Production Operator at AnaBio Technologies Ltd
Carrigtwohill, County Cork, Ireland -
Full Time


Start Date

Immediate

Expiry Date

11 Nov, 25

Salary

0.0

Posted On

12 Aug, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Gmp

Industry

Pharmaceuticals

Description

WHAT WILL I BE DOING?

o Equipment Operation: Operate, monitor, and control equipment used in the manufacturing process. Follow established procedures and guidelines to ensure accurate and efficient operation.
o Process Monitoring: Monitor process parameters, including temperature, pressure, flow rates, and levels, to maintain optimal operating conditions. Identify and troubleshoot process deviations or abnormalities and take appropriate corrective actions in consultation with Production and Engineering personnel.
o Compliance with GMP: Adhere to GMP guidelines and regulatory requirements throughout the manufacturing process. Follow standard operating procedures (SOPs) and work instructions to ensure product quality, safety, and traceability. Maintain accurate and up-to-date documentation and records as required.
o Safety and Environmental Compliance: Comply with all safety protocols, including the proper use of personal protective equipment (PPE)
o Cleaning and Maintenance: Perform routine cleaning and maintenance activities on equipment, process areas, and production lines as per SOPs. Keep the work area clean, organized, and free from potential hazards. Identify and report any equipment malfunctions or maintenance requirements promptly.
o Collaboration and Communication: Work closely with other team members, including R&D, Engineering and QA, to ensure smooth operation and troubleshooting of processes. Communicate effectively, both verbally and in writing, to report issues, document process changes, and participate in shift handovers.
o Continuous Improvement: Identify opportunities for process optimization, efficiency improvements, and cost savings. Participate in investigations of process deviations, incidents, or non-conformances and contribute to root cause analysis and corrective actions.
o Inventory Management: Perform incoming & outgoing inspection, stock transfer and management of materials, equipment, consumables, documentation, and packaging.

Responsibilities

As a Process Operator in a Good Manufacturing Practice (GMP) area, your primary responsibility is to ensure the safe and efficient operation of manufacturing processes in compliance with established GMP standards. You will be responsible for operating and monitoring equipment, executing production procedures, and maintaining documentation in accordance with regulatory requirements. Your attention to detail, adherence to standard operating procedures (SOPs), and commitment to maintaining a clean and organized work environment will be crucial to your success in this role.

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