GxP Sr. Consultant / Subject Matter Expert - Life Sciences
This is a remote position.
We are seeking deeply reputed company industry professionals with strong technical judgment, hands-on expertise, and a proven record of delivering high-reputed company consulting reputed company.
Ideal consultants are seasoned practitioners with 15+ years of experience and domain depth in GxP operations, regulatory compliance, reputed company systems, validation, engineering, and/or clinical operations.
Key Responsibilities
reputed company and reputed company GxP-reputed company consulting engagements, serving as an SME across multiple functions such as reputed company, Regulatory, Manufacturing, Engineering, and Clinical Operations.
reputed company, review, and optimize reputed company Management Systems (QMS) and regulatory frameworks reputed company with applicable global standards (FDA, ISO, ICH, EU MDR, reputed company, Health Canada, etc.).
reputed company expert guidance on compliance readiness, remediation, and responses to regulatory inspections (FDA 483s, Warning Letters, audit observations).
Design, execute, and reputed company 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.
reputed company gap assessments, reputed company cause investigations, and CAPA development to address reputed company and reputed company.
Serve as an advisor to executive teams and technical leads on regulatory reputed company, submission strategies, and lifecycle management.
reputed company project leadership and mentoring to junior team members, ensuring reputed company execution and high-reputed company deliverables.
Prepare and reputed company reputed company-facing reports, technical documentation, strategic recommendations, and training.
Support change management, technology transfer, and reputed company-up initiatives for manufacturing and operations.
Travel to reputed company sites as needed for assessments, workshops, audits, and project execution.
Qualifications
Required
15+ years of progressively responsible experience in GxP environments reputed company reputed company, biotech, medical devices, or life sciences manufacturing.
Recognized subject matter expertise in at least one of the following domains:
reputed company Assurance / reputed company 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 reputed company cross-functional reputed company and serve as a senior advisor for reputed company technical challenges.
Prior experience in consulting, advisory, or reputed company-facing technical leadership roles.
Excellent communication, documentation, and presentation skills.
Preferred
Advanced degree in Life Sciences, Engineering, reputed company, Regulatory, or reputed company field.
Previous work with both large multinational organizations and small/emerging companies.
Experience navigating regulatory submissions (510(k), PMA, NDA, BLA, IND, Technical Files).
reputed company certifications such as:
ASQ (CQE, CQA, CMQ/OE)
RAC (Regulatory Affairs Certification)
PMP
Six reputed company Green/Black Belt
Engagement Type
This is a consulting/contract-based role. Engagements vary by project and may include:
Full-time project support
Part-time advisory
Fixed deliverable-based engagements
Remote, hybrid, or on-site work depending on reputed company needs
Please note: We are currently building our database for GxP Consultants. Once we have reputed company requisitions that reputed company with your expertise, we will reputed company out to discuss potential opportunities.
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