2026 Graduate Manufacturing Process Specialist at Johnson Johnson
Cork, County Cork, Ireland -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

0.0

Posted On

05 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Process Engineering, Cell Culture, Delta V, Equipment Installation

Industry

Mechanical or Industrial Engineering

Description

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 DESCRIPTION:

ROLE TITLE: Graduate Manufacturing Process Specialist
START DATE: September 2026
LOCATION: Cork, Ireland

POSITION SUMMARY:

Reporting to Operations Manager, this position is responsible for representing operations on capital project teams and supporting first line troubleshooting of the day-to-day activities within Operations - These activities include but are not confined to:

Responsibilities
  • 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.
  • Participate in/ Lead Cross Functional teams when required.
  • Support of Commissioning and Qualification activities.
  • Preparation and updating of Batch Records, Procedures and Work Instructions.
  • Provide 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.
  • Completion of all documentation in compliance with site procedures and GDP.
  • Lead, support and participate in commissioning and qualification activities both current and future projects (and annual re-qualification activities.
  • Prioritize and schedule activities to support business needs and to meet requirements of Master Production Schedule.
  • Support ongoing studies by Validation, OTS and other support functions.
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