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Quality Controller, Leeds, West Yorkshire
Client: Advanced Medical Solutions
Location: Leeds, West 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 through its ActivHeal brand. Since 2019, the Group has made seven acquisitions, expanding its product portfolio and global presence. AMS's products are manufactured in several countries and sold worldwide through various channels. The Group has R&D hubs in the UK, Ireland, Germany, France, and Israel. Established in 1991, it employs over 1,500 staff. For more information, visit www.admedsol.com.
AMS is committed to equal employment opportunities and values diversity, ensuring no 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 through appropriate channels.
* Product release planning, performing goods receiving inspections and testing, process inspections, and final product release testing.
* Develop, generate, maintain, and audit documentation supporting an effective and compliant Quality Management System, including Device History Records, Material and Product Specifications, Test Records, and In-process & Product Release Testing.
* Update and maintain Quality procedures, test methods, and instructions. Train others as required.
Qualifications and Skills:
* Experience in a manufacturing environment (medical device preferred), with appropriate qualifications such as 5 GCSEs including Maths and English.
* Ability to read, analyze, and understand drawings, procedures, and standards.
* Ability to represent the department in cross-functional interactions.
* Desirable: Experience in the medical device industry, knowledge of ISO 13485 & FDA QSR requirements, City & Guilds 743 or equivalent, statistical knowledge, knowledge of quality techniques and implementation, GMP, GLP, and Quality Systems, strong attention to detail, good organizational and communication skills, flexibility, and adaptability.
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