Quality Controller

JR United Kingdom; Bournemouth; On-site; GBP 25,000 - 40,000; Full time

Job summary

A leading company in innovative tissue-healing technology seeks a Quality Assurance professional to conduct QA/QC functions in a manufacturing setting. The ideal candidate will have experience in the medical device industry, along with the ability to maintain quality processes and documentation. This role requires strong organizational and communication skills to ensure compliance with quality standards.

Qualifications

• Experience in a manufacturing environment (medical device preferred).
• Ability to read and understand drawings, procedures, and standards.
• Preferably has knowledge of ISO 13485 & FDA QSR.

Responsibilities

• Conduct QA/QC functions and prioritize demands.
• Product release planning and goods receiving inspection.
• Develop, maintain, and audit documentation for the Quality Management System.

Skills

Attention to detail

Organizational skills

Effective time management

Good communication skills

Flexibility and adaptability

Education

5 GCSEs including Maths/English

City & Guilds 743 or equivalent

Job description

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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 the UK, Germany, France, the Netherlands, Thailand, India, the Czech Republic, and Israel, and are sold globally. The Group has R&D hubs in the UK, Ireland, Germany, France, and Israel. Established in 1991, the Group employs over 1,500 staff. For more info, visit www.admedsol.com

AMS provides 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 and prioritize demands.
• Work according to SOPs and PWIs, report non-conformances or deviations.
• Product release planning, goods receiving inspection & testing, in-process inspection, and final product testing.
• Develop, maintain, and audit documentation supporting the Quality Management System, including Device History records, specifications, test records, and testing data.
• Update and maintain quality procedures, test methods, and instructions. Train others as needed.

Qualifications & Skills:

• 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, and standards.
• Ability to represent the department in cross-functional interactions.
• Preferred: Experience in the medical device industry, knowledge of ISO 13485 & FDA QSR, City & Guilds 743 or equivalent, statistical knowledge, and familiarity with quality techniques and GMP/GDP standards.
• Strong attention to detail, organizational skills, effective time management, and good communication skills. Flexible and adaptable to change.