Documentation Specialist

Details of the offer

Job Title: Documentation Specialist Location: Princeton, NJ (Hybrid) Duration: 04 Months Work location – onsite or remote? Princeton Headquarter _ Hybrid : 3 days on site (Tuesday, Wednesday, Thursday) Working Days/Hours? 8 hours per day – day time Top 3 qualities you are looking for in this worker. Team work and collaboration, following established rules and attentive to details, ability to communicate at various level of the hierarchy Job and Competencies requirements (education, technical organizational and relational skills, etc…) • A minimum of a bachelor's degree in a Science/Engineering Mathematics, Computer Sciences or other relevant discipline • A minimum of 1-3 years of overall experience in the medical device/pharmaceutical industry. • Demonstrated knowledge of QSR/GMP (21 CFR Part 820) regulations and ISO (ISO 13485) standards is required. • Knowledge of 21 CFR Part 11 and Computer/Quality System Software validation, preferred. • Strong oral and written communication skills and effective interpersonal skills. • Ability to multitask, prioritize and meet deadlines. • Proficiency in Microsoft Office (SharePoint, PowerPoint, Word, Excel, Adobe Acrobat, etc.) is required. • Proficiency in training management and product lifecycle management (Agile) systems preferred. Responsibilities • The position is responsible for facilitation quality system document control activities in compliance with U.S. and International requirements as defined in FDA Regulations, ISO Standards, European Medical Device Directives, and other International Regulations. • Facilitates Document Change Orders for corporate quality system documents including document changes and training. • Collaborates with document authors to release and implement of Global Standard Operating Procedures (GSOPs). • Participate to Change Review Board meetings. • Operate in Integra's corporate document control and training systems to transact changes to quality system documents. • Support quality system training and management of quality system training requirements in LMS • Execute change orders in alignment with quality system priorities and the global QMS Roadmap • Participate to projects linked with corporate Doc Control activities. Work in collaboration with process owner to update corporate documents (policies and procedures). Make sure that the changes are processed in the Electronic Document Management system in compliance with internal procedural requrements. Collaborate with the other team members to have the change reviewed and appropriate training assigned: Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions.


Nominal Salary: To be agreed

Source: Talent2_Ppc

Job Function:

Requirements

Payer Process Coordinator - Ur Revenue Cycle

Payer Process Coordinator - UR revenue cycle Location: Pennsauken - 6991 North Park Dr. Employment Type: Employee Employment Classification: Regular Time ...


Virtua Medical Group - New Jersey

Published 6 days ago

Administration Md - Travel - - Excellent Benefits 2024-11-18

LocumJobsOnline is working with VieMed Healthcare Staffing to find a qualified Administration MD in New Jersey, New Jersey, 08037! About The Position Ready t...


Locumjobsonline - New Jersey

Published 6 days ago

Bilingual Store Associate (Spanish)

Store associates work closely with wholesale and retail customers to determine their needs, answer their questions about Sherwin-Williams products, and recom...


Sherwin-Williams - New Jersey

Published 4 days ago

Administrative Assistant

The Advisor & Site Support Role serves as a key player in driving team initiatives, internal and external correspondence, and maintaining exceptional client ...


Barnum Financial Group - New Jersey

Published 7 days ago

Built at: 2024-11-24T06:19:25.563Z