Global Regulatory and Compliance In Semester Graduate Intern

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences diagnostics and biotechnology

At Cytiva one of Danahers 15 operating companies our work saves livesand were all united by a shared commitment to innovate for tangible impact.

Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement you help turn ideas into impact innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines new medicines and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us working on challenges that truly matter with people that care for each other our customers and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

The Global Regulatory and Compliance Graduate Intern is responsible to evaluate development of regulatory frameworks collaborate with interdisciplinary team to develop standard work and contribute to development projects under mentorship. At Cytiva our vision is to advance future therapeutics from discovery to delivery.

This position is part of the Global Regulatory Compliance team located in Marlborough MA and will be onsite with possibility of hybrid. Must have reliable transportation to and from site. This role is Part Time during the semester asking for 15-20 hours per week. Start date is scheduled for November/December 2025 going through end of May 2026.

Hourly Rate: $25-30 per hour with possibility of scheduling your own hours

What you will do:

• Evaluate the development of regulatory frameworks and regulatory initiatives in health and life sciences particularly as related to cell and gene therapy as well as other regenerative medicines to evaluate the impact of regulation on complex biologics development.
• Collaborate with our interdisciplinary team to generate standard operating procedures and templates related to regulatory document preparation and submission.
• Contribute to existing or new product development projects from regulatory perspective under mentorship.

Who you are:

• Currently Enrolled in a Masters or Graduate program related to Regulatory Affairs in drug and/or medical device Biopharma Engineering or Biopharma Statistics.
• Experience from FIELD/TASK/SYSTEM is an advantage
• Comfortable working with MS Office tools
• Full professional fluency in English
• Exceptional interpersonal verbal communication and writing skills
• Strong quantitative analytical problem solving and conceptual skills
• Accomplishment of teamwork adaptability innovation and integrity

At Cytiva we believe in designing a better more sustainable workforce. We recognize the benefits of flexible remote working arrangements for eligible roles and are committed to providing enriching careers no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.

Join our winning team today. Together well accelerate the real-life impact of tomorrows science and technology. We partner with customers across the globe to help them solve their most complex challenges architecting solutions that bring the power of science to life.

For more information visit .

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race color national origin religion sex age marital status disability veteran status sexual orientation gender identity or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process to perform essential job functions and/or to receive other benefits and privileges of employment please contact:1- or .