Quality Assurance Inspector

Actalent; Los Angeles (CA); On-site; Full time

Job summary

Actalent is seeking a Quality Assurance Inspector for a pharmaceutical company in Northridge, CA. The role involves performing inspections, maintaining documentation, and ensuring compliance with GMP standards. Ideal candidates have at least one year of experience in quality control and possess strong attention to detail. This entry-level position offers the chance to gain valuable laboratory experience in the pharmaceutical field.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Employee Assistance Program

Qualifications

• 1 year of experience in GMP regulated QC experience.
• Experience with visual inspection and measurements.
• Basic understanding of GMPs.

Responsibilities

• Perform inspection and measurements of packaging materials.
• Conduct instrumental analysis including FTIR.
• Maintain accuracy and calibration of laboratory testing equipment.

Skills

Attention to detail

Basic math skills

Good documentation practices

Good mechanical aptitude

Education

High School diploma or GED

Tools

Calipers

Measuring tools

Job description

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Material Inspection

Pharmaceutical company in Northridge is hiring an inspection technician to join their laboratory! Great opportunity to gain Lab Technician experience in the Pharmaceutical Industry!

Material Inspection

Pharmaceutical company in Northridge is hiring an inspection technician to join their laboratory! Great opportunity to gain Lab Technician experience in the Pharmaceutical Industry!

Job Description

The Quality Inspector provides analytical support and services for all aspects of Raw Material Testing to support commercial manufacturing. This includes but is not limited to raw material and hard good testing as well as sampling.

Responsibilities

• Perform inspection and measurements of hard goods and packaging materials, including color match, caliper, and ruler measurements.
• Perform instrumental analysis, including FTIR.
• Participate in basic quality control procedures and inventory management.
• Maintain good record-keeping practices while adhering to quality and safety programs.
• Maintain accuracy and calibration of laboratory testing equipment.
• Use LIMS and other relevant computer software programs to collect or input data and information.
• Maintain accurate and up to date training records.
• Ability to work flexible hours as needed to support production demands.
• Work well in both team and individual environments.
• Other duties as assigned.
  
  

Essential Skills

• 1 year of experience in GMP regulated QC experience
• Experience with visual inspection and measurements
• Basic math skills
• Good documentation practices
• Experience with calipers, measuring tools, and inspection tools
• High School diploma or GED
• Basic understanding of GMPs
• Good mechanical aptitude and skills
• Attention to detail and strong organizational skills
  
  

Additional Skills & Qualifications

• Experience in inspection procedures and/or the product line
• Ability to perform basic math (addition, subtraction, etc.)
• Experience with finished in-process inspection and packaging
• Experience using hand tools such as calipers and rulers
  
  

Work Environment

GMP environment with shifts available from 8am-5pm, 7am-4pm, and 9am-6pm. The role involves the use of laboratory equipment and requires adherence to safety and quality standards. The position offers long-term opportunities and the chance to gain pharmaceutical experience.

Pay and Benefits

The pay range for this position is $18.80 - $20.00/hr.

Requirements

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 Panorama City,CA 91402.

Application Deadline

This position is anticipated to close on Jun 30, 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 [e-mail] for other accommodation options.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Quality Assurance

• Industries

  Business Consulting and Services

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