DQA – Deputy Manager – Development Quality Assurance | Morepen Laboratories Limited | Gandimaisamma, Hyderabad, Telangana, India
Morepen Laboratories Limited is hiring a Deputy Manager – Development Quality Assurance at its Gandimaisamma, Hyderabad, Telangana, India facility. This full-time opportunity is ideal for professionals with 4 to 8 years experience in development quality assurance within the Pharmaceutical industry in India. The role focuses on ensuring quality compliance during product development stages, reviewing documentation, and supporting regulatory readiness.
Location
Gandimaisamma, Hyderabad, Telangana, India
Employment Type
Full-time
Experience Required
4 to 8 years experience in development quality assurance
Compensation & Benefits
Salary not disclosed aligned with Pharmaceutical industry in India standards.
About Morepen Laboratories Limited
Morepen Laboratories Limited operates within the Pharmaceutical industry in India focusing on API and formulation development supported by strong quality systems.
Position Overview
The DQA Deputy Manager will oversee development quality processes, documentation review, and compliance monitoring during product lifecycle stages.
Key Responsibilities
- Review development documentation.
- Ensure compliance with GMP standards.
- Support validation activities.
- Coordinate cross-functional teams.
- Conduct quality reviews.
- Monitor audit readiness.
- Maintain quality records.
- Support regulatory submissions.
- Identify compliance gaps.
- Implement corrective actions.
Required Skills & Competencies
- Development QA expertise.
- Regulatory compliance knowledge.
- Documentation review skills.
- GMP understanding.
- Analytical thinking ability.
- Communication skills.
- Problem-solving capability.
- Quality systems knowledge.
- Team coordination skills.
Educational Qualification
MPharm or MSc
About the Project & Industry
This role strengthens pharmaceutical development quality systems within the Pharmaceutical industry in India.
Why Join Morepen Laboratories Limited?
Opportunity to contribute to regulated pharmaceutical product development environments.
How to Apply
jobs@morepenpdr.com
