Quality Assurance Officer

SGS; Remote; GBP 34,000 - 53,000; Full time

Job summary

A leading testing and certification company is looking for a Quality Assurance Specialist to maintain its medical device internal quality management system. The role involves managing documentation under regulatory schemes and performing quality assurance checks. Ideal candidates should have a degree in Biomedical Sciences or similar, as well as strong knowledge of quality management systems. This position offers remote flexibility and the opportunity to work within a multinational environment, supporting personal and professional development.

Benefits

Flexible schedule

Hybrid work model

Continuous learning options

Global company environment

Qualifications

• Good working knowledge of quality management systems including CAPA management.
• Detail-oriented with strong organizational skills.
• Ability to work in a team and write clear procedures.

Responsibilities

• Maintain the internal quality management system.
• Manage complaints and compliance queries.
• Perform quality assurance checks on system documents.

Skills

Quality management systems knowledge

Detail-oriented

Strong organizational skills

Ability to organize workload

Teamwork ability

Fluent in English

Education

Bachelor's degree in Biomedical Sciences or similar

Tools

MS Office (Word, Excel, Outlook)

Job description

We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

At SGS, we have an open corporate and international culture. We offer a dynamic work environment in a leading global company. Our high professional standards and our sustainability approach guarantee you a future-oriented work environment. We invest in our employees for the long term and are committed to supporting your development within the company. Our business principles include: Integrity, Health, Safety & Environment, Quality & Professionalism, Respect, Sustainability, and Leadership.

Job Description

Main Purpose of Role

Maintenance of the NB 1639 medical device internal quality management system.

Managing of daily QA tasks

• Updating and maintenance of documents under the MDD, MDR and IVDR scheme,
• Management the IF database,
• Collaboration on generic scheme documents,
• Publishing of documents on the SGS website,
• Bizzmine (Quality Management System); user communication and maintenance.

This role will report to the Quality & Regulatory Manager, Business Assurance.

It is remote based, and we are open to candidates located everywhere across Europe. But they must hold a valid work permit for their country of residency.

Key Accountabilities

• Management of complaints, compliance queries and appeals,
• Management of continual improvement,
• Management of document control and records,
• Perform quality assurance check on updated quality management system documents,
• Release of updated quality management system documents in Bizzmine,
• Build a good working relationship with the Global Medical Device Certification / Competency / Technical and Clinical Manager(s), and other Global Medical Device Team members,
• Undertake personal professional development and ensure appropriate training records are updated,
• Provide technical support to all parts of the business,
• Maintain a full knowledge and understanding of SGS procedures, regulations, guidance documents (e.g., MDCG) and external approval criteria,
• Support the development and maintenance of combined scheme documents.

Qualifications

Skills & Knowledge

• Good working knowledge of quality management systems including CAPA management, document control and good documentation practices (GDP),
• Detail oriented,
• Strong organisational skills,
• Ability to organise own workload considering priorities set by the global medical device quality manager,
• Ability to adapt quickly and demonstrate flexibility,
• Ability to work in a team,
• Ability to write clear procedures,
• Good working knowledge of the main MS office tools (Word, Excel, Outlook),
• Fluent written and spoken English.

A nice to have:

• Detailed understanding of global medical device regulations MDR and IVDR, and medical
• Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001.

Experience

• Significant work experience in a position with QA responsibility.

Another nice to have:

• Experience working with medical devices,
• Auditing experience against recognised standards.

Qualifications (academic)

• Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., pharmacy, bioengineering, nurse, ...)

Additional nice to have:

• Medical device training on MDD, MDR, IVDR or ISO 13485

Performance Indicators

• Turnaround time for compliance issues/complaints/ appeals,
• Efficient running of QMS and release of quality management documents.

Please send your CV in English

Additional Information

Why SGS?

• Global and very stable company, world leader in the TIC (Testing, Inspection and Certification) industry.
• Flexible schedule and hybrid model.
• SGS university and Campus for continuos learning options.
• Multinational environment where you will work with colleagues from multiple continents.
• Benefits platform.

Join Us:At SGS we believe in innovation, collaboration, and continuous improvement. We offer a supportive and inclusive work environment that encourages professional growth and personal development.

Job Location