APDM Pharmaceuticals Private Limited has its office in Ahmedabad with all QA and regulatory support staffs for managing CDO and CDMO projects ,vendor Audits, BA BA monitoring, project and Engg team. We are a global pharmaceutical service providers with a vast global network of CMO’s, CDMO’s and CRO’s. We have more than 100 years of CDMO, 50 years of R&D and decades of regulatory and QA experience in our company.
Post : Sr. Officer / Executive
Department : Formulation Development (Parenteral & Ophthalmic)
Experience Required : 3–5 Years
Qualification : M.Pharm in Pharmaceutics with relevant experience in Formulation Development
Job Summary
• Development and optimization of parenteral and ophthalmic formulations.
• Planning and execution of formulation development trials.
• Scale-up and technology transfer activities.
• Troubleshooting of formulation and process-related issues.
• Preparation and review of development documents, including PDR and related technical reports.
• Coordination with Analytical, QA, Production and other cross-functional teams.
Desired Skills
• Hands-on experience in Parenteral and Ophthalmic formulation development.
• Exposure to development of products for US, Europe and ROW markets.
• Experience developing 505(b)(2) products would be an advantage.
• Familiarity with US FDA, EMA/European and other international regulatory requirements for pharmaceutical product development.
• Good problem-solving, analytical thinking, technical documentation and communication skills.
Share your resume at : career@apdmpharma.com
Last Date to Apply : 10/09/2026
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