
Manager Formulation Development and Research
2 days ago
Experience - 12 to 16 Years
Qualification - M Pharm
Responsibilities
- Design and optimize manufacturing processes with technical improvements for regulated markets (US, Canada, EU) within allotted timelines.
- Evaluate manufacturing processes using DoE and QbD to define design space, control strategy, critical/ key parameters, and identify process risks.
- Screen manufacturing sites based on formulation and process complexity/feasibility
- Lead Technology transfer function with adequate project management skills to ensure successful scale-up of new products and effective launches with stipulated time.
- Define procedures for seamless product transfers between development and manufacturing (in-house and external), ensuring robust scale-up, accurate filings, and successful launches.
- Serve as SME for pharmaceutical processes and technologies, providing guidance in tech transfer, troubleshooting, and investigations to ensure robust performance and timely supply.
- Define and implement standards for formulation technology transfer and be the point contact for formulation technology transfer activities, with CFTs.
- Initiate, drive and facilitate capacity enhancement, cost reduction and time cycle reduction projects.
- Review and approve departmental SOPs to ensure compliance with cGMP and CQA guidelines, technical changes, change control, deviations and relevant documents. .
Desired Skills
- Expertise in formulation development of various dosage forms with strong knowledge of process optimization.
- Hands-on experience in technology transfer and scale-up
- Strong understanding of regulatory guidelines such as USFDA, EMA, WHO.
- Excellent documentation, communication, and analytical skills
- Ability to work in a fast-paced, dynamic environment
- Project management and cross-functional coordination
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