Document Control Specialist

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500 employees globally, with over 30 locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.

Company: One of Our Clients

Job Title: Document Control Coordinator

Location: Chaska, MN 55318

Contract Duration: 10 Months (Possible Extension)

Shift: Shift M-F 8:00 AM-4:30 PM

Pay Rate: $28-$32.00/hr on W2

Top 3 must have:

• Meticulous attention to detail and strong organizational skills.
• Skilled at prioritizing in a demanding and fast paced environment while producing error free work and meeting required deadlines.
• Adept at multitasking and troubleshooting while appropriately addressing issues as they arise.

Job Responsibilities:

• Implement changes based on red-lines and format engineering documents per documentation standards
• Ensure guidelines and definitions are consistently applied across templates and documents.
• Review all documentation for accuracy, completeness and consistency incontent, format, files and authorizations.
• Filing, scanning, copying and electronic notification and distribution of released documentation.
• Store and control archived documentation.

Success Factors

• Meticulous attention to detail and strong organizational skills.
• Skilled at prioritizing in a demanding and fast paced environment while producing error free work and meeting required deadlines.
• Adept at multitasking and troubleshooting while appropriately addressing issues as they arise.
• Ability to work independently.
• Well versed in good documentation practices
• Team Player – Thrives in a team environment to achieve a shared goal or outcome

Education and/or Work Experience Requirements:

• 2-3 years of relevant experience
• Graduate from a recognized program in QA preferred
• Previous QA and QMS experience
• Previous experience working within a GMP manufacturing environment would be an asset.
• Experience working with Electronic Document Management System.
• Knowledge of ISO 9001 standard required; knowledge of ISO 13485 is an advantage·
• Prior experience with documentation of Life Science or Medical Device products.
• Strong word processing skills using Microsoft Office products including application and editing of Word multilevel lists, pagination, headers/footers, tables and track changes.
• Strong communication skills, both written and verbal.
• Experience with design document engineering change orders.
• Knowledge of document control procedures including database storage, maintenance, and revision control

Regards,

Prateek Pampattiwar

Recruitment Specialist

Net2Source Inc.

Global HQ Address –270 Davidson Ave, Suite 704, Somerset, NJ 08873, USA

Office: (201) 340-8700 x 324 | Cell: (551) 220 3007| Fax: (201) 221-8131| Email: Pampattiwar.Prateek@net2source.com