Pharmaceutical Packaging Technician (ONSITE- 1st/2nd Shift) at NetSource, Inc.

PLEASE DO NOT APPLY IF YOU ARE NOT LOCAL TO WEST POINT, PA.

MUST HAVES:
Experience in product packaging, clinical packaging experience in a regulated environment
GMP experience in regulated environment
Able to wear appropriate respiratory protection to work with potent compounds
Experience/ Able to work in a climate-controlled environment (example 2-8 degrees C but could vary)
Cleaning experience within a regulated environment
ERP system/ SAP
Proficiency with computer programs, Experience with Outlook and Teams
Ability to stand or sit for prolonged periods of time and capable of lifting up to 50lbs

Requirements: Must have 1-2 years working in GMP operations Experience in Clinical Supply Packaging Operations preferred B.S. degree preferred. Additional experience required without B.S. degree

Please note that this is a 1 year contract position.

First Shift- 6AM-2:30PM
Second Shift- 2:30PM-10:30PM

Pharmaceutical/ Medical Device Industry experience.

BS or BA Preferred; Experience in Clinical Supply Packaging Operations preferred
This role plays a critical part in the supply chain for critical trials. In this position you are assigned daily projects and will be the one packaging medication into the proper package while working closely with the label and warehouse teams.
GMP experience, previous experience following SOPs and proper documentation practices
"Close attention to detail
Timeliness (complete projected by deadline)
Able to work independently or with a small team"

Summary: Work as part of a Team to execute clinical packaging and labeling activities, including material, room and equipment staging, execution and documentation of operations, and room clearance and cleaning. Support additional operational activities in support of sampling and material transfer. Performs all tasks related to clinical label printing production. Maintain training and compliance with site safety and quality requirements.

Selected Responsibilities: Maintain cGMP and safety training to site requirements Follow cGMP and safety requirements in all activities Stage materials for operations, handling products with restricted time out of environment requirements Set-up, operate, disassemble and clean area equipment Perform and document de-packaging, packaging, labeling and sampling activities Report potential quality events, non-conformance to GMPs/SOPs when observed Ensures that each component or bulk material used in label production is properly identified, not expired, verified throughout processing and corresponds to the written information on the work order before proceeding to the next step. Print, inspect, proof, and perform accountability for clinical product labels. Process labeling/packaging batch paperwork according to GMP/GDP. Verifies before use that equipment calibration date has not been exceeded. Maintain label inventory. Carries out all the appropriate periodic quality inspections during the printing process to ensure the integrity. Clean facility and equipment including cleaning of packaging rooms and general housekeeping and perform verification procedures Stocking of PPEs, disinfectants, cleaning wipes and other consumables for the facility and packaging rooms Physically capable to don and wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE are essential for the health and safety of employees Ability to lift, carry, push, and pull up to 50 lbs.

Applicants must provide their phone number. Reference job number A4320.