Description
HIGHLIGHTS OF QUALIFICATIONS 1. Many years of pharmaceutical leadership experience in a Biotech and parenteral drug-manufacturing environment. 2. Diversified experience in sterile manufacturing including bulk manufacturing, aseptic filling, component sterilization, freeze drying, environmental monitoring, inspection and packaging. 3. Knowledge of governmental cGMP, OSHA, DEA regulations and procedures, experience with FDA, EU and other regulatory agencies inspections. 4. Prepared production and system change controls. Authored SOP's and production batch record in necessary detail to control and record operation activity. 5. Experienced in chemical testing which including HPLC, Ph, specific gravity, conductivity meters, spectrophotometer, chlorine concentration in water, etc. 6. Experienced in biological testing which including LAL test for endotoxin determination, bio-burden bulk sampling, environmental monitoring etc. 7. Excellent in planning, organizing, managing and administrating the company's resources 8. Enjoy learning new technologies and committed to on-going skill development 9. Self-motivated, hard-working, dedicated, reliable & a consistent performer 10. More than 4 years of experience in solid dosage manufacturing including granulation and compression.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| (Confidential) | Senior Supervisor | 1/2001 - Present |
| Hoffmann La Roche. | Production Specialist | 1/1988 - 1/2001 |
| Bristol Meyers Squibb | Material Supervisor | 1/1984 - 1/1987 |
| Efroze Chemicals Indus. | Production Supervisor | 1/1982 - 1/1984 |
Accomplishments
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