IPM - Assistant Manager – IPM | Morepen Proprietary Drug Research | Gagillapur, Hyderabad, Telangana, India
Morepen Proprietary Drug Research is inviting applications for the position of IPM - Assistant Manager at its pharmaceutical research and manufacturing facility in Gagillapur, Hyderabad, Telangana, India. This full-time opportunity is ideal for professionals with 6 to 10 years of experience in IPM operations, pharmaceutical manufacturing systems, project management coordination, compliance processes, and regulated production environments. The selected candidate will manage IPM activities, coordinate production planning operations, supervise documentation systems, and ensure compliance with pharmaceutical quality and operational standards. Candidates with expertise in process coordination, manufacturing workflows, GMP systems, and cross-functional team management within pharmaceutical environments will be preferred. This role provides valuable exposure to advanced pharmaceutical operations, production management systems, and regulated industrial environments focused on operational efficiency, quality assurance, and compliance excellence.
Location
Gagillapur, Hyderabad, Telangana, IndiaEmployment Type
Full-timeExperience Required
6 to 10Compensation & Benefits
Competitive compensation package with opportunities for leadership exposure, pharmaceutical operational management experience, and long-term career development.About Morepen Proprietary Drug Research
Morepen Proprietary Drug Research is engaged in pharmaceutical manufacturing, research-driven healthcare operations, formulation development, and regulated industrial production systems.Position Overview
The IPM - Assistant Manager will manage IPM operations, manufacturing coordination activities, and process compliance systems within pharmaceutical operations.Key Responsibilities
- Coordinate IPM and pharmaceutical production activities.
- Monitor operational planning and manufacturing schedules.
- Ensure compliance with GMP and regulatory standards.
- Maintain production and process-related documentation.
- Coordinate with quality assurance and production departments.
- Support process improvement and operational efficiency initiatives.
- Review reports related to production and operational performance.
- Supervise workflow coordination and resource utilization.
- Assist in audit preparation and compliance management.
- Support training and operational guidance for teams.
Required Skills & Competencies
- Knowledge of pharmaceutical manufacturing operations.
- Understanding of IPM and process coordination systems.
- Leadership and team management capabilities.
- Strong communication and reporting skills.
- Problem-solving and operational analysis expertise.
- Awareness of GMP and regulatory compliance systems.
- Ability to manage documentation and workflow processes.
- Time management and organizational abilities.
- Attention to detail and process accuracy.
- Capability to work in regulated pharmaceutical environments.