Jobs in Lowell | Careers in Government

26Jobs found

Direct Hire SR Manager Regulatory Affairs
- Lowell, Massachusetts
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Pilot
- Lowell, Indiana
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$144718.046875
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Experienced Customs and Border Protection Officer – Sign-On and Retention Incentives ($60K)
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Information Systems Technician
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- Lowell, Arkansas
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$
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- Administration and Management
Pilot
- Lowell, Indiana
- U.S. Navy
$
- Full Time
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Pilot
- Lowell, Michigan
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$
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Licensed Professional Counselor (Virtual)
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FEATURED JOBS

Featured Employers

Direct Hire SR Manager Regulatory Affairs
- Lowell, Massachusetts 01852 United States
- Adecco
- Jun 05, 2026
- Full Time
Adecco

Government jobs offer stability, competitive benefits, and the chance to make a meaningful impact on your community and country. Whether you’re starting your career or seeking new opportunities, these roles provide pathways for growth, security, and service. Explore positions across a wide range of fields and take the first step toward a rewarding future in public service.
Read more ›
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Job Details
- Full Time
- Jun 05, 2026
Job Description
Senior Manager Regulatory Affairs Salary Range: $128,000 - $145,000 + 15% bonus Hybrid (3 days a week) Full benefits, Medical, Dental, Vision, 401k - 4% match, Flex PTO

Position Summary:
The Senior manager, Regulatory Affairs is responsible for developing and executing regulatory strategies for assigned product portfolios and projects across North America (US and Canada). This role leads the planning, preparation, and submission of regulatory filings (e.g., Pre-Submissions, 510(k)s, PMAs, PMA Annual Reports, IDEs, and License Applications) and serves as a key regulatory partner to cross-functional teams.

The Senior Manager provides strategic regulatory guidance to support product development, commercialization, and lifecycle management while ensuring compliance with FDA and Health Canada requirements. This role collaborates closely with global regulatory counterparts within the Company's Group and may supervise regulatory staff and/or lead complex regulatory projects.

Job Responsibilities:
This position is responsible for, but not limited to, the following:
Develop and execute regulatory strategies for assigned products and projects in alignment with North America and global regulatory objectives
Lead the planning, preparation, and submission of regulatory submissions (e.g., Pre-Submissions, 510(k)s, PMAs, IDEs, and Health Canada License Applications) to support product approvals and lifecycle management
Serve as the NAM regulatory representative on cross-functional project teams, providing guidance on regulatory requirements, risks, and timelines
Lead interactions with FDA and Health Canada reviewers for assigned submissions, including responding to questions and managing communications in alignment with leadership
Assess the regulatory impact of product changes and define appropriate regulatory pathways and documentation strategies
Review and approve regulatory documentation, including submissions, Memos-to-File, labeling, and promotional materials to ensure compliance with applicable regulations
Partner with global regulatory teams to ensure alignment on regulatory strategies, submissions, and change management activities
Monitor evolving regulatory requirements, guidance documents, and industry trends to inform regulatory strategy and maintain compliance
Contribute to regulatory intelligence activities, including competitive landscape assessments and interpretation of new regulations and standards
Support regulatory operations activities as needed, including establishment registrations, device listings, and import/export compliance
Manage the regulatory release of new products and address any regulatory import/export issues.
Ensure regulatory deliverables are completed in accordance with project timelines and quality expectations
Identify risks and proactively propose mitigation strategies to support successful regulatory outcomes
Monitor for and lead opportunities with FDA and Health Canada to participate in relevant pilot programs and Experiential Learning Programs.
May represent Regulatory Affairs in internal audits and support external inspections as needed
Mentor junior regulatory staff and contribute to building regulatory capabilities within the organization
Develop and monitor appropriate metrics to track regulatory and process improvement.
Develop and deliver training regarding NAM Regulatory Affairs activities for Company Group globally and support cross-country projects as needed.
Other duties as assigned.
Management Responsibilities:
This position manages the following positions on a daily basis.
Direct: 1 to 3 Regulatory Affairs Specialists
Physical Attributes:
General office environment. May sit for extended periods of time.
Physically able to bend, crouch and reach continuously while performing required job tasks.
Utilize dexterity abilities to perform typing, operate a computer and other office equipment, to perform filing, and related job responsibilities and attention to detail competence.
Physically able to spend significant time reading both on paper and on a computer.
Travel less than 5% both domestically and internationally.
Minimum Qualifications:
Bachelor's Degree in a scientific, engineering, or related discipline.
7-10 years of experience in a medical technology company with regulatory, quality, or clinical experience.
5+ years of people management or demonstrated team leadership experience
Preferred Qualifications:
Experience developing regulatory strategies and leading FDA and Health Canada submissions for all device classes
Strong working knowledge of FDA and Health Canada regulation and guidance
Experience negotiating and interfacing with FDA and Health Canada
Strong project management and organizational skills with the ability to manage multiple priorities
Excellent written and verbal presentation skills.
Strong analytical and problem solving skills with a solutions-oriented mindset.
Experience across multiple device types (e.g., capital equipment, consumables, implants, software as a medical device, etc.)
If you meet the above qualifications and would like to apply for this position, please click APPLY NOW and upload your most current resume or you may email your resume to our recruiter, Dee Shider at; Please include "Reg Manager" on the subject line of any e-mail correspondence. Questions regarding this position can be addressed by emailing. Thank you in advance for applying, however, only qualified candidates will be contacted. The Adecco Group is a Fortune Global 500 company and the global leader in Human Resource Solutions. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your Professional Career. For great opportunities near you, go to today! Equal Opportunity Employer/Veterans/Disabled. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit

Pay Details: $128,000.00 to $145,000.00 per year

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
The California Fair Chance Act
Los Angeles City Fair Chance Ordinance
Los Angeles County Fair Chance Ordinance for Employers
San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Senior Manager Regulatory Affairs Salary Range: $128,000 - $145,000 + 15% bonus Hybrid (3 days a week) Full benefits, Medical, Dental, Vision, 401k - 4% match, Flex PTO

Position Summary:
The Senior manager, Regulatory Affairs is responsible for developing and executing regulatory strategies for assigned product portfolios and projects across North America (US and Canada). This role leads the planning, preparation, and submission of regulatory filings (e.g., Pre-Submissions, 510(k)s, PMAs, PMA Annual Reports, IDEs, and License Applications) and serves as a key regulatory partner to cross-functional teams.

The Senior Manager provides strategic regulatory guidance to support product development, commercialization, and lifecycle management while ensuring compliance with FDA and Health Canada requirements. This role collaborates closely with global regulatory counterparts within the Company's Group and may supervise regulatory staff and/or lead complex regulatory projects.

Job Responsibilities:
This position is responsible for, but not limited to, the following:
Develop and execute regulatory strategies for assigned products and projects in alignment with North America and global regulatory objectives
Lead the planning, preparation, and submission of regulatory submissions (e.g., Pre-Submissions, 510(k)s, PMAs, IDEs, and Health Canada License Applications) to support product approvals and lifecycle management
Serve as the NAM regulatory representative on cross-functional project teams, providing guidance on regulatory requirements, risks, and timelines
Lead interactions with FDA and Health Canada reviewers for assigned submissions, including responding to questions and managing communications in alignment with leadership
Assess the regulatory impact of product changes and define appropriate regulatory pathways and documentation strategies
Review and approve regulatory documentation, including submissions, Memos-to-File, labeling, and promotional materials to ensure compliance with applicable regulations
Partner with global regulatory teams to ensure alignment on regulatory strategies, submissions, and change management activities
Monitor evolving regulatory requirements, guidance documents, and industry trends to inform regulatory strategy and maintain compliance
Contribute to regulatory intelligence activities, including competitive landscape assessments and interpretation of new regulations and standards
Support regulatory operations activities as needed, including establishment registrations, device listings, and import/export compliance
Manage the regulatory release of new products and address any regulatory import/export issues.
Ensure regulatory deliverables are completed in accordance with project timelines and quality expectations
Identify risks and proactively propose mitigation strategies to support successful regulatory outcomes
Monitor for and lead opportunities with FDA and Health Canada to participate in relevant pilot programs and Experiential Learning Programs.
May represent Regulatory Affairs in internal audits and support external inspections as needed
Mentor junior regulatory staff and contribute to building regulatory capabilities within the organization
Develop and monitor appropriate metrics to track regulatory and process improvement.
Develop and deliver training regarding NAM Regulatory Affairs activities for Company Group globally and support cross-country projects as needed.
Other duties as assigned.
Management Responsibilities:
This position manages the following positions on a daily basis.
Direct: 1 to 3 Regulatory Affairs Specialists
Physical Attributes:
General office environment. May sit for extended periods of time.
Physically able to bend, crouch and reach continuously while performing required job tasks.
Utilize dexterity abilities to perform typing, operate a computer and other office equipment, to perform filing, and related job responsibilities and attention to detail competence.
Physically able to spend significant time reading both on paper and on a computer.
Travel less than 5% both domestically and internationally.
Minimum Qualifications:
Bachelor's Degree in a scientific, engineering, or related discipline.
7-10 years of experience in a medical technology company with regulatory, quality, or clinical experience.
5+ years of people management or demonstrated team leadership experience
Preferred Qualifications:
Experience developing regulatory strategies and leading FDA and Health Canada submissions for all device classes
Strong working knowledge of FDA and Health Canada regulation and guidance
Experience negotiating and interfacing with FDA and Health Canada
Strong project management and organizational skills with the ability to manage multiple priorities
Excellent written and verbal presentation skills.
Strong analytical and problem solving skills with a solutions-oriented mindset.
Experience across multiple device types (e.g., capital equipment, consumables, implants, software as a medical device, etc.)
If you meet the above qualifications and would like to apply for this position, please click APPLY NOW and upload your most current resume or you may email your resume to our recruiter, Dee Shider at; Please include "Reg Manager" on the subject line of any e-mail correspondence. Questions regarding this position can be addressed by emailing. Thank you in advance for applying, however, only qualified candidates will be contacted. The Adecco Group is a Fortune Global 500 company and the global leader in Human Resource Solutions. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your Professional Career. For great opportunities near you, go to today! Equal Opportunity Employer/Veterans/Disabled. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit

Pay Details: $128,000.00 to $145,000.00 per year

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
The California Fair Chance Act
Los Angeles City Fair Chance Ordinance
Los Angeles County Fair Chance Ordinance for Employers
San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Apply Now View job
Share this job:
Please mention you found this employment opportunity on the CareersInGovernment.com job board.
Adecco

Government jobs offer stability, competitive benefits, and the chance to make a meaningful impact on your community and country.

Whether you’re starting your career or seeking new opportunities, these roles provide pathways for growth, security, and service.

Explore positions across a wide range of fields and take the first step toward a rewarding future in public service.
Adecco
- https://careersingovernment.com/categories/1138/federal-government-jobs/
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Search Jobs In Lowell

26 Jobs in Lowell

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Job Details

Job Description

Adecco

Adecco