Ethicon Inc., a member of Johnson & Johnson Family of Companies, is recruiting for a Senior Scientist to join our world-class team, located in Cornelia, GA!
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/ .
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to build a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to tackle the world's most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities, and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
The Senior Scientist will report directly to the Laboratory Supervisor or Laboratory Manager and will perform sophisticated testing in compliance with laboratory test methods and procedures to support the manufacturing and timely delivery of product to customers (75 to 100%).
Work will be well defined and will be reviewed for accuracy upon completion.
The role requires application of standard practices and techniques in specific situations and to recognize discrepancies in results and follow operations through a series of detailed steps and processes and be able to serve as an expert in technical areas.
Key Responsibilities: Operating in accordance with current GMPs, including the ability to understand and apply SOPs and use GMPs for documenting, testing, and maintaining accurate laboratory records.
Performing daily calibrations/verifications and routine maintenance of laboratory instrumentation and equipment according to current SOPs.
Supporting the Lifecycle Management Process for Instrument and the Software.
Following all job-specific safety procedures as well as quality system requirements as defined within procedures and instructions.
Performing data reviews and investigations supporting qualification pertaining to product development, validation, and test methods.
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