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Quality Controller, Watford, Hertfordshire
Client: Advanced Medical Solutions
Location: Watford, Hertfordshire, 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, foams, and more through its ActivHeal brand and white label.
The Group has made several acquisitions since 2019, expanding its product range and global presence, with manufacturing in multiple countries and products sold worldwide. Established in 1991, AMS employs over 1,500 staff and invests in R&D hubs across Europe and Israel. For more information, visit www.admedsol.com.
AMS is committed to equal employment opportunities, valuing diversity and prohibiting discrimination based on gender, race, age, nationality, disability, or other protected characteristics.
Role Responsibilities:
* Conduct QA/QC functions, prioritize demands, work according to SOPs and PWIs, report non-conformances or deviations.
* Product release, including planning, performing goods receiving inspections, in-process and final product testing.
* Develop, generate, maintain, and audit documentation supporting the Quality Management System, such as Device History Records, Material and Product Specifications, Test Records.
* Update and maintain quality procedures, test methods, instructions; train others as required.
Candidate Requirements:
* Experience in a manufacturing environment, preferably medical devices, with appropriate qualifications (e.g., 5 GCSEs including Maths/English).
* Ability to read and understand drawings, procedures, standards, and represent the department in cross-functional interactions.
* Desirable: Experience in the medical device industry, knowledge of ISO 13485 & FDA QSR, City & Guilds 743 or equivalent, statistical knowledge, understanding of quality techniques, GMP, GCP, and quality systems.
* Strong attention to detail, organizational skills, effective time management, good communication skills, and adaptability.
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