Jeff Line Email & Phone Number

Please, feel free to message me. Let's talk about amino acid analysis, spectrophotometry, or electroporation/electrofusion and how these methods can be applied into a peptide or protein production workflow.

Greater Los Angeles Area

Installations, preventative maintenance, and technical support on Biochrom laboratory instruments. Troubleshooting support, on-site repair, validation, and end user training.

Greater Los Angeles Area

Review and edit quality control standard operating procedures and validation protocols.

Carson, Ca

Designed and commissioned analytical and microbiology testing laboratories. Managed validation of incubators, autoclave, and storage chambers. Implement validation protocols for IQ, OQ, and PQ of analytical instruments. Oversee development, optimization, and validation of analytical methods using HPLC, GC, AA and FT-IR. Design equipment preventative maintenance procedures and manage calibration schedule.Reviewed existing quality systems to ensure analyst follow GLP and GMP practices to comply with FDA and USP requirements. Investigate reoccurring out of specifications for root cause and implement CAPAs to resolve issues.Communicate with management team and executives to design systems to stream line production activities while maintaining quality compliance through change control procedures.Manage nine analysts and technicians. Conduct training on quality systems and GMP compliance. Evaluated and restructured quality team based on individual strengths and competence.

Greater Los Angeles Area

Advise on quality control operations; specifically in analytical method development, validation protocols, training protocols, and establishing standard operating procedures. Experience in biotech, nutraceutical, and cosmetic industries.

San Fernando, Ca

Supervise validation and metrology group. Author and execute equipment Installation, Operation and Performance Qualification protocols. Author and execute cleaning validation protocols. Manage and maintain calibration schedule for all production equipment and analytical instruments. Manage all equipment commissioning, in house calibration, and discrepancies. Work directly and meet with company executives to discuss on going projects and department goals.

HPLC Method validation. Product active ingredient(s) analysis.

Part Time; author/revise SOPs, assist with laboratory set-up.

Analyzed in-process and final products. HPLC, Endotoxin, ELISA, electrophoresis. Assay transfer and method validation. Author and revised SOPs.

Greater San Diego Area

Environmental Monitoring

Bachelor, Microbiology

Aa, Performing Arts / Sound Engineer