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Sr. Subcontract Administrator; INF

Job in Coos Bay, Coos County, Oregon, 97458, USA
Listing for: LanceSoft Inc
Full Time position
Listed on 2026-01-12
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Engineering, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 42 - 50 USD Hourly USD 42.00 50.00 HOUR
Job Description & How to Apply Below
Position: Sr. Subcontract Administrator (INF)

Title :
Sr. Subcontract Administrator
Duration : 06 Months
Pay Range : $42.00 – $50.00/hr on W2
Work type :
Remote

Job Description
  • Quality Engineers lead and drive process and product improvements and provide specialized quality-related services to R&D, Quality Assurance, Manufacturing Engineering, Production, Procurement, and Marketing.
  • They develop, implement, and evaluate tools and equipment for quality assurance and product/process improvement.
Additional responsibilities will include
  • Drives quality assurance activities related to batch review, change control, NCRs, Deviations, CAPAs, Audits, and supports Product Complaints technical investigations for the relevant product platforms.
  • Support 3rd party audit of site through audit prep and participating in the front/back room.
  • Apply advanced Quality Assurance and Scientific Method techniques and principles to daily tasks and activities.
  • Apply relevant regulations, standards, GxP requirements, and industry best practices to assignments.
  • Plan and conduct projects and activities with moderate to high technical responsibility, complexity, and strategic feedback.
  • Act as an SME in quality assurance and scientific matters as applicable.
  • Develop and drive key strategic quality assurance initiatives throughout the organization.
  • Contributes to the development of new projects/programs/processes.
  • Lead/drive root cause investigations for multiple issues, including complaints, NCRs, Deviations, OOS, etc.
  • Leads projects requiring representation of the organization to internal and/or external customers or others, providing expertise, and promoting solutions.
Job Requirements
  • Bachelor’s or Master’s Degree in biology, chemistry, biotechnology, engineering, or a related field, or equivalent experience.
  • Post-graduate, Quality Assurance Certifications, such as Six Sigma, CQE, CQA, etc., is preferred.
  • 4+ years of experience in a similar position within the Life science industry.
  • Familiarity with medical device regulations, such as ISO 13485, FDA 21 CFR part 820, and IVDR 2017/746 is required.
  • Strong organizational and analytical skills with a focus on finding effective and efficient solutions in compliance with the regulations.
  • An effective communicator at all levels, both internally and externally.
  • Team player with the ability to make independent decisions within the framework and guidelines of the organization.
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