Description

In need of quality assurance technicians that can come in and help with their QA functions. Will be held responsible for:

Reviewing and editing batch records

Assisting in Document Change Control and reviewing history records for compliance.

Working with Non conformances, discrepancies and dispositions.

Assist with investigations for Environmental Monitoring- surface sampling, air sampling, etc.

Perform lab work as needed within microbiology and chemistry

Perform OS investigations

Perform work within quality systems as needed. Examples include supplier management, internal audits, non conformances, risk analysis.

Assist with Handling Customer Complaints, support regulatory audits

Help with following up with office and lab personnel on documentation.

Skills

Gmp, Quality assurance, batch record review, Capa, Audit, non conforming

Top Skills Details

Gmp,Quality assurance

Additional Skills & Qualifications

Education: Bachelor of Science degree in related field or comparable additional experience. Associates okay with 2 years of FDA quality experience, Bachelors at least 1 year.

Pharmaceutical experience preferred

FDA/cGMP Experience - 1 year

Experience with Microsoft office suite

Master control experience is preferred.

Pay and Benefits

The pay range for this position is $25.00 - $37.00/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Santa Ana,CA.

Application Deadline

This position is anticipated to close on Aug 29, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.