Product Release Specialist II
Johnson & Johnson is currently seeking a Product Release Specialist II to join our Deliver Team in Jacksonville, FL.
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 create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve 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.
Our Product Release Specialists will be responsible for release of batch records from Quality Operations through review of electronic and/or manual device history to ensure quality standards are met. They will follow prescribed steps to document issues and follow-up corrective actions as needed. Document batch release process and mentors less experienced staff on implementation. Makes recommendations and provides support to corrective actions. Administers requests for rework and destruction of materials. Adheres to environmental policy and procedures and supports department environmental objectives.
Duties and Responsibilities:
- Review electronic and manual records pertinent to device history and sterilization. Investigates and resolves discrepancies (80%)
- Participates in training and development of Product Release staff (5%)
- Responsible for manual DHR documents to be filed for storage per procedure (10%)
- Participates in the development and implementation of new systems directly and indirectly impacting Product Release (5%)
