The Senior Manager will partnercrossfunctionallywith Quality, Regulatory Affairs, Operations, R&D, ... R&D. * Communicate audit results, risk assessments, and improvement opportunities to senior ...
The Senior Manager will partnercrossfunctionallywith Quality, Regulatory Affairs, Operations, R&D, ... R&D. * Communicate audit results, risk assessments, and improvement opportunities to senior ...
The Senior Manager will partner cross-functionally with Quality, Regulatory Affairs, Operations ... R&D. * Communicate audit results, risk assessments, and improvement opportunities to senior ...
The Senior Manager will partner cross-functionally with Quality, Regulatory Affairs, Operations ... R&D. * Communicate audit results, risk assessments, and improvement opportunities to senior ...
Land Acq & Ent Director-FG
Lakeville, MN · On-site
$120 - $190/hr
The Company's strategic relationship with D.R. Horton, the nation's largest homebuilder ... Manage due diligence process on land acquisition opportunities and meet all entitlement needs ...
Land Acq & Ent Director-FG
Lakeville, MN · On-site
$120 - $190/hr
The Company's strategic relationship with D.R. Horton, the nation's largest homebuilder ... Manage due diligence process on land acquisition opportunities and meet all entitlement needs ...
Senior Manager, R&D
Saint Paul, MN · On-site
The role has direct management responsibilities over R&D engineering functions within Abbott Vascular R&D. This individual will play a role in technical stewardship of Abbott Vascular's product ...
Senior Manager, R&D
Saint Paul, MN · On-site
The role has direct management responsibilities over R&D engineering functions within Abbott Vascular R&D. This individual will play a role in technical stewardship of Abbott Vascular's product ...
The role has direct management responsibilities over R&D engineering functions within Abbott Vascular R&D. This individual will play a role in technical stewardship of Abbott Vascular's product ...
The role has direct management responsibilities over R&D engineering functions within Abbott Vascular R&D. This individual will play a role in technical stewardship of Abbott Vascular's product ...
The role has direct management responsibilities over R&D engineering functions within Abbott Vascular R&D. This individual will play a role in technical stewardship of Abbott Vascular's product ...
The role has direct management responsibilities over R&D engineering functions within Abbott Vascular R&D. This individual will play a role in technical stewardship of Abbott Vascular's product ...
Sales Area Manager
Lakeville, MN · On-site
D.R. Horton, Inc., the largest homebuilder in the U.S. , was founded in 1978 and is a publicly ... The right candidate will manage, train and motivate sales staff in a specific geographic area.
Sales Area Manager
Lakeville, MN · On-site
D.R. Horton, Inc., the largest homebuilder in the U.S. , was founded in 1978 and is a publicly ... The right candidate will manage, train and motivate sales staff in a specific geographic area.
Dairy Product R&D-Fermentation and Biotechnology Emphasis Design, execute, and analyze microbial ... Dairy Management Inc. is proud to be an Equal Employment Opportunity Employer. Qualified applicants ...
Dairy Product R&D-Fermentation and Biotechnology Emphasis Design, execute, and analyze microbial ... Dairy Management Inc. is proud to be an Equal Employment Opportunity Employer. Qualified applicants ...
Dairy Product R&D-Fermentation and Biotechnology Emphasis · Design, execute, and analyze microbial ... Dairy Management Inc.™ is proud to be an Equal Employment Opportunity Employer. Qualified ...
Quick apply
Dairy Product R&D-Fermentation and Biotechnology Emphasis · Design, execute, and analyze microbial ... Dairy Management Inc.™ is proud to be an Equal Employment Opportunity Employer. Qualified ...
Trade Classification Lead
$120K - $204K/yr
KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... This role serves as the primary technical liaison between engineering, product management, supply ...
Trade Classification Lead
$120K - $204K/yr
KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... This role serves as the primary technical liaison between engineering, product management, supply ...
Support product trials, field test programs, and new product introductions in coordination with Technical Services, Sales, Product Management, and R&D. * Provide accurate product recommendations and ...
Quick apply
Support product trials, field test programs, and new product introductions in coordination with Technical Services, Sales, Product Management, and R&D. * Provide accurate product recommendations and ...
Support product trials, field test programs, and new product introductions in coordination with Technical Services, Sales, Product Management, and R&D. * Provide accurate product recommendations and ...
Support product trials, field test programs, and new product introductions in coordination with Technical Services, Sales, Product Management, and R&D. * Provide accurate product recommendations and ...
Trade Classification Lead
$120K - $204K/yr
KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... This role serves as the primary technical liaison between engineering, product management, supply ...
Trade Classification Lead
$120K - $204K/yr
KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... This role serves as the primary technical liaison between engineering, product management, supply ...
Trade Classification Lead
$120K - $204K/yr
KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... This role serves as the primary technical liaison between engineering, product management, supply ...
Trade Classification Lead
$120K - $204K/yr
KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... This role serves as the primary technical liaison between engineering, product management, supply ...
Handle R&D-related legal work, including: * Pre-clinical research agreements * Sponsored research ... Strong drafting, negotiation, and stakeholder management skills Compensation: The estimated total ...
Handle R&D-related legal work, including: * Pre-clinical research agreements * Sponsored research ... Strong drafting, negotiation, and stakeholder management skills Compensation: The estimated total ...
Manager
Roseville, MN · On-site
R.I.D.E. values, Passion, Representing the Brand, Interpersonal Skills, Delivering Results, and ... Prior management experience in a retail environment preferred. * Strong leadership, coaching, and ...
Manager
Roseville, MN · On-site
R.I.D.E. values, Passion, Representing the Brand, Interpersonal Skills, Delivering Results, and ... Prior management experience in a retail environment preferred. * Strong leadership, coaching, and ...
R.I.D.E. values, Passion, Representing the Brand, Interpersonal Skills, Delivering Results, and ... Prior management experience in a retail environment preferred. * Strong leadership, coaching, and ...
R.I.D.E. values, Passion, Representing the Brand, Interpersonal Skills, Delivering Results, and ... Prior management experience in a retail environment preferred. * Strong leadership, coaching, and ...
Manager R D information
See Saint Paul, MN salary details
$23.3K - $30.6K
4% of jobs
$30.6K - $37.9K
10% of jobs
$43.8K is the 25th percentile. Wages below this are outliers.
$37.9K - $45.2K
14% of jobs
$45.2K - $52.5K
16% of jobs
The median wage is $58.8K / yr.
$52.5K - $59.8K
7% of jobs
$59.8K - $67.1K
10% of jobs
$70.8K is the 75th percentile. Wages above this are outliers.
$67.1K - $74.4K
29% of jobs
$74.4K - $81.7K
4% of jobs
$81.7K - $89K
3% of jobs
$89K - $96.4K
1% of jobs
$96.4K - $103.7K
2% of jobs
$23.3K
$62K
$103.7K
How much do manager r&d jobs pay per year?
Is research and development stressful as a career?
What are the key skills and qualifications needed to thrive as a Manager R&D, and why are they important?
Is a manager R&D a good job?
What is the difference between Manager R&D vs R&D Engineer?
| Aspect | Manager R&D | R&D Engineer |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Engineering, Management experience | Bachelor's or Master's in Engineering or related field |
| Work Environment | Leads teams, oversees projects, strategic planning | Designs, develops, tests products or processes |
| Employer & Industry Usage | Common in tech, manufacturing, pharmaceuticals | Found across similar industries, often in product development |
The main difference is that a Manager R&D oversees research teams and strategic projects, while an R&D Engineer focuses on technical development and product design. Managers handle leadership and planning, whereas Engineers execute technical tasks within projects.
How much do research and development managers make in the US?
What are some common challenges faced by a Manager R&D when leading cross-functional innovation projects?
What is a Manager R&D?
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The top searched job categories for Manager R&D jobs in Saint Paul, MN are:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 8 days ago
Medtronic rating
7.9
Based on 176 frontline employees who took The Breakroom Quiz
161st of 540 rated manufacturers
Job description
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the LifeBusiness Group: Global Quality / Enterprise Quality
Location: Flexible (U.S. or Global Medtronic Location)
The Senior Manager, Compliance & Internal Auditis responsible forleading and advancing Medtronic's globalinternalaudit program to ensure compliance with applicable regulatory requirements and quality management standards. This role provides strategic leadership for internal audits aligned with the Medical Device Single Audit Program (MDSAP), FDA Quality Management System Regulation (QMSR), ISO 13485, and other applicable global regulatory frameworks.
The Senior Manager will partnercrossfunctionallywith Quality, Regulatory Affairs, Operations, R&D, and functional leadership to assess enterprise compliance,identifysystemic risks, and strengthen the effectiveness of the Medtronic Quality Management System. This role plays a keypartin driving inspection readiness and supporting continuous improvement across the enterprise.
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
Key Responsibilities
Internal Audit Program Leadership
Lead and manage enterprise internal audit activities aligned with global regulatory requirements including MDSAP, QMSR, and ISO 13485.
Develop and executeriskbasedauditschedule, auditplans across Medtronic operating units, manufacturing sites, andenterprisefunctions.
Serve as Lead Auditor for complex orhighimpactcompliance audits.
Ensure audits are conductedin accordance withinternal procedures, regulatory expectations, and recognized auditing standards.
Regulatory Compliance & Risk Oversight
Provide subject matterexpertiseon regulatory quality requirements and global compliance expectations.
Evaluate the effectiveness and maturity of quality system processes across the organization.
Identify systemic compliance risks and provide recommendations for mitigation.
Inspection and Audit Readiness
Support enterprise preparation for regulatory inspections and external audits.
Leadand/orparticipateinmock inspections and readiness assessments to strengthen organizational preparedness.
Partner with site leadership to address compliance gaps and ensure sustainable remediation.
Corrective Action & Compliance Monitoring
Review audit findings and ensureappropriate rootcause analysis and corrective actions.
Monitor effectiveness of CAPA activities related tointernalaudit observations.
Track compliance trends and escalate systemic risks to leadership asappropriate.
Stakeholder Engagement
Collaborate with global stakeholders including Quality, Regulatory Affairs, Manufacturing, Supply Chain, and R&D.
Communicate audit results, risk assessments, and improvement opportunities to senior leadershipas per defined intervals andin management reviews.
Provide guidance on interpretation of regulatory requirements and quality system expectations.
Continuous Improvement
Identifyenterprise trends and opportunities for quality system improvement based on audit data.
Enhance audit methodologies, tools, and analytics capabilities.
Contribute to strengthening a proactive culture of compliance and quality.
Leadership & Talent Development
Mentor and develop internal auditors andcrossfunctionalaudit team members.
Provide training and coaching on regulatory audit techniques and compliance practices.
Minimum Qualifications
Bachelor's degree plus 7+ years of experience in quality, regulatory affairs, compliance, or related functions in the medical device or regulated healthcare industry.
Minimum3years of experience conducting or managing internal or regulatory audits.
Minimum 5 years ofmanagerialexperience
Demonstratedexpertisein:
MDSAP audit model
FDA QMSR / 21 CFR Part 820 transition to ISO 13485
ISO 13485 Quality Management Systems
Certified Lead Auditor or equivalent auditing certification.
Experience interacting with regulatory agencies or supporting regulatory inspections.
Preferred Qualifications
Bachelor's degree in engineering, Life Sciences, Quality, Regulatory Affairs, or related field.Advanced degree (MS, MBA, or related field).
Experience with global regulatory frameworks including EU MDR, Health Canada, PMDA, TGA, and ANVISA.
MDSAP auditing experience.
ASQ certifications (CQA, CQE, or equivalent).
Experience leadingenterpriselevelcompliance or audit programs.
Leadership Competencies (Medtronic Leadership Expectations)
Strategic mindset with the ability to assessenterpriselevelcompliance risks.
Strong stakeholder engagement and influencing skills across global organizations.
Ability to translate regulatory requirements into practical operational improvements.
Datadrivendecision making and risk management.
Commitment to developing talent and building strong audit capabilities.
Travel Requirements
Ability to traveldomestically andinternationally up to10-20% to Medtronic sites.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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