Calibration Technician

Job Description

Job Description

Calibration Technician III

Location: San Diego, CA (Onsite)

Duration: 12-Month Contract with Potential for Extension and Full-Time Conversion

Schedule: Monday-Friday, 8:00 AM-5:00 PM

Position Summary

We are seeking an experienced Calibration Technician III to support calibration, maintenance, troubleshooting, and documentation activities for critical inspection, measurement, and test equipment in a highly regulated medical device manufacturing environment. This role is responsible for ensuring equipment accuracy, reliability, and compliance with quality system requirements while collaborating with Engineering, Quality, Manufacturing, and Facilities teams.

The ideal candidate brings strong hands-on calibration expertise, experience working within GMP-regulated environments, and a proven ability to troubleshoot complex instrumentation issues while maintaining compliance with cGMP and 21 CFR Part 820 requirements.

Key Responsibilities

• Perform precision calibration, adjustment, and verification of:
  • Electronic instruments
  • Mechanical measuring devices
  • Dimensional equipment
  • Pressure systems
  • Temperature and thermal measurement devices
  • Humidity monitoring equipment
• Execute preventive maintenance activities to ensure equipment performance and reliability.
• Troubleshoot calibration discrepancies and equipment performance issues, identifying root causes and supporting corrective actions.
• Review calibration certificates, service reports, and vendor documentation for accuracy, completeness, and compliance.
• Maintain calibration records, equipment histories, and quality documentation in accordance with cGMP and FDA quality system requirements.
• Coordinate calibration and service activities with internal stakeholders and external vendors.
• Support investigations, root cause analyses, and CAPA activities related to measurement and calibration systems.
• Utilize IBM Maximo or similar CMMS/asset management systems to manage calibration schedules and equipment records.
• Partner with Manufacturing, Quality Assurance, Engineering, Facilities, Maintenance, and R&D teams to ensure equipment readiness and regulatory compliance.
• Contribute to continuous improvement initiatives focused on calibration processes, documentation, and equipment reliability.

Required Qualifications

• High school diploma or equivalent required.
• 2-4+ years of related technical experience required.
• Strong hands-on experience calibrating and troubleshooting:
  • Electronic equipment
  • Mechanical instruments
  • Pressure systems
  • Temperature and humidity monitoring equipment
  • Thermal and dimensional measurement devices
• Working knowledge of cGMP regulations and quality systems.
• Experience maintaining calibration records and reviewing calibration certificates.
• Ability to investigate equipment issues and support root cause analysis and corrective action activities.
• Strong technical documentation and communication skills.
• Proficiency with Microsoft Office Suite (Word, Excel, Outlook, PowerPoint).

Preferred Qualifications

• 5-7+ years of calibration experience in a GMP, GxP, medical device, biotechnology, or pharmaceutical manufacturing environment.
• Experience working under FDA-regulated quality systems and 21 CFR Part 820 requirements.
• Pharmaceutical or medical device industry experience.
• Familiarity with IBM Maximo or similar asset management systems.
• ASQ Certified Calibration Technician (CCT) certification.
• Experience supporting specialized or proprietary calibration processes.
• Background in CAPA, preventive maintenance, equipment qualification, and compliance-driven environments.

Physical Requirements

• Ability to stand and walk for extended periods.
• Ability to move between facilities and work areas as needed.
• Ability to independently lift and carry equipment weighing up to 20 pounds.

Why Join the team?

• Opportunity to work with advanced medical device manufacturing technologies.
• Exposure to both standard and specialized calibration processes.
• Collaborative environment with Engineering, Quality, Manufacturing, and R&D teams.
• Long-term contract opportunity with strong potential for extension or direct hire conversion.
• Meaningful role supporting product quality, compliance, and patient safety.

If you have a strong calibration Background within a regulated manufacturing environment and are looking to join a high-performing team, we'd love to hear from you.

Job Type & Location

This is a Contract position based out of San Diego, CA.

Pay and Benefits

The pay range for this position is $30.00 - $35.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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 San Diego,CA.

Application Deadline

This position is anticipated to close on Oct 7, 2026.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email View email address on us.fitly.work for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.