Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory ... May direct interaction with regulatory agencies on defined matters. * Recommends strategies for ...
Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory ... May direct interaction with regulatory agencies on defined matters. * Recommends strategies for ...
Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory ... May direct interaction with regulatory agencies on defined matters. * Recommends strategies for ...
Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory ... May direct interaction with regulatory agencies on defined matters. * Recommends strategies for ...
Therefore, we are looking fora passionate Senior Regulatory Affairs Specialist who has direct ... Provide regulatory support for currently marketed products, including reviewing labeling and ...
Therefore, we are looking fora passionate Senior Regulatory Affairs Specialist who has direct ... Provide regulatory support for currently marketed products, including reviewing labeling and ...
Therefore, we are looking fora passionate Senior Regulatory Affairs Specialist who has direct ... Provide regulatory support for currently marketed products, including reviewing labeling and ...
Therefore, we are looking fora passionate Senior Regulatory Affairs Specialist who has direct ... Provide regulatory support for currently marketed products, including reviewing labeling and ...
Director, Enterprise EH&S
Minneapolis, MN · On-site
$133K - $219K/yr
... Labeling and Packaging (CLP) regulations. Key Accountabilities Enterprise EH&S Strategy and ... Direct and oversee the work of external consultants and specialized technical resources supporting ...
Director, Enterprise EH&S
Minneapolis, MN · On-site
$133K - $219K/yr
... Labeling and Packaging (CLP) regulations. Key Accountabilities Enterprise EH&S Strategy and ... Direct and oversee the work of external consultants and specialized technical resources supporting ...
Fragrance Director
Minneapolis, MN · On-site
$130K - $175K/yr
Fragrance Director Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an ... with fragrance regulatory and safety frameworks, such as IFRA standards and allergen labeling.
Fragrance Director
Minneapolis, MN · On-site
$130K - $175K/yr
Fragrance Director Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an ... with fragrance regulatory and safety frameworks, such as IFRA standards and allergen labeling.
Fragrance Director
Minneapolis, MN · On-site
$150 - $200/hr
Fragrance Director Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an ... with fragrance regulatory and safety frameworks, such as IFRA standards and allergen labeling.
Fragrance Director
Minneapolis, MN · On-site
$150 - $200/hr
Fragrance Director Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an ... with fragrance regulatory and safety frameworks, such as IFRA standards and allergen labeling.
Fragrance Director
Minneapolis, MN · On-site
Fragrance Director Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an ... with fragrance regulatory and safety frameworks, such as IFRA standards and allergen labeling.
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Fragrance Director
Minneapolis, MN · On-site
Fragrance Director Duke Cannon Supply Co. is a growth-oriented CPG company that operates with an ... with fragrance regulatory and safety frameworks, such as IFRA standards and allergen labeling.
Director of Quality
Plymouth, MN · On-site
$190K - $250K/yr
Ensuring that quality and regulatory requirements are established implemented and maintained in ... labeling and drug product; * Oversee review and approval or rejection of all controlled documents ...
Director of Quality
Plymouth, MN · On-site
$190K - $250K/yr
Ensuring that quality and regulatory requirements are established implemented and maintained in ... labeling and drug product; * Oversee review and approval or rejection of all controlled documents ...
Assistant Director of International Student Life
Northfield, MN · On-site
$60 - $80/hr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... hazardous labels.***Note:** This position description is not intended to be all-inclusive.
Assistant Director of International Student Life
Northfield, MN · On-site
$60 - $80/hr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... hazardous labels.***Note:** This position description is not intended to be all-inclusive.
Senior Director, Global Medical Safety, Global Pharmacovigilance (psychedelics)
Saint Paul, MN · On-site
Represent Global Safety in regulatory interactions; presenting and defending safety findings ... Represents GPV CS&PV at Labeling Committee/ Executive Committee discussions on new information ...
Senior Director, Global Medical Safety, Global Pharmacovigilance (psychedelics)
Saint Paul, MN · On-site
Represent Global Safety in regulatory interactions; presenting and defending safety findings ... Represents GPV CS&PV at Labeling Committee/ Executive Committee discussions on new information ...
Assistant Director of International Student Life
Northfield, MN · On-site
$59K - $61K/yr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... and hazardous labels. Note: This position description is not intended to be all-inclusive.
Assistant Director of International Student Life
Northfield, MN · On-site
$59K - $61K/yr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... and hazardous labels. Note: This position description is not intended to be all-inclusive.
Assistant Director of International Student Life
Northfield, MN · On-site
$60 - $80/hr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... and hazardous labels. Note: This position description is not intended to be all-inclusive.
Assistant Director of International Student Life
Northfield, MN · On-site
$60 - $80/hr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... and hazardous labels. Note: This position description is not intended to be all-inclusive.
Assistant Director of International Student Life
Northfield, MN · On-site
$60 - $80/hr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... labels.Note: This position description is not intended to be all-inclusive. Employees may perform ...
Assistant Director of International Student Life
Northfield, MN · On-site
$60 - $80/hr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... labels.Note: This position description is not intended to be all-inclusive. Employees may perform ...
Assistant Director of International Student Life
Northfield, MN · On-site
$59K - $61K/yr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... and hazardous labels. Note: This position description is not intended to be all-inclusive.
Assistant Director of International Student Life
Northfield, MN · On-site
$59K - $61K/yr
Provide cultural, personal, and regulatory advising to a diverse set of international students with ... and hazardous labels. Note: This position description is not intended to be all-inclusive.
Retail Pharmacy Technician (certified)
Hallock, MN · On-site
$21 - $31/hr
Count, Prepare and label medications under the direct supervision of a licensed pharmacist. * Perform duties in accordance with the Minnesota Board of Pharmacy regulations. * Prepare refill requests ...
Retail Pharmacy Technician (certified)
Hallock, MN · On-site
$21 - $31/hr
Count, Prepare and label medications under the direct supervision of a licensed pharmacist. * Perform duties in accordance with the Minnesota Board of Pharmacy regulations. * Prepare refill requests ...
Cook - Part-time, Truman Senior Living
Truman, MN · On-site
$16 - $20.72/hr
The cook will follow dietary regulations and any dietary restrictions. Benefit Summary: Heartland ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Cook - Part-time, Truman Senior Living
Truman, MN · On-site
$16 - $20.72/hr
The cook will follow dietary regulations and any dietary restrictions. Benefit Summary: Heartland ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Dietary Cook, FT - Minnewaska Lutheran Home
Starbuck, MN · On-site
$14.25 - $18.25/hr
The cook will follow dietary regulations and any dietary restrictions. Qualifications: Must be able ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Dietary Cook, FT - Minnewaska Lutheran Home
Starbuck, MN · On-site
$14.25 - $18.25/hr
The cook will follow dietary regulations and any dietary restrictions. Qualifications: Must be able ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Cook - Part-time, Truman Senior Living
$14.25 - $18.50/hr
The cook will follow dietary regulations and any dietary restrictions. Benefit Summary: Heartland ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Cook - Part-time, Truman Senior Living
$14.25 - $18.50/hr
The cook will follow dietary regulations and any dietary restrictions. Benefit Summary: Heartland ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Cook - Traverse Care Center
Wheaton, MN · On-site
$19.50 - $26/hr
The cook will follow dietary regulations and any dietary restrictions. Qualifications: Must be able ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Cook - Traverse Care Center
Wheaton, MN · On-site
$19.50 - $26/hr
The cook will follow dietary regulations and any dietary restrictions. Qualifications: Must be able ... Report any missing MSDS labels to Director. * Ensure that food and supplies for the next day are ...
Director Regulatory Labeling information
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Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 4 days ago
Medtronic rating
7.9
Based on 180 frontline employees who took The Breakroom Quiz
155th of 546 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 LifeMedtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices focusing on a diverse line of Sutures (absorbable/non-absorbable, coated/uncoated). Regulatory support will focus on sustaining globalization, international submissions, commercial support, manufacturing support, systems improvement, and other responsibilities aligned with global medical device regulations and the goals of the Wound Management business.Responsibilities may include the following and other duties may be assigned.
- Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and inspections.
- Leads or compiles all materials required in submissions, license renewal and annual registrations.
- Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance.
- Monitors and improves tracking / control systems.
- Keeps abreast of regulatory procedures and changes.
- May direct interaction with regulatory agencies on defined matters.
- Recommends strategies for earliest possible approvals of clinical trials applications.
To be considered for this role, you must have:
Bachelor's degree required
Minimum of 2 years of relevant experience, or advanced degree with a minimum of 0 years of relevant experience.
Preferred qualifications include:
Experience with U.S. FDA and international regulatory requirements for medical devices
Familiarity with EU MDR, MDD, ISO 13485, ISO 14971, and related standards
Experience supporting regulatory submissions, audits, or inspections
Strong written and verbal communication skills
Strong organizational skills with the ability to manage multiple priorities
Experience collaborating in a cross-functional, fast-paced environment
Familiarity with medical device product development or lifecycle management
RAC certification or progress toward certification
Experience working with Notified Bodies or global regulatory agencies.
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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