Are you an experienced Quality Inspector eager to advance your career in the aerospace and medical device sectors? If so, I have an excellent opportunity with a well-established, ISO 13485 certified company. With over 35 years of expertise and advanced fabrication capabilities, this leading organization delivers top-quality products from a state-of-the-art, 53,000-square-foot facility.
The ideal candidate has a minimum of 2-3 years of experience in Quality Inspection, with expertise in First Article, In-Process, and Final Inspections. Skilled in reading blueprints, including GD&T, and proficient in using precision tools such as dial indicators, drop gauges, and measurement microscopes, including Keyence microscopes. Familiarity with basic Microsoft Office Suite for reading and reporting is also essential.
The Role Offers:
· Competitive salary and benefits including medical, dental, eyecare, and life insurance
· Family-owned company with 43 years in business
· No layoffs in company history
· Resilient and recession-proof with 20% annual growth
· High growth opportunities
· Opportunities for overtime
· Flexible working hours
· Offers work-life balance
If this sounds like you, please send a copy of your resume in a Word document. The company is interviewing as soon as this week, so I will be in touch ASAP!
Summary:
Seeking a detail-oriented Quality Inspector to join our team. The ideal candidate will be responsible for ensuring that our fluid control devices meet the highest standards of quality and compliance within the medical device and life sciences industries. As part of our ISO 13485 certified company, the Quality Inspector will play a critical role in maintaining our commitment to exceptional product quality and customer satisfaction.
Key Responsibilities:
· Inspect Incoming Materials: Evaluate and verify the quality of incoming raw materials and components to ensure compliance with specifications.
· Perform In-Process Inspections: Conduct regular inspections during the manufacturing process to identify defects or inconsistencies in products, including precision bore syringes, rotary valves, and tubing assemblies.
· Conduct Final Inspections: Assess finished products to ensure they meet design specifications, quality standards, and regulatory requirements prior to shipment.
· Document Inspection Results: Maintain accurate records of inspection results, documenting any non-conformities and collaborating with production and engineering teams to address issues.
· Collaborate with Teams: Work closely with manufacturing and engineering teams to troubleshoot quality issues and suggest improvements to processes and products.
· Utilize Inspection Tools: Operate and maintain various measurement instruments, such as calipers, micrometers, and Keyence microscopes, to ensure accurate assessments.
· Maintain Compliance: Adhere to company policies, procedures, and quality standards in alignment with ISO 13485 certification requirements.
· Report and Analyze Data: Analyze inspection data to identify trends and areas for improvement, presenting findings to management as necessary.
Qualifications:
· Proven experience as a Quality Inspector or similar role in the medical device or manufacturing industry.
· Familiarity with quality control standards and ISO 13485 regulations.
· Proficiency in reading blueprints and technical documents, including GD&T specifications.
· Strong analytical skills and attention to detail, with the ability to identify and resolve quality issues effectively.
· Experience using inspection tools and measurement devices, as well as basic Microsoft Office software for documentation and reporting.
Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria.
Equal Opportunity Employer/Veterans/Disabled. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit. The Company will consider qualified applicants with arrest and conviction records.
Pay Details: $50,000.00 to $70,000.00 per year
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
The California Fair Chance Act
Los Angeles City Fair Chance Ordinance
Los Angeles County Fair Chance Ordinance for Employers
San Francisco Fair Chance Ordinance
