Manager LCM

Johnson & Johnson is currently seeking a Manager LCM to join our Medical Device Business Services, Inc.

located in West Chester, PA.

There is an internal pre-identified candidate for consideration.

However, all applications will still be reviewed.

Remote work options may be considered on a case-by-case basis and if approved by the Company.

About Johnson & Johnson

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.

Job Summary

Manages the operational function in medical affairs to achieve organizational objectives.

Provides life cycle management of the marketed product.

This role will provide expertise in support of the Medical Strategy in concert with Operating Entity Medical Leaders.

Provides Strategic Medical support for cross-platform Orthopaedics.

Duties & Responsibilities


* Provide consultation in analysis, review, and conclusions for Clinical Evaluation Reports (CER) and related documents (i.e.: SOA; CEP; Literature Review, SSCP, PMCF).


* Provide Lifecycle Management for marketed products including labelling updates, medical support and accountability for technical files and documents and medical support to Quality groups.


* Collaborate closely with the Medical Directors in support of business responsibilities.


* Research, prepare and document responses to Medical Information Requests from Healthcare providers.


* Review and approve medical content in Copy Approval process; consults with Medical Director when needed.


* Provide medical oversight of publication strategy for selected marketed products in close collaboration with the Medical Affairs team.


* Prepare and/or manage preparation of presentations and manuscripts around clinical data as well as medical and sc...