Staff Global Regulatory GPO in United States at Jobgether

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Staff Global Regulatory GPO in United States.

This role sits at the heart of global regulatory strategy within a leading diagnostics environment, ensuring that products, documentation, and marketing materials meet complex international regulatory requirements. You will define and execute regulatory frameworks that support the full product lifecycle, from registration and labeling to compliance for promotional and scientific content. Working across global, cross-functional teams, you will help standardize processes and strengthen alignment between regulatory affairs, commercial functions, and business units. The position requires a strong ability to interpret evolving global regulations and translate them into actionable strategies and governance models. You will also contribute to audit readiness, inspection support, and continuous improvement of regulatory systems and tools. This is a high-impact leadership role for a regulatory expert who thrives in a matrixed, global, and highly regulated life sciences environment.

• Develop and execute global regulatory strategies ensuring compliance across product lifecycle management and international markets
• Oversee regulatory requirements for product labeling, ensuring accuracy, consistency, and adherence to global standards
• Manage regulatory review and approval processes for marketing, advertising, training, and scientific materials
• Maintain and optimize regulatory systems, tools, and workflows supporting lifecycle and compliance activities
• Interpret and assess global regulations, evaluating their impact on products, processes, and business operations
• Support internal and external audits, inspections, and compliance reviews across global regions
• Collaborate with Business Unit and Commercial Regulatory Affairs teams to align processes and share best practices
• Prepare regulatory documentation, assessments, and stakeholder-ready presentations to support decision-making
• Drive cross-functional initiatives to improve regulatory efficiency, standardization, and governance

• Bachelor’s degree with 9+ years, Master’s degree with 7+ years, or Doctoral degree with 4+ years in life sciences, biomedical engineering, chemistry, or related field
• Extensive experience in regulatory affairs, ideally within in-vitro diagnostics, medical devices, or other highly regulated industries
• Strong ability to interpret global regulatory frameworks and apply them to product and business operations
• Experience managing labeling, product registration, and regulatory lifecycle processes
• Excellent written and verbal communication skills with ability to simplify complex regulatory concepts
• Strong presentation and stakeholder management skills across global, cross-functional teams
• Proficiency in Microsoft Office tools and regulatory documentation systems
• Experience working in matrixed and multicultural environments
• Strong analytical thinking, attention to detail, and ability to manage complex regulatory challenges
• Ability to influence, drive alignment, and support decision-making in dynamic environments

• Competitive annual salary range of $140,000–$170,000 depending on experience
• Performance-based bonus and incentive eligibility
• Comprehensive medical, dental, and vision insurance coverage
• 401(k) retirement savings plan
• Paid time off and holiday benefits
• Flexible remote work arrangement (with occasional travel requirements)
• Career development opportunities within a global life sciences organization
• Inclusive and innovation-driven work culture focused on impact and continuous improvement.