Lonza, one of the world’s leading life sciences manufacturing companies, has announced an exciting Quality Associate โ 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
| Particular | Details |
|---|---|
| Company | Lonza |
| Position | Quality Associate โ 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 โ 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:
- Bachelor’s or Master’s degree in:
- B.Pharm
- M.Pharm
- B.Sc
- M.Sc
- Biotechnology
- Microbiology
- Life Sciences
- Related Scientific Discipline
Candidates should have knowledge of:
- 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
Preferred Skills
- Strong analytical thinking
- Excellent documentation practices
- Audit coordination experience
- Problem-solving abilities
- Cross-functional communication
- Stakeholder management
- Continuous improvement mindset
- Regulatory compliance knowledge
Why Join Lonza?
Lonza offers employees:
- Competitive compensation
- Global career opportunities
- Inclusive workplace culture
- Continuous learning programs
- Cross-functional international exposure
- Professional development
- Ethical work environment
- Opportunity to work with cutting-edge pharmaceutical manufacturing
Why This Role is a Great Career Opportunity
This Quality Associate role provides hands-on exposure to several highly sought-after pharmaceutical quality domains, including:
- GMP Compliance
- Data Integrity
- Vendor Qualification
- Regulatory Audits
- CAPA
- Quality Management Systems
- Document Control
- Change Control
- Inspection Readiness
These skills are highly valued across pharmaceutical, biotechnology, CDMO, CRO, API, biologics, and medical device companies worldwide.
How to Apply
