Life Sciences Jobs at Lonza | Candidates Apply Now
Are you looking for Life Sciences Jobs or QA Jobs with a leading global pharmaceutical company? Lonza Careers has announced an excellent opportunity for the position of Quality Associate – GMP & DI Compliance in Rewari, Haryana. If you have a background in Pharmacy or Life Sciences and are passionate about Quality Assurance, GMP compliance, regulatory audits, and quality systems, this is your chance to build a rewarding career with one of the world’s leading life sciences organisations.
Job Description
- Location: Rewari, Haryana, India
- Reference: R77753
Key Responsibilities
- Ensure compliance with applicable regulatory requirements, customer expectations, Halal standards, and internal quality procedures.
- Coordinate and support regulatory inspections, customer audits, certification audits, and follow-up actions to ensure successful outcomes.
- Maintain and manage the Approved Vendor List and support vendor qualification activities in accordance with quality and compliance standards.
- Plan, perform, and coordinate vendor audits to evaluate compliance and identify opportunities for improvement.
- Develop, implement, and monitor training programs to ensure personnel competency and compliance with GMP and quality requirements.
- Administer the Document Management System (DMS) and ensure effective document control practices across the site.
- Lead and execute self-inspection programs to identify compliance gaps and drive corrective and preventive actions.
- Develop, monitor, and continuously improve the site Data Integrity Program and Data Integrity Matrix across systems and processes.
- Participate in and manage Change Control activities, ensuring appropriate risk assessment, documentation, and implementation.
Qualifications
Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related scientific discipline.
Experience
Experience within Quality Assurance, Quality Management Systems, Compliance, or regulated manufacturing environments.
Skills Needed
- Strong understanding of GMP principles, quality systems, regulatory requirements, and compliance expectations.
- Knowledge of audit management, vendor qualification, document control, change management, CAPA, and data integrity practices.
- Experience working with Document Management Systems (DMS) and quality management processes.
- Strong analytical and problem-solving skills with the ability to identify risks and drive effective corrective actions.
- Excellent communication and stakeholder management skills with the ability to collaborate across functions.
What You Will Get
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance.
- Opportunities to collaborate with global cross-functional teams.
- Ongoing learning and professional development opportunities.
If you are searching for Life Sciences Jobs, QA Jobs, or exciting opportunities through Lonza Careers, this Quality Associate – GMP & DI Compliance role offers an excellent opportunity to grow your career in Quality Assurance, GMP compliance, regulatory audits, and quality management systems with a globally recognized life sciences company. Apply today and take the next step in your professional journey.
