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Quality Assurance Specialist II; Operations

Job in Huntsville, Madison County, Alabama, 35824, USA
Listing for: Valid8 Financial, Inc.
Full Time position
Listed on 2026-02-01
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Quality Assurance Specialist II (Operations) - (2026-009-104)

Responsibilities

  • Works on problems of diverse scope in which analysis of data requires evaluation of identifiable factors.
  • Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
  • Normally receives no instructions on routine work, general instructions on new assignments.
  • Participates in the disposition of batches, including resolution of investigations and deviations to meet lot release time lines.
  • Conduct manufacturing and packaging batch record review for accuracy and data integrity (ALCOA+) compliance.
  • Performs line clearance and checks for product and packaging activities.
  • Author, review and approve Documents in EDMS system to ensure compliance.
  • Participate and provide analytical documentation review to support in the release of raw materials.
  • Review CofA’s, stability data and release testing documentation in support of final product release.
  • Compile Product Quality Reports (i.e. annual product reports, batch review summary report).
  • Contribute to quality improvement initiatives.
  • Gathers and collates quality metric data.
  • Participates in regulatory inspections by assisting in the coordination of readiness activities and inspection logistics.
  • Performs data audits and report review as required.
  • Supports in quality investigations utilizing QA tools and follows up on corrective actions to closeout.
  • Performs other duties as assigned.
  • A minimum of a Bachelors degree in a scientific discipline is required.
  • Equivalent experience may be accepted.
  • A minimum of 3 years related experience is required.
  • A minimum of 2 years experience in the pharmaceutical industry working in a GMP environment is required.
  • Must have a demonstrated working knowledge of scientific principles. Laboratory instrumentation experience (NMR, HPLC, GC, etc.) a plus.
  • Requires strong oral and written communication skills. Knowledge of FDA regulations and cGMPs for drugs are a must.
  • Ability to work and coordinate activities with multiple functional groups with sense of urgency.
  • Ability to organize, prioritize, plan and schedule.
  • Ability to work with minimal supervision.
  • Physical Requirements
  • Must be able to pass pre-employment drug screening and background check for employment consideration.
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