PHARMAFull-time
Quality Specialist (QMS, Documentation)
By Admin · Quality Assurance & Quality Control
BANGALORE (IN)ONSITEPOSTED: 8/27/2026
PHARMAFull-time
HIRING ORGANIZATIONMERCKScience and Technology; Pharmaceuticals and Life Science
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities
Oversee quality assurance processes within the Life Science division in India.
Develop, implement, and maintain the Quality Management System (QMS) in accordance with applicable regulatory requirements and industry standards.
Lead and manage quality assurance activities, including audits and investigations.
Collaborate with cross-functional teams to maintain product quality throughout the complete product lifecycle.
Monitor and analyze quality metrics to identify trends, risks, and areas requiring improvement.
Prepare and review quality documentation, including Standard Operating Procedures (SOPs), validation protocols, and quality reports.
Provide training and guidance to staff on quality assurance practices and regulatory compliance.
Drive continuous-improvement initiatives focused on product quality and operational efficiency.
Regulatory & Quality Standards
Apply knowledge of regulatory requirements including FDA, EMA, NABL, and ANAB expectations.
Apply quality standards such as ISO and GMP within quality-assurance processes.
Support compliance, audit readiness, investigation management, documentation control, and quality-system effectiveness.
Qualifications & Experience
Master's degree in Life Sciences, Chemistry, Engineering, or a related field.
7–9 years of experience specified for the role.
Minimum 7 years of quality-assurance experience in the pharmaceutical, chemical, life-sciences, or biotechnology industry.
Strong analytical, problem-solving, and communication skills.
Ability to work collaboratively in a fast-paced, team-oriented environment.
Work Environment & Company Context
Full-time position based in Jigani, Bangalore, India.
Role sits within Merck's Life Science division and contributes to maintaining quality and regulatory compliance across products and processes.
Merck emphasizes inclusion, belonging, professional development, and opportunities for employees to grow at their own pace.
REQUIRED VERIFIED SKILLS
Master's Degree in Life Sciences
Chemistry or Engineering
7-9 years experience
Quality Assurance
Pharmaceutical Industry
Chemical Industry
Life Sciences
Biotechnology
Quality Management Systems
QMS
Regulatory Compliance
FDA
EMA
NABL
ANAB
ISO
GMP
Audits
Investigations
Quality Metrics
SOPs
Validation Protocols
Quality Documentation
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Merck is actively hiring for this position.
INDUSTRY: Science and Technology; Pharmaceuticals and Life Science
RECOMMENDED TRAINING
1/5
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