Quality Engineer at Jedco Inc
Grand Rapids, MI 49505, USA -
Full Time


Start Date

Immediate

Expiry Date

03 Dec, 25

Salary

70000.0

Posted On

03 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Training, Customer Requirements, Manufacturing Processes

Industry

Pharmaceuticals

Description

JOB SUMMARY:

The Quality Engineer will have responsibility reviewing internal and external engineering documentation to assure all customer contractual items regarding product quality are met. Additionally, this individual will exercise Accept/Reject authority over documents presented for review and provide guidance to other individuals within Jedco to ensure compliance with customer contracts. This role will represent Jedco Quality Organization during internal or external review functions regarding product quality, including product process development and/or non-conformance investigations communicating directly with Engineering, Quality, Manufacturing, and other individuals in the Jedco Organization, along with Customer representatives.

QUALIFICATIONS:

· Must exhibit working knowledge of manufacturing processes utilized at Jedco and customer requirements associated with those processes.
· Must have excellent communication and organizational skills aligned with essential duties and responsibilities.
· To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
· The requirements listed below are representative of the knowledge, skill, and/or ability required.

EDUCATION AND/OR EXPERIENCE:

· High School Diploma (minimum), bachelor’s degree or equivalent technical/engineering training preferred. (Documented experience in a Quality or Engineering background may also be considered.)
· Extensive PPAP experience.
· Proficient in Microsoft Office applications.
· Experience or training in risk management and analysis techniques (SPC, DOE, FMEA).
Job Type: Full-time
Pay: From $70,000.00 per year
Work Location: In perso

How To Apply:

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Responsibilities

· Reviews customer and internal documents as required to ensure manufacturing processing complies to all applicable regulatory, customer, contractual or accreditation body standards.
· Facilitates internal document revisions, additions or subtractions with applicable departments/personnel as directed by VP of Quality or as a result of individual research or discovery.
· Initiates external document request when applicable through the review of invoked requirements.
· Attends and contributes to new product review and development as required.
· Creates or oversees the creation of Quality Plans for use during manufacturing process verification/validation. Including: Firat Article, Inspection Method Sheets (IMS) and statistical plans, as required. Creates or oversees the creation of customer documents for the purpose of communicating found non-conformances for customer review/disposition.
· Creates or oversees the creation of customer documents for the purpose of communicating non-conformance Corrective Action for customer review/disposition.
· Oversees the performance of delegated Quality related studies or functions (non-conformance investigation, gage R&R, etc.).
· Maintains reporting, management and distribution of data associated with product quality as applicable to regulatory, customer, contractual or accreditation body standards.

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