Quality Assurance Document Specialist

4 weeks ago


Lancaster, United States Nutramax Laboratories Full time
Job Description

Summary of the Position: We are seeking a skilled Quality Assurance (QA) Document Specialist to join our team at Nutramax Laboratories. This role will be responsible for ensuring the accuracy and completeness of documentation related to batch records, forms, and other pertinent cGMP documents and logbooks.

Key Responsibilities:

  • Perform batch record reviews and document control tasks with high attention to detail.
  • Ensure all documentation is accurate and complete before releasing to production and/or customer consumption.
  • Communicate effectively with various departments within the organization to ensure timely issuance, execution, and correction of records in the quality system.
  • Assist in maintaining quality control documents and spreadsheets.

Requirements:

  • Minimum of 2 years of experience in a GMP or pharmaceutical manufacturing environment.
  • Strong mathematical background and organizational skills.
  • Proficient in MS Office Suite, specifically Word and Excel.
  • Detail-oriented with a strong ability to handle multiple projects.

Educational Requirements: Associate Degree or a minimum of two years' experience in QA related to food, pharmaceutical, or other government-related industry.



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