Quality Controller

JR United Kingdom; Basingstoke; On-site; GBP 28,000 - 40,000; Full time

Job summary

A leading company in the medical device sector seeks a Quality Control Specialist to oversee product release planning and ensure compliance with quality standards. The role demands experience in a manufacturing setting, proficiency in documentation, and knowledge of relevant regulatory requirements. Successful candidates will excel in organizational skills and possess a detail-oriented mindset, contributing to the production of high-quality healthcare products.

Qualifications

• Experience in a manufacturing environment with QC/QA expertise.
• Ability to analyze and understand technical documentation.

Responsibilities

• Conduct product release planning, inspection, and testing.
• Maintain and audit documentation for the Quality Management System.
• Generate and update quality procedures and instructions.

Skills

Attention to Detail

Organisational Skills

Communication

Education

5 GCSE’s or equivalent including Maths/English

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, an Israeli developer of innovative internal sealants, Biomatlante, a French developer and manufacturer of surgical biomaterials, Raleigh, a leading UK coater and converter of woundcare and bio-diagnostics materials, AFS Medical, an Austrian specialist surgical business, Connexicon, an Irish tissue adhesives specialist, Syntacoll a German specialist in collagen-based absorbable surgical implants and Peters Surgical a global provider of specialty surgical sutures, mechanical haemostasis and internal cyanoacrylate devices. AMS's products, manufactured in the UK, Germany, France, the Netherlands, Thailand, India, the Czech Republic and Israel, are sold globally via a network of multinational or regional partners and distributors, as well as via AMS's own direct sales forces in the UK, Germany, Austria, France, Poland, Benelux, India, the Czech Republic and Russia. The Group has R&D innovation hubs in the UK, Ireland, Germany, France and Israel. Established in 1991, the Group has more than 1,500 employees. For more information, please see www.admedsol.com

AMS provides equal employment opportunities for all applicants. We highly value and encourage diversity across our workforce meaning that no one will be discriminated against because of their gender, race, age, nationality, disability, or any other protected characteristic as prohibited by law.

What will this role involve?

• Product Release Planning / performing Goods Receiving inspection & testing. In-process inspection and testing, and testing for final product release. Any other reasonable requirement as required to meet the business objectives.
• Develop, generate, maintain and audit documentation to support an effective and compliant Quality Management System including; Device History records, Material and Product Specifications, Test records, In-process & product release testing, accurately recording data, calculation of results.
• Generate, update and maintain Quality procedures, test methods, instructions. To train others as required.

Qualifications and experience:

• Ground in a manufacturing environment (medical device preferred), previous QC/QA experience, with appropriate qualifications of 5 GCSE’s or equivalent including Maths/English.
• Ability to read, analyze, and understand drawings / procedures / standards.
• Ability to represent the department in cross-functional interactions.

Desirable:

• Experience in medical device industry / Knowledge of ISO13485 & FDA QSR requirements.
• City & Guilds 743 or equivalent.
• Statistical knowledge.
• Knowledge of world class quality techniques and implementation.
• Knowledge of Good Manufacturing Practice, Good Laboratory Practice and Quality Systems.
• Strong attention to detail.
• Good organisational skills.
• Able to manage own time effectively, prioritise tasks and deliver to critical deadlines.
• Good communication skills; written, verbal and presenting.
• Flexible and adaptable to changing work environment.