Compliance Specialist – Grant, Sponsoring & Donation Process

Flexsis; Risch-Rotkreuz; On-site; CHF 90,000 - 130,000; Full time

Job summary

Roche Diagnostics in Rotkreuz, Switzerland, seeks a reliable Compliance Specialist to manage the GSD process for grants, sponsorships, and donations. You will oversee the complete lifecycle, ensuring audit-ready documentation and adherence to internal Roche policies and Swiss medtech rules.

You will screen requests, draft agreements (German primarily, some English), coordinate with vendors and internal stakeholders, and support due diligence.

Qualifications

• Bachelor’s degree required; Master’s preferred in Law, Compliance, Business Administration, or related field.
• 3–5 years of healthcare compliance or sponsorship management experience.
• Solid knowledge of Swiss Medtech Code and MedTech Europe guidelines.
• Understanding of Swiss healthcare law (TPA/HMG, TPO/VAM) and IVDR familiarity.
• Business fluency in German and English (written and spoken).

Responsibilities

• Manage sponsorship lifecycle from initial approval through archiving for audit trail.
• Screen sponsorship requests and prepare sponsorship/engagement agreements in German and English.
• Evaluate requests against Roche policies and Swiss Medtech Code.
• Set up vendors/creditors and create Purchase Orders.
• Track financial steps through to invoice verification and approvals.
• Serve as main contact for external sponsors and doctors' associations and internal teams.

Skills

Compliance

Stakeholder management

German fluency

English fluency

Attention to detail

Education

Bachelor's degree

Master's degree preferred

Tools

MS Office

Purchase Orders

SOPs

Job description

Flexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting.

For our client Roche Diagnostics in Rotkreuz, we are looking for a reliable and motivated (m/f/d)

Compliance Specialist – Grant, Sponsoring & Donation (GSD) Process

Start Date: 16th December 2026

End Date: 1 year after start

Extension: possible

Workload: 80–100%

• You manage commercial and medical sponsoring activities throughout their entire lifecycle—from initial approval and contract support to gathering, reviewing, and archiving all required documentation (attendee lists, event reports, photos, receipts) to ensure a complete audit trail.
• You screen incoming sponsorship requests and supporting documents (official request letters, detailed agendas, overall event budgets, up-to-date HCP CVs). Review compliance due diligence checks for HCOs and HCPs, and prepare sponsorship and engagement agreements (mostly in German, some in English) using standard templates.
• You evaluate requests against internal Roche policies and the Swiss Medtech Code. Screen for key risk factors (e.g., events held during ski season, purely tourist destinations, inappropriate entertainment or side programs, and gifts to HCPs).
• You set up new vendors/creditors (HCOs, HCPs, event agencies) and create/approve Purchase Orders (POs).
• You track and coordinate financial steps through to invoice verification and approval workflows.
• You act as the key point of contact for external sponsoring requesters and doctors' associations (coordinating event logistics/approvals), as well as internal business owners, event management, marketing, medical affairs, and local/global compliance teams.

• You have a minimum of a Bachelor’s degree (Master’s degree preferred), ideally in Law, Compliance, Business Administration, or a related field, to effectively engage with highly educated stakeholders.
• You have 3–5 years of proven experience in healthcare compliance, ethics compliance, legal operations, or sponsorship management within the Pharma or MedTech industry.
• You bring solid working knowledge of the Swiss Medtech Code (mandatory—legal background alone is not sufficient) and MedTech Europe guidelines.
• You have a good understanding of relevant Swiss healthcare law (e.g., TPA/HMG, TPO/VAM) and basic familiarity with broader regulatory frameworks (such as IVDR).
• You are business fluent in both German and English (written and spoken), as most contracts are in German (with some English contracts for the French-speaking region).
• You have proficiency in MS Office; highly self-driven, flexible, detail-oriented, and pragmatic project/stakeholder manager with strong communication skills.

Nice-to-Haves

• You bring prior experience with internal Roche systems, processes, and compliance policies.
• You have hands-on experience opening/onboarding new suppliers and creating/managing Purchase Orders (POs).
• You have practical experience with disclosing transfers of value under Swiss Medtech and MedTech Europe rules.
• You speak French