This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
We are looking for a skilled Sr Compliance Specialist to join our team in Mounds View, Minnesota. In this contract position, you will play a vital role in ensuring adherence to compliance standards and regulatory requirements within the organization. If you are passionate about quality management and have a strong background in compliance, this is an excellent opportunity to contribute to impactful projects.
Job Responsibility:
Develop and implement compliance strategies to ensure organizational adherence to internal and external regulations
Monitor quality management systems to identify and address any gaps or inefficiencies
Collaborate with cross-functional teams to manage cost centers and oversee financial aspects of compliance-related initiatives
Conduct detailed analyses related to capital management and expense accounts to support project goals
Ensure accurate documentation and reporting of compliance activities and findings
Serve as a point of contact for compliance audits and field actions, providing necessary information and support
Assist in the development and execution of compliance-related training programs
Drive improvements in compliance processes by evaluating current practices and recommending enhancements
Support the PMO team in aligning compliance efforts with organizational objectives
Stay updated on industry trends and regulations to proactively address potential compliance challenge
Requirements:
Bachelors Degree in a relevant field (Life Sciences, Engineering, Business, or similar)
Minimum 4 years’ experience in the medical device or pharmaceutical industry
Strong knowledge of regulatory standards and compliance processes
Proficiency in managing financial aspects such as cost centers and expense accounts
Familiarity with tools and methodologies such as R Code and PMO frameworks
Direct experience managing or supporting Field Corrective Actions (FCA), recalls, or similar post-market activities
Experience supporting audits (internal, external, or regulatory)
In-depth knowledge of industry regulations (FDA, EU MDR, ISO standards)
Advanced proficiency in documentation and tracking tools (e.g., SharePoint, Smartsheet, Excel)