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Haleon

GxP (GCP, GLP, GVP) Quality Assurance Associate Director

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Job type

Full Time

Experience

Executive · 10 years

Location

India - Andra Pradesh - Hyderabad

Workplace

Remote

Posted

2026-08-17

Job board

workday

GeneralQuality Assurance JobsHealthcare Services Jobs

Benefits

Competitive salaryEquityHealthcarePTORetirementLearning budgetParental leaveWellnessVisa/relocationRemote flexibilityStipendsBonus/commissionPaid holidays

Education

Doctoral degree

Full Job Description

Role Overview This role provides independent Quality Assurance oversight, auditing, inspection support, and strategic compliance advice across Haleon GxP activities, with an integrated scope covering GVP, GCP, GLP and related GCLP activities. The role supports the protection of patients, consumers, and research participants, reinforces data integrity and regulatory compliance, and helps drive continuous improvement across Consumer Safety, Clinical Development, and broader R&D processes. What You Will Do Plan, lead, and conduct GVP, GCP, GLP/GCLP audits independently or as part of a broader audit team. Support functional activities across pharmacovigilance, clinical and non-clinical development to ensure compliance with applicable regulatory requirements, guidelines, laws, and Haleon quality standards. Why It Might Be a Fit The ideal candidate will have strong knowledge of applicable GVP, GCP, GLP and related regulatory requirements, guidelines, industry expectations, and company policies and procedures. They will be able to influence, negotiate and build credibility with internal and external stakeholders, including senior leaders, technical experts, audit auditees, vendors and partners. Requirements Bachelor of Science degree, or equivalent qualification / relevant professional experience 10+ years of pharmaceutical, consumer healthcare, R&D, Quality or related industry experience, including significant experience (minimum 3 years) in Quality Assurance and auditing across at least one major GxP area Strong knowledge of applicable GVP, GCP, GLP and related regulatory requirements, guidelines, industry expectations, and company policies and procedures Broad scientific, pharmaceutical, consumer healthcare or R&D background with relevant understanding of pharmacovigilance, clinical development, non-clinical research and associated quality systems Benefits Competitive salary Equity Healthcare PTO Retirement Learning budget Parental leave Wellness Visa/relocation Remote flexibility Stipends Bonus/commission Paid holidays

Skills and Technologies

Quality AssuranceAuditingRegulatory compliancePharmacovigilanceClinical developmentNon-clinical researchQuality systemsGCPGLPGVPGCLPQuality Assurance JobsHealthcare Services Jobs

Visa sponsorship is indicated for this role.