Company

Pl DevelopmentsSee more

addressAddressPiedmont, SC
type Form of workFull-Time
CategoryManufacturing

Job description

Job Description

Work Schedule: Weekend Shift - Friday to Sunday 6am-6:30pm

JOB QUALIFICATIONS:

  • Previous experience with QA helpful
  • Ability to read and write English
  • Basic knowledge and understanding of cGMP
  • Ability to work in a fast paced environment
  • Ability to multi task
  • Basic math skills
  • Ability to work with limited supervision

POSITION RESPONSIBILITIES:

  • Inspection of initial product produced as it is bottled and released off the production line, checking for correct content, volume fill level, bottle size, verification of label, correct batch number, expiration date, verification packaging conforms to customer purchase order specs
  • Report any errors or discrepancies to the line leader, Supervisor, Director of Quality and/or General Manager
  • QA pallets of product in the quarantine area
  • Identify with proper paper work all pallets cleared for the move to Distribution Center
  • Receive bank from production any unused labels
  • Participate on an as need basis with the taking of monthly inventory

PHYSICAL REQUIREMENTS:

  • Standing, walking
  • Minimal amount of lifting and over head lifting
  • Reaching, pushing, pulling, bending, squatting, climbing and proper use of a step stool / ladder for blender inspection
  • Comfortable with exposure to strong chemical smells and confined areas
Company Description
PL Developments is an over-the-counter pharmaceutical manufacturing and packaging company, headquartered in New York. We have an excellent work environment, truly invest in our people, and believe in great work/life balance. We offer a comprehensive benefits package.
PLD participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Refer code: 8612699. Pl Developments - The previous day - 2024-03-17 18:12

Pl Developments

Piedmont, SC
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