Senior Process Specialist

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:
Supply Chain Engineering

Job Sub Function:
Process Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Athens, Georgia, United States of America

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Senior Process Specialist to be in Athens, GA!

The Sr.

Process Specialist is responsible for providing technical support for the Active Pharmaceutical Ingredient and Monomer manufacturing processes.

Technical support includes safety, quality, efficiency improvements and issue resolution to ensure products are manufactured compliantly and efficiently.

They also support capital projects, site wide initiatives, or other projects as needed as a project lead or subject matter authority.

Key Responsibilities:


* Drive day-to-day manufacturing technical implementation focusing on safety, quality (manufacturability) and product cost.


* Implement processes and methodologies that support the sharing of standard processes.


* Own process improvements related to safety, environmental, quality, compliance, productivity, yield, and cost.


* Lead multi-functional teams in the identification and performance of cost and process improvements.


* Investigate complex technical problems and provide solutions for process improvement and cost reduction.


* Own corrective/preventative measures to improve compliance and reduce repeat occurrences.


* Serve as Subject Matter Authority during internal and external regulatory audits (including FDA, EMEA, DEA).


* Provide documentation support for SOP/ Batch Record revisions.

Qualifications:

Education:


* Minimum of High School Diploma/GED plus two years formal technical education/training or equivalent is required.

Bachelor’s Degree in science preferred

Required:


* Minimum six (6) years of professional experience


* Experience within Chemical, Pharmaceutical, Medical Device, or similarly regulated manufacturing industry


* Ability to lead and coordinate multi...