Top 123 Medical affairs Jobs in Cincinnati Oh

Regulatory Affairs Specialist
AtriCure —Mason, OH
- $85,000 - $104,000 a year
- Hybrid work
- Background check
- Pass drug screening
- Mid-level
- Paid parental leave
- Health insurance
Physician (Gastroenterology)
US Veterans Health Administration —Cincinnati, OH
- $315,000 - $400,000 a year
- Online Application
- Background check
- Medicine
- Management
- Paid holidays
- Dental insurance
CDL-A OTR & Regional Truck Driver
USA Truck —Covington, KY
- $1,437 - $1,725 a week
- Full-time
- Dedicated
- No touch freight
- CDL A
- Health savings account
- AD&D insurance
Quick Apply
CDL-A Dedicated Truck Driver
USA Truck —Ohio
- $1,580 - $1,775 a week
- Full-time
- Dedicated
- No touch freight
- CDL A
- Health savings account
- AD&D insurance
Quick Apply
Medical Education Program Manager
Mammotome —Cincinnati, OH
- $100,000 - $120,000 a year
- Full-time
- Sales
- Marketing
- 5 years
- Health insurance
- Dental insurance
Senior Regulatory Affairs Specialist
AtriCure —Mason, OH
- $106,000 - $130,000 a year
- Background check
- Pass drug screening
- Analysis skills
- Paid parental leave
- Health insurance
Territory Manager, Cincinnati
Deciphera Pharmaceuticals —Cincinnati, OH
- $176,000 - $243,000 a year
- Full-time
- Remote
- 5 years
- Driver's License
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Medical Instrument Technician (Electrocardiograph Technician-EKG)
US Veterans Health Administration —Cincinnati, OH
- $52,559 - $68,328 a year
- Online Application
- Background check
- Pass drug screening
- English
- Paid parental leave
- Paid holidays
Coordinator GME Application & Student Placement Specialist
St. Elizabeth Healthcare —Edgewood, KY
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Health insurance
- Tuition reimbursement
10d
Medical Instrument Technician (EKG/Monitor Watcher)
US Veterans Health Administration —Cincinnati, OH
- $47,298 - $68,328 a year
- 12 hour shift
- Hybrid work
- Background check
- BLS Certification
- Pass drug screening
- Paid parental leave
- Paid holidays
7d
Senior Consultant, Strategic Communications
ERM Group —Cincinnati, OH
- $78,500 - $99,100 a year
- Full-time
- Hybrid work
- Spanish
- Bachelor of Science
- Research
- AD&D insurance
- Health insurance
11d
Medical Science Liaison / Senior Medical Science Liaison, North Central
Acadia Pharmaceuticals Inc. —Cincinnati, OH
- $143,400 - $220,000 a year
- Medicine
- Microsoft Excel
- Microsoft Outlook
- Paid parental leave
- Employee stock purchase plan
3d
Regulatory Affairs Specialist (510(k))
Vein360 —Blue Ash, OH
- Full-time
- Mid-level
- 3 years
- In-person
Quick Apply
9d
Donation Support Services Evaluation Coordinator (7p-7a)
Network For Hope —Cincinnati, OH
- Full-time
- Mid-level
- High school diploma or GED
- LPN
- Disability insurance
- Health insurance
Quick Apply
11d
Medical Support Assistant (Advanced)
US Veterans Health Administration —Middletown, OH
- $51,437 - $67,271 a year
- Online Application
- Background check
- Writing skills
- Pass drug screening
4d
Clinical Liaison
Liberty Station Health Campus —Township of Liberty, OH
- Full-time
- Sales
- Mid-level
- Driver's License
- Paid parental leave
- Health savings account
Hospice Clinical Liaison
Dignity Care Partners Hospice Blue Ash —Blue Ash, OH
- Full-time
- RN License
- Mid-level
- 3 years
Quick Apply
Institutional Review Board Coordinator
TriHealth —Cincinnati, OH
- Full-time
- Microsoft Excel
- Hospital
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Liaison (PRN)–ARU – Anderson Hospital
Mercy Health —Cincinnati, OH
- PRN
- Master of Social Work
- Nursing
- Hospital
- Health savings account
- Disability insurance
Specialist Oncology Clinical Ops - Cancer Center
St. Elizabeth Healthcare —Edgewood, KY
- Full-time
- Hospital
- 5 years
- Mid-level
- Health insurance
- Tuition reimbursement

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Regulatory Affairs Specialist

AtriCure -
Mason, OH

Apply Now

Job Details

$85,000 - $104,000 a year

Benefits

Paid parental leave
Health insurance
On-site gym
Dental insurance
Parental leave
401(k) matching
Volunteer time off
Pet insurance

Qualifications

Productivity software

Full Job Description

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure's Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure's AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure's Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure's cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.

We foster a culture of inclusion by embracing diverse experiences and individuals where everyone's authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.

POSITION SUMMARY:

This position will originate appropriate documents to obtain and maintain marketing privileges consistent with applicable government requirements where AtriCure conducts business. This position will also maintain internal documentation of such approvals and handle requests for documentation from our international distributors and customers. This position is responsible for practicing Quality System Manual procedures and complying with its requirements, and carrying out responsibilities as outlined in safety, health and environmental policies.

ESSENTIAL FUNCTIONS OF THE POSITION:

Support global regulatory pre-market applications for geographies included but not limited to: Taiwan, Singapore, Australia, Brazil, Korea, UAE, EU, UK, U.S, Japan, and Canada. Submission support may include but is not limited to: IDEs, PMA submissions and supplements or 510k for US, EU Technical Documentation, and/or Japan Shonin.
Support global regulatory post-market activities for the responsible geographies above, such as updating 510(k) letters to file, Technical Files and Design Dossiers on an annual basis, preparing and submitting product renewals, and annual/post-approval reports.
Support product marketing in additional geographies, as necessary, with international regulatory submissions, product renewals, tender bids, and fulfilling custom requirements.
Request Certificates to Foreign government and Free Sale Certificates as new products are approved
Obtain notarization and legalization of documents as required
Maintain, update and track open regulatory requests. Provide periodic status updates on open and closed requests
Review of product and manufacturing changes for compliance with applicable regulations (Change Control)
Work with Regulatory Affairs staff, engineers and technical experts to resolve potential regulatory issues, deficiencies and questions from regulatory agencies
Maintain submission correspondence files and other regulatory files in a complete manner
Maintain regulatory files for product compliance
Perform other related duties as assigned in support of regulatory activities
Assist in interacting with reviewers from regulatory agencies on specific projects
Provide support during internal and external audits
Maintain current knowledge of worldwide regulatory requirements

ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION:

Regular and predictable work performance
Ability to work under fast-paced conditions
Ability to make decisions and use good judgement
Ability to prioritize various duties and multitask as required
Ability to successfully work with others
Additional duties as assigned
Hybrid environment (with remote possibilities)
Travel responsibilities to AtriCure facilities for team functions and activities when needed

BASIC QUALIFICATIONS:

Bachelor's degree in a technical/scientific/life science discipline required or 3+ years of Regulatory experience in the medical device industry
Proficient on programs within Microsoft Office
Written and verbal communication skills
Problem solving and/or troubleshooting experience

PREFERRED QUALIFICATIONS:

Minimum of 2 years of experience in the medical device industry
Basic knowledge of U.S. and/or European/International regulations and standards
Strong understanding of documentation within a quality management system
Team oriented and able to effectively manage and prioritize multiple projects
General knowledge of medical terminology

OTHER REQUIREMENTS:

Ability to regularly walk, sit, or stand as needed
Ability to occasionally bend and push/pull as needed
Ability to pass pre-employment drug screen and background check
Occasional travel may be required

MN Hiring Range:

$85,000-104,000

#LI-JH1

AtriCure has a variety of benefits available for US based employees and their families. Examples include Medical & Dental beginning day 1 of employment, 401K plus match, 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads, Volunteer Time off, Pet Insurance, and more. Corporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website: https://www.atricure.com/careers-atricure/benefits.

AtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here https://www.e-verify.gov AtriCure is an Equal Employment Opportunity/Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s).

You may access our global privacy policy here: https://www.atricure.com/privacy

Apply Now

Refine Your Search

medical affairs jobs in cincinnati oh

Regulatory Affairs Specialist

Physician (Gastroenterology)

CDL-A OTR & Regional Truck Driver

CDL-A Dedicated Truck Driver

Medical Education Program Manager

Senior Regulatory Affairs Specialist

Territory Manager, Cincinnati

Medical Instrument Technician (Electrocardiograph Technician-EKG)

Coordinator GME Application & Student Placement Specialist

Medical Instrument Technician (EKG/Monitor Watcher)

Senior Consultant, Strategic Communications

Medical Science Liaison / Senior Medical Science Liaison, North Central

Regulatory Affairs Specialist (510(k))

Donation Support Services Evaluation Coordinator (7p-7a)

Medical Support Assistant (Advanced)

Clinical Liaison

Hospice Clinical Liaison

Institutional Review Board Coordinator

Clinical Liaison (PRN)–ARU – Anderson Hospital

Specialist Oncology Clinical Ops - Cancer Center

I want to receive the latest job alert for medical affairs in cincinnati oh

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