Validation Associate (Quality Department) Needed in Moorpark (in-person only)
Industry: Health and Beauty products
Pay: $21 - $23/hour
Monday - Friday
8:00am - 4:30pm
QUALIFICATIONS
· Minimum of 2 years of experience in quality. Experience in the cosmetic/pharmaceutical industry is preferred.
· High School Graduate or General Education Degree (GED) is required.
· BA or BS Degree in applicable field (Engineering, Quality, etc.) preferred.
· Basic algebra and statistics.
· Working knowledge of Microsoft Word, Excel and Outlook.
POSITION SUMMARY
As part of the quality team, the Validation Associate will be responsible for Quality Control functions and monitor all aspects of the manufacturing operations to assure adherence to current Good[RF1] Manufacturing Practices (cGMP) regulations.
JOB DUTIES AND RESPONSIBILITIES
Validation Associate's responsibilities will include, but are not limited to the following:
· Assist in validation activities such as conducting IQ/OQ and PQ study, process batching verification of flow meters etc.
· Manage Vendor Qualification program.
· Maintain SDS binders / electronic files.
· Maintain Facility Temperature & Humidity Logs.
· Maintain Wastewater pH Log & Treatment Process.
· Collect DI water samples when necessary and submit to an outside Lab.
· Conduct Fire Extinguishers Monthly Inspection
· Conduct weighing scales calibration verification.
· Cleaning verification using a luminometer.
· Check the weight of the bulk after transfer (calculate the yield and verify label information after transferring bulk).
· Verify critical raw material used during batching (includes active pharmaceutical ingredient and DI water).
· Prepare and submit samples for validation study.
· Monitor equipment maintenance & repair log quarterly per SOP.
· Maintain an awareness of cGMP, Good Laboratory Practices (GLP), good housekeeping and safety in the laboratory.
· Communicate any discrepancies and OOS's with Laboratory Manager, assist and/or issue OOS investigations, deviations and issue non-conformance material reports (NCMR) per established SOP.
· Maintain inventory of lab supplies.
· Support and enforce all company policies, procedures, and guidelines.
· Other duties as assigned.
All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.
