BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a contract to potential hire Quality Assurance Inspector to work for a leading contract manufacturing company.

Contract: 6-12 months with potential to hire

Pay Rate: $20-24/hr

Shift: 2nd shift (between 2:30PM-12AM)

Responsibilities (Duties may include, but are not limited to, the following):

• Inspect packaging components, finished goods, and/or other items as required.
• Produce and maintain complete and accurate records of inspections.
• Exercise and monitor GMP compliance in work environment.
• Audit / Verify Production Checks & Balances at Startup, in-process and at end of each production run.
• Review and release quality inspection records.
• Interpret Fill & Assembly Instructions (routers).
• Perform non-routine experimentation/problem solving with minimal supervision.
• Understand and exercise all company safety requirements and procedures.
• Ensure procedures are followed and documentation needs are adequately met.
• Responsible to maintain retain sample storage and controls.
• Communicate non-conformances to support quality needs.
• Support quality alert investigations and CAPAs, as needed.
• Performs other duties as assigned.

Physical Requirements:

• Ability to lift and pull a minimum of 30 lbs. using proper lifting techniques.
• Requires walking and standing for lengthy periods of time.
• Certain areas require the use of safety equipment.
• Requires bending, pulling, pushing, reaching above shoulder/below waist levels and climbing of stairs.

Experience/Requirements:

• High School Diploma or equivalent required
• 1+ years of experience in an OTC drug & cosmetic care manufacturing environment (preferred).
• Excellent English written and verbal communication skills.
• Familiar with calculator, rulers/other measuring devices, scales and digital/spring torque meters desirable.
• Some line inspection and documentation experience in manufacturing (preferred).
• Additional QA experience and FDA regulation knowledge (preferred).
• Knowledge of computer applications (i.e. Microsoft Office).

Please send resumes to and visit our website at for additional job opportunities!!!