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Gcp Compliance & Qa Consultant.

Propharma
5+ years
INR 18-28 LPA
United States
10 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Role Overview

The Clinical Quality Assurance (CQA) Consultant provides expert quality and compliance consulting services to pharmaceutical, biotechnology, and healthcare organizations.

The role focuses on:

  • GxP Compliance

  • Quality Management Systems (QMS)

  • Auditing

  • Regulatory Compliance

  • CAPA Management

  • SOP Development

  • Quality Risk Management

  • Client Consulting

This is a senior-level consulting role requiring strong expertise in FDA, EMA, MHRA, ICH, GMP, GDP, and GCP regulations.


Experience Required

Educational Qualification

Minimum

✅ Bachelor's Degree in a Scientific Discipline

Examples:

  • Pharmacy

  • Biotechnology

  • Life Sciences

  • Microbiology

  • Biochemistry

  • Chemistry

  • Biomedical Sciences


Preferred

✅ MSc

✅ PhD

✅ Advanced Scientific Degree


Additional Preferred Qualifications

  • Qualified Person (QP)

  • Responsible Person (RP)

  • Responsible Person Import (RPi)

(Particularly relevant for EU/UK candidates)


Key Responsibilities

1. Quality Assurance Consulting

  • Provide quality and compliance consultation to clients

  • Support pharmaceutical and biotech organizations

  • Deliver quality assurance projects

  • Act as Subject Matter Expert (SME)


2. Regulatory & GxP Compliance

  • Ensure compliance with:

    • FDA Regulations

    • ICH Guidelines

    • EMA Regulations

    • MHRA Requirements

    • GMP Standards

    • GDP Standards

    • GCP Standards

  • Provide regulatory compliance guidance


3. Quality Management System (QMS) Support

  • Develop Quality Management Systems

  • Improve quality processes

  • Implement quality frameworks

  • Support quality system optimization


4. Auditing Activities

  • Lead internal audits

  • Conduct supplier audits

  • Conduct vendor audits

  • Perform compliance assessments

  • Prepare audit reports

  • Track audit findings and actions


5. CAPA & Deviation Management

  • Investigate deviations

  • Analyze non-conformances

  • Develop CAPAs

  • Support root cause analysis

  • Monitor CAPA effectiveness


6. SOP Development & Training

  • Write SOPs

  • Review SOPs

  • Update quality procedures

  • Deliver quality training programs

  • Educate teams on compliance requirements


7. Client Project Management

  • Manage multiple consulting projects

  • Estimate project scope and effort

  • Ensure project delivery timelines

  • Maintain client satisfaction


8. Business Development Support

  • Support proposal development

  • Participate in sales discussions

  • Provide technical expertise during client engagements

  • Identify consulting opportunities


9. Continuous Improvement

  • Monitor regulatory updates

  • Develop subject matter expertise

  • Promote quality culture

  • Drive operational excellence initiatives


Required Technical Skills

Quality & Compliance

✔ GxP Compliance

✔ GMP

✔ GDP

✔ GCP

✔ Quality Risk Management

✔ Inspection Readiness


Quality Systems

✔ QMS Development

✔ SOP Writing

✔ CAPA Management

✔ Deviation Investigation

✔ Change Control

✔ Non-Conformance Management


Auditing

✔ Internal Audits

✔ Supplier Audits

✔ Vendor Audits

✔ Audit Reporting

✔ Compliance Assessments


Regulatory Affairs

✔ FDA Regulations

✔ EMA Regulations

✔ MHRA Requirements

✔ ICH Guidelines

✔ CFR Knowledge


Key Competencies

Leadership Competencies

  • Client relationship management

  • Stakeholder engagement

  • Consulting mindset

  • Influencing skills

Analytical Competencies

  • Root cause analysis

  • Risk assessment

  • Problem solving

  • Data interpretation

Communication Competencies

  • Technical writing

  • SOP writing

  • Presentation skills

  • Training delivery

Personal Competencies

  • Attention to detail

  • Quality orientation

  • Accountability

  • Adaptability

  • Continuous learning mindset


Career Progression

Typical career path:

  1. QA Specialist

  2. Senior QA Specialist

  3. CQA Consultant

  4. Senior CQA Consultant

  5. Principal Consultant

  6. Associate Director – Quality

  7. Director – Quality & Compliance

  8. Vice President – Quality & Regulatory Affairs


Ideal Candidate Profile

A quality and compliance professional with 5+ years of pharmaceutical, biotechnology, or CRO experience, strong expertise in GxP regulations, auditing, CAPA management, SOP development, and regulatory compliance consulting.

Candidates with previous consulting experience, FDA/EMA inspection exposure, and strong audit leadership skills will be highly competitive.


Overall Assessment

Job Level

Mid-Senior to Senior Quality Professional

Experience Required

5+ Years

Function

Quality Assurance & Regulatory Compliance

Industry

Pharmaceutical / Biotechnology / CRO / Consulting

Specialization

GxP Compliance, Quality Systems, Auditing, Regulatory Quality

Best Suited For

Quality Assurance Specialists, GMP/GCP Auditors, Regulatory Compliance Professionals, Quality Managers, and consultants seeking a client-facing global quality assurance role with significant exposure to international pharmaceutical and biotechnology projects.