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- Manage all aspects of CMC activities for pharmaceutical and consumer health products, encompassing formulation development, process optimization, and analytical methods.
- Develop and maintain precise technical documentation, including CMC regulatory submissions (INDs, NDAs, MAA, Food supplement dossier, Cosmetics etc.).
- Create and update product specifications, master batch records, and standard operating procedures.
- Serve as the primary point of contact between the organization and manufacturing sites.
- Collaborate closely with manufacturing teams to ensure alignment with CMC strategies and objectives.
- Work collaboratively with QA and QC teams to implement and maintain quality standards throughout the manufacturing process.
- Participate in the development and execution of quality initiatives.
- Stay abreast of regulatory changes and industry trends impacting CMC requirements.
- Ensure ongoing compliance with relevant regulations and guidelines.
- Prepare and review CMC sections of regulatory submissions to health authorities.
- Identify opportunities for process improvements and efficiency enhancements in collaboration with manufacturing teams.
- Implement changes to enhance the robustness and reliability of manufacturing processes.
- Collaborate with supply chain teams to manage inventory levels and ensure timely production and distribution.
- Implement strategies to enhance the reliability of the supply chain for pharmaceutical and consumer health products.
- Bachelor's or advanced degree in a relevant scientific or engineering discipline.
- Proven experience in CMC management within the consumer health or related industries.
- Technical writing expertise with the ability to articulate complex CMC concepts in regulatory submissions.
- In-depth knowledge of formulation development, process optimization, and analytical methods in a consumer health context.
- Familiarity with regulatory requirements and guidelines related to consumer health products.
- Project management skills to oversee CMC processes and timelines.
- Effective communication skills to liaise with manufacturing, QA, QC, and regulatory teams.
- Collaborative mindset with the ability to work across functional areas.
- Knowledge of quality systems and practices in the pharmaceutical or consumer health sector.
- Adaptability to evolving industry standards and regulatory landscapes.
- Growth Opportunities for strong performers
- Flexible working schedule
- Chance to work on cutting edge technology
- Fun working culture
CMC Manager - Delhi, India - Vita Green Health Product Company Limited
Description
Job Purpose:
The position will be overseeing Chemistry, Manufacturing, and Controls (CMC) activities, ensuring the highest quality and compliance standards. Responsibilities will encompass a range of tasks, including technical writing, collaboration with manufacturing sites, and close coordination with Quality Assurance (QA) and Quality Control (QC) functions.
Main Tasks:
CMC Oversight:
Technical Writing:
Manufacturing Site Liaison:
Quality Assurance/Quality Control Collaboration:
Regulatory Compliance:
Process Optimization:
Supply Chain Coordination:
Requirements
Benefits
We offer you..