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Quality Associate – GMP & DI Compliance

REWARI (IN)ONSITEPOSTED: 7/13/2026
PHARMAFull-time
HIRING ORGANIZATIONLONZALife Sciences / Pharmaceutical Manufacturing / Healthcare Technology
Lonza

ROLE DEFINITION & RESPONSIBILITIES

Lonza, one of the world’s leading life sciences manufacturing companies, has announced an exciting Quality Associate – GMP & Data Integrity (DI) Compliance opportunity at its Rewari, Haryana facility. This is an excellent opportunity for candidates with experience in Quality Assurance (QA), Quality Management Systems (QMS), GMP Compliance, Data Integrity, CAPA, Document Management Systems (DMS), Vendor Qualification, and Regulatory Compliance.

If you’re looking to build your career in pharmaceutical quality systems, GMP compliance, regulatory inspections, and quality management, this Lonza career opportunity offers excellent professional growth within a globally recognized organization.

Job Overview

Company: Lonza
Position: Quality Associate – GMP & DI Compliance
Department: Quality Assurance / QMS
Location: Rewari, Haryana, India
Job Type: Full-Time
Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc, Biotechnology, Microbiology, Life Sciences or related discipline
Experience: Experience in QA, QMS, Compliance or Regulated Manufacturing
Industry: Pharmaceutical / Life Sciences
Shift: As per company requirement

Key Responsibilities

As a Quality Associate – GMP & DI Compliance, you will

Support and maintain the Quality Management System (QMS).
Ensure compliance with GMP, regulatory requirements, customer expectations, and Halal standards.
Coordinate regulatory inspections and customer audits.
Support certification audits and audit follow-up activities.
Manage Approved Vendor List (AVL) and vendor qualification activities.
Perform and coordinate vendor audits.
Administer the Document Management System (DMS).
Maintain document control and GMP documentation.
Execute self-inspection programs.
Drive CAPA implementation and continuous improvement initiatives.
Manage Change Control activities using risk-based approaches.
Develop and monitor Data Integrity (DI) programs.
Maintain the Data Integrity Matrix across systems.
Coordinate GMP and Quality training programs.
Collaborate with Manufacturing, Engineering, Regulatory Affairs, Supply Chain, and Quality teams.

Required Qualifications

Applicants should possess a Bachelor’s or Master’s degree in:

B.Pharm
M.Pharm
B.Sc
M.Sc
Biotechnology
Microbiology
Life Sciences
Related Scientific Discipline

REQUIRED VERIFIED SKILLS

GMP Guidelines
Quality Assurance
Quality Management System (QMS)
Data Integrity (DI)
CAPA
Change Control
Vendor Qualification
Vendor Audit
Regulatory Compliance
Document Management Systems (DMS)
Risk Assessment
Regulatory Inspections

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Lonza offers competitive compensation, global career opportunities, an inclusive workplace culture, continuous learning programs, cross-functional international exposure, and robust professional development.

ORGANIZATION CONTEXT & CULTURE

Lonza is actively hiring for this position.

INDUSTRY: Life Sciences / Pharmaceutical Manufacturing / Healthcare Technology

EXPECTED CAREER ROADMAP

This Quality Associate role provides hands-on exposure to several highly sought-after pharmaceutical quality domains. These skills are highly valued across pharmaceutical, biotechnology, CDMO, CRO, API, biologics, and medical device companies worldwide, offering a strong pathway for global career progression.

APPLICATION ADVISORY

Ensure your resume prominently highlights your practical experience in QA, QMS, and Regulated Manufacturing. Be prepared to discuss specific scenarios involving CAPA implementation, data integrity maintenance, and audit coordination during the interview.
RECOMMENDED TRAINING
1/5
GCP Audit & Compliance Crash Course

GCP Audit & Compliance Crash Course

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.