Job Description
- You will be responsible for the smooth running of the production line and the quality of output. - Ensure GMP compliance of manufacturing of products contracted out. - Ensure all aspects of product manufacturing and/or testing complies with established standard operating procedures (SOPs) and the applicable marketing authorizations. - Involve in many activities related to Contract Manufacturing Unit in the company. - Maintaining a positive and constructive relationship with the contractor employees. - study and learn deeply the production procedures. The ability to direct personnel towards maximum performance is much appreciated. Decision-making and problem-solving will take up a part of your job. - Report and provide an evaluation of issues such as deviations and equipment failures to determine a cause and corrective action. Leads root cause investigation of process deviations within the process operations and obtaining solutions. - Ability to fulfill the 100% travel schedule (duration of coverage between 4-14 overnight stays)
Requirements
- BS/MS in Chemical Engineering, Chemistry, or any related discipline is preferred. - Proficient computer skills including Microsoft Word and Excel. - Language Skills: Good command of English (written /reading). - No experience is needed, but having experience in the pharmaceutical industry is appreciated. - Be highly capable of working in a team environment with a positive attitude under some supervision, thus having good team work and communicational skills is needed - No experience is needed, but having experience in the pharmaceutical industry is appreciated. - Being enthusiastic, energetic, quick learner, self-motivated and able to work in cross-functional teams is necessary. - Ideal Age: 22 – 35 years
Employment Type
- Full Time
Job Category
Seniority
Details
Employment type
- Full Time
Job Category
Educations
Seniority
