QA/RA Professionals @ HaMaDa - August 2019

18 August 2019
Location: Flexible

Job Description:

HaMaDa, an established and fast growing consulting firm serving the Medical Device & Digital Health industries is looking for consultants at different career levels with experience in Regulatory Affairs, Quality Assurance, Clinical Affairs or Auditing, for a part- or full-time position.

With the objective to help our customers to obtain, maintain or expand market access worldwide, you as a consultant, may build the requested documentation and design dossiers in support of CE marking, FDA submissions including 510(k), PMA, Q-subs, or similar approval processes.

Depending on your background and experience, your activities may also include Strategy Planning, review and/or develop Technical Files, Clinical Evaluations and Quality Management Systems, conduct internal or supplier Audits, deliver QA/RA management, or help improve our customers Quality Processes.

Required Qualifications:

Our Job Requirements

  • Technical or scientific degree (BSc, MSc or PhD)
  • Minimal 5 years working experience in the field of Medical Devices
  • Knowledge of Medical Device Regulations (CE, FDA, PAL, TGA, etc.) and/or Quality Assurance.
  • Communicative and service oriented, supporting a wide variety of clients from small start-ups to larger firms
  • Strong organizational skills, detailed oriented to deal with various projects at the same time.
  • Very good personal skills
  • Fluent in English.
  • Additional languages an advantage
  • Willing to travel abroad
Apply to This Job Here: HaMaDa email