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  • Quality Manual
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    • GP-001 Documents and records control
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    • 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
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      • 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
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    • GP-200 Remote Data Acquisition in Clinical Investigations
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  • Deprecated
  • JD-002 Sales Manager 2022_001

JD-002 Sales Manager 2022_001

Education​

University degree: Bachelor's degree in engineering or equivalent.

Experience​

>=2 years

Skills​

  • Sales and marketing management.
  • Social media.
  • Knowledge of medical device and/or healthcare sector.
  • Communicative, proactive, organised and engaged.

Responsibilities​

  • To manage the communication and marketing plan of the company.
  • To manage the sales and sales plan of the company.
  • To contact customers, evaluate and study the product needs.
  • To elaborate offers to clients.
  • To supervise the sale conditions to clients.
  • Customer support.
  • To evaluate customer satisfaction.
  • To obtain new clients and fields of action.
  • To supervise commercial forecasts and participate in their preparation.
  • To propose new markets.
  • To manage social media and corporate communications.
  • To represent the company in congresses and events.
  • To create the necessary documents for the correct communication and advertising of the company.
  • 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 JD-004 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

Taig Mac Carthy

446B9ECEF0B3DBCFAA27A2618D6C4DD8

Signer name: Taig Mac Carthy

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

Reason: Accepted

JD-001 General ManagerJD-004 Quality Manager
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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.)