Manufacturing/Production Associate
Location: Princeton New Jersey, New Jersey
Type: Contract
Contractor Work Model: Onsite
Hours: 1st Shift 6 AM- 2:30 PM M-F Responsibilities
The Manufacturing/Production Associate will perform GMP activities associated with producing, cleaning, and packaging.
- Works in a Class 8 cleanroom environment
- Weighs out raw chemicals and ingredients and charges into fill tanks
- Operates fill equipment, filling devices per batch record and SOP instructions
- Records operating data such as production numbers, process conditions, test results and instrument readings
- Makes adjustment to operating settings, as needed
- Handles hazardous materials and hazardous waste in compliance with local, federal, and company guidelines
- Draws samples of products and materials for laboratory analysis
- Performs basic tests on filled devices
- Completes batch record and SOP documentation according to cGMP requirements
- Enters data into electronic software systems (i.e. ERP)
- Cleans work areas and fill station per SOP requirements
- Other duties as assigned
- High School graduate with 3+ years of manufacturing experience in pharmaceutical or medical device cGMP compliant production/pilot plant or recent college graduate with 0 years of experience.
- Must be capable of wearing required PPE
- Must be capable of working in a cleanroom environment and meeting necessary hygiene requirements.
- Good written and verbal language skills and ability to follow SOPS
- Computer literacy
- Basic math skills
- Ability to lift 50 pounds
- Ability to climb staircases
- Ability to stand for long periods of time (i.e. 1 hour).
- Flexibility and attention to detail
- cGMP and/or clean room experience is a plus
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