Incoming Quality Assurance Technician

Siemens Mobility; Greater Sudbury; On-site; CAD 60,000 - 80,000; Full time

Job summary

A leading medical technology company located in Ontario is seeking an Incoming Quality Assurance Technician. In this role, you will be responsible for inspecting and ensuring that all incoming materials meet stringent quality standards before they are used in production. This position requires effective communication with suppliers and documentation of inspection processes to maintain compliance. Ideal candidates will have a strong background in quality management systems and effective use of measurement equipment. Join a diverse team dedicated to healthcare solutions.

Benefits

26 days' holiday with option to buy/sell 5 more

Up to 10% employer pension contribution

Share and bonus scheme

Flexible benefits from private medical insurance to dental cover

Corporate Social Responsibility opportunities including 2 paid volunteering days

Qualifications

• Proficiency in measurement verification of incoming materials.
• Understanding of documentation practices and regulations.
• Experience in quality assurance processes across manufacturing sites.

Responsibilities

• Conduct inspections of incoming materials to ensure quality compliance.
• Communicate effectively with suppliers about material quality issues.
• Document all received materials and their inspection results.

Skills

Ability to read drawings & associated design specifications

Knowledge of Quality Management Systems, ISO 13485, 21 CFR 820

Ability to use various measurement equipment

Understanding of GDP & GMP

Tools

CATSWEB

SAP

Documentum

Job description

Siemens Healthcare Diagnostics Manufacturing Ltd

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

Apply now for the position of Incoming Quality Assurance Technician and you will be responsible for completing inspection, control and disposition of all incoming materials across the Sudbury manufacturing sites, completing all relevant documentation and traceability processes to applicable quality standards. The IQA Technician ensures that incoming materials to be used by production meet all quality requirements.

Your Role:

• Carry out inspection of incoming goods across the Sudbury sites using measurement equipment, specifications and quality control plans (QCP's). Ensuring all incoming materials fully conform to requirements prior to assembly, completing all associated documentation/records and following GDP (Good Documentation Practices).
• Provide input to the process for the control and disposition of any non-conforming materials, completing tasks, documentation and segregating materials as required within documented working practices.
• Effectively communicate with both internal & external suppliers/stakeholders. Be point of contact for part quality related enquiries, elevate issues as required, ensuring consistency and adherence to processes.
• Complete assigned training within the defined timescales.
• Provide support to other Quality functions within Sudbury as required, covering in-process testing and/or inspections and final product release processes. Provide support for both Internal and 3rd party site audits.
• Participate in SQDIP meetings, provide accurate and timely reports and take responsibility for the achievement of target KPI's for the role.
• Establish & maintain supplier 'Quality Approved' samples for relevant attributes (colours, finishes)
• Actively use business systems such as CATSWEB, CERDAAC, SAP, Documentum & Learn4U.

Your Expertise:

• Ability to read drawings & associated design specifications and reference standards.
• Ability to use various measurement equipment and process for verification of incoming materials.
• Knowledge of Quality Management Systems, ISO 13485, 21 CFR 820.
• GDP & GMP (Good Documentation Practices & Good Manufacturing Practices).
• 26 days' holiday with the option to buy or sell an additional 5
• Up to 10% employer pension contribution
• Share and bonus scheme
• Access to our flexible benefits from private medical insurance to dental cover
• Corporate Social Responsibility opportunities including 2 paid volunteering days per year and support from our 24/7 employee assistance programme

Who we are:

We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

How we work:

When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

As an equal opportunity employer, we welcome applications from individuals with disabilities.

We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities.

To all recruitment agencies:

Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated.