Senior Medical Device Documentation Coordinator

SGS UK Ltd; West Midlands; Presencial; GBP 30 000 - 36 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Bonus program

Private medical cover

Pension & Life Assurance

Generous annual leave

Birthday day off

Retailer discounts

Parental leave pay

Christmas vouchers

Wellbeing initiatives

Gym membership

Resumo da oferta

SGS UK Ltd is seeking a Senior Technical Medical Device Coordinator for the Birmingham area. This permanent, office-based role runs Monday to Friday 8.30am–5pm with a salary up to £33,000 per year.

You will oversee Technical Documentation reviews, assist with complaints, and support key clients through calls and meetings. The ideal candidate will have practical experience with Medical Device Regulations or Auditing Regulations, plus strong MS Office skills and documented control experience.

Qualificações

• Experience with Medical Device Regulations or Auditing Regulations.
• Proven experience working in an office environment.
• High level of computer literacy in MS Office and databases.
• Minimum NVQ 3 in Customer Service and/or Administration.
• Experience producing professional written communications.

Responsabilidades

• Manage processes related to Technical Documentation (TD) reviews.
• Assist with management of complaints.
• Support client calls and meetings to strengthen relationships with Key Clients.
• Raise purchase orders for invoicing clients.

Conhecimentos

Medical device regs

Auditing regs

Technical documentation

Office experience

Written communications

Formação académica

NVQ 3 in Customer Service/Administration

Ferramentas

MS Office Suite

Databases

PowerPoint

Teams

Descrição da oferta de emprego

SGS UK Ltd is seeking a Senior Technical Medical Device Coordinator for the Birmingham area. This permanent, office-based role runs Monday to Friday 8.30am–5pm with a salary up to £33,000 per year.

You will oversee Technical Documentation reviews, assist with complaints, and support key clients through calls and meetings. The ideal candidate will have practical experience with Medical Device Regulations or Auditing Regulations, plus strong MS Office skills and documented control experience.