Chemist - Analytical

KDC One•Chatsworth, CA

7d•Onsite

About The Position

The Analytical Chemist is responsible for performing assay testing on OTC or cosmetic bulk/ finished product and assist in stability assay study in compliance with Quality Control Specifications, and regulatory requirements. Specific Responsibilities & Duties: Promotes a safe working environment and adheres to Health, Safety and Environmental procedures, company safety rules, Good Laboratory Practices (GLD’s), Current Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) at all times. Perform analytical tests on Bulk, finished products, stability samples, raw materials, and contract manufactured material in compliance with GMP and as directed by the QC Specifications. Perform variety of analytical methods using HPLC, GC, ICP, FTIR, UV/Vis, and variety of wet chemistries following SOP of internal test method, USP or customer specified methods. Responsible for maintenance and troubleshooting of analytical instrument and clearly communicating the problems with Sr. Lead Chemist or Lab Director. Perform method validation following established test methods. Participate in method validation, method development and method transfer as needed. Perform calibration and routine maintenance of laboratory equipment as directed by the Quality Assurance Director. Conduct laboratory work and associated record keeping in a safe manner and in keeping with generally recognized GLP, GMP and company & customer’s SOP. Follow internal and customer specification. Write OOS report and Investigate problems presented in test results. Physical Requirements: Capable of lifting up to 25 lbs. Capable of standing, walking, and sitting for extended periods Qualifications: High school education or equivalent. Bachelor of science; Chemistry field preferred. Must have a minimum of 3-year experience in Quality Control preferably in analytical filed Must be able to maintain a clean, sanitary, and organized work area. Maintains housekeeping in conformance with Good Laboratory Practices (GLD’s), Current Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) Full knowledge of working with and troubleshooting analytical instrumentation. Good time-management skills Good English communications skills: speaking, reading, and writing. Advance PC Knowledge i.e. MS Office Suite (Excel, Word, Outlook) is preferred Flexibility to work long hours during peak season or special schedules as needed to satisfying job requirements. Ability to multi-task and follow through on project assignments Ability to quickly remedy procedural problems Good interpersonal and customer service skills Excellent organizational and planning skills Makes suggestions for improvements Communicates and collaborates with management Work Environment: Laboratory environment Noise level is low to moderate Proper lighting and ventilation

Requirements

High school education or equivalent.
Bachelor of science; Chemistry field preferred.
Must have a minimum of 3-year experience in Quality Control preferably in analytical filed
Must be able to maintain a clean, sanitary, and organized work area.
Maintains housekeeping in conformance with Good Laboratory Practices (GLD’s), Current Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s)
Full knowledge of working with and troubleshooting analytical instrumentation.
Good time-management skills
Good English communications skills: speaking, reading, and writing.
Advance PC Knowledge i.e. MS Office Suite (Excel, Word, Outlook) is preferred
Flexibility to work long hours during peak season or special schedules as needed to satisfying job requirements.
Ability to multi-task and follow through on project assignments
Ability to quickly remedy procedural problems
Good interpersonal and customer service skills
Excellent organizational and planning skills
Makes suggestions for improvements
Communicates and collaborates with management

Responsibilities

Promotes a safe working environment and adheres to Health, Safety and Environmental procedures, company safety rules, Good Laboratory Practices (GLD’s), Current Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) at all times.
Perform analytical tests on Bulk, finished products, stability samples, raw materials, and contract manufactured material in compliance with GMP and as directed by the QC Specifications.
Perform variety of analytical methods using HPLC, GC, ICP, FTIR, UV/Vis, and variety of wet chemistries following SOP of internal test method, USP or customer specified methods.
Responsible for maintenance and troubleshooting of analytical instrument and clearly communicating the problems with Sr. Lead Chemist or Lab Director.
Perform method validation following established test methods.
Participate in method validation, method development and method transfer as needed.
Perform calibration and routine maintenance of laboratory equipment as directed by the Quality Assurance Director.
Conduct laboratory work and associated record keeping in a safe manner and in keeping with generally recognized GLP, GMP and company & customer’s SOP.
Follow internal and customer specification.
Write OOS report and Investigate problems presented in test results.