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Quality Associate Engineer

Kinetic Personnel Group Tustin, CA (Onsite) Full-Time

Quality Associate Engineer 

Role Overview

The Quality Associate Engineer is a key contributor to the Quality Assurance team, responsible for managing  Change Management System and supporting manufacturing and testing activities in compliance with cGMP regulations. This role partners closely with cross-functional teams to ensure changes are properly assessed, documented, and implemented while maintaining the highest quality standards.

Key Responsibilities

  • Author and maintain change control records to support Quality Assurance activities.
  • Develop impact assessments, risk analyses, and change action plans in collaboration with QA and cross-functional partners.
  • Track and manage the status of change controls to ensure timely execution and closure.
  • Participate in Change Control Review Board meetings and document meeting minutes.
  • Support senior engineers with the implementation of new or modified systems.
  • Review and approve calibration and preventive maintenance records for manufacturing equipment, analytical instruments, facilities, and critical utilities.
  • Collaborate with cross-functional teams to ensure accurate and timely review of reports and records in accordance with established SOPs.
  • Evaluate and approve calibration out-of-tolerance events, including participating in investigations to assess potential product impact.
  • Author, review, and revise quality system SOPs and forms to support continuous improvement.
  • Support regulatory inspections and quality audits as needed.
  • Communicate potential quality or regulatory risks to Quality Management in a timely manner.
  • Perform other related duties as assigned.

Minimum Qualifications

  • Bachelor of Science degree in Biology, Chemistry, Biochemistry, or a related scientific discipline.
  • Minimum of 2 years of experience in the pharmaceutical or biopharmaceutical industry.
  • Prior experience in Quality Engineering preferred.
  • Working knowledge of FDA cGMP regulations, ICH guidelines, and quality compliance standards.
  • Strong interpersonal and collaboration skills with the ability to work effectively in a team environment.
  • Flexibility in work schedule to meet business needs.

Physical Demands & Work Environment

  • Occasional exposure to electrical hazards, chemicals, vibrations, fumes, wet or humid conditions, and moving mechanical parts.
  • Noise levels may occasionally be loud.
  • Ability to sit, stand, walk, and use hands for handling and reaching.
  • Occasional climbing, balancing, stooping, kneeling, crouching, or crawling.
  • Regular lifting up to 10 pounds; occasional lifting up to 20 pounds.
  • Vision requirements include close, distance, and color vision.
  • Reasonable accommodations may be made to enable individuals to perform essential job functions.

Who You Are

  • A positive, team-oriented professional with a proactive, “can-do” mindset.
  • A clear and confident communicator, both verbally and in writing.
  • Highly organized with strong multitasking abilities and exceptional attention to detail.
  • Skilled at building strong working relationships across teams and with external partners.

Salary Range: $55K to $72K annually, based on experience and qualifications.
 We also provide opportunities for professional growth in a supportive and inclusive work environment.

KPG123

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Job Snapshot

Employee Type

Full-Time

Location

Tustin, CA (Onsite)

Job Type

Other

Experience

Not Specified

Date Posted

02/04/2026

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