Quality Controller

JR United Kingdom; Sheffield; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading company in innovative tissue-healing technology is seeking a Quality Controller for a 12-month contract in Sheffield. This role involves conducting quality assurance functions, planning product releases, and maintaining quality documentation. Ideal candidates will have experience in the medical device industry and strong attention to detail.

Qualifications

• Experience in a manufacturing environment (medical device preferred).
• Knowledge of ISO13485 & FDA QSR.
• Statistical knowledge and quality systems understanding.

Responsibilities

• Conduct QA/QC functions and report non-conformances.
• Develop and maintain documentation supporting Quality Management System.
• Train others on quality procedures.

Skills

Attention to detail

Organizational skills

Communication skills

Adaptability

Education

5 GCSEs including Maths/English

City & Guilds 743 or equivalent

Job description

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Quality Controller, Sheffield, South Yorkshire

Client: Advanced Medical Solutions

Location: Sheffield, South Yorkshire, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

2

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

Quality Controller - 12 month Contract

Who are Advanced Medical Solutions? AMS is a world-leading independent developer and manufacturer of innovative tissue-healing technology, focused on quality outcomes for patients and value for payers. AMS has a wide range of surgical products including tissue adhesives, sutures, haemostats, internal fixation devices, and internal sealants, marketed under brands like LiquiBand, RESORBA, and others. AMS also supplies wound care dressings such as silver alginates, foam dressings, and more. Since 2019, the Group has made seven acquisitions, expanding its product portfolio and global presence. AMS products are manufactured in multiple countries and sold worldwide through various channels. The Group has R&D hubs in the UK, Ireland, Germany, France, and Israel, and employs over 1,500 staff.

AMS is committed to equal employment opportunities, valuing diversity and non-discrimination based on gender, race, age, nationality, disability, or other protected characteristics.

Role Responsibilities:

• Conduct QA/QC functions, prioritize tasks according to demands, work to SOPs and PWIs, report non-conformances or deviations.
• Product release planning, goods receiving inspection, testing, and final product release.
• Develop, maintain, and audit documentation supporting the Quality Management System, including Device History Records, specifications, test records, and release testing data.
• Update and maintain quality procedures, test methods, and instructions; train others as required.

Candidate Requirements:

• Experience in a manufacturing environment (medical device preferred), with relevant qualifications (e.g., 5 GCSEs including Maths/English).
• Ability to read and understand drawings, procedures, standards; represent the department in cross-functional interactions.
• Experience in the medical device industry, knowledge of ISO13485 & FDA QSR, City & Guilds 743 or equivalent, statistical knowledge, and understanding of quality systems and practices.
• Strong attention to detail, organizational skills, ability to manage time and prioritize, good communication skills, and adaptability.