratory.
• Complete and submit laboratory testing and/or data analysis per protocol or procedure requirements into LIMS.
• Verifies calibrations and preventive maintenance of laboratory equipment is complete before use.
• Maintain organized, legible laboratory notebook.
• Perform proper labeling of samples and equipment per procedure.
• Execute the receipt, storage and chamber pulls for Stability samples.
• Respond to temperature and humidity control of stability chambers and take appropriate action per direction.
• Document chamber maintenance, repairs and excursions in logbooks per direction.
• Maintain accurate inventory and chain of custody records for all products.
• Provide samples to the laboratories on a scheduled and as-needed basis per procedure.
• Perform database management, data quality assurance, and data set creation using internal data sources.
• Execute computer system validation (CSV.)
• Ability to execute database queries.
• Maintain individual training completion in a compliant state.
• 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
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• 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 of (2) years of experience work experience in a lab

Required Skills & Experience:

• Work in a team-oriented environment that embraces change, risk, and flexibility.
• Excellent verbal and written communication skills.
• Good interpersonal relationship and people skills.
• Ability to follow management guidance/direction.
• Prior experience working with current Good Manufacturing Practices (cGMP) related to the QC laboratory.
• Ability to support multiple priorities daily.
• Ability to read and execute documents such as SOPs, work instructions, test methods and protocols.
• Experienced with Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
• Experienced in document management systems (PLMs)
• Experienced in environmental monitoring systems (preferably EMS and Amegaview.)
• Experienced in database administration of LIMS (preferably LabWare.)

Preferred Skills & Experience:

• Prior experience in stability laboratories
• Prior experience with LIMS (preferably LabWare.)

Other:

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

The anticipated base pay range for this position is ($50,500) to ($60,000)

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

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.

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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