Before joining Navigos Search, Tuyen had already have headhunting experience at a major agency where she performed exceptionally well. She is currently a recruitment consultant in the Industrial and Manufacturing team, who has already achieved great successes since recently joining Navigos Search.
Tuyen is passionate about career consulting as she loves working directly with people and helping them with their problems. Her love for this profession has made her a trusted advisor for both clients and job-seekers. In addition, she is also a curious individual who never stops learning to improve herself and to contribute more to the job market.
At Navigos Search, Tuyen has successfully recruited senior positions of high technical requirements such as Export Sales Manager, Production Director, Senior Engineering Manager, Costing Manager,…
DUTIES & RESPONSIBILITIES
- Coordinate workload for all employee in the Research & Development Chemical Formulations;
- Develop the research methodology, perform pharmaceutical research samples and valid for procedure for manufacturing to ensure the timetable;
- Monitor the stability of research samples and raw materials of new suppliers;
- Establish registration dossiers (Part Pharmacy) for new product or improve product;
- Provide technical support to solve problems on the production line;
- Responsibility for optimizing the manufacturing processes and increasing productivity;
- Provides solutions in trouble-shooting on production and decrease costs;
- Cooperate with QA, QC and Production Department to organize the effective validation;
- Cooperate with Production to supervise manufacturing of scale up and technical transfers;
- Maintain orderly batch record files for each product and correspond with samples;
- Interact with QA, QA manager to conduct investigation of customer’s complains about unusual incidents and returned products.
Growth opportunity
Your Challenge
Will be given in interview
Promotion Opportunity
Will be given in interview
- PhD degree in Pharmacy, Bio-Chemical, Biotechnology, Biology, Chemical, have deep knowledge in generic pharmaceutical industry, and knowledge of WHO-GMP, PIC/S, TGA, FDA specification;
- At least 3 year-experience in management level;
- English: communication
- Deep knowledge in GMP, GLP, GSP, GDP, regulatory affairs and issue related;
- Experienced in human resource management and quality management for infusion and injection drug;
- Experience in pharmaceutical research and development and scientific report;
- Self-motivated and proactive.