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Cleanroom manufacturing technician

Fermoy
Occupop
Manufacturing technician
Posted: 23h ago
Offer description

Job information
Fermoy, County Cork, Ireland
Company: Bitrecruit
Client / Employer: Occupop
Job reference: d7c6df7586b6ecec243b9601d3583e5d
Listing type: Basic
EU work permit required: No
Posted: 20.05.2026
Role Overview
The Technician supports the operation of a biomanufacturing facility by performing routine and specialised production tasks to manufacture products in compliance with Good Manufacturing Practices (GMP) and safety regulations. This role involves operating and maintaining production equipment, monitoring process parameters, recording data, and performing in‑process quality checks to ensure consistent product quality and batch integrity.
Shifts

Day Shift – Monday to Friday 06:00–14:30
Evening Shift – Monday to Friday 14:00–22:30
Night Shift – Monday night to Saturday morning 22:00–06:30

Level of Responsibility

Operates within clearly defined SOPs and work instructions under close to moderate supervision.
Responsible for product quality during assigned production stages.
Reports deviations, defects, or equipment issues immediately.
Might assist with training of new operators.

Responsibilities

Perform routine and specialised production tasks.
Operate and maintain production equipment.
Monitor process parameters.
Record data accurately.
Conduct in‑process quality checks.
Ensure compliance with GMP and safety regulations.
Document and report process deviations.

Qualifications

Experience in GMP or regulated manufacturing (preferred). Background in ISO or GMP environments also advantageous.
Basic mechanical aptitude and familiarity with manufacturing environments.
Strong attention to detail and product safety awareness.
Postsecondary technical training preferred.
Leaving Certificate or equivalent required.
GMP training certification advantageous.
0–2 years of experience in manufacturing, packaging, or assembly.
Prior cleanroom or sterile assembly experience beneficial.

Knowledge, Skills & Abilities

Knowledge of GMP, GDP (Good Documentation Practices), and basic regulatory requirements.
Familiarity with cleanroom classifications, gowning, and contamination control principles.
Understanding of standard manufacturing and assembly processes in a regulated environment.

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