Home PageWho We Are and What We DoPhilosophyCareerContact Us
Core Competencies Workforce Solutions IT Service Products GSA

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)
---------------------------------------------------------------------------------------------------------------------

Position Title: 12116989-Document Control Associate
Location: 11 Cabot Blvd, Mansfield, MA 02048

Pay Rate: $21/hr.

Contract Duration: Till Jan 2021

Job Title- Document Control Associate

Duration-Till Jan 2021

Location- Mansfield, MA

Responsibilities
• Responsible for supporting the maintenance of the document control system
• Responsible for formatting, proper spelling and clarity of text for any written documents submitted to document control
• Review all electronic documents submitted to document control for correct formatting, spelling and clarity of text before releasing as approved documents
• Maintains all ISO/FDA standard operating procedures, work instructions and forms
• Maintains revision and approval status of all documents
• Maintains official copies (either hard copy or electronic) of all approved documentation
• Maintains appropriate form templates for access
• Updates computerized documents with data from change control documents and maintains archive of changed ISO/FDA controlled documents
• Manages circulation of documents for management approval
• Tracking, follow-up and implementation of, including but not limited to, ECOs, validation records, batch records and notebooks.
• Responsible for supporting record retention activities (collection, shipment and retrieval to/from offsite storage)

 Requirements

Qualifications
• Minimum of 1-2 years’ experience in document management using electronic document management systems
o Preferred experience with Agile and /or Adaptiv PLM systems
• Minimum of 1-2 years’ experience in a Quality Systems / Regulatory Compliance environment with a working knowledge preferably in the medical device, diagnostics or pharmaceutical industries.  Familiarity with FDA regulations and ISO series of quality standards preferred
• Capable of both written and verbal effective communication skills including presentations as assigned.
• Proficient in the Microsoft Office suite of products.
• Solid organizational and document management skills

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.


------------------------------------------------------------------------------------------------------

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 - Harshitha@norlandgroup.com and copy: 12116989-Document Control Associate to the email Subject Line.

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

Job Posted Date: 1/25/2019