We are looking for experienced GxP Quality & Compliance professionals with strong pharmaceutical experience across quality management, audits, compliance assessments and regulated technology environments.Key ResponsibilitiesSupport GxP compliance and quality management initiativesConduct periodic reviews, audits and control maturity assessmentsSupport Change Management, Deviation Management and Supplier Management processesReview validation and compliance documentationPerform risk assessments and identify compliance gapsSupport regulatory and quality requirements for pharmaceutical applicationsWork with SAP, QMS, DMS, EDC, CTMS and regulatory platformsSupport SaaS and cloud qualification activitiesCoordinate with QA, IT, business and regulatory stakeholdersManage multiple projects in complex Life Sciences environmentsWhat We’re Looking For4–14 years of relevant Pharmaceutical / Life Sciences experienceStrong understanding of GxP, 21 CFR Part 11 and GAMP 5Experience in Quality, Compliance, CSV or IT AuditHands-on experience with audits and compliance assessmentsKnowledge of risk management and quality processesExperience with Change, Deviation and Supplier ManagementExposure to clinical / regulatory applications is an advantageStrong stakeholder management and communication skillsIT background preferred⭐ Experience in pharmaceutical consulting, digital transformation or regulated technology environments will be an added advantage.ONLY IMMEDIATE JOINERS📩 Interested candidates can share their updated resume with passport pics attached at: csv.staffing@mazars.co.in and Harshita.sengar@mazars.co.in - mark all of them with your profile summary (Linkedin ID Link) along with details of their notice period and current location, CTC (Fixed + Variable) & Expected CTC

GxP Quality & Compliance Professional (Pharma/CSV, Quality, Audits, Compliance)

Emma

Responsibilities

Skills wanted:

Language(s) required:

Pooja Gupta

Pooja Gupta

About Forvis Mazars:

www.forvismazars.com/group/en

Admin access needed