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Job Details

QC Engineer III

Company name
Thermo Fisher Scientific Inc.

Location
Pleasanton, CA, United States

Employment Type
Full-Time

Industry
Engineering, Quality

Posted on
Oct 03,2019

Valid Through
Jan 16,2020

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Job Description

Job Title: QC Engineer III

Requisition ID: 104865BR

When you are part of the team at Thermo Fisher Scientific, you’ll do important work, bringing families together, reduce crime and supporting safer communities. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

Location/Division Specific Information

US-California-Pleasanton / GSD Human Identification

How will you make an impact?

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of more than $24 billion and approximately 70,000 employees globally. Our mission is to enable our customers to make the world healthier, cleaner and safer. Being part of HID you will have the ability to make your communities safe and allowing families to connect with their loved ones.

What will you do?

Performing raw material Quality Control physical Inspection of instrument and consumable parts, documentation, review test results, C of A review and raw material release.

Maintaining accurate and complete records of inspection activities in compliance with ISO 9001, ISO 13485 and good documentation practices

Assure compliance to internal SOPs

Providing Quality oversight for issues of significant scope and complexity across multiple functional groups in order to ensure adherence to ISO standards.

Creating problem reports/ NCMR’s and Deviations for nonconforming raw material

Ensuring discrepancies are thoroughly identified, defined and properly assessed.

Interacting with interdepartmental contacts on change and discrepancy assessment, resolution, and quality approval.

Providing timely information to Operation.

Update and meet metrics

Identifying opportunities for continuous improvement of the Quality Systems and participate on implementation.

Revise procedures as needed.

Hands-on laboratory duties and have the willingness to learn new techniques and equipment

Maintain calibrated tools and equipment

Be able to communicate technical issues and inspection results orally and in writing.

Ability to work independently and as part of the IQC team

Sense of urgency with completion of projects and tasks

Serves as a backup for other Quality positions as needed

Other duties and responsibilities as assigned

Knowledge to interpret and inspect specifications per ANSI/Y14.5/ASME for mechanical parts, electrical parts such as PCAs, electrical units, electrical cables per IPC/MHMA-A-620, Class 2, to inspect and process C of A for chemical IQC

Capable to use all precision inspection tools to perform test methods, equipment acquisition, sample plan definition, and validation development. Equipment includes calipers, micrometers, drop indicator, height gauge, comparator, CMM, Vision system, Keyence and pin gauge technique and other QC inspection tools.

Convert units between English and metric systems (such as INCH to mm)

Use various numbering methods, such as scientific notation, decimals, and fractions, and convert the values between these methods.

May need to walk on a continuous basis, bend and lift to 40 lbs.

Be able to read and interpret blueprints, SOPs and WINs and able to define critical, major, and minor characteristics.

How will you get here?

Education:

BS in Engineering or AA with related industry experience.

Experience

Minimal of 2 to 5 years of hands on experience as quality control inspector in biotechnology or pharmaceutical desired.

Demonstrated experience in a wide range of methods used in Engineering, instrumentation and tools used in Engineering related fields.

Knowledge, Skills, Abilities

Attention to details, desire to be hands-on and excellent bench work management.

Experience with Agile and Track-Wise is preferred

Proficient in data analysis and a working knowledge of SAP and excel is a plus.

The candidate must have solid technical writing, interpersonal and communication skills and be a team player.

Knowledge of International Standards ISO-9001, ISO-13485 and/or 21 Code of Federal Regulations (CFR) Part 820 Food and Drug Administration (FDA) Quality Systems Regulation (QSR) is a plus

This position does not have relocation assistance

At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds have a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process,

click here

for further assistance.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Company info

Thermo Fisher Scientific Inc.
Website : http://www.thermofisher.com

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