QC FG Lab Technician I

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

Job Function:
Quality

Job Sub Function:
Quality Control

Job Category:
Business Enablement/Support

All Job Posting Locations:
San Angelo, Texas, 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

An internal pre-identified candidate for consideration has been identified.

However, all applications will be considered.

 

We are searching for the best talent for QC FG Lab Technician I to be in San Angelo, TX.

Job Summary

Responsible for inspecting Batch Records and Final Release of materials to ensure quality standards are met and following prescribed steps to document issues and follow-up on corrective actions.

Responsible for inspecting Batch Records and Final Release of materials to ensure quality standards are met and following prescribed steps to document issues and follow-up on corrective actions.

Duties & Responsibilities

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:


* Assures optimum control of quality so that raw material and/or finished products conform to existing requirements, standard operation procedures, and governmental regulations and adheres to all Quality Systems Requirements (QSR) and ISO standards.


* Performs raw material, in-process, Sterilization Run Record and/or finished goods reviews.


* Meets functional area goals and yearly strategic imperative project timelines.


* Cross-trains to support other functional review areas.


* Utilizes Standards of Leadership and the Credo.


* Performs other work-related duties assigned by Supervisor.


* Follows current compliance regulations and standards and all federal regulated programs.


* Ensures safe working conditions and practices in the department.


* Complies with all applicable quality management system, environmental, safety and occupational health policies.

(for example, ISO 13485, ISO14001 & OSHAS18001),


* Responsible for communicating business related issues or opportunities to next management level


* Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulat...