Process Technician

STERIS; Westport; On-site; EUR 32,000 - 42,000; Full time

Job summary

STERIS in Westport, Ireland, is seeking a Process Technician to verify product release, perform process assurance activities and maintain QA systems in line with GMP.

The role involves dosimetry reading, documentation, customer support, and aiding the validation loads, with emphasis on accuracy, teamwork and adherence to ISO 13485 standards. Two years of GMP experience preferred; strong MS Office skills and ability to liaise with customers, operators and management are essential.

Qualifications

• Two years or more of work in GMP environment.
• Good communication and interpersonal skills.
• Understanding and appreciation of Good Manufacturing Practice and
• Quality Assurance programmes such as ISO 13485
• Experience in Healthcare manufacturing environment.
• Careful attention to detail. Ability to follow documented procedures.
• Proficient with MS Office suite
• Liaise with customers, operators, managers and STERIS
• Ability to motivate and co ordinate team approach to continuous improvement and problem solving.

Responsibilities

• Verify product release by routine dosimetry.
• Preform all process assurance activities.
• Perform defined administrative duties regarding dosimetry and process records.
• Maintain all aspects of the process quality assurance system to achieve customer requirements consistent with STERIS policies.
• Perform dosimetry reading and release product within defined specification limits and follow documented procedures.
• Provide logistic information and customer support in response to customer query or request, received by email or telephone taking care of their needs in a timely, efficient and friendly manner.
• Prepare production administration paperwork including certificates of processing, dosimetry reports, letters, routine reports and shipping documents. Issue paperwork and follow up as necessary within limit of authority as specified by Management.
• Setup up validation load with dosimetry requirement as per validation department or customer validation protocol
• Setup Dose Audit where required by customer
• Collecting dosimeters from routine and validation loads following processing during working hours and weekend where applicable.
• Reinforce impression of a quality G.M.P. Healthcare company by maintaining work areas clean and tidy.
• Undertake other duties, tasks and responsibilities as may be assigned by the Management from time to time.
• Provide operational support where required by Manager

Skills

Good communication

MS Office

Team coordination

Problem solving

Quality mindset

Education

Vocational/Technical

Tools

MS Office

Job description

Position Summary

Process Technician position will be involved

• Verify product release by routine dosimetry.
• Preform all process assurance activities.
• Perform defined administrative duties regarding dosimetry and process records.
• Maintain all aspects of the process quality assurance system to achieve customer requirements consistent with STERIS policies.

Duties

• Perform dosimetry reading and release product within defined specification limits and follow documented procedures.
• Provide logistic information and customer support in response to customer query or request, received by email or telephone taking care of their needs in a timely, efficient and friendly manner.
• Prepare production administration paperwork including certificates of processing, dosimetry reports, letters, routine reports and shipping documents. Issue paperwork and follow up as necessary within limit of authority as specified by Management.
• Setup up validation load with dosimetry requirement as per validation department or customer validation protocol

Duties - cont'd

• Setup Dose Audit where required by customer
• Collecting dosimeters from routine and validation loads following processing during working hours and weekend where applicable.
• Reinforce impression of a quality G.M.P. Healthcare company by maintaining work areas clean and tidy.
• Undertake other duties, tasks and responsibilities as may be assigned by the Management from time to time.
• Provide operational support where required by Manager

Education Degree

Vocational/Technical

Required Experience

Two years or more of work in GMP environment.

Specific Work Requirements

• Good communication and interpersonal skills
• Understanding and appreciation of Good Manufacturing Practice and
• Quality Assurance programmes such as ISO 13485
• Experience in Healthcare manufacturing environment.
• Careful attention to detail. Ability to follow documented procedures.
• Proficient with MS Office suite
• Liaise with customers, operators, managers and STERIS
• Ability to motivate and co ordinate team approach to continuous improvement and problem solving

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com.

STERIS strives to be an Equal Opportunity Employer.