Quality Systems Documentation Specialist (4-month contract) at large consumer goods client

Location: Branchburg Township, New Jersey
Type: Contract
Level: not_specified

Description

Four-month role responsible for supervising the development, creation, and revision of controlled documentation in compliance with client procedures, current GMP, 21 CFR 820, ISO 13485, and AATB standards. The position partners with managers and supervisors across local and global functions and collaborates with Change Control and Quality Investigations/CAPA teams. The employer, location, compensation, education requirements, and experience requirements are not specified in the provided excerpt.

Required Skills

Document control
Current GMP
21 CFR 820
ISO 13485
AATB standards
Change control
CAPA investigations
Cross-functional collaboration

Additional Information

Preferred Qualifications: Experience with regulated medical-device or biologics quality systems and applicable GMP, 21 CFR 820, ISO 13485, and AATB standards would be beneficial
Experience collaborating with change control and quality investigations/CAPA teams would be beneficial