
Job Description
Job Description:
Supervision of the contract manufacturing process from 0 to 100 (site selection, technology transfer, production monitoring)
Cooperation in the transfer, optimization and control of pharmaceutical formulation at production sites
Supervision and control of how to carry out all stages of product production
Technical evaluation of production equipment and machinery and their adaptation to product needs
Mastery of GMP principles, including quality assurance of the process and production equipment, documentation and reporting
Mastery of all production line devices (solids, liquids and softgels)
Manage relationships with contract factories and negotiate for appropriate financial and operational conditions
Monitor product quality and supervise the implementation of GMP standards and legal requirements
Control the schedule, costs and risk management of contract projects
Periodic visits to factories and submission of technical and management reports
Identify and evaluate new factories to develop the contract manufacturing network
Interdepartmental cooperation with R&D, QC, supply and commercial units to advance projects
Qualifications:
A degree in chemistry or related fields
Sufficient knowledge of pharmaceutical formulation and production processes
Technical familiarity with pharmaceutical manufacturing industrial machinery
Knowledge of the pharmaceutical industry and contract manufacturing plants
High ability in negotiation, bargaining and communication management
Responsible, organized, with a team spirit and the ability to manage time
Readiness to periodically visit factories
Employment Type
Job Category
Educations
Seniority
Details
Employment type
Job Category
Educations
Seniority
