GxP Senior Consultant – Subject Matter Expert

Pharmavise Corporation

Consultant with 15+ years of experience in GxP operations and regulatory compliance. Leading consulting engagements with pharmaceutical and biotech clients on quality systems and compliance issues.

Posted 6/3/2026full-timeRemote • 🇺🇸 United StatesSeniorWebsite

About the role

Key responsibilities & impact

Lead and deliver GxP-focused consulting engagements, serving as an SME across multiple functions such as Quality, Regulatory, Manufacturing, Engineering, and Clinical Operations.
Develop, review, and optimize Quality Management Systems (QMS) and regulatory frameworks aligned with applicable global standards (FDA, ISO, ICH, EU MDR, MHRA, Health Canada, etc.).
Provide expert guidance on compliance readiness, remediation, and responses to regulatory inspections (FDA 483s, Warning Letters, audit observations).
Design, execute, and oversee validation and qualification programs: Process validation Equipment qualification (IQ/OQ/PQ) Software/CSV (21 CFR Part 11) Cleaning and sterilization validation Computerized systems validation.
Support product development programs, ensuring adherence to design control, risk management, verification/validation, and DHF/technical documentation requirements.
Perform gap assessments, root cause investigations, and CAPA development to address quality and compliance risks.
Serve as an advisor to executive teams and technical leads on regulatory pathways, submission strategies, and lifecycle management.
Provide project leadership and mentoring to junior team members, ensuring structured execution and high-quality deliverables.
Prepare and deliver client-facing reports, technical documentation, strategic recommendations, and training.
Support change management, technology transfer, and scale-up initiatives for manufacturing and operations.
Travel to client sites as needed.

Requirements

What you’ll need

15+ years of progressively responsible experience in GxP environments within pharma, biotech, medical devices, or life sciences manufacturing.
Recognized subject matter expertise in at least one of the following domains: Quality Assurance / Quality Systems Regulatory Affairs Validation & Engineering (Process, Equipment, Automation, CSV) Manufacturing Operations / Tech Transfer Clinical Operations & Compliance Risk Management (ISO 14971) Design Controls (21 CFR 820, ISO 13485)
Strong working knowledge of global GxP regulations and standards (FDA 21 CFR, EU MDR/IVDR, ISO 13485, ICH Q-series, GAMP 5, ISO 9001/62304/17025, etc.).
Proven ability to lead cross-functional projects and serve as a senior advisor for complex technical challenges.
Prior experience in consulting, advisory, or client-facing technical leadership roles.
Excellent communication, documentation, and presentation skills.

Benefits

Comp & perks

Equal Opportunity Employer

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Quality Management Systems (QMS)regulatory frameworkscompliance readinessvalidation programsprocess validationequipment qualificationsoftware validationcleaning validationcomputerized systems validationrisk management

Soft Skills

project leadershipmentoringcommunicationdocumentationpresentationadvisory skillscross-functional collaborationstrategic recommendationsclient-facing skillschange management