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QA Release Officer (FTC)
Llanberis | Contract | www.cv-library.co.uk |
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 QA Release Officer and you will ensure products made available for sale comply with Manufacturing and testing requirements/In-process and release specifications. This is a Fixed Term Contract (Ending September 2025) and will be site based at our Llanberis facility.
Your Role:
Reviewing manufacturing documentation to confirm that the product was manufactured in line with the requirements of the DMR to ensure both customer and regulatory requirements are met
Assigning of Kit Literature included with each product released in line with the DMR requirements to ensure that customers are supplied with the appropriate Kit Literature when using the product
Liaise with document owners to resolve issues or non-compliances identified during the review process and ensure that they are resolved prior to release to ensure only compliant products are released
Produce and publish reports on the quality of the documentation reviewed to provide feedback on current performance and drive future improvements
Liaising with documentation owners to identify documentation improvement opportunities to increase the quality and compliance of generated documents
Continually assess the processes used within the QA Release Group for appropriateness and identification of non value added activities to ensure compliance and continuous improvement of the QA Release process Your Expertise:
Educated to 'A' level standard / equivalent vocational training and/or have equivalent time served experience within a Quality, Scientific or Engineering environment.
Awareness of working in a GMP environment
Ability to communicate with all areas of an organisation
Perform work in compliance with established procedures
Understanding of computer software including Word, Excel and Access
Must be able to demonstrate a good attention to detail Benefits:
A competitive salary
Annual Bonus Scheme
Generous pension contributions
26 days holiday
Access to our flexible benefits from private medical insurance to dental cover
Corporate Social Responsibility opportunities including 2 paid volunteering days per year
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
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 QA Release Officer and you will ensure products made available for sale comply with Manufacturing and testing requirements/In-process and release specifications. This is a Fixed Term Contract (Ending September 2025) and will be site based at our Llanberis facility.
Your Role:
Reviewing manufacturing documentation to confirm that the product was manufactured in line with the requirements of the DMR to ensure both customer and regulatory requirements are met
Assigning of Kit Literature included with each product released in line with the DMR requirements to ensure that customers are supplied with the appropriate Kit Literature when using the product
Liaise with document owners to resolve issues or non-compliances identified during the review process and ensure that they are resolved prior to release to ensure only compliant products are released
Produce and publish reports on the quality of the documentation reviewed to provide feedback on current performance and drive future improvements
Liaising with documentation owners to identify documentation improvement opportunities to increase the quality and compliance of generated documents
Continually assess the processes used within the QA Release Group for appropriateness and identification of non value added activities to ensure compliance and continuous improvement of the QA Release process Your Expertise:
Educated to 'A' level standard / equivalent vocational training and/or have equivalent time served experience within a Quality, Scientific or Engineering environment.
Awareness of working in a GMP environment
Ability to communicate with all areas of an organisation
Perform work in compliance with established procedures
Understanding of computer software including Word, Excel and Access
Must be able to demonstrate a good attention to detail Benefits:
A competitive salary
Annual Bonus Scheme
Generous pension contributions
26 days holiday
Access to our flexible benefits from private medical insurance to dental cover
Corporate Social Responsibility opportunities including 2 paid volunteering days per year
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
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