Regulatory Affairs Lead
Company: Experis
Location: South Saint Paul
Posted on: January 8, 2026
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Job Description:
Our client, a leading organization in the medical device and
pharmaceutical industry, is seeking a Regulatory Affairs Lead to
join their team. As a Regulatory Affairs Lead, you will be part of
the Laboratory / Technical Family supporting regulatory and
environmental compliance initiatives. The ideal candidate will have
strong analytical skills, excellent communication abilities, and a
proactive approach, which will align successfully in the
organization. Job Title: Regulatory Affairs Lead Location:
Maplewood, MN Duration: 3 months (Potential to extend) What's the
Job? Lead regulatory and environmental compliance activities within
the organization, ensuring adherence to applicable regulations and
standards. Support the development and implementation of regulatory
strategies for product approvals and post-market changes.
Coordinate and conduct global regulatory change assessments and
manage associated activities for assigned products. Assist in risk
management activities, vigilance reporting, and other quality
initiatives with minimal oversight. Communicate technical results
effectively to cross-functional teams through reports,
presentations, and documentation. What's Needed? Bachelor’s Degree
in a scientific discipline such as Chemistry or Chemical
Engineering. Minimum of five (5) years of experience in regulatory
affairs within the pharmaceutical or medical device industry,
including experience with combination medical devices. Experience
authoring regulatory submissions, technical documentation, and
regulatory strategies. Proficiency in regulatory support for wound
dressings, surgical products, or related medical devices. Strong
organizational skills, stakeholder management, and proficiency in
Office Suite and Regulatory Management Software. What's in it for
me? Opportunity to work with a diverse and innovative global team.
Engage in impactful projects that influence regulatory strategies
and product development. Develop your professional skills in a
dynamic environment. Be part of a company committed to compliance
and quality excellence. Remote work flexibility within the United
States. Upon completion of waiting period consultants are eligible
for: Medical and Prescription Drug Plans Dental Plan Vision Plan
Health Savings Account Health Flexible Spending Account Dependent
Care Flexible Spending Account Supplemental Life Insurance Short
Term and Long Term Disability Insurance Business Travel Insurance
401(k), Plus Match Weekly Pay If this is a role that interests you
and you'd like to learn more, click apply now and a recruiter will
be in touch with you to discuss this great opportunity. We look
forward to speaking with you! About ManpowerGroup, Parent Company
of: Manpower, Experis, Talent Solutions, and Jefferson Wells.
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions
company, helps organizations transform in a fast-changing world of
work by sourcing, assessing, developing, and managing the talent
that enables them to win. We develop innovative solutions for
hundreds of thousands of organizations every year, providing them
with skilled talent while finding meaningful, sustainable
employment for millions of people across a wide range of industries
and skills. Our expert family of brands – Manpower, Experis, Talent
Solutions, and Jefferson Wells – creates substantial value for
candidates and clients across more than 75 countries and
territories and has done so for over 70 years. We are recognized
consistently for our diversity - as a best place to work for Women,
Inclusion, Equality and Disability and in 2023 ManpowerGroup was
named one of the World's Most Ethical Companies for the 14th year -
all confirming our position as the brand of choice for in-demand
talent.
Keywords: Experis, Minneapolis , Regulatory Affairs Lead, Science, Research & Development , South Saint Paul, Minnesota
