Top 773 Director of regulatory affairs Jobs in Remote(us)

Director, Quality Systems & Regulatory Affairs (Remote - East Coast)
CEFALY Technology —Darien, CT
- Full-time
- Remote
- Engineering
- Analysis skills
- Mentoring
- Paid holidays
- Disability insurance
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Associate Director, Regulatory Affairs
BeiGene —Remote
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- Full-time
- Microsoft Outlook
- Computer literacy
- 8 years
- Health savings account
- Employee stock purchase plan
Director, Regulatory Affairs (Fractional)
Lexitas Pharma Services —Remote
- $300 - $350 an hour
- Remote
- Ability to walk for extended periods
- Senior level
- Ability to stand for extended periods
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Director, Regulatory Affairs - Development Strategy
Insmed Incorporated —Bridgewater, NJ
- $185,000 - $252,500 a year
- Full-time
- Remote
- 5 years
- Business development
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
Director, Clinical Research Regulatory Affairs
MD Anderson —Houston, TX
- $70.43 - $105.53 an hour
- Full-time
- Remote
- Medicine
- Master's degree
- Supervising experience
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Director, Regulatory Affairs CMC
Neurogene Inc. —Remote
- Remote
- Writing skills
- Bachelor's degree
- Doctor of Philosophy
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Director, Regulatory Affairs
Argon Medical Devices Inc —Plano, TX
- Full-time
- Remote
- Bachelor of Science
- 8 years
- Analysis skills
Sr Manager/Assoc Director, CMC Regulatory Affairs
Erasca —South San Francisco, CA
- $175,000 - $205,000 a year
- Remote
- 5 years
- Bachelor's degree
- Quality control
- Health savings account
- AD&D insurance
Global Regulatory Affairs Director - Inflammation and Rare Disease
Amgen —Remote
- $189,632.45 - $256,561.55 a year
- Remote
- Doctoral degree
- Master's degree
- Bachelor's degree
- Disability insurance
- Health insurance
Associate Director or Director, CMC Regulatory Affairs
Atsena —Durham, NC
- Full-time
- Remote
- 7 years
- Writing skills
- Doctor of Philosophy
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Director of Value Based Care Regulatory Compliance
Agilon Health —Remote
- $153,000 - $191,300 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- 5 years
12d
Director, Head of Regulatory Affairs -
Allstate —Remote
- $187,000 - $260,000 a year
- Remote
- 11+ years
- Presentation skills
- Bachelor's degree
12d
Executive Director, Regulatory Affairs
Kyverna Therapeutics —Remote
- $270,000 - $300,000 a year
- Full-time
- Remote
- 11+ years
- Bachelor's degree
- Mentoring
Director, Regulatory Affairs
Grid United —Remote
- Full-time
- Remote
- Up to 50% travel
- Engineering
- 8 years
- Health insurance
- 401(k)
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Director, Regulatory Affairs, Strategy
LeonaBio, Inc. —Bothell, WA
- $220,000 - $260,000 a year
- Full-time
- Remote
- Medicine
- 8 years
- Doctor of Philosophy
Quick Apply
4d
Director, Regulatory Affairs Advertising and Promotion
Ultragenyx Pharmaceutical —Novato, CA
- $214,100 - $264,500 a year
- Full-time
- Remote
- 5 years
- Bachelor of Science
- Bachelor's degree
- Gym membership
10d
Senior Director Biostatistics - REMOTE
Penfield Search Partners —Remote
- Remote
- Doctor of Philosophy
- Neurology
- Mentoring
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Associate Director, Market Access & Reimbursement - Alpharetta, GA or Remote
Avanos Medical —Alpharetta, GA
- $160,000 - $185,000 a year
- Full-time
- Remote
- Windows
- Analysis skills
- Bachelor's degree
- Health insurance
- 401(k) matching
Executive Medical Director, Neurology, Clinical Development (Remote)
Penfield Search Partners —Fairfield, CT
- Contract
- Remote
- Medicine
- 5 years
- Doctor of Philosophy
Quick Apply
Associate Director, Regulatory Affairs
Insmed Incorporated —Bridgewater, NJ
- $164,000 - $213,000 a year
- Full-time
- Remote
- Microsoft Outlook
- 5 years
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
4d

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Director, Quality Systems & Regulatory Affairs (Remote - East Coast)

CEFALY Technology
Darien, CT

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Job Details

Full-time

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance
Retirement plan

Qualifications

Corrective and preventive actions (CAPA)
Biomedical regulatory compliance
Supplier quality assurance (SQA)
Customer complaint resolution

Full Job Description

Director, Quality Systems & Regulatory Affairs

Department: Quality & Regulatory Affairs
Reports To: SVP, Operations
Location: Remote or Hybrid - East Coast ONLY
FLSA Status: Exempt, Full-Time

Position Summary

CEFALY Technology is seeking an experienced Quality Systems & Regulatory Affairs leader to strengthen and scale the organization's quality and regulatory infrastructure. This individual will serve as the functional lead for Quality Systems and Regulatory Affairs and will be responsible for improving organizational compliance, strengthening audit readiness, and reducing quality system risk through robust process ownership and execution.

A critical priority for this role will be optimizing and expanding the company's electronic Quality Management System (eQMS), conducting comprehensive assessments of quality documentation and system effectiveness, and driving sustainable process improvements across the organization. This position will provide experienced leadership during notified body audits and regulatory inspections and will help build long-term organizational capability through mentorship and process maturity.

The role serves as a strategic and hands-on partner across Operations, Supply Chain, Customer Service, Product Development, and leadership teams to ensure compliance excellence and scalable growth.

Essential Responsibilities

Quality Management System (QMS) & eQMS Leadership

Serve as system owner and business lead for the organization's eQMS platform including optimization, implementation expansion, workflow design, governance, and user adoption.
Assess current eQMS utilization and develop a roadmap for full implementation and process maturity.
Own and administer day-to-day QMS and eQMS activities and processes.
Lead continual improvement initiatives across quality system processes and documentation.
Lead comprehensive audits of controlled documentation and quality records to identify inconsistencies, gaps, obsolete content, and systemic documentation deficiencies.
Establish processes and controls ensuring consistency across SOPs, work instructions, forms, labels, templates, and quality records.
Drive document control processes including creation, revision workflows, review cycles, training assignments, archival activities, and change management.
Develop sustainable document governance practices to reduce repeat nonconformances and improve inspection readiness.
Monitor quality metrics and identify opportunities for process improvements.
Support and improve CAPA, nonconformance, complaint handling, change control, risk management, and supplier quality processes.
Ensure QMS alignment with ISO 13485, FDA Quality System Regulation (21 CFR Part 820/QMSR), EU MDR, and applicable global requirements.
Lead initiatives to improve quality system effectiveness, data integrity, and organizational compliance maturity.
Maintain ongoing inspection and audit readiness.

Audit & Compliance Leadership

Act as primary Quality and Regulatory lead during notified body audits, FDA inspections, supplier audits, and external quality assessments.
Lead audit preparation strategy, evidence collection, coordination activities, and response management.
Drive audit finding remediation through root cause analysis and sustainable CAPA implementation.
Support management review processes and quality reporting.
Maintain a continuous state of organizational inspection readiness.

Regulatory Affairs Leadership

Independently lead FDA and international regulatory submissions and agency interactions.
Prepare, coordinate, and execute regulatory filings and lifecycle submissions.
Conduct regulatory impact assessments related to product, process, manufacturing, supplier, labeling, and operational changes.
Provide regulatory strategy recommendations and communicate business impact to leadership.
Support registrations, renewals, amendments, and post-market regulatory activities.
Interpret changing regulatory requirements and proactively communicate implications.
Maintain regulatory records and submission archives.

Leadership & Cross-Functional Partnership

Mentor and help develop junior QA/RA personnel.
Provide quality and regulatory leadership across Operations, Supply Chain, Customer Service, Product Development, and leadership teams.
Act as an internal subject matter expert for QMS and regulatory requirements.
Support employee training initiatives related to quality systems and compliance.
Provide guidance during business, operational, and product decisions.

Qualifications

Education

Bachelor's degree in Engineering, Life Sciences, Regulatory Affairs, Quality, or related field required.
Advanced degree preferred.

Experience

8–12+ years of progressive Quality and Regulatory Affairs experience within medical devices.
Demonstrated experience serving as lead quality or regulatory representative during notified body audits and regulatory inspections.
Proven experience owning, implementing, or significantly improving an electronic QMS platform; Greenlight Guru experience strongly preferred.
Demonstrated experience identifying and remediating systemic documentation and quality system deficiencies.
Experience independently leading FDA submissions and EU MDR activities.
Experience with CAPA, complaint handling, risk management, supplier quality, document control, and change management systems.
Demonstrated success improving audit outcomes and quality system maturity.
Prior people leadership or mentoring experience strongly preferred.
Experience supporting Class II and/or Class III medical devices preferred.

Knowledge & Skills

Deep understanding of ISO 13485, FDA Quality System Regulation (21 CFR Part 820/QMSR), EU MDR, and related global regulations.
Strong understanding of quality systems architecture and eQMS administration.
Excellent technical writing and documentation skills.
Strong project management and organizational capabilities.
Strong leadership presence during audits and external interactions.
Ability to manage multiple priorities within fast-paced environments.
Excellent communication and cross-functional influencing skills.
Strong analytical, problem-solving, and systems-thinking abilities.

Preferred Certifications

RAC, CQE, CQA, ASQ certifications, or equivalent preferred.

Success in this role includes:

Complete a comprehensive assessment of current QMS and eQMS state.
Develop and execute a Greenlight Guru optimization roadmap.
Conduct a full controlled-document audit and remediation initiative.
Reduce repeat audit observations and documentation inconsistencies.
Improve notified body audit readiness and inspection confidence.
Strengthen quality system governance and documentation control processes.
Improve organizational QA/RA capability and mentorship support.
Build scalable infrastructure supporting future growth.

Why This Role Matters

This role is being added to strengthen organizational quality and regulatory capabilities, reduce single-point dependency risk, improve QMS sustainability, and establish scalable systems supporting long-term growth and compliance excellence.

Benefits

Health insurance (80% employer-paid)
Employer-paid Dental and Vision
Short-Term and Long-Term Disability
Group Life Insurance
IRA with company match (no vesting period)
Paid PTO
Paid company holidays

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Refine Your Search

director of regulatory affairs jobs in remote(us)

Director, Quality Systems & Regulatory Affairs (Remote - East Coast)

Associate Director, Regulatory Affairs

Director, Regulatory Affairs (Fractional)

Director, Regulatory Affairs - Development Strategy

Director, Clinical Research Regulatory Affairs

Director, Regulatory Affairs CMC

Director, Regulatory Affairs

Sr Manager/Assoc Director, CMC Regulatory Affairs

Global Regulatory Affairs Director - Inflammation and Rare Disease

Associate Director or Director, CMC Regulatory Affairs

Director of Value Based Care Regulatory Compliance

Director, Head of Regulatory Affairs -

Executive Director, Regulatory Affairs

Director, Regulatory Affairs

Director, Regulatory Affairs, Strategy

Director, Regulatory Affairs Advertising and Promotion

Senior Director Biostatistics - REMOTE

Associate Director, Market Access & Reimbursement - Alpharetta, GA or Remote

Executive Medical Director, Neurology, Clinical Development (Remote)

Associate Director, Regulatory Affairs

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