Regulatory Affairs Intern at Werfen North America | Life Sciences | Earn Upto $30/hr | Apply Now
Securing a Regulatory Affairs Intern position at Werfen is an elite entry point for students looking to influence the safety and efficacy of medical diagnostics on a global scale. Based in the innovation hub of Bedford, MA, this Life Sciences Job offers more than just a typical internship; it provides a front-row seat to the complex regulatory pathways that bring life-saving diagnostic assays from the lab to the hospital bedside. If you are searching for high-impact Jobs in USA that blend technical engineering with legal strategy, Werfen’s 2026 program is designed to turn your academic potential into professional leadership.
- Job Position: Regulatory Affairs Intern
- Location: Bedford, MA
About the Company
Werfen is a family-owned, innovative giant founded in 1966 in Barcelona, Spain. Today, it is a worldwide leader in specialized diagnostics, with a workforce of over 7,000 employees and an annual revenue of approximately $2 billion. Werfen dominates the markets for Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant medicine. Operating directly in 30 countries and over 100 territories, Werfen ensures that healthcare professionals have the tools to improve hospital efficiency and patient care worldwide. The company’s success is built on a relentless dedication to innovation and quality, making a Regulatory Affairs Intern a vital part of their operational integrity.
Key Responsibilities Of a Regulatory Affairs Intern
In this Regulatory Affairs Intern role, you will act as the bridge between engineering innovation and health authority compliance. You won’t just be observing; you will be executing “hands-on” professional tasks that define the success of new product launches.
Regulatory Documentation and Submission Support
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Health Authority Filings: Assist in compiling critical documentation for FDA 510(k) submissions in the U.S. and IVDR Technical Files in Europe.
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Change Orders: Create and manage Change Orders to update regulatory documentation and Standard Operating Procedures (SOPs) as diagnostic technologies evolve.
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Database Management: Support the organization and maintenance of regulatory files within Werfen’s electronic Regulatory Affairs Database to ensure “audit-ready” compliance.
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Quality Assurance: Adhere to the company’s quality system requirements, ensuring all projects meet strict federal and state guidelines.
Candidate Profile: Qualifications for this Life Sciences Job
Werfen is looking for high-achieving students who can combine analytical strength with creative problem-solving abilities.
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Education: Currently enrolled in a Bachelor’s or Graduate degree program. Ideal majors include Regulatory Affairs and Life Sciences or Engineering.
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Experience Level: Candidates should have at least two college semesters completed and a proven track record of academic excellence.
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Key Attributes:
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Multitasking: The ability to handle multiple priorities and assignments simultaneously in a fast-paced environment.
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Technical Proficiency: Strong skills in Microsoft Office (Excel, Word, and PowerPoint).
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Interpersonal Skills: Excellent communication skills to collaborate with cross-functional teams in Bedford and beyond.
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Compensation and Career Growth For Regulatory Affairs Intern
Werfen values the leadership potential of its interns and offers a competitive package to support your professional development.
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Hourly Range: $22/hr to $30/hr, depending on your relevant experience and academic grade level.
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Hands-on Mentorship: This Regulatory Affairs Intern role is designed to provide meaningful experience that sets the foundation for a long-term Life Sciences Job career.
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Location: Bedford, MA is a premier location for Jobs in USA within the biotech and medical device sectors, offering a vibrant community for young professionals.
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Diversity and Inclusion: Werfen is an Equal Opportunity employer committed to a diverse workplace, strictly prohibiting discrimination and fostering an environment where every unique background is valued.
In summary, a Regulatory Affairs Intern position at Werfen is one of the most comprehensive ways to launch a career in the medical device industry. By joining a company with $2 billion in annual revenue and a focus on specialized diagnostics, you gain exposure to international regulatory standards that are highly sought after in the global market. This Life Sciences Job in Bedford, MA, offers the perfect blend of technical challenge and professional reward, ensuring that you are not just building a resume, but building the future of patient care. Among Jobs in USA, Werfen stands out as a place where you are constantly learning and being challenged on a daily basis.
