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Quality Document Specialist

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GForce Life Sciences

2021-12-04 02:00:03

Job location Irving, Texas, United States

Job type: fulltime

Job industry: HR / Recruitment

Job description

Job Title : Engineering - Non-Degreed I/Quality Doc Specialist

Location : Irving, TX

Duration: months Contract


Education:

High School Diploma with 2-3+ years of exp.

Associate: 1+ years

Bachelors: Preferred


Quality Document Specialist with experience in Design History Files (DHF); Medical Device/ regulated Industry Preferred

Any Quality Documentation Experience can work


Responsibilities:

Receive and coordinate requests for processing and approval of engineering design documents in a controlled product lifecycle management system.

Complete assigned tasks by monitoring progress and performing follow-up activities to ensure successful completion of document control activities.

Perform evaluation of engineering documentation supporting identified projects.

Resolve document control issues and discrepancies.

Ensure compliance to site level policies and procedure by promptly reporting non-compliance issues to the department manager or team leads.

Must be able to work independently and effectively with various quality and engineering functions.

Performs other duties and tasks as required.

Preferred Experience:

Knowledge and proficiency of electronic document control systems.

Knowledge of engineering documents and change control processes will enhance execution of the deliverables.

Proficiency with Outlook, Word, Excel, PowerPoint, Acrobat, and other software tools, you will efficiently track engineering packages

Strong verbal, written, organizational, time management and interpersonal skills.

Responsible for the evaluation and administration of electronic controlled quality records in accordance with regulatory requirements and company policies.

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