Senior Quality Assurance Officer

JR United Kingdom; Lincoln; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading company in the medical device sector is seeking a Senior Quality Assurance Officer to manage design assurance activities as part of a maternity cover role. You will oversee NPD and ensure compliance with international quality standards while closely collaborating with regulatory teams. This 12-month temporary position is based on-site in Lincoln and requires expertise in IVD devices and regulatory affairs.

Qualifications

• Experience with IVD medical device new product development.
• Extensive knowledge of international IVD quality systems including 21 CFR 820 and ISO 13485.
• Experience with increasing responsibility in medical device Quality Assurance.

Responsibilities

• Support projects for New Product Development or Product Lifecycle Management.
• Conduct design assurance duties to ensure business delivery is on budget and schedule.
• Collaborate with Regulatory Affairs on global regulatory submissions.

Skills

Design controls for regulated products

Medical device quality systems

Regulatory submissions

Education

Bachelor’s degree in science, medical or technical field

Job description

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Senior Quality Assurance Officer, lincoln

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Client:

Jackson Hogg

Location:

lincoln, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

04.06.2025

Expiry Date:

19.07.2025

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Job Description:

This temporary 12-month position (for maternity cover) reports to the Manager of Quality Assurance (Design) and is part of the Quality Assurance and Regulatory Compliance Department located in Newcastle-upon-Tyne and will be an on-site position.

In this role, you will have the opportunity to:

• Work on site projects to support the progression of the most viable commercial/strategic opportunities for New Product Development (NPD) or Product Lifecycle Management (PLCM)
• Plan, organise and conduct duties related to design assurance and ensuring executions of tasks ensuring the delivery to the business is within budget and on schedule
• Work closely with Regulatory Affairs on deliverables for global regulatory submissions, including FDA 510(k)s and PMAs and IVDR CE certifications

The essential requirements of the job include:

• Working knowledge of design controls for regulated products
• Experience in IVD medical device new product development and design controls
• Extensive knowledge of international IVD medical device quality systems including but not limited to 21 CFR 820 and ISO 13485
• Bachelor’s degree in science, medical or technical field and experience with increasing responsibility in medical device Quality Assurance

It would be a plus if you also possess previous experience in:

• Experienced with higher classification IVD/Medical devices and companion diagnostics
• IVD medical device regulatory affairs experience a distinct advantage