QC Technologist I

Werfen•San Diego, CA

12d•$24 - $29•Onsite

About The Position

The QC Lab Technologist I is responsible for the execution of a broad range of bench test procedures used in the QC testing of finished goods prior to release, assisting with investigations of product performance, routine validation studies, and housekeeping within the Quality Control (QC) laboratory. The QC Lab Technologist I maintains the documentation of approved QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. This is a 1st shift position. Hours: Monday-Friday, 5:00am-1:30pm. This is a 6-month temporary assignment, with potential for extension or conversion depending on individual performance and business needs. The base hourly range for this role is currently $24.00/hr. to $29.00/hr. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.

Requirements

High school diploma required
Basic skills with common laboratory techniques, such as pipetting and use of balances.
Basic skills with Microsoft Office suite.
Must occasionally lift up to 25 lbs.
Basic ability to pay close attention to detail is required
Work is accurate and completeness of records
Demonstrated ability to meet department goals
Good written and verbal communication skills.
Acts Honest, Loyal, trustworthy
Basic ability to Juggle Priorities, and support changing business needs
Basic ability to actively develop a network to bring best solutions to the team or customer
self-motivated
Must demonstrate professionalism during all interactions within company, customer and third parties
Serves as a role model for “Quality First”
Promptly and effectively handles basic issues and problems

Nice To Haves

Bachelor’s degree in Science or equivalent experience preferred.
Understanding of Good Laboratory Practices (GLP) preferred.
Previous experience in a Quality Control (QC) lab and/or Quality Assurance (QA) role within regulated medical device manufacturing or In-Vitro Diagnostic device (IVD) manufacturing preferred.
Phlebotomy certification a plus.
Knowledge of FDA-GMP/QSR and ISO standards for quality a plus.
Basic skills with Large Enterprise Resources Planning (ERP) a plus.

Responsibilities

Perform testing of finished goods per relevant SOP.
Assist with testing as required for product validation and process validation on existing products.
Maintain proper laboratory housekeeping and ensure adequacy of supply levels in the QC laboratory by informing appropriate personnel of low supply levels as required.
Document all finished goods test results and maintain appropriate records in QC (including electronic records), as required.
Maintain product testing database and trending associated with product specifications as specified in laboratory SOPs.
As required, assist with testing for investigation and resolution of complaints, non-conforming material, and product performance issues.
Perform testing and prepare basic out-of-specification reports, as required.
Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes.
Other duties as assigned.