Quality Control Associate

Job Description

This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformance's, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues.

Multiple Shifts Available:

202112-137366 Quality Control Specialist (Tuesday - Saturday, 4:30pm - 1:30am)
202112-137371 Quality Control Specialist I (Monday - Friday, 1pm-9:30pm)
202112-137375 Quality Control Specialist I (Monday - Friday, 1pm-9:30pm)
202112-137372 Quality Control Specialist I (Monday - Friday, 11:30am-8pm)
202112-137377 Quality Control Specialist I (Monday - Friday, 5:30am - 1pm)
202112-137373 Quality Control Specialist I (Monday-Friday, 8am - 4:30pm)

Your key responsibilities

• Completes batch records while maintaining good documentation practices

• Prepares/formulates QC test solutions following standard operating procedures and guidelines given by supervisor; solutions include aqueous solutions containing salts, organics, acids, bases and/or modified DNA and organic solutions

• Conducts QC testing following standard operating procedures and guidelines given by supervisor

• Under direction, perform validation and stability studies, execute protocols, analyze data, generate reports, initiate non-conformances for MRB

• Responsible for on-time completion of scheduled work orders

• Monitors inventory levels on a daily basis

• Participates in departmental projects—works with QC members on OOS/NCR/CAPA investigations as needed

• Understanding of molecular techniques (DNA extraction, PCR Amplification)

• Adheres to the requirements of working in a GMP, ISO certified or FDA workplace

• Assists with special projects as requested and perform additional duties as required

Who you are

• B.S. degree required, in basic sciences, life sciences, or engineering and/or two (2) years of relevant experience in a QC capacity

• Technical knowledge of molecular biology, including principles of nucleic acid hybridization, probe and primer design, and enzymatic amplification of specific gene sequences

• Knowledge of safety precautions required for working with biohazards and bloodborne pathogens

• Knowledge of the Quality System; able to execute change orders under the guidance of higher level employees

• Knowledge of basic statistics relevant to interpretation and analysis of scientific data

Job Type: Full-time

Pay: $23.00 - $24.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift

Supplemental Pay:

• Bonus pay

Ability to commute/relocate:

• Carlsbad, CA 92008: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

• Please briefly describe your laboratory experience.

Experience:

• Laboratory: 1 year (Required)

Work Location: One location