- Reporting to CEO
- Execute the current under-license/Tech Transfer/contract manufacturing projects
- Handle the upcoming local/contract manufacturing projects which have recently exited business development pipeline in association with Kimiara's overseas partners
- Develop new projects in both RX and OTC segments in collaboration with business development and marketing departments
- Recruit, train, and manage subordinates needed to be teamed up for the projects
- Facilitate the regulatory procedure in collaboration with the regulatory department and the technical manager
- Support and follow implementation of any studies (BE, Clinical studies) pertaining to the products and projects
- Negotiate with local pharmaceutical companies to expand the number of contract manufacturing partners
- Maintain productive relationship with the rest of the team in different departments
- Analyze production process, CMOs, Suppliers data and identify trends, problems, and opportunities for improvement.
Requirements
- Pharma D. / Pharmaceutics
- Minimum of 3 years of supervisory/leadership experience in production/manufacturing environment in pharmaceutical industry
- Decent profile of practical experience in industry / Manufacturing procedures
- Capable of planning and executing defined plans
- Creativity rising from a background of mastering the current situation and trend(s) of the market and industry
- Familiarity with regulatory procedures and the prevailing regulations of the MOH/IFDA
- Mastering all the steps of manufacturing pharmaceuticals and the pertinent requirements
- Familiarity with Technology transfer and Under License Manufacturing
- Good command of English
- Negotiation skills & Good communication (verbal and written) skills, along with demonstrated positive leadership skills with experience in team-building/motivating practices.
- A general perception of business development and its core elements
- Good at necessary IT skills