Assistant Manager - Formulation Development

Drlogy; India; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Drlogy is seeking an Innovative Assistant Manager - Formulation Development in India. This role involves managing pharmaceutical formulation development projects and ensuring compliance with quality standards. The ideal candidate will lead formulation trials, coordinate technology transfer activities, and enhance product development.

Strong experience in formulation research, process optimization, and cross-functional collaboration is essential. A commitment to continuous improvement and training staff on compliance practices will be critical for success in this role.

Qualifications

• Experience in formulation development and product optimization.
• Knowledge of GMP and pharmaceutical quality standards.
• Ability to train staff on formulation procedures.

Responsibilities

• Manage formulation development and product optimization activities.
• Ensure compliance with GMP and pharmaceutical quality standards.
• Support validation and exhibit batch manufacturing activities.

Skills

Formulation development

Process optimization

Analytical coordination

Regulatory documentation

Cross-functional collaboration

Risk assessment

Job description

Overview

Innovative Assistant Manager - Formulation Development responsible for managing pharmaceutical formulation development projects, process optimization, and technology transfer activities. Skilled in formulation research, scale-up operations, analytical coordination, and regulatory documentation. Adept at supporting product development and ensuring compliance with pharmaceutical quality standards.

Responsibilities

• Manage formulation development and product optimization activities.
• Conduct formulation trials and process evaluation studies.
• Coordinate scale-up and technology transfer operations effectively.
• Ensure compliance with GMP and pharmaceutical quality standards.
• Review formulation reports and technical documentation accurately.
• Coordinate with QA, QC, production, and regulatory teams.
• Monitor formulation performance and product quality parameters.
• Investigate formulation deviations and implement corrective actions.
• Support validation and exhibit batch manufacturing activities.
• Conduct risk assessments and process evaluation studies.
• Maintain formulation development records and project documentation.
• Participate in audits and regulatory inspection activities.
• Train staff on formulation procedures and compliance practices.
• Support continuous improvement and product enhancement initiatives.
• Contribute to successful commercialization of pharmaceutical products.

Qualifications

• Experience in formulation development and product optimization activities.
• Experience in formulation trials, process evaluation, scale-up and technology transfer.
• Knowledge of GMP and pharmaceutical quality standards.
• Ability to review formulation reports and technical documentation.
• Strong cross-functional collaboration with QA, QC, production, and regulatory teams.
• Experience in risk assessment and process evaluation studies.
• Experience supporting validation and batch manufacturing activities.
• Ability to train staff on formulation procedures and compliance practices.
• Commitment to continuous improvement and product enhancement.
• Contribute to commercialization of pharmaceutical products.