Senior Executive / Assistant Manager Formulation R&D

Cronus Pharma; Hyderabad; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Cronus Pharma Specialities India Pvt. Ltd. is seeking experienced professionals for the Formulation Research & Development team in Hyderabad. Position: Senior Executive / Assistant Manager Formulation R&D with 6–9 years of experience and an M.Pharm in Pharmaceutics or Pharmaceutical Sciences.

Location: Hyderabad / Shamshabad. Immediate joiners preferred. You will work across liquid oral and OSD formulations, scale-up, DoE, QbD, and technology transfer, coordinating with Analytical R&D,

Qualifications

• M.Pharm (Pharmaceutics / Pharmaceutical Sciences) degree required.
• Hands-on experience in liquid oral and OSD formulations.
• Development from lab scale to pilot/commercial scale.
• Exposure to QbD, DoE and risk assessment.
• GMP knowledge and regulatory awareness.

Responsibilities

• Develop and optimize liquid oral and OSD formulations from lab to pilot and commercial scale.
• Coordinate with Analytical R&D, Production, QA, QC and Tech Transfer teams.
• Prepare development protocols, reports and technical documentation.
• Troubleshoot formulation and manufacturing-related challenges.
• Ensure GMP compliance and regulatory alignment during development.

Skills

Liquid oral formulations

OSD formulations

Formulation development

QbD

DoE

Process development

Education

M.Pharm (Pharmaceutics / Pharmaceutical Sciences)

Job description

Cronus Pharma Specialities India Pvt. Ltd. is looking for experienced professionals to join our Formulation Research & Development team.

Position: Senior Executive / Assistant Manager Formulation R&D
Department: Formulation Research & Development
Experience: 6 9Years
Qualification: M.Pharm ( Pharmaceutics / Pharmaceutical Sciences)
Location: Hyderabad / Shamshabad

Key Experience Required:

• Hands-on experience in Liquid Oral Formulations & OSD formulations
• Formulation development from lab scale to pilot/commercial scale
• Experience in pre-formulation, formulation optimization and process development
• Strong exposure to QbD, DoE and risk assessment
• Experience in scale-up, technology transfer and process optimization
• Preparation and review of development protocols, reports and technical documentation
• Troubleshooting formulation and manufacturing-related challenges
• Coordination with Analytical R&D, Production, QA, QC and Technology Transfer teams
• Exposure to excipients selection, compatibility studies and formulation characterization
• Knowledge of GMP, regulatory requirements and pharmaceutical development practices

Immediate Joiners / Short Notice Candidates are highly preferred.