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2nd Shift QA Manufacturing Specialist

Harrow, Inc.
Location
Ledgewood, New Jersey
Posted
1 month ago
Department
QA
What they actually want (must-haves)
  • 3-5 years of progressive experience in cGMP quality operations and FDA regulations
  • High school degree
  • Three-plus years of experience with aseptic drug product manufacturing
  • Fundamental knowledge of safety, quality systems, and quality assurance concepts
  • Strong familiarity with manufacturing processes and operations
  • Ability to complete tasks with little direction
Nice to have
  • BS in the Scientific field preferred
What the job really is

The 2nd Shift QA Manufacturing Specialist at Harrow will oversee quality assurance in the manufacturing and production areas, ensuring compliance with cGMP standards. Daily responsibilities include monitoring compounding, filling, inspection, and labeling/packaging processes, as well as conducting reviews of in-process activities and documentation. The role requires active participation in regulatory audits and generating necessary quality control documentation.

Things to weigh
  • No salary listed
  • On-site position with potential for rotating shifts and weekend hours
  • Work hours may vary significantly based on workload demands
Job score2.6/5
Benefits1/5
Freshness4/5
Career value4/5
Role clarity4/5
Pay transparency0/5

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