Quality Controller

JR United Kingdom; Watford; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading company in medical device manufacturing is seeking a Quality Controller for a 12-month contract in Watford. The role involves performing quality assurance and control functions to maintain high standards of production. Candidates should have experience in a manufacturing environment and a background in medical devices is preferred. Strong attention to detail, organizational skills, and the ability to work collaboratively are key for success in this role.

Qualifications

• Experience in a manufacturing environment, preferably medical devices.
• Ability to read and understand drawings and procedures.
• Desirable: Knowledge of ISO 13485 & FDA QSR.

Responsibilities

• Conduct QA/QC functions, prioritizing demands and reporting non-conformances.
• Perform goods receiving inspections, in-process and final product testing.
• Develop and maintain documents supporting Quality Management System.

Skills

Attention to detail

Organizational skills

Time management

Communication skills

Adaptability

Education

5 GCSEs including Maths/English

City & Guilds 743 or equivalent

Job description

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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.