# Manufacturing Process Specialist at Johnson & Johnson

Johnson & Johnson is hiring a Manufacturing Process Specialist in Cork, Ireland. It pays €43k-€69k a year and Level rates it Little AI ●○○○; you can [apply on Johnson & Johnson](https://jobsbylevel.com/go/1c98e002-d1ce-4c93-ab89-ebc166ba62fd?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Ringaskiddy, Cork, Ireland.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Ringaskiddy, Cork, Ireland
- Salary: €43k-€69k
- Posted: November 4, 2026
- Apply: https://jobsbylevel.com/go/1c98e002-d1ce-4c93-ab89-ebc166ba62fd?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=manufacturing-process-specialist-at-johnson-johnson-c159c4

## Prepare for this job

The job page lists 5 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/manufacturing-process-specialist-at-johnson-johnson-c159c4

## 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 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: Supply Chain Manufacturing Job Sub Function: Manufacturing Deployment 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 talents for the Manufacturing Process Specialist roles 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. As a Manufacturing Process Specialist, you will: General Activities Represent 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 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. 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 with Manufacturing and general site procedures at all times. Completion of all documentation in compliance with site procedures and GDP. Execution of activities as necessary to meet operational and business needs. Lead, support and participate in commissioning and qualification activities both current and future projects (and annual re-qualification activities). Also support to validation activities. Prioritize and schedule activities to support business needs and to meet requirements of Master Production Schedule. Lead and Support investigation and resolution of problems on plant. Participate in and lead Cross-Functional teams as necessary. Generate and assist with generation, review, and revision of Manufacturing documentation as necessary. Ensure that personal training requirements are completed in

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