Pharmaceutical manufacturing and research co. (Sacramento, CA) seeks qualified professional to
design & execute analytical method validation protocols and reports of active pharmaceutical
ingredients and drug products (finished products). Work with SOPs for instruments processes
and methodologies used to achieve product. Follow Good Laboratory Practices and perform
analytical method development and validation for API and finished products. Send resumes to:
HRD, Nivagen Pharmaceuticals Inc., 3050 Fite Circle, Suite 100, Sacramento, CA 95827
I am looking forward for a Chemist position in Quality Control department. I expect a career which is different yet unique, my intelligence is continuously nourished by challenges and constant quest for knowledge is honed on the newest of technologies. Looking forward to a challenging career in an organization where I can sharpen my professional skills and experience and work at a position where my ability for innovative decision making could be tapped.
Summary: A self motivated, creative, hard working and resourceful individual with strong analytical, investigative, technical problem solving, decision making, interpersonal and communication skills.
Having over 11 years hands-on laboratory experience in chemist quality testing of pharmaceutical and biological drug substance (s) / product (s). Currently working as a Team Lead in General testing laboratory, Quality Control at a Biologicals Company named Human Biologicals Institute, a division of Indian Immunologicals Ltd., (Subsidiary of National Dairy Development Board).
Mob No:+91- 9787791770
Mail ID: email@example.com