Quality Assurance Coordinator at SGS
EPC3, , United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

09 Dec, 25

Salary

0.0

Posted On

09 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

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

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

Responsibilities

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.
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