QC Microbiologist Analyst

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 jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Quality

Job Sub Function:
Quality Control

Job Category:
Professional

All Job Posting Locations:
Gurabo, Puerto Rico, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness.

Learn more at https://www.jnj.com/medtech

Johnson & Johnson is currently recruiting for multiple QC Microbiologist Analyst positions (4 openings).

These positions will be located in Gurabo, Puerto Rico.

Purpose:

Reporting to the Quality Control leadership team, the QC Microbiologist Analyst is responsible for supporting microbiological testing activities within the Biosynthetic and Parenteral manufacturing operations.

This role provides microbiological oversight and technical support to ensure compliance with GMP requirements, regulatory standards, and company quality systems.

The analyst performs routine and non-routine microbiological testing, supports investigations, validations, environmental monitoring programs, and contributes to the timely release of high-quality products while maintaining compliance with all applicable procedures and regulations.

You will be responsible for:



* Monitor activities of the Biosynthetic facility during third shift operations, included but not limited to: viable, surface and non-viable air sampling, water and compressed gases monitoring and testing.


* Provide support to the microbiological aspects of the manufacture, validations and projects related to the parenteral area.


* Conduct Laboratory tests in support of parenteral production such as Bacterial Endotoxin Tests (finished product, raw materials, WFI and Clean Steam), Bioburden and in process product tests, Sterility tests, Biological Indicators (BIs) testing, Environmental Monitoring of aseptic manufacturing areas, isolates identification (IDs).


* Support equipment qualification activities and new technology introduction.


* Provide technical knowledge to make decisions related to product quality from t...