Job Description
Support and develop forms for inspections of raw materials, components, and finished products to verify compliance with quality specifications and standards. Use various inspection tools and equipment to measure and assess product attributes as needed to support the inspection team. Develop and implement robust quality control procedures, work instructions, and job aids as assigned. Ensure product processes adhere to established quality standards and guidelines. Monitor and document data throughout the production process. Identify and document defects, nonconformances, or deviations from quality standards. Implement corrective actions to prevent recurrence of defects as needed. Participate in root cause analysis and continuous improvement activities. Use statistical methods and quality tools (e.g., Pareto analysis) to identify opportunities for process enhancement. Schedule and record calibration and preventive maintenance of equipment to ensure accuracy and reliability. Comply with ISO Quality Management System, FDA 21 CFR Part 820 Quality System Requirements (QSR), and medical device industry requirements. Assist in the implementation of the quality management system.
ResponsibilitiesSupport and develop forms for inspections of raw materials, components, and finished products.Use various inspection tools and equipment to measure and assess product attributes.Develop and implement quality control procedures, work instructions, and job aids.Ensure product processes adhere to established quality standards and guidelines.Monitor and document data throughout the production process.Identify and document defects, nonconformances, or deviations from quality standards.Implement corrective actions to prevent recurrence of defects as needed.Participate in root cause analysis and continuous improvement activities.Use statistical methods and quality tools to identify opportunities for process enhancement.Schedule and record calibration and preventive maintenance of equipment.Comply with ISO Quality Management System, FDA 21 CFR Part 820 QSR, and medical device industry requirements.Assist in the implementation of the quality management system.Essential SkillsExperience with Nonconformance Material Report (NCMR) processes.Proficiency in document control.Knowledge of Geometric Dimensioning and Tolerancing (GD&T).Experience with Corrective and Preventive Actions (CAPA).Familiarity with ISO 9001 quality management standards.Additional Skills & QualificationsBachelor’s degree in engineering or a related field (e.g., mechanical engineering, industrial engineering, quality control) or 4-8 years of relevant experience preferred.Experience with quality control and quality assurance processes in the relevant industry preferred.Experience with quality control software and data analysis tools is an advantage.Work Environment
The position requires working standard hours from 8 AM to 5 PM in an office and manufacturing environment. The role is 100% onsite.
Send resume to dfarrand @ actalentservices.com
Pay and BenefitsThe pay range for this position is $30.00 - $40.00
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 Carlsbad,CA.
Application Deadline
This position will be accepting applications until Jan 21, 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.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.