Manufacturing 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 Manufacturing

Job Sub Function:
Manufacturing Process Improvement

Job Category:
Professional

All Job Posting Locations:
Ringaskiddy, Cork, Ireland

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 the Manufacturing Process Specialist role to be in Cork, Ireland.

Purpose:

The manufacturing process specialist will be responsible for representing operations on capital project teams and supporting first line troubleshooting of the day-to-day activities within operations.

You will be responsible for:


* Representing Operations on cross functional project implementation teams.


* Monitoring and troubleshooting of the manufacturing process and equipment issues and process optimization



* Monitoring and reporting of process performance using statistical process control


* Troubleshooting of DCS (e.g Delta V) and PLC control systems


* Investigating and resolving issues raised within the Manufacturing Department


* Participateing in/ Leading Cross Functional teams when required.


* Supporting of Commissioning and Qualification activities


* Preparation and updating of Batch Records, Procedures and Work Instructions


* Providing process and equipment related training as required within the Manufacturing Department


* Completion of assigned tasks to support manufacture of quality biomedicines in accordance with cGMP and EHS requirements.

General Scope of Responsibilities:



* Lead by example and strive to perform to high standards at all times.


* Responsible and accountable for assuring the safe accomplishment of job activities, following good environmental practices and procedures.  Commit to and demonstrate safe behavior in every activity.


* Carry out routine and non-routine tasks delegated by the Operations Manager according to appropriate procedures, values, and standards.


* Carry out all activities in compliance with corporate and cGMP/EHS regulatory requirements.


* Compliance ...