Sr. Quality System Specialist ??? Document Control (154606) Position Available In Bergen, New Jersey

Job Description:

A-Line Staffing is now hiring a Sr. Quality System Specialist??? Document Control for a major medical device manufacturer. ThisSr. Quality System Specialist position is a full-time, remoteopportunity offering competitive pay, long-term potential, and thechance to support a major organizational transition within a globalhealthcare leader. If interested, please send your resume toLKOPASZ@ALINESTAFFING.com Sr. Quality System Specialist ???Document Control Compensation The pay for this position is $34.20per hour Sr. Quality System Specialist ??? Document ControlHighlights This is a contract position (not contract-to-hire)

Schedule:

Standard business hours, Monday ???

Friday Shift:

Dayshift (Exact schedule to be confirmed)??????????????????????????????????????????????????????????????? Sr.

Quality System Specialist ??? Document Control ResponsibilitiesServe as the primary support for converting Quality SystemProcedures and Records from IDS to SM business unit formats Executehigh-volume document conversion in Microsoft Word, including layoutand content updates Perform policy and procedure updates due toorganizational changes Ensure accuracy and compliance with internalquality standards and external regulatory requirements Supportcontinuous improvement of Quality Systems through processdocumentation and revision Maintain detailed records of allchanges, ensuring proper documentation workflows are followedCollaborate with cross-functional teams to ensure consistency andaccuracy of documentation May contribute to or lead other assignedquality documentation tasks as needed Sr. Quality System Specialist??? Document Control Requirements Bachelor???s degree in science,engineering, or a relevant discipline Minimum of 5 years ofrelevant experience in quality systems or document control Highproficiency in Microsoft Word and Document Management tools isrequired Strong attention to detail and high degree of accuracy inediting/revising documents Familiarity with FDA and internationalquality system regulations , including 21 CFR Part 820, ISO 13485,MDSAP, EU

MDR/IVDR

Ability to work independently under minimalsupervision Experience working within a regulated industry (medicaldevices preferred) Preferred Qualifications Experience with BDquality systems such as SAP, Trackwise, and PEGA Certified QualityAuditor (CQA) or Transactional Six Sigma Green Belt is a plusStrong organizational skills and the ability to manage largevolumes of documentation in a fast-paced environment If you thinkthis Sr. Quality System Specialist ??? Document Control position isa good fit for you, please reach out to me ??? feel free to call,e-mail, or apply to this posting! If interested, please send yourresume to LKOPASZ@ALINESTAFFING.com