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.

The QA Technician will be responsible for performing product release activities across the Sudbury manufacturing sites, ensuring all processes and relevant documentation are completed to applicable quality standards. The QA Technician ensures that products released for distribution from the Sudbury Sites meet all quality requirements. This is a permanent role, working from Monday to Friday (Days).

Job Responsibilities:

• Carry out quality control and documentation checks of manufactured product across the Sudbury sites, following GDP (Good Documentation Practices) and ensuring all Product conforms to specification prior to release.
• 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 stakeholders. Escalate issues as required, ensuring consistency and adherence to processes.
• Provide support to other Quality functions within Sudbury as required.
• 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.
• Represent the business in customer audits and regulatory inspections to demonstrate that we have compliant systems.
• Maintain compliance with Data Integrity Regulations, GAMP standards, 21 CFR Part 11 and applicable regulatory guidelines.

Skills and Experience:

• You will have a flexible approach and ability to adapt according to workload.
• You are self-motivated, reliable, able to work on own initiative, manage time effectively and possess a desire to succeed.
• You will be an effective team member and able to communicate across functions.
• You will be curious - keen to understand, learn and try new things, and possess excellent written and oral communication skills.
• Experience in a manufacturing environment.
• IT literate with strong knowledge of Microsoft Office packages.
• GDP & GMP (Good Documentation Practices & Good Manufacturing Practices).

Our Benefits:

• 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.

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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.