Quality Technician

Quality Operations Technician

Location: Cork

Duration: 12 months

Hours: 40 hours

Quality Operations Support role for all Manufacturing Value Streams and supporting  functions. 

As a Quality Operations Technician, this role will play a crucial part in ensuring the quality  and efficiency of our medical device manufacturing processes. You will actively contribute  to the overall operational success of our manufacturing facility, with a specific focus on  maintaining high-quality standards, adhering to regulatory requirements, and supporting  the continuous improvement of our manufacturing operations

Roles and Responsibilities

• Maintain the standard of Good Manufacturing Processes and housekeeping  requirements in line with Regulatory requirements 

• Documentation and Record-Keeping: Assist in maintaining accurate and up-to-date  documentation related to manufacturing processes, quality controls, and compliance  activities. 

• Review product on Quality Hold, investigate and determine disposition as required. 

• Completion of non-conformance reports and associated investigations with the support  of the quality engineers. 

• Monitor manufacturing processes to identify any deviations from established standards  and promptly report any issues or non-compliance 

• Support Quality System activities within value streams and across the site such as GMP  process walks, complaint investigations and NR’s 

• Ensure that all relevant Quality KPI Data is recorded, reported and actioned in an  efficient manner. (CAPA, NR, etc.) 

• Identify and carry out required Quality training including certification of production  associates and roll out of quality alerts when required. 

• Participate in training programs to enhance knowledge of manufacturing processes,  quality systems, and regulatory compliance requirements. 

• Ensure all Manufacturing Areas comply with GMP, ISO and QSR requirements.

• Ensure that all Health, Safety and Environmental requirements are fulfilled.

• Continuous Improvement: Collaborate with cross-functional teams to identify areas for  improvement and support initiatives aimed at enhancing operational processes,  product quality, and overall efficiency 

• Data Analysis: Assist in the analysis of manufacturing data to identify trends, patterns,  and areas for improvement, contributing to process optimization and efficiency  enhancement efforts. 

• Responsible for communicating business related issues or opportunities to next management level 

• Responsible for following all Company guidelines related to Health, Safety and Environmental  practices as applicable. 

• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all  Company guidelines related to Health, Safety and Environmental practices and that all  resources needed to do so are available and in good condition, if applicable 

• Responsible for ensuring personal and Company compliance with all Federal, State, local and  Company regulations, policies, and procedures 

• Performs other duties assigned as needed 

How to Succeed

• Level 7 Degree/Diploma and or 1 to 3 years Medical Device Manufacturing experience  Working knowledge of Quality Systems (FDA/ISO) within a regulated environment. 

• Ability to interpret Engineering drawings/specifications

Benefits

This role offers a very competitive hourly rate. This contract will run for 12 month.

about DePuy Synthes

DePuy Synthes is the orthopaedic and neurological businesses of Johnson & Johnson - the world's most comprehensive and broadly-based healthcare company. At DePuy Synthes we specialise in our innovations in healthcare products, services and programs that make a real difference to millions of people across the world. We specialise in joint reconstruction, trauma, extremities, craniomaxillofacial, spinal surgery and sports medicine, and also the VELYS™ Digital Surgery portfolio. Contribute to the next healthcare breakthrough with your next project at DePuy Synthes. 

https://www.jnjmedtech.com/en-US/companies/depuy-synthes

https://www.jnjmedtech.com/en-GB/companies/depuy-synthes

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, LTD & Umbrella options are available. 

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.