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Incoming Associate (Quality Control) - Pharmaceuticals
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NPAworldwide Recruitment Network
 
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Job Location: Lancaster, SC
JOB DESCRIPTION

Job #: 43112
Title: Incoming Associate (Quality Control) - Pharmaceuticals
Job Location: Lancaster, South Carolina - United States
Remote Job: Unknown
Employment Type:
Salary: $35,000.00 - $50,000.00 - US Dollars - Yearly
Employer Will Recruit From: Nationwide
Relocation Paid?: NO

WHY IS THIS A GREAT OPPORTUNITY?

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.

JOB DESCRIPTION

  • 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.
QUALIFICATIONS

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

Education:
University - Associate`s Degree/Graduate Diploma/2 Years




How to Apply:


 
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