We are looking for an Incoming Associate to follow current Good Manufacturing Practices (cGMP) and current Good Documentation Practices (cGDP) to record all procedures in a timely manner. The Associate will understand and follow Standard Operating Procedures (SOP) in all functions executed and report any deviations where necessary.
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.
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