About Dexcom:

Dexcom empowers people to take control of diabetes through innovative continuous glucose monitoring (CGM) systems. Headquartered in San Diego, California, Dexcom has emerged as a leader of diabetes care technology.

We invite you to become a part of a fast growing, purpose driven team in our newly established business centre in Vilnius!

Summary:

This role will support the implementation of Dexcom’s Corporate Compliance Program for EMEA. This includes partnering with business stakeholders on key compliance initiatives, communicating compliance program requirements to employees, and helping to foster Dexcom’s culture of ethics and compliance in the region. In addition, this role offers the opportunity to be involved in all elements of a Compliance Program, including risk assessments, training, monitoring, investigations, and third-party due diligence.

Essential Duties and Responsibilities:

• Assist with managing day to day operations of compliance in the region.
• Assist with the implementation of regional and local policies, guidelines, and procedures.
• Assist with delivering Corporate Compliance training pertaining to the Company’s policies and procedures and applicable laws and regulations, and reporting systems.
• Track the completion status of compliance training modules and liaise with relevant stakeholders to ensure their timely completion.
• Assist with the execution of the annual monitoring plan by supporting the compliance monitoring reviews in key risk areas, for compliance with applicable rules and regulations and compliance program effectiveness for the region.
• Understand and keep up to date with changes to relevant regional and local laws, regulations and codes of conduct and ethics.
• Assist with ensuing operating manuals and procedural documents stay current when regulations change.
• Assist with Compliance system implementation.
• Assist with the EMEA Compliance Sub-Committee and EMEA Grants Committee meetings.

About You:

• Up to 3 years of work experience, including experience in a compliance, legal, auditing or investigation role in life sciences, preferably in the biotechnology, medical device, and/or pharmaceutical industries.
• Have knowledge of healthcare law (fraud and abuse, Anti-Kickback, transparency, etc.) and medical device regulations.
• Have strong customer focus, work ethic and integrity.
• Have experience of working in a fast-paced environment.
• You must have good interpersonal and communication skills and demonstrated ability to work effectively as part of a team, with a positive attitude.
• Be critical thinking with sound judgment and decision-making skills.
• Be self-directed, proactive, motivated, and a fast learner.
• Able to work independently.
• Excellent written and oral communication skills.
• Be able to work confidently within groups in a multinational company and respond to global/cultural sensitivities.
• Communicate effectively in English.
• Have excellent time management.

We offer:

• Opportunity to work in global, innovative, fast-growing company with 7,000+ awesome colleagues.
• Flexible work.
• 5 additional vacation days.
• Health, Life and Accident insurance.
• Health and Wellness programs.
• Private Pension plan.
• Access to the best-in-class training and development programmes.
• Team buildings and events.
• Competitive salary and additional bonuses.

Monthly base salary for this position is from 2,452 EUR gross.
*The final offer will depend on your qualifications, competencies, and professional experience

Sounds like you? Apply!