Regulatory Affairs Specialist

For immediate consideration, please email resume to-jonukwugha@actalentservices. com to schedule an employment screening!

Job Description

Medtronic is seeking a Regulatory Affairs Specialist to provide contract support for regulatory change assessments related to U.S. FDA and EU MDR requirements. This role will focus on evaluating manufacturing and design changes, preparing regulatory submission documentation, and supporting global regulatory strategies throughout active development and production programs. The specialist will work cross‑functionally with engineering, manufacturing, and quality teams while serving as a key regulatory resource onsite. Experience with medical device regulatory submissions, change assessments, and FDA/EU compliance is required.

Day-to-Day: Work with Manufacturing/Engineering to process changes to machining, capital equipment, and tooling. Ensuring these changes align with US FDA & EU MDR regulatory standards.

Skills

Engineering Changes, regulatory reporting, change order, medical device, US FDA, EU MDR, manufacturing process

Top Skills Details

Engineering Changes,regulatory reporting,change order,medical device

Additional Skills & Qualifications

Experience with ISO 11607‑1 and ISO 11607‑2, including packaging system design and process validation for terminally sterilized medical devices

Familiarity with packaging standards such as ASTM and ISTA

Working knowledge of FDA 21 CFR Part 820 and general Quality System Regulation requirements

Prior experience interfacing with Notified Bodies on EU MDR change notifications

Experience supporting cross‑functional teams during design or manufacturing changes in a regulated medical device environment

Experience Level

3-5 years of experience in the medical device industry preferred

This is a Contract position based out of North Haven, CT.

The pay range for this position is $35.00 - $50.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in North Haven,CT.

This position is anticipated to close on Apr 15, 2026.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

About Actalent

Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000 extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Salary : $35 - $50