Skip to main content
QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
    • GP-001 Documents and records control
    • GP-002 Quality planning
    • GP-003 Audits
    • GP-004 Vigilance system
    • GP-005 HR and training
      • Deprecated
        • JD-001 General Manager 2022_001
        • JD-002 Sales Manager 2022_001
        • JD-003 Design & Development Manager 2022_001
        • JD-004 Quality Manager and Person Responsible for Regulatory Compliance (PRRC) 2022_001
        • JD-005 Technical Manager & Person Responsible for Regulatory Compliance (PRRC) 2022_001
        • JD-006 HR Manager 2022_001
        • R-005-001 Training plan 2022_001
        • R-005-003 Training plan 2023_001
        • R-005-003 Training plan 2024_001
        • R-005-003 Training plan 2024
      • R-005-003 Training plan 2025
      • Product development hiring schedule
      • R-005-006 GDPR training
    • GP-007 Post-market surveillance
    • GP-009 Sales
    • GP-010 Suppliers
    • GP-012 Design, Redesign and Development
    • GP-018 Infrastructure and facilities
    • GP-019 Software validation
    • GP-023 Change control management
    • GP-050 Data Protection
    • GP-051 Security violations
    • GP-052 Data Privacy Impact Assessment (DPIA)
    • GP-200 Remote Data Acquisition in Clinical Investigations
  • TF_Legit.Health_Plus
  • Licenses and accreditations
  • External documentation
  • Records
  • Records
  • GP-005 HR and training
  • Deprecated
  • JD-003 Design & Development Manager 2022_001

JD-003 Design & Development Manager 2022_001

Education​

Bachelor's degree in engineering or equivalent.

Experience​

>=2 years

Skills​

  • Knowledge of artificial intelligence applications in the healthcare sector.
  • Communicative, organised, resolute and goal oriented.

Responsibilities​

  • To coordinate the product design and development processes.
  • To manage the product technical aspects with suppliers and subcontractors.
  • To support the monitoring of the medical device during its entire life cycle.
  • To verify that the developed products meet the requirements of the applicable regulations.
  • To prepare the design and development documentation.
  • To provide the COO with all the information required for the drafting of the medical device technical documentation.
  • To support the maintenance of the risk management report.
  • To notify the JD-004 Quality Manager or the JD-005 Technical Manager & Person Responsible for Regulatory Compliance (PRRC) of any non-conformity, deviation, need or abnormality.
  • To request training from the Quality Manager and attend said training.
  • To notify the existence of non-conforming products or materials to the JD-004 Quality Manager for their correct identification, documentation, segregation, evaluation and control.
Approved byAccepted by

E-Signature (Appfire integration):

Signature logo

Andy Aguilar

077475E323E2B048966060431C67F749

Signer name: Andy Aguilar

Signing time: Sun, 11 Sep 2022 14:01:42 GMT

Reason: Approved

E-Signature (Appfire integration):

Signature logo

Gerardo Fernandez

0CB46CA5BDE79B7F072BCCDFC99B4CA1

Signer name: Gerardo Fernandez

Signing time: Sun, 11 Sep 2022 14:01:42 GMT

Reason: Accepted

JD-001 General ManagerJD-003 Design & Development Manager
Previous
JD-002 Sales Manager 2022_001
Next
JD-004 Quality Manager and Person Responsible for Regulatory Compliance (PRRC) 2022_001
  • Education
  • Experience
  • Skills
  • Responsibilities
All the information contained in this QMS is confidential. The recipient agrees not to transmit or reproduce the information, neither by himself nor by third parties, through whichever means, without obtaining the prior written permission of Legit.Health (AI LABS GROUP S.L.)