QC Scientist (3rd shift)

Johnson & Johnson is currently seeking a QC Scientist (3 rd shift) to join Janssen Ortho LLC organization located in Gurabo, PR.

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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.

The QC Scientist is responsible for performing and reviewing all chemical and physical testing of raw materials, bulk, finished, combination products and utilities (i.e.

water, etc.) according with internal and compendia specifications.

Performs and participate on investigations when questionable analytical results have been generated.

Operates and maintains laboratory instrumentation following the established methods and procedures.

Prepares testing solutions and samples according to written instructions.

Documents accurately all raw data in a legible manner at time of execution, following the Good Documentation Practices.

Maintains complete and accurate records.

Takes training of methods and procedures prior to execution.

Performs any special task assigned by QC Management in support of Order Release Department.

Assures the compliance to all quality control policies, procedures and systems to ensure the timely release of high quality product in support the supply chain process.

Key Responsibilities:


* Performs all laboratory analysis and activities in accordance with cGMP's practices, internal and external regulations and policies, and consistent with supply chain cycle time goals.

Responsible for following laboratory priority report and in-process boards to support manufacturing rhythm wheels and business rules.

Complies with all Laboratory Schedules for raw materials, drug product and/or combination product testing and special projects.

Assures to follow QC initiatives and requirements.


* Verifies (Peer Reviewer) documen...