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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, which it markets under its brands LiquiBand, RESORBA, LiquiBandFix8, LIQUIFIX, Peters Surgical, Ifabond, Vitalitec and Seal-G. AMS also supplies wound care dressings such as silver alginates, alginates, and foams through its ActivHeal brand as well as under white label. Since 2019, the Group has made seven acquisitions: Sealantis, Biomatlante, Raleigh, AFS Medical, Connexicon, Syntacoll, and Peters Surgical. AMS's products are manufactured in multiple countries and sold globally via a network of partners and direct sales forces. 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 provides equal employment opportunities to all applicants, valuing diversity and ensuring no discrimination based on gender, race, age, nationality, disability, or other protected characteristics.
Role Responsibilities:
* Conduct all QA/QC functions and prioritize demands.
* Work according to SOPs and PWIs, report non-conformances or deviations through appropriate channels.
* Product release planning, goods receiving inspection, and testing.
* Perform in-process and final product testing for release.
* Develop, generate, maintain, and audit documentation supporting an effective and compliant Quality Management System, including Device History Records, Material and Product Specifications, and Test Records.
* Update and maintain quality procedures, test methods, and instructions.
* Train others as required.
Qualifications and Skills:
* Experience in a manufacturing environment, preferably medical devices, with relevant qualifications (e.g., 5 GCSEs including Maths/English).
* Ability to read and understand drawings, procedures, and standards.
* Ability to represent the department in cross-functional interactions.
* Desirable: Experience in the medical device industry, knowledge of ISO13485 & FDA QSR, City & Guilds 743 or equivalent, statistical knowledge, understanding of quality techniques, GMP, GLP, and QMS.
* Strong attention to detail, organizational skills, and ability to manage time effectively.
* Good communication skills, flexible and adaptable to change.
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