Quality Technician

STERIS IMS; Northampton; On-site; GBP 25,000 - 35,000; Full time

Job summary

A global leader in healthcare solutions is seeking a Quality Inspector in Northampton. You'll assist in quality investigations, inspect medical devices, and ensure compliance in a fast-paced environment. Candidates should possess at least 1 year of relevant experience and have proficiency in Excel and Word. Strong attention to detail and teamwork skills are essential. This role offers the opportunity to contribute to patient safety and product quality.

Qualifications

• Minimum 1 year of experience in a regulated manufacturing or repair environment.
• Ability to work in a fast-paced environment with strict deadlines.
• Detail-oriented with a focus on continuous improvement.

Responsibilities

• Assist in production line Quality investigations.
• Perform inspection of Rigid and Flexible Endoscopes.
• Coordinate and conduct in-process and final QC product acceptance testing.

Skills

Attention to detail

Flexibility

Teamwork

Integrity

Accountability

Education

TVQ or NVQ Level 2 in Decontamination or equivalent experience

Tools

Excel

Word

Job description

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

HOW YOU WILL MAKE A DIFFERENCE

Do you want to spend your working time making a difference in the world around you? Are you passionate about supporting the medical industries? Do you care about keeping patients and people safe? If so, then a career with Steris could be a great fit for you.

At STERIS we are the trusted experts and global leaders in medical device repair services and surgical instrument manufacturing

We are dedicated to enabling patient safety and driving improvements in quality outcomes and efficiency across all our products and services.

What's involved

Assists in production line Quality investigations and associated problem-solving activities.

Performs inspection of Rigid and Flexible Endoscopes

May coordinate and conduct in-process and final QC product acceptance testing, depending on facility.

Investigates production line stoppages to identify corrective actions.

Identifies and documents product and process non-conformances.

Participates on a Material Review Board to review and process non conformance reports.

Reviews DHR’s and supports batch record release.

Enters and retrieves Quality data from local and global systems.

Performs site calibration activities and recordkeeping.

Executes environmental monitoring processes and recordkeeping.

Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release.

Complete other duties as assigned.

Required Experience

Ability to work in a fast-paced environment with strict deadlines

Ability to generate detailed, high-quality documentation.

Ability to work with others in analyzing and solving technical problems.

Teamwork: Collaborates with others. Works in a professional manner to support team actions.

Effectively manages work tasks. Is detail oriented and strives for continuous improvement.

PC experience and working familiarity of common desktop applications including Excel and Word.

Minimum 1 year of experience in a regulated manufacturing or repair environment or other technical production environment

Ideally will have Quality Inspection experience

Preferred Experience

• TVQ or NVQ Level 2 in Decontamination or equivalent experience.
• Previous experience in Sterile Services and/or health related products.

Skills

• Flexibility
• Teamwork
• Integrity
• Working under pressure
• Accountability
• Attention to detail

STERIS plc provides employment and advancement opportunities without regard to age, disability, gender reassignment, marriage or civil partnership, pregnancy and maternity, race, religion/belief, sex (gender), sexual orientation or any other legally protected characteristic as defined by UK employment law.