Team Leader – Manufacturing / QMS Job Opening at Dr. Reddy’s Laboratories, Hyderabad
Dr. Reddy’s Laboratories Ltd. has announced an exciting career opportunity for an experienced pharmaceutical professional for the position of Team Leader – Manufacturing / QMS in Hyderabad, Telangana. The position is suitable for professionals with extensive experience in pharmaceutical manufacturing, Quality Management Systems (QMS), GMP documentation, investigations, CAPA, change control and regulatory compliance.
With a strong focus on quality, compliance and continuous improvement, this role offers an opportunity to work in a dynamic pharmaceutical manufacturing environment with a globally recognised organisation.
Job Details
| Particular | Details |
|---|---|
| Company | Dr. Reddy’s Laboratories Ltd. |
| Position | Team Leader – Manufacturing / QMS |
| Location | Hyderabad, Telangana |
| Department | Production – OSD / Manufacturing / QMS |
| Experience | 10+ Years |
| Qualification | Pharmacy / Science / Biotechnology or related field |
| Industry | Pharmaceutical |
| Employment Type | Full-time |
About the Role
The selected candidate will be responsible for managing and supporting key quality documentation and compliance activities within the pharmaceutical manufacturing environment.
The role involves preparation and review of GMP documentation, coordination with Quality Assurance and cross-functional teams, management of investigations and CAPAs, support for audits and inspections, and ensuring timely completion of quality-related activities.
The candidate will also contribute to maintaining a strong culture of compliance and continuous improvement across the organisation.
Key Responsibilities
The major responsibilities associated with this position include:Preparing, reviewing and updating GMP-related documents such as SOPs, investigations, CAPAs, risk assessments, URS and qualification documents.
Coordinating with Quality Assurance and cross-functional teams for document review, approval and implementation.
Conducting periodic documentation audits to ensure compliance with current GMP requirements.
Supporting audit preparation, audit responses and regulatory inspection readiness.
Monitoring and ensuring timely closure of quality notifications, CAPAs and change controls through relevant QMS/SAP systems.
Performing incident, OOS and OOT investigations and supporting effective root-cause analysis.
Preparing appropriate CAPAs and monitoring their effectiveness.
Coordinating departmental training activities and ensuring timely completion of SOP and GMP-related training.
Supporting safety and ESG initiatives within the department.
Maintaining proper control, accessibility and archival of quality-related documents.
Promoting continuous improvement and a strong compliance culture within the manufacturing environment.
Educational Qualification
Candidates applying for this position should preferably possess:Graduation in Pharmacy; or
Post Graduation in Pharmacy; or
A degree in Science, Biotechnology or a related discipline.
Additional certifications in areas such as Pharmaceutical IPQA, CDSCO Compliance, Pharmaceutical Quality Auditing or equivalent fields may be advantageous.
Experience Required
The position requires a minimum of 10+ years of relevant professional experience.
Candidates with strong exposure to pharmaceutical manufacturing, Quality Management Systems, GMP documentation, regulatory compliance, investigations and quality improvement activities may be particularly suitable for this opportunity.
Key Skills
Applicants should have strong knowledge and practical exposure to areas including:Current Good Manufacturing Practices (cGMP)
Good Documentation Practices (GDP)
Quality Management Systems
Change Control
CAPA Management
Incident Management
OOS/OOT Investigations
Risk Management
Regulatory Compliance
Audit Planning and Execution
Technical Documentation
Pharmaceutical Manufacturing
Continuous Improvement
QMS Software
Preferred Experience
Experience in the following areas will be considered an added advantage:Automated QMS software used in pharmaceutical manufacturing.
Internal inspections and compliance audits.
Non-conformance and CAPA management.
Quality document control and archival.
Deviation and incident management.
Market complaint handling.
Impact assessment related to compliance.
Quality improvement initiatives.
Alignment of manufacturing processes with current quality standards and industry best practices.
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company headquartered in Hyderabad, India. The organisation operates across global markets with a focus on making affordable and innovative medicines accessible to patients.
The company has research and development centres, manufacturing facilities and commercial operations across numerous countries and employs thousands of professionals worldwide.
Dr. Reddy’s Laboratories promotes a workplace based on diversity, inclusion, professional development and equal employment opportunities.
Benefits and Career Development
According to the company, employees may have access to a range of benefits and professional development opportunities, which may include:Learning and development programmes.
Career growth opportunities.
Joining and relocation support, where applicable.
Family support benefits.
Medical coverage for employees and eligible family members.
Life coverage.
Professional learning opportunities.
Benefits may vary according to the position, location and applicable company policies.
Who Should Apply?
This opportunity may be suitable for experienced pharmaceutical professionals who have a strong background in manufacturing, QMS, GMP compliance and quality documentation and are looking to take their careers to the next level.
Candidates should carefully review the eligibility requirements and experience criteria before submitting an application.
How to Apply
Interested and eligible candidates are advised to apply through the official Dr. Reddy’s Laboratories career portal.
Official Careers Website:
https://careers.drreddys.com/job/team-leader-manufacturing-qms-in-hyderabad-jid-5190
Candidates should verify the current vacancy status, eligibility requirements and application instructions directly on the official careers portal before applying.
Final Note
This job information is published by Helbert Solutions for educational and career-information purposes. Helbert Solutions is not the employer or recruitment agency for this vacancy. Candidates should independently verify the vacancy and all recruitment-related information through the official company website before submitting personal information or making any payment.
For more pharmaceutical jobs, internships, training opportunities and career updates, continue visiting Helbert Solutions.
