IPQA Associate Level I - 2nd shift

Job ID 19-00033

Industry Pharma

Job Type Permanent

Location Dayton, NJ


Conducts and verifies line clearances (Rooms / Equipment)  and components verification
Performs  in- process checks and finish goods inspections to ensure product conforms batch record specifications
Performs AQL Sampling
Verify that temperature/humidity and Magnehelics are all in range/good working condition
Collects and submits Stability Samples from Manufacturing and Packaging operations
Collection and storage of retain samples
Perform water readings and instruments verification
Verify and confirm issuances and reconciliation of product and components
Checks calibration tags/stickers on process equipment
Inspects and releases printed packaging materials
 Inspects incoming and outgoing materials for proper identification and conformance with specifications
Regularly review and maintain logbooks and forms
Initiates Deviation & CAPAs as needed
Handle various requests from departments for developmental or investigative reasons
Provides support to complete Annual Product Review


High School Diploma or equivalent GED
Ability and willingness to learn manufacturing/packaging procedures and federal regulations pertaining to manufacturing process
Experienced in proper documentation and correction practices
Read, write and speak English

Minimum of 1-2 years of experience performing in-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment.
Must be a Team player able to effectively communicate with QA Supervisor, IPQA, Quality Control, Production, and Supply Chain to meet finished product release goals
Be able to work long hours to support production requirements
Be available for overtime, including weekends, as needed for production support

Physical requirement:
Stand/walk for the majority of the shift.
Must be able to bend at the waist and knees as well as twist at the trunk.
Must practice good personal hygiene
Must be able to lift up to 30 lbs.