Technology Transfer Formulation & Development (OSD & Liquid) Executive/Asst. Manager
Location:
Kamothe, Navi Mumbai
only Male candidate
About Raptech Pharmatechnologies Pvt. Ltd.:
Our activities range from R&D, manufacturing & marketing of finished pharmaceutical formulations of Niche therapeutic segments. Our mission is to be the finest in our line of work and help save and enhance even more lives through our innovations around the globe is what we envisage. We aim to progress towards horizontal and vertical integration in pharmaceutical generic product development. Our state-of-the-art R&D centre is at the forefront of developing high-quality generic formulations to meet unmet medical needs globally. We foster a collaborative and dynamic environment where scientific excellence and professional growth are paramount.
Job Summary:
The Technology Transfer Executive/Asst. Manager will be a key contributor to our R&D team, responsible for scale up, manufacturing process validation and transfer to production site (e.g., solid oral, liquid oral, parenteral, etc.). This role involves hands-on production and pilot plant handling experience, manufacturing & scale up of pilot/Pivotal/exhibit batches, and and documentation in a cGMP-compliant environment. The successful candidate will possess a strong understanding of pharmaceutical sciences, formulation principles, and an ability to troubleshoot and innovate.
Key Responsibilities:
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Formulation Design & Development including Technology Transfer:
Develop and optimize various dosage forms, including but not limited to tablets, capsules, injectables, suspensions, solutions, creams, gels, and transdermal patches.
Oversee Technology Transfer including finalization of Technology Transfer documentation and Technology Transfer Reports
Monitor batches formulated at RnD
Oversee the stability charging program for batches developed in-house
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Process Development & Optimization:
Develop robust and scalable manufacturing processes for developed formulations.
Optimize critical process parameters (CPPs) and critical material attributes (CMAs) to ensure product quality and manufacturability.
Troubleshoot formulation and process challenges, implementing effective solutions.
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Documentation & Compliance:
Maintain meticulous laboratory notebooks and detailed records of the development process, observations, and results.
Ensure all work is conducted in compliance with cGMP, ICH guidelines, and company policies.
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Collaboration & Communication:
Work collaboratively with cross-functional teams including Analytical Development, Process Development, Quality Assurance, Regulatory Affairs, and Manufacturing.
Present scientific findings and project updates effectively to internal teams and management.
Stay updated with the latest scientific literature, industry trends, and regulatory requirements related to pharmaceutical formulation.
Qualifications:
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Education:
B.Pharm, M.Pharm
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Experience:
7-9 years of hands-on experience in pharmaceutical formulation technology transfer to manufacturing, pilot plant handling
Experience with solid and liquid oral dosage forms is highly preferred.
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Skills & Competencies:
Strong theoretical and practical knowledge of pharmaceutical formulation principles, physical pharmacy, and drug delivery systems.
Proficiency in operating equipment relevant to formulation development.
Ability to work independently and as part of a team in a fast-paced environment.
Job Types: Full-time, Permanent