Nutramax Laboratories

Incoming Associate (2nd Shift)


  • Inspecting and sampling materials appropriately.  All samples taken will be accurately documented and deducted from inventory.  This person will reference Finished Product and Material Specifications for specific sampling instructions.
  • Responsible for reading and understanding all the accompanied paperwork, which includes but is not limited to: Packing Slips, Bills of Lading, Certificates of Analysis (CoA), Certificate soft Compliance (Coca), Printed Material Proofs, & Material Safety Data Sheets (MSDS). The QCIA will inspect all received materials for identity, quantity, and damage.
  • Processing and bookkeeping of all materials received, which includes but is not limited to: generating the Inspection Form, appropriate disposition labels, inventory sheets, assigning sequential lot numbers, & updating the receiving/sampling logs.
  • Updating and navigating through the Navision software program. The QCIA will report and rectify any discrepancies with the QC Management or QCIT.
  • Following current Good Manufacturing Practices (cGMP) documentation guidelines to record all procedures in a timely fashion. This person will follow Standard Operating Procedures (SOP) in all functions executed and report any deviations where necessary.
  • Maintaining a safe working environment by following all safety guidelines/regulations and wearing Personal Protective Equipment (PPE) as appropriate. This person will ensure that all equipment used in sampling is cleaned, calibrated, and properly maintained.
  • Must be able to effectively communicate with other departments and function within a team environment.
  • Perform other assigned duties as may be required in meeting company objectives
  • Communicate effectively with other departments within the organization and function within a team environment.


Minimum Requirements:  Requires proficiency in MS Office Suite.  Ability to lift and maneuver material. Good written and oral communication skills


Education and Experience A high school diploma or General Educational Development (GED) .Minimum of one year of experience in a regulated cGMP environment

Computer / Internet / Technology

Tagged as: compliance, documentation, samples