Company 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:
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:
Skills & Knowledge
Essential:
Essential:
Additional Information
Why SGS?
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.
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 /
- Undertake personal professional development and ensure appropriate training records are
- Provide technical support to all parts of the business,
- Maintain a full knowledge and understanding of SGS procedures, regulations, guidance
- Support the development and maintenance of combined scheme documents.
Skills & Knowledge
Essential:
- Good working knowledge of quality management systems including CAPA management,
- Detail oriented,
- Strong organisational skills,
- Ability to organise own workload considering priorities set by the global medical device quality
- 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.
- Detailed understanding of global medical device regulations MDR and IVDR, and medical
- Knowledge of accreditation standard ISO 17021-1:2015, ISO 13485, ISO 9001.
Essential:
- Significant work experience in a position with QA responsibility.
- Experience working with medical devices,
- Auditing experience against recognised standards.
- Bachelor’s degree (or higher) in Biomedical Sciences or similar field (e.g., pharmacy, bioengineering, nurse, ...)
- Medical device training on MDD, MDR, IVDR or ISO 13485
- Medical device auditor
- Turnaround time for compliance issues/complaints/ appeals,
- Efficient running of QMS and release of quality management documents.
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.