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Vacancy Details

Engineering & Technical

Manufacturing Technician I – Mayo - Unknown - 104628

Contract Type: Permanent
Location: Unknown
Date: 17/06/2019
Job Reference: 104628
Contact Name: Tommy McKeown
Contact Email:

Job Description

Manufacturing Technician I – Mayo - Unknown - 104628
Manufacturing Technician I – Mayo

Part of the Core 1 area upgrade for the commercialisation of an Ophthalmic parenteral and support of ongoing PFS preparations Roles are required across a 2 shift pattern, 1st shift and 2nd shift.

Knowledge and Experience

• Degree in a Science or Engineering discipline and or three years of applied experience in Pharma /
• Experience with commercial & / or clinical manufacture.
• Excellent technical writing and communication skills.
• Proven ability to problem solve.
• Must be a self-starter with a pro-active approach
• Experience with interacting in project teams.
• Experience with single use technologies
• Understanding of autoclave sterilisation, depyrogenation, filter integrity testing essential
• Knowledge of lyophilisation and freeze dryer operations
• Flexibility of working hours may be required
• Experience with GMP regulatory inspections


• Assist in all aspects of batch manufacturing activities, in accordance with SOPs and batch record
instruction for multiple products
• Perform sterile filtration and filter integrity testing.
• Updating / generation of SOPs and manufacturing documentation
• Coordination of calibration / revalidation activities
• Support installation of new equipment as required
• Knowledge of equipment validation and SDLC an advantage.
• Completion of quality records
• Implementation of product dedicated controls for the Core 1 area
• Support regulatory inspections as required

Skills and requirements

• Good technical writing skills.
• Excellent communication skills
• Good time management and organisational skills.
• Understanding of autoclave sterilisation, depyrogenation, filter integrity testing essential
• Understanding of aseptic practices in clean room environment
• Understanding of Single Use Technology and Single use system validation.
• Working knowledge of Quality Management System (QMS)
• Knowledge of clinical development phases
• Understanding requirements of cross contamination controls in multi product facility
• Working knowledge of Lean Six Sigma, yellow/green belt desirable.

For further information on this please contact Tommy Mckeown on 086 0100903 /

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