Join Dr. Reddy’s Laboratories as Cleaning Validation Specialist | Regulatory Affairs Jobs
Looking to build a rewarding career in the pharmaceutical industry? Explore Regulatory Affairs Jobs and exciting opportunities with Dr Reddy’s career in India. Dr. Reddy’s Laboratories Ltd., a global leader in Pharmaceutical Jobs, is hiring for a Cleaning Validation Specialist position at its Hyderabad facility. This role offers the chance to contribute to a world-class organization that’s accelerating access to affordable and innovative medicines — because Good Health Can’t Wait.
Job Details:
- Job Title: Cleaning Validation Specialist / Associate
- Location: Hyderabad, India
- Department: IPDO / Global Manufacturing Organization (GMO)
Job Description For Regulatory Affairs Jobs
The Cleaning Validation Specialist plays a vital role in implementing cleaning validation procedures, ensuring compliance with regulatory standards and GMP. This position contributes to Regulatory Affairs Jobs excellence by preparing and reviewing SOPs, validation plans, and reports while supporting the Quality Management System (QMS) and compliance efforts within Dr Reddy’s career framework.
Key Responsibilities :Pharmaceutical Jobs at Dr Reddy’s
- Prepare, review, and approve Cleaning Master Validation Plans, Validation Protocols, Reports, and Acceptance Criteria documents while focusing on regulatory affairs in these jobs.
- Ensure implementation of cleaning validation SOPs and master plans in compliance with cGMP and regulatory standards.
- Compile and summarize data for validation reports and periodic monitoring.
- Review and approve QMS documents like change controls and incident reports.
- Participate in internal and external audits related to validation.
- Support risk assessment and design qualification activities.
- Provide training and support digitalization initiatives within the cleaning validation framework.
Qualifications
- Education: Bachelor of Pharmacy or Master’s in Science/Pharmacy.
- Experience: 3–7 years in Cleaning Validation, preferably in solid dosage manufacturing.
Technical Skills:
- Hands-on experience in validation protocols and swab sampling for regulatory affairs jobs.
- Knowledge of PDA Tech Report 29, ISPE, APIC, and other relevant guidelines.
- Proficiency in CLEEN software and data interpretation.
Behavioral Skills:
- Excellent communication, analytical, and problem-solving skills.
- Team collaboration and a commitment to continuous learning.
About the Department – Regulatory Affairs Jobs in Global Manufacturing Organisation (GMO)
At Dr. Reddy’s Laboratories, the GMO division drives precision manufacturing and compliance excellence. With 19 state-of-the-art facilities across India, Mexico, and the UK, GMO supports Pharmaceutical Jobs that shape the future of healthcare. Recognized by the World Economic Forum’s Global Lighthouse Network, GMO exemplifies sustainability, innovation, and digitalization — key pillars of Dr Reddy’s career development.
Benefits Offered
- Competitive salary with relocation and family support.
- Comprehensive medical and life coverage.
- Maternity, paternity, and professional learning programs for continuous growth.
Why Join This Company?
At Dr. Reddy’s, Good Health Can’t Wait is more than a motto it’s a mission. The organization fosters an inclusive culture rooted in empathy, innovation, and teamwork. Employees pursuing roles in regulatory affairs jobs or broader Pharmaceutical Jobs find endless opportunities for growth and purpose within Dr Reddy’s career ecosystem.
