Top 14 Regulatory affairs manager Jobs in Durham, Nc

Regulatory Affairs Manager
bioventus —Durham, NC
- Full-time
- 5 years
- Senior level
- Communication skills
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases
Chiesi Farmaceutici —Cary, NC
- $121,000 - $182,000 a year
- Overtime
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Health insurance
Sr. Director, Strategic Regulatory Affairs and UDI
Teleflex —Morrisville, NC
- $203,000 - $253,000 a year
- 11+ years
- Office
- Analysis skills
- Disability insurance
- Health insurance
Regulatory Affairs Manager - CMC & Labeling
United Therapeutics —Research Triangle Park, NC
- Full-time
- Hybrid work
- Office
- Master's degree
- Project management
- Paid parental leave
- Employee stock purchase plan
US Regulatory Manager
UPL ltd —Cary, NC
- Full-time
- 5 years
- Mid-level
- Presentation skills
Senior Manager, Regulatory Affairs
Azurity Pharmaceuticals - US —Raleigh, NC
- Full-time
- Hybrid work
- Bachelor of Science
- Office
- Microsoft Office
- Fuel card
- Health insurance
8d
Planned Activity Project Manager - Cary, NC
Siemens Healthineers —Cary, NC
- $74,350 - $102,234 a year
- Full-time
- Microsoft Outlook
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
6d
Head of US Crop Protection Regulatory Affairs - Research Triangle Park, NC (preferred)
BASF —Research Triangle Park, NC
- Full-time
- Hybrid work
- Bachelor of Science
- 11+ years
- Bachelor's degree
- Adoption assistance
- Parental leave
Senior Manager, Project Management
Grifols —Durham, NC
- Full-time
- Office
- Master's degree
- Doctor of Philosophy
Public Regulatory Analyst I
State of North Carolina - Commerce —Wake County, NC
- $63,927 - $87,899 a year
- Full-time
- Engineering
- Mid-level
- Office
- Paid holidays
- Health insurance
14d
Project Lead - RUA92307
IQVIA —Raleigh, NC
- $200,000 - $225,000 a year
- Full-time
- Nursing
- Driver's License
- Travel
Senior Associate, Regulatory CMC
HUMACYTE GLOBAL INC —Durham, NC
- Full-time
- Remote
- Bachelor of Science
- Writing skills
- Bachelor's degree
- Paid parental leave
- Paid holidays
Quick Apply
Senior Corporate Counsel/ Associate Director, Compliance #4927
GRAIL —Durham, NC
- $205,000 - $260,000 a year
- Full-time
- Hybrid work
- 8 years
- Continuous improvement
- Travel
- Health insurance
- Dental insurance
Quick Apply
4d

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Regulatory Affairs Manager

bioventus -
Durham, NC

Apply Now

Job Details

Full-time

Qualifications

FDA submissions
Presentations for conferences or internal meetings
Biomedical regulatory compliance

Full Job Description

Are you ready to work for a more active world?

At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.

The Regulatory Affairs Manager is responsible for developing and executing global regulatory strategies to plan, prepare, and obtain approvals and compliance with national and international regulatory requirements (e.g. U.S FDA, Health Canada, EU notified bodies, etc.), as well as work collaboratively with R&D/Engineering and Operations, Clinical/Medical Affairs, and other functional areas to provide regulatory expertise. The position will ensure that company policies, procedures and practices follow appropriate regulatory requirements.

Key Responsibilities:
1. Prepare, provide direction and oversee documentation packages for submission to global regulatory authorities to register new and/or maintain global approvals/clearances for assigned products.

2. Develop and maintain outstanding relationships with all regulatory and compliance agencies. Provide appropriate interface with global regulatory agencies in a variety of pre- and post-market forums. Provide guidance, interpretation, and opinions on complex regulatory matters (particularly related to submission pathways), outlining the different outcomes.
3. Prepares, collects, reviews, and assembles technical documentation required for writing regulatory and clinically-related submissions such as US 510K, PMAs, IDEs, NDAs, INDs, or international dossiers for new and modified products.
4. Liaises with project teams to develop regulatory strategies, testing requirements and other documentation to ensure regulatory data requirements are met. .
6. Works with stakeholders to serve as a point person for regulatory agency interactions, including preparation of briefing packages, including presentations, and strategy for meetings, and response to agency letters pertaining to assigned products.

7. Monitor proposed and current global regulations and standards; assess impact of changes to such on assigned biologics product lines

8. Maintains awareness of global regulatory legislation and assesses its impact of development and manufacturing initiatives.

9. Evaluates design, manufacturing and labeling changes to ensure compliance with FDA, international, and other applicable governmental regulations.

10. Identifies and facilitates in the remedy of inefficiencies in Quality systems and processes.

11. Contribute to the Regulatory and/or Quality perspective on due diligence activities to identify issues related to the targeted product’s development and/or its manufacture.

12. Holds oneself and others accountable to conduct business in a manner compliant with Bioventus’ Code of Compliance and Ethics, policies and procedures and internal controls applicable to their role.

13. All other duties or projects as assigned.

Education and Experience (Knowledge, Skills & Abilities)

Bachelor’s degree required (study area in Engineering or life sciences preferred, but other degrees may be considered)
Knowledge & experience working with biologics
Extensive knowledge of FDA and applicable international regulations required.
Working knowledge of US Quality Systems Regulations (QSRs) and/or Good Manufacturing Practices (GMPs), along with ISO 13485.
Minimum of 5 – 7 years of Regulatory and Quality regulations experience and submission experience required. Class II medical device experience required, Class III medical device and/or PMA / BLA/NDA submissions experience desired.
Excellent written, verbal communication and presentation skills are required, including the ability to communicate clearly, concisely and effectively verbally and in writing
Solid interpersonal skills including the ability to remain calm, professional, diplomatic, and positive
Being detail-oriented while having the ability to handle multiple projects/tasks
Experience interacting with US FDA is required

Are you the top talent we are looking for?

Apply now! Hit the “Apply” button to send us your resume and cover letter.

Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.

Apply Now

Refine Your Search

regulatory affairs manager jobs in durham, nc

Regulatory Affairs Manager

Senior Manager, CMC Regulatory Affairs, Global Rare Diseases

Sr. Director, Strategic Regulatory Affairs and UDI

Regulatory Affairs Manager - CMC & Labeling

US Regulatory Manager

Senior Manager, Regulatory Affairs

Planned Activity Project Manager - Cary, NC

Head of US Crop Protection Regulatory Affairs - Research Triangle Park, NC (preferred)

Senior Manager, Project Management

Public Regulatory Analyst I

Project Lead - RUA92307

Senior Associate, Regulatory CMC

Senior Corporate Counsel/ Associate Director, Compliance #4927

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