Quality Inspector-Night Shift Galway

Posted: 8th August, 2024

Title: Quality Inspector-Night Shift

Department: Manufacturing

Location: Galway, Ireland

 

Responsibilities

Inspection and Testing:

1. • Perform incoming, in-process, and final inspection of medical device components and finished products.
   • Conduct inspections using various tools and equipment to verify dimensions, tolerances, and visual characteristics.
   • Utilize testing equipment to verify product functionality and performance.

Documentation:

1. • Document and record inspection and test results accurately and in compliance with regulatory requirements.
   • Maintain detailed inspection records, including batch/lot numbers, inspection dates, and results.

Compliance with Standards:

1. • Ensure products conform to established quality standards, industry regulations, and company procedures.
   • Stay updated on relevant standards and regulations applicable to medical devices.

Root Cause Analysis:

1. • Participate in investigations to identify the root cause of quality issues or non-conformities.
   • Collaborate with other departments to implement corrective and preventive actions.

Calibration and Maintenance:

1. • Verify and ensure that inspection and testing equipment are calibrated and maintained according to schedule.
   • Report any equipment malfunctions and take appropriate actions.

Training and Development:

1. • Ensure your training is always up to date
   • Provide training to production and other relevant personnel on quality standards and inspection processes.

Communication:

1. • Communicate quality issues and non-conformities to relevant stakeholders.
   • Collaborate with cross-functional teams, including engineering and production, to address quality concerns.

Continuous Improvement:

• Participate in continuous improvement initiatives to enhance quality processes and systems.
• Propose and implement efficiency improvements in inspection and testing procedures.

Regulatory Compliance:

• Ensure that all quality inspection activities comply with regulatory requirements such as ISO 13485, and other applicable standards.

 Record Keeping:

• Maintain organized and complete records of all inspection and testing activities for audit purposes.

Risk Management:

• Contribute to risk management activities, including identifying and assessing potential risks associated with product quality.
• Other duties outlined by your manager

Qualifications & Experience

Leaving Cert or equivalent, Minimum 1-2 years’ experience in a manufacturing environment is required and quality assurance experience is desired

The successful candidate will possess the following key attributes:

• Must have excellent MS Excel skills and be proficient in Microsoft Office
• Strong attention to detail
• Strong verbal and written communications skills.
• Excellent attendance record.
• Understanding/awareness of Customer requirements in terms of quality and delivery.
• Ability to impart knowledge in clear concise manner.
• Demonstrate working as part of a team with common goals.
• Take ownership for behaviour, workmanship.
• Decision-making and Reporting skills
• Good attendance record

The above list of job responsibilities is not exclusive or exhaustive and the post holder will be required to undertake such tasks as may reasonably be expected within the scope of the post.

FOR INTERESTED APPLICANTS: If you are interested in this position, please send a brief cover letter, resume, please state the job title applying for and any other relevant material for the candidacy to GalwayHR@nelipak.com. Thank you!

Browse More Opportunities