Quality Technician (2nd)

Job Description

Job Description

Job Title: Quality Technician (2nd Shift) Job Description

The Quality Technician performs incoming, in-process, and final inspections of components and assemblies in accordance with control and quality plans. This role reviews and approves final release documentation, completes accurate quality records within company and GMP guidelines, and ensures all materials and products meet defined specifications and regulatory requirements.

• Perform incoming inspections of received materials in accordance with control and quality plans and documented procedures.
• Conduct in-process inspections of components and assemblies to verify conformance to engineering drawings, schematics, and specifications.
• Carry out final inspections of completed products and assemblies and approve or reject items based on defined quality standards.
• Inspect incoming or production materials for conformance to engineering drawings, schematics, process standards, and production or process plans.
• Perform incoming testing of components and monitor results for conformance to design, test specifications, or standards.
• Accept or reject materials or articles and clearly identify, document, and communicate non-conformances to appropriate personnel.
• Refer and document unusual inspection problems to supervision, leads, or Project Quality Engineers for resolution.
• Use a variety of measuring tools, including electrical test sets, multimeters, fixed and limit gauges, plug gauges, steel rules, scales, micrometers, calipers, and surface plates, to verify product dimensions and performance.
• Assist in writing, reviewing, and updating inspection procedures, protocols, and checklists to improve clarity and effectiveness.
• Transfer, release, or quarantine material physically in accordance with inspection status and documented procedures.
• Document and maintain accurate inspection and test records in compliance with GDP and GMP requirements.
• Review and approve final release documentation to ensure completeness, accuracy, and compliance with quality standards.
• Understand and apply lot numbering and traceability requirements to maintain product history and accountability.
• Apply ISO quality assurance standards and maintain supporting documentation as required.
• Maintain a safe and clean work environment by keeping shelves, workstations, and equipment neat and by complying with procedures, rules, and regulations.
• Complete all required paperwork and electronic documentation accurately and in a timely manner.
• Communicate effectively with cross-functional teams to resolve quality issues and support continuous improvement.
• Follow written work instructions and standard operating procedures (SOPs) to ensure consistent and compliant inspection activities.

• Ability to read and understand mechanical drawings and dimensions.
• Ability to read and interpret drawing notes and understand configuration management and revision control.
• Proficiency in using basic measuring tools such as calipers, go/no-go gauges, torque wrenches, and similar instruments.
• Experience working with an ERP system and performing accurate data entry.
• Proficiency with Outlook and Microsoft Office applications.
• Strong communication and organizational skills.
• Solid math fundamentals and the ability to comprehend written work instructions.
• Ability to communicate clearly in both written and oral form.
• Knowledge of medical device manufacturing processes.
• Working understanding of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).
• Excellent documentation skills with strong attention to detail and accuracy.
• Ability to perform quality control activities including blueprint reading, SOP adherence, and visual inspection.
• Experience using inspection tools such as microscopes, micrometers, calipers, and other precision measurement devices.
• Ability to identify non-conforming materials and document non-conformances appropriately.
• Understanding of product conformity requirements and their importance in a regulated environment.
• Understanding of lot numbers, traceability, and related documentation requirements.
• Familiarity with ISO quality assurance standards and associated documentation.

• Experience with electrical test sets, multimeters, and vision measuring systems is a plus.
• Experience in a cleanroom or controlled manufacturing environment is beneficial.
• IPC-A-610 certification is recommended for inspection of electronic assemblies.
• Experience with medical device quality control and inspection processes.
• Demonstrated ability to work as a team player and collaborate effectively across functions.
• Flexibility to multitask and manage multiple priorities in a fast-paced environment.

You will join a quality-focused organization that values precision, compliance, and continuous improvement in a regulated manufacturing environment. The company offers the opportunity to grow your skills in medical device quality, contribute directly to product safety and reliability, and work closely with experienced professionals in a supportive team setting. You will benefit from a structured environment with clear procedures, strong emphasis on documentation excellence, and the potential to transition into a long-term, direct role as you demonstrate your capabilities and commitment.

This role operates in a cleanroom environment that follows strict cleanliness, safety, and contamination control procedures. You will work primarily on the 2nd shift from approximately 2:30 p.m. to 11:00 p.m., supporting inspection activities throughout the production process. The position involves frequent use of precision measuring tools, microscopes, electrical test equipment, and computer systems including ERP and Microsoft Office. You will follow documented procedures, rules, and regulations to maintain a safe, organized, and compliant work area, with an emphasis on proper handling of materials and adherence to Good Manufacturing Practices and ISO quality standards.

This is a Contract to Hire position based out of Carlsbad, CA.

The pay range for this position is $26.00 - $28.00/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)

This is a fully onsite position in Carlsbad,CA.

This position is anticipated to close on Oct 19, 2026.

Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.

Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

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

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

Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall 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 applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.