QA/RA Associate

Posted: Wednesday, 27 November 2024
Valid Thru: Friday, 27 December 2024
Index Requested on: 11/27/2024 19:15:21
Indexed on: 11/27/2024 19:15:21

Location: White Plains, NY, 10601, US

Industry: Advertising and Public Relations
Occupational Category: 13-0000.00 - Business and Financial Operations
Type of Employment: FULL_TIME

Zeiss Group is hiring!

Description:

Join the Zeiss team in White Plains, NY, as a Quality Assurance/Regulatory Affairs (QA/RA) Associate. You will support the Quality Department in meeting regulatory obligations (e.g.: FDA reporting, Rad. Health reporting) and the maintenance of the various activities related to sustaining an ISO 9001/13485 Quality Management System including document control, complaint & CAPA processing, and audit planning. This is a Hybrid (3/2) position, working in the office, and remotely.

Job Functions:
  • Administers complaint process, including review and logging of incoming complaints, preliminary investigation and follow-up to closure
  • Assists process owners with development/review of Standard Operating Procedures for RMS and IQS
  • Provides Regulatory support, including guidance, review and preparation of filings for initial, supplemental and annual CDRH reports (including, but not limited to RMS, IQS, XRM, SBE, and SMT)
  • Maintains FDA establishment registrations, renewals and device listings
  • Administers corporate document control process and updates QMS database
  • Administers Corrective Action/ Preventive Action System
  • Administers internal audit plan and scheduling
  • Prepares graphs or charts of data and/or analyzes data
  • Assist in internal and external audits
  • Participates in preparation of Management Review data and presentations
  • Other QA/regulatory duties and other duties as assigned


  • Bachelors Degree with 2 years experience in an ISO certified or QSR compliant environment
  • Working knowledge of FDA Quality System Regulation and CDRH reporting requirements
  • Working knowledge of ISO requirements, specifically ISO 9001 or ISO 13485 Medical Devices
  • ISO 9001 Auditor Certification a plus
  • Effective verbal and written communication skills
  • Strong Computer Skills (MS Word, Excel, PowerPoint, etc.)
  • Ability to schedule and handle multi-tasking to meet deadlines
  • Ability to interact positively and professionally at all levels of the organization
  • Ability to work independently or as part of a team


The annual salary range for this contingent position (temp - to - hire) is $65 - 70K.

The salary offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, complexity/specialization/scarcity of talent.

Your ZEISS Recruiting Team:
Steve Warner

Responsibilities:

Please review the job description.

Educational requirements:

  • high school

Desired Skills:

Please see the job description for required or recommended skills.

Benefits:

Please see the job description for benefits.

Apply Now