Compliance Administrative Assistant

Posted 7 Days Ago
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Plan-Les-Ouates, Genève, CHE
In-Office
Mid level
3D Printing • Healthtech • Robotics • Manufacturing
The Role
Provides administrative support to Legal and Compliance operations within a regulated medical device company. Responsibilities include managing contracts and third-party information, preparing transparency reports and regulatory filings, maintaining compliance records, managing shared mailboxes, organizing meetings, and drafting minutes. The role requires strong organization, attention to detail, confidentiality, French and English fluency, Microsoft Office proficiency, and preferably experience with CLM systems and regulated healthcare industries.
Summary Generated by Built In

Are you passionate about maintaining the highest standards of compliance and administrative excellence?
Do you want to join an innovative medical device company where you will play a key role in supporting regulatory processes, ensuring documentation accuracy, and upholding our commitment to integrity?


                                                                           If yes, come to join our legal team!

                                                                            As Compliance Administrative Assistant

You will provide administrative support to the Legal & Compliance department in all activities related to interactions with Healthcare Professionals (HCPs), including contracts, transparency reporting, and other compliance-related requirements.


Your main responsibilities will be:


Contract management

  • Prepare, track, and archive contracts, including consultant agreements, Non-Disclosure Agreements (NDAs), sponsorships, hospitality agreements, grants, and other related documents.
  • Review supporting documentation for completeness and accuracy prior to approval.
  • Follow up on contract execution and signature processes.

Transparency and compliance

  • Prepare and submit regulatory disclosures and filings (CNOM, EPS, MDEON, Transparency reporting, etc.).
  • Collect and maintain information required to meet transparency reporting obligations.
  • Monitor and track compliance-related files to ensure completeness and timely processing.

Systems Management

  • Enter, update, and maintain contract and Third-Party information within the Contract Lifecycle Management (CLM) system.

Administrative Support

  • Manage the Legal & Compliance and Grants shared mailboxes.
  • Organize meetings, take meeting notes, and draft meeting minutes.
  • Provide general administrative support to the Compliance team.

Your profile:

  • 2 to 5 years of experience in an administrative support role, preferably within the medical device, pharmaceutical, healthcare, or other regulated industries.
  • Advanced proficiency in Microsoft Office applications;
  • Experience with a Contract Lifecycle Management (CLM) system is highly desirable.
  • Fluent in French and English, with excellent written and verbal communication skills.
  • Proficiency in one or more additional European languages is a plus.
  • Excellent organizational and follow-up skills.
  • Strong attention to detail and commitment to accuracy.
  • Proactive mindset and ability to adapt to changing priorities.
  • Reliable and able to manage responsibilities effectively.
  • Professional discretion and strong respect for confidentiality.
  • Ability to work independently as well as collaboratively within a team.

Skills Required

  • 2 to 5 years of experience in an administrative support role
  • Experience in the medical device, pharmaceutical, healthcare, or another regulated industry
  • Advanced proficiency in Microsoft Office applications
  • Experience with a Contract Lifecycle Management system
  • Fluency in French and English
  • Excellent written and verbal communication skills
  • Excellent organizational and follow-up skills
  • Strong attention to detail and commitment to accuracy
  • Proactive mindset and ability to adapt to changing priorities
  • Professional discretion and respect for confidentiality
  • Ability to work independently and collaboratively within a team
  • Proficiency in one or more additional European languages
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The Company
370 Employees
Year Founded: 2005

What We Do

Spineart is a privately held Swiss medical device company dedicated to accelerating technology adoption and elevating the standard of spinal care. As a global leader in spine surgery, the company provides innovative, patented, and clinically validated technologies in minimally invasive surgery, motion preservation, 3D-printed implants, and robotic guidance, supporting surgeons and hospitals in over 60 countries to improve patient outcomes worldwide.

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