The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work ...
The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work ...
The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work ...
The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work ...
Senior Quality Analyst - FDA Regulated Manufacturing
Rochester, MN · On-site
$85K - $128K/yr
Responsibilities The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst ...
Senior Quality Analyst - FDA Regulated Manufacturing
Rochester, MN · On-site
$85K - $128K/yr
Responsibilities The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst ...
The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work ...
The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work ...
The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst directs the work to ...
The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst directs the work to ...
Quality Analyst - FDA Regulated Manufacturing
Rochester, MN · On-site
$78K - $117K/yr
Responsibilities The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst ...
Quality Analyst - FDA Regulated Manufacturing
Rochester, MN · On-site
$78K - $117K/yr
Responsibilities The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst ...
The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst directs the work to ...
The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst directs the work to ...
The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst directs the work to ...
The Quality Analyst, FDA Regulated Manufacturing is responsible for implementation of quality and regulatory compliance for product manufacturing activities. The Quality Analyst directs the work to ...
Are you an experienced Wastewater Operator or looking for a new career? PeopleService is hiring in the Litchfield, MN area! Our First District Association location has a newly built ...
Are you an experienced Wastewater Operator or looking for a new career? PeopleService is hiring in the Litchfield, MN area! Our First District Association location has a newly built ...
Wastewater Operator/Maintenance Tech - FDA
Litchfield, MN · On-site
$20 - $30/hr
Description Are you an experienced Wastewater Operator or looking for a new career? PeopleService is hiring in the Litchfield, MN area! Our First District Association location has a newly built ...
Wastewater Operator/Maintenance Tech - FDA
Litchfield, MN · On-site
$20 - $30/hr
Description Are you an experienced Wastewater Operator or looking for a new career? PeopleService is hiring in the Litchfield, MN area! Our First District Association location has a newly built ...
Principal Regulatory Affairs Specialist
Eden Prairie, MN · On-site
$120K - $135K/yr
FDA medical device regulations, FDA guidance documents, 21 CFR Parts 807, 801, 820/QMSR, and 830, ISO 13485, ISO 14971, and other applicable standards to execute regulatory strategies, submissions ...
Principal Regulatory Affairs Specialist
Eden Prairie, MN · On-site
$120K - $135K/yr
FDA medical device regulations, FDA guidance documents, 21 CFR Parts 807, 801, 820/QMSR, and 830, ISO 13485, ISO 14971, and other applicable standards to execute regulatory strategies, submissions ...
Principal Regulatory Affairs Specialist
Eden Prairie, MN · Hybrid
$120K - $135K/hr
FDA medical device regulations, FDA guidance documents, 21 CFR Parts 807, 801, 820/QMSR, and 830, ISO 13485, ISO 14971, and other applicable standards to execute regulatory strategies, submissions ...
Principal Regulatory Affairs Specialist
Eden Prairie, MN · Hybrid
$120K - $135K/hr
FDA medical device regulations, FDA guidance documents, 21 CFR Parts 807, 801, 820/QMSR, and 830, ISO 13485, ISO 14971, and other applicable standards to execute regulatory strategies, submissions ...
FDA-regulated Medical Device Software/Systems Validation Position Overview The Computer Systems Validation Engineer will be responsible for validating software and equipment in compliance with FDA ...
FDA-regulated Medical Device Software/Systems Validation Position Overview The Computer Systems Validation Engineer will be responsible for validating software and equipment in compliance with FDA ...
VP Global Quality and Regulatory
$220K - $225K/hr
Oversee FDA listings, EU conformity declarations, etc., to ensure clearance to distribute products. * Oversee product listings, declarations and regulatory approvals (ie 510(k), ISO, CE, CMDCAS) are ...
VP Global Quality and Regulatory
$220K - $225K/hr
Oversee FDA listings, EU conformity declarations, etc., to ensure clearance to distribute products. * Oversee product listings, declarations and regulatory approvals (ie 510(k), ISO, CE, CMDCAS) are ...
Oversee FDA listings, EU conformity declarations, etc., to ensure clearance to distribute products. * Oversee product listings, declarations and regulatory approvals (ie 510(k), ISO, CE, CMDCAS) are ...
Oversee FDA listings, EU conformity declarations, etc., to ensure clearance to distribute products. * Oversee product listings, declarations and regulatory approvals (ie 510(k), ISO, CE, CMDCAS) are ...
Provide comprehensive documentation (specifications and validation/qualifications) per the division's policy to meet FDA regulations. Your Responsibilities Include: * Define the development of ...
Provide comprehensive documentation (specifications and validation/qualifications) per the division's policy to meet FDA regulations. Your Responsibilities Include: * Define the development of ...
Vice President, Quality Assurance & Regulatory Affairs
Fridley, MN · On-site
$154K - $204K/yr
The company's Vivistim ® Paired VNS™ Therapy is the first and only FDA-approved implantable solution designed to improve function in chronic ischemic stroke survivors with moderate to severe upper ...
Vice President, Quality Assurance & Regulatory Affairs
Fridley, MN · On-site
$154K - $204K/yr
The company's Vivistim ® Paired VNS™ Therapy is the first and only FDA-approved implantable solution designed to improve function in chronic ischemic stroke survivors with moderate to severe upper ...
Senior Regulatory Affairs Specialist
$113K - $165K/yr
Ensures relevant International, ISO and FDA Export requirements are met, as required and ensures accuracy of submission information. 6. Initiates FDA export approval requires and product release ...
Senior Regulatory Affairs Specialist
$113K - $165K/yr
Ensures relevant International, ISO and FDA Export requirements are met, as required and ensures accuracy of submission information. 6. Initiates FDA export approval requires and product release ...
Senior Regulatory Affairs Specialist
Plymouth, MN · On-site
$113K - $165K/yr
Ensures relevant International, ISO and FDA Export requirements are met, as required and ensures accuracy of submission information. 6. Initiates FDA export approval requires and product release ...
Senior Regulatory Affairs Specialist
Plymouth, MN · On-site
$113K - $165K/yr
Ensures relevant International, ISO and FDA Export requirements are met, as required and ensures accuracy of submission information. 6. Initiates FDA export approval requires and product release ...
Manufacturing Engineer
Minneapolis, MN · On-site
$76K - $98K/yr
Ensure compliance with FDA regulations, GMP, ISO 13485, and company quality standards. * Participate in CAPA investigations, root cause analysis, and implementation of corrective actions. * Support ...
Quick apply
Manufacturing Engineer
Minneapolis, MN · On-site
$76K - $98K/yr
Ensure compliance with FDA regulations, GMP, ISO 13485, and company quality standards. * Participate in CAPA investigations, root cause analysis, and implementation of corrective actions. * Support ...
Fda information
See Minnesota salary details
$13.08 - $18.68
11% of jobs
$23.22 is the 25th percentile. Wages below this are outliers.
$18.68 - $24.29
18% of jobs
$24.29 - $29.90
16% of jobs
The median wage is $32.70 / hr.
$29.90 - $35.50
12% of jobs
$35.50 - $41.11
11% of jobs
$45.31 is the 75th percentile. Wages above this are outliers.
$41.11 - $46.71
12% of jobs
$46.71 - $52.32
9% of jobs
$52.32 - $57.92
5% of jobs
$57.92 - $63.53
3% of jobs
$63.53 - $69.13
2% of jobs
$69.13 - $74.74
2% of jobs
$13
$38
$74
How much do fda jobs pay per hour?
Is it hard to get hired by the FDA?
How much do you make working for FDA?
What are some typical challenges faced by professionals working at the FDA, and how can they be managed?
What are the key skills and qualifications needed to thrive as an FDA (U.S. Food and Drug Administration) Regulatory Affairs Specialist, and why are they important?
What does an FDA (Food and Drug Administration) professional do?
Does FDA have remote jobs?
What is the highest paying job at the FDA?
What is the difference between Fda vs Food Scientist?
| Aspect | Fda | Food Scientist |
|---|---|---|
| Required Credentials | Typically a degree in health, science, or related field; certifications vary | Bachelor's or master's in food science, microbiology, or related |
| Work Environment | Regulatory agencies, laboratories, inspection sites | Food manufacturing facilities, laboratories, research settings |
| Employer & Industry Usage | U.S. Food and Drug Administration, government agencies | Food companies, research institutions, government agencies |
| Common Search & Comparison Intent | Understanding regulatory roles, compliance, and enforcement | Food safety, product development, research |
While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

Full-time
Medical, Dental, Vision, Retirement
Posted 4 days ago
Mayo Clinic rating
7.8
Based on 692 frontline employees who took The Breakroom Quiz
104th of 890 rated healthcare providers
Job description
The Sr. Quality Analyst, FDA Regulated Manufacturing is responsible for oversight of quality and regulatory compliance for product manufacturing activities. The Sr. Quality Analyst directs the work to identify and reduce regulatory, accreditation, and compliance risk by continuous monitoring and evaluating current facility policies and practices to ensure compliance is built into the operational systems. Oversees manufacturing compliance by making interpretations and developing executive summaries of regulatory and compliance information, maintaining registration information, communication with external regulatory and accreditation agencies. The Sr. Quality Analyst communicates and works effectively with leadership to take necessary actions to mitigate identified risks; Is accountable for the effective implementation of the Quality Management System (QMS); and serves as the subject matter expert on the policies, processes and procedures of the QMS by developing a broad knowledge of the practice, business and technology as it relates to product manufacturing.
Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic.
- Medical: Multiple plan options.
- Dental: Delta Dental or reimbursement account for flexible coverage.
- Vision: Affordable plan with national network.
- Pre-Tax Savings: HSA and FSAs for eligible expenses.
- Retirement: Competitive retirement package to secure your future.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law". Mayo Clinic participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization.
A master's degree in product manufacturing medicine, business, regulatory compliance, or management and 5 years' experience in a quality related field is preferred or a bachelor's degree and 5 years' experience supporting FDA regulated product manufacturing, quality, regulatory, or compliance. Knowledge and experience in the application of laws, regulations, and guidance documents related to FDA regulated industries (biologics, pharmaceuticals, etc.) and previous experience with FDA GMPs, EU regulations, and/or ISO certification for product manufacturing is required. Demonstrated ability to interpret regulations and translate them into compliant, inspection-ready operational practices is highly desired. Exceptional human relations and communication (written, verbal, and listening) skills are required. Organizational project management skills are essential, along with analytical and critical thinking skills. Must be flexible and capable of adapting to and facilitating change. Should be very detail-oriented and have the ability to work independently and productively with minimal direction and routinely exercise initiative and sound judgment. Must have the ability to lead, motivate, and influence others. Compliance issues may create difficult situations for the individuals involved; therefore, objectivity and professionalism is essential. Must be experienced in conducting audits. Remains abreast of current, new, and developing industry trends, regulations, and legal positions related to FDA regulated manufacturing, patient care, and information management. Possesses strong human relations skills and problem-solving skills in order to influence all levels of the organization toward regulatory and accreditation compliance. Possesses strong written and verbal communication skills. Works independently with minimal direction and is self-motivated.
Must have demonstrated capacity to comprehend complex protocols, programs, and situations. The ability to exercise good judgment in ambiguous situations while under pressure and tight deadlines, and strong coping skills are required. Must be flexible in adapting to a variety of responsibilities, work assignments, and priorities. Must also be flexible with work schedule as needed to meet customer needs. Experience working in a research environment is preferred. Must be self-motivated and able to independently schedule workday activities with minimal direction. ASQ certification in quality and/or GMP principles (e.g., quality process analyst, quality improvement associate, etc.) is strongly encouraged.
What Mayo Clinic employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Mayo Clinic
Sourced by ZipRecruiter
Mayo Clinic is the largest integrated, not-for-profit medical group practice in the world. We're building the future, one where the best possible care is available to everyone — and more people can heal at home. Our relentless research turns into earlier diagnoses and new cures. That's how we inspire hope in those who need it most. At Mayo Clinic, experts work together to solve the most challenging unmet needs of patients. Our history of innovation dates back almost 150 years, when brothers Will and Charlie Mayo pioneered an integrated, team-based approach to medicine. Today, that trailblazing spirit drives innovations like Mayo Clinic Platform — which powers new technologies to change how care is delivered to all.
Industry
Hospitals
Company size
10,000+ Employees
Headquarters location
Rochester, MN, US
Year founded
1919