Product Quality Inspector 2

Teledyne Scientific & Imaging Portsmouth , NH 03801

Posted 4 days ago

Company Overview

Teledyne DGO designs connection systems that transmit signals, data or power through challenging media, such as subsea oil wells; and through pressure barriers, such as the hull of a submarine. Because the cost of failure is so high, Teledyne DGO designs and manufactures its products to deliver total reliability. We engineer and manufacture our products as if lives and fortunes depended on them. Because they do.

Teledyne DGO offers our employees an excellent benefit package including:

  • Medical & Dental Insurance

  • Life Insurance

  • Voluntary Personal Accident Insurance

  • Business Travel Accident Insurance

  • Employee Stock Purchase Program

  • Voluntary Short & Long Term Disability

  • 401(K) Plan

  • Flexible Health & Dependent Spending Accounts

  • Employee Assistance Program

  • Paid Vacations & Sick Time

  • College Tuition Reimbursements

Teledyne DGO is a fast growing division of Teledyne Technologies and is looking to add highly motivated and skilled individuals to our team. Teledyne DGO is dedicated to providing an environment that fosters excellence in teamwork, and includes every Employee, Supplier, Business Partner and Customer as a valued member of our team. Our employees are treated with respect, professionalism and the opportunity for career advancement in a safe work environment.

Position Summary and Responsibilities

Essential Duties and Responsibilities:

  • Performing mechanical inspection, of completed product, to verify compliance to the Customer's drawings, specifications and contract.

  • Validation that all Customer quality requirements have been met by reviewing in-process inspection, assembly and test records.

  • Creation of Objective Quality Evidence document packages for presentation to the Customer.

  • Frequent interface with customer source inspectors, during their performance of source inspection.


Education and Experience:

  • A minimum of 2 years' experience in the Manufacturing/Quality field.

  • Experience with contract/purchase order requirements review a plus.

  • Ability to apply common sense in performing job

  • Ability to understand and follow basic instructions and guidelines

  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals

  • Ability to use basic high school math skills

Job Knowledge, Skills and Abilities:

  • Working knowledge of manufacturing processes, or equivalent education.

  • The ability to read and interpret engineering drawings.

  • Experience using precision measuring equipment for mechanical inspection.

  • Proficiency using MS Windows, MS Office and Adobe (Professional) software.

  • ERP system experience preferred

  • Must be well organized and detail oriented

Training Requirements:

  • IFS Overview/Administration

  • Hazardous Communications

  • Quality Management Systems

Physical Demands:

  • Be capable of lifting up to 40 pounds on a regular basis.

  • Pass a vision screening (Jaeger/Ishihara Color Scale).

  • This job will require bending, standing in various positions and walking.

Work Environment:

  • This position will mainly work in a manufacturing production floor environment

  • Required to work on the production floor with proper PPE

Required to perform other duties as requested, directed or assigned.

Citizenship RequirementsDue to the type of work at the facility and certain access restrictions, successful applicants must be a "U.S. Person" (US citizens, US nationals, lawful permanent residents, asylees or refugees). Teledyne is an Affirmative Action/Equal Opportunity EmployerAll qualified applicants will receive consideration for employment without regard to race,color,religion,religious creed,gender,sexual orientation,gender identity,gender expression,transgender,pregnancy,marital status,national origin,ancestry,citizenship status,age,disability,protected Veteran Status,genetics or any other characteristic protected by applicable federal,state,or local law. If you need assistance or an accommodation while seeking employment,please email or call (805)373-4545. Determinations on requests for reasonable accommodation will be made on a case-by-case basis. Please note that only those inquiries concerning a request for reasonable accommodation will receive a response.

icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Quality Control Inspector


Posted 2 days ago

VIEW JOBS 3/21/2019 12:00:00 AM 2019-06-19T00:00 This position is responsible for supporting Novocure's quality inspection activities in the Portsmouth, NH facility. This includes conducting inspection acceptance activities, form reviews (document inspections), and some operational activities as needed. Essential Duties and Responsibilities: Responsible for acceptance activities for all products and components. Signs off to releasing medical products for use by Novocure customers. Inspect incoming, in-process, finished products for conformance to standards. Identify non-conforming materials and initiate NCMR's. Review completed records to ensure accuracy and conformance to Good Documentation Practices (GDP's). Accurately document incoming, in-process, and final inspection data for trending. Work with other personnel to resolve discrepancies. Assist with operational processes, such as labeling, packaging, product cleaning, and shipping, as needed. Qualifications: HS Diploma 2 plus years of Quality Control Inspection experience, preferably in an ISO 9001, ISO 13485, and/or FDA regulated environment Knowledge of medical device quality system requirements (21CFR Part 820, ISO 13485) highly desirable. Proficient in Microsoft Office applications Experience working in computer systems (e.g., databases) Knowledge/Skills/Abilities: Must be have high attention to detail and be able to document work accurately Must have good written and oral communication skills Must be able to work in a team environment Must be able to execute responsibilities with minimal direct supervision. Knowledge of FDA and ISO standards for Medical Devices is a plus Ability to multi-task, perform efficiently, and independently Working Condition: Standing and sitting for extended periods Lifting up to 30 pounds #LI-POST Novocure Newington NH

Product Quality Inspector 2

Teledyne Scientific & Imaging