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I am a strong contributor performing routine tasks and other duties assigned under cGMP and GLP methods. I am a versatile individual with keen attention to details and provide input to increase productivity and quality. I participate in IQ, OQ and PQ in
As a technician, I would bring focus on quality and ease of use to your system development. Furthermore, I am eager and determined to work as team in order to achieve success.
Machine Operator
About Me
Industry: |
Manufacturing & Production |
|---|---|
Occupation: |
Machine Operator |
Highlights: |
Over 10 years experience in clean room. Demonstrated interpersonal skill to increase productivity, quality and safety at work. Motivated by opportunities to learn and meet unprecedented challenges. Extensive background in pharmaceutical manufacturing, design and development of equipment fixtures and special tools. Other areas of expertise: • Provided ideas to improve production yield, throughput and quality |
Ideal Companies: |
Bio-tech, Pharmaceuticals, engineering |
Education level: |
Associate |
Will Relocate: |
No |
Location: |
San Jose, CA |
Work Experiences
5/2007 - 1/2009
Alexza Pharmaceuticals
Individual Contributor
- • Material requisition and reconciliation
• Drug formulation
• Line clearance
• Equipment set-up operate, and cleaning of processing equipment.
• Final assembly of drug delivery device
• Batch record review
• Measurement of parts using caliper, micrometer and other measuring instruments for analysis.
• Demonstrated team leadership to ensure that daily production timelines are met as needed.
• Responsible for training of new manufacturing technicians and ensuring that training records were accurate and up to date.
• Collaborated on Competency Based Training program.
• Suggested modification of set up jigs and fixture to increase productivity, quality and safety.
• Assisted R&D in mixing Slurry, weighing, washing and coating of foils.
• Collaborated and contributed in process development group to conduct, execute experimental protocols.
• Ensured manufacturing protocols to enable timely cGMP compliant production of quality.
• Manufactured supplies for non-clinical, pre-clinical and clinical studies under cGMP method.
5/2003 - 4/2007
Aleza Corporation
Individual Contributor
- • Independently performed Aseptic manufacturing tasks from washing, sterilization, and depyrogenation of parts to be used in sterile filtration, final sterile drug fill, assembly, and inspection of Viadur for any deficiency
• Performed injection molder Set-up and troubleshooting.
• Performed setup, operation and inspection of small parts.
• Performed set-up, operation and troubleshooting of sub assembly equipments
• Ensured safety and cGMP compliance in work assignments.
• Contribute to continuous improvement opportunities
12/2000 - 12/2002
