Head of Quality & Regulatory Compliance (Director Level)

Posted 4 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
150K-180K Annually
Senior level
Healthtech • Information Technology • Software • Biotech
The Role
The Head of QRC oversees quality and regulatory programs, ensuring compliance with global standards and fostering innovation in AG Mednet's SaaS offerings.
Summary Generated by Built In

Description

Overview:

AG Mednet is a software platform company operating at the intersection of clinical trials, data integrity, and regulatory compliance, supporting life sciences customers worldwide. We are seeking a Head of Quality & Regulatory Compliance (QRC) to provide strategic leadership and oversight of our quality and regulatory programs. 

The QRC function plays a pivotal role in ensuring that AG Mednet's products and services align with global regulations and standards relevant to the Life Science sector (e.g., 21 CFR Part 11, Computer System Validation, ICH GCP, HIPAA, GDPR, etc.), as well as safeguarding data through appropriate controls (SOC 2, NIST, ISO/IEC 27000 series standards, etc.).

Position Summary:

The Head of QRC is a senior leadership role responsible for owning and scaling AG Mednet’s Quality Management System (QMS) and regulatory compliance strategy across our cloud-based SaaS products and services. 

The ideal candidate brings deep experience supporting regulated B2B SaaS platform development and delivery and proactively translates regulatory and compliance requirements into practical, risk-based guidance that enables product innovation and business growth. 

Responsibilities:

  • Serve as a player-coach by combining hands-on ownership of quality, compliance, and regulatory activities with leadership and mentorship of the QRC team.
  • Actively monitor regulatory and compliance developments, assess applicability to AG Mednet, and proactively advise leadership and cross-functional stakeholders.
  • Maintain embedded quality and compliance oversight across the software development lifecycle, including validation strategy, change management, and release readiness and approval. 
  • Develop and implement sustainable systems and processes that support organizational growth while adhering to global regulations and standards.
  • Establish streamlined procedures, metrics, and indicators to measure and continually enhance processes.
  • Monitor the effectiveness of quality management and lead the management review process, reporting to senior leadership.
  • Support commercial and customer-facing activities, including RFP/RFIs and client discussions, as a senior quality and regulatory representative. 
  • Manage and support customer audits and inspections, as needed, and oversee vendor compliance activities (e.g., tool qualification) to ensure alignment with customer regulatory requirements.
  • Manage the CAPA / Quality Event program in collaboration with department managers.
  • Create training plans and oversee the administration of the employee Training program.
  • Collaborate with the Security Office to attain and maintain SOC 2 certification and enhance the company's security assurance program.
  • Act as the company Privacy Officer, including developing and implementing privacy policies, procedures, and training, addressing privacy concerns, reviewing contracts related to privacy and data protection, investigating potential breaches, and cooperating with regulatory authorities.
  • Maintain AG Mednet’s Privacy Shield certification and monitor the privacy regulatory landscape for relevance to AG Mednet.

Requirements

Qualifications & Experience

  • Bachelor's degree in a relevant field (Regulatory Affairs, Life Sciences, Computer Science, or similar)and/or 7-10+ years of relevant experience in quality, regulatory compliance, and/or risk management roles supporting cloud-hosted software or enterprise SaaS platforms within the pharmaceutical/biotech or life sciences industries.
  • Demonstrated experience building and/or leading high performing QRC teams, and supporting individual member’s professional growth.
  • Profound knowledge of regulations and controls (e.g., 21 CFR Part 11, CSV, ICH GCP, HIPAA, GDPR, SOC 2).
  • Strong project management experience with a track record of successfully leading and completing quality and compliance improvement projects.
  • Demonstrated ability to influence cross-functional stakeholders and communicate complex regulatory topics clearly and pragmatically.
  • Excellent organizational, document management, and communication skills.
  • Proficiency in prioritizing, managing, and delivering on multiple projects concurrently, coupled with a strong motivation to excel in a dynamic, fast-paced environment. A team player with a proactive problem-solving approach.
  • Demonstrated capability and interest in transforming how you work by leveraging AI

Preferred Tools & Skills:

  • Familiarity with modern SaaS architectures and cloud environments
  • Experience with Atlassian products (Jira and Confluence), learning management system (LMS) and document management system (DMS) platforms

Salary Range: 150,000 - 180,000

Skills Required

  • Bachelor's degree in a relevant field or 7-10+ years of relevant experience in quality, regulatory compliance, and/or risk management
  • Demonstrated experience building and/or leading high performing QRC teams
  • Profound knowledge of regulations and controls (e.g., 21 CFR Part 11, CSV, ICH GCP, HIPAA, GDPR, SOC 2)
  • Strong project management experience leading quality and compliance improvement projects
  • Ability to influence cross-functional stakeholders and communicate complex regulatory topics clearly
  • Excellent organizational, document management, and communication skills
  • Proficiency in prioritizing and managing multiple projects in a fast-paced environment
  • Interest in transforming work processes by leveraging AI
  • Familiarity with modern SaaS architectures and cloud environments
  • Experience with Atlassian products (Jira and Confluence), LMS and DMS platforms
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
0 Employees

What We Do

AG Mednet, Inc. provides AI-powered clinical trial workflow management software. Their platform, Judi, streamlines processes for regulated research, aiming to accelerate execution from protocol to submission and enable clinical trial leaders to focus on developing breakthrough treatments.

Similar Jobs

Cox Enterprises Logo Cox Enterprises

Search Engine Optimization Specialist

Artificial Intelligence • Automotive • Greentech • Information Technology • Machine Learning • Software • Cybersecurity
Remote or Hybrid
United States
50000 Employees
22-33 Hourly
Hybrid
Boston, MA, USA
130 Employees
150K-170K Annually
Hybrid
Boston, MA, USA
130 Employees
170K-200K Annually

Pfizer Logo Pfizer

Senior Manager, AI, and Data Engineering

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Hybrid
4 Locations
121990 Employees
139K-232K Annually

Similar Companies Hiring

Golden Pet Brands Thumbnail
Digital Media • eCommerce • Information Technology • Marketing Tech • Pet • Retail • Social Media
El Segundo, California
178 Employees
Kepler  Thumbnail
Fintech • Software
New York, New York
6 Employees
Onshore Thumbnail
Artificial Intelligence • Fintech • Software • Financial Services
New York City, NY
100 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account