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This position requires - Clear Background, Drug Test, and Education Check.
Must be authorized to work in the US for any employer without Sponsorship.
(Principal Only! No Corp to Corp)
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Position Title: 9385-Document Control Specialist
Location: San Jose CA

Pay Rate: $22.50

Position Title: Document Control Specialist

Location: San Jose CA

Pay Rate : DOE

1 year contract

 

 **BACKGROUND CHECK AND DRUG TEST IS REQUIRED*

Desc:

Duration: 1 year contract

Job Description
Position Summary: Document Control Specialist
The Document Control Specialist works with a small team responsible for part number assignments, revision control of documents/drawings, processing engineering change orders and product data entry and coordination in several electronic databases. This position supports and interfaces with R&D Engineering, Manufacturing, Operations, Purchasing, Planning, and Quality functions. The ability to consistently and accurately complete daily work assignments with a moderate degree of independence per standard work instructions with a moderate degree of independence per standard work instructions is a fundamental requirement for success, along with initiating communication (verbal, email, etc.) and applying corrections as required to clarify, complete or resolve data and process compliance.
Minimum Requirements/Qualifications:
Associate Degree in Electrical or Manufacturing Engineering or Computer Sciences or equivalent through work experience. One to three years of experience as a Document Control Specialist or Engineering Services/Product Data administrator is required. Must have the ability to create and edit Microsoft Word, Excel, PowerPoint files; be familiar with SAP ERP (create material, BOM and run reports; and have knowledge of at least one of the following Product Data Management software tools: ProductCenter, Agile, Arena, Documentum, or equivalent. Previous employment in a high-technology company
(electronic/electro-mechanical system-level products/instrumentation) is preferred as well as the basic understanding of ISO 9000 requirements. Knowledge of FDA requirements for medical devices is preferred.
Desirable:
Previous employment with a life sciences or biotechnology company; certification/training related to process improvement (e.g., 8-Step, PPI, Six-Sigma, Lean Manufacturing, etc.); the basic knowledge of electronic and/or mechanical components; participation in RoHS compliance activities; the ability to perform edit-level tasks Using Auto CAD, Pro/Engineer, or SolidWorks; experience working in ISO 13485 environment.

 

 

If you're qualified and interested in this position, please reply to the following questions:

 

1. An attachment of your updated resume in MS Word document format

2. Your desire pay rate?

3. Your availability for interview, if selected?

4. When can you start?

The Norland Group is proud to be an Affirmative Action/Equal Opportunity Employer. We encourage all qualified applicants to apply for any open position for which they feel they are qualified. Norland does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. Norland maintains a drug-free workplace and perform pre-employment substance abuse testing and background checks.


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If you are interested in this position, please submit your resume in a Word Document with the month and year that you have worked at each previous position to - Karen@norlandgroup.com and copy: 9385-Document Control Specialist to the email Subject Line.

Or click this email link and attach your resume in a MS Word Document format

Job Posted Date: 3/25/2019