JT898 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN NS

New Albany, OH

Temporary

Biopharmaceutical

Entry Level

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

Routinely perform moderately-complex to complex processes according to Standard Operating Procedure (SOP).
Maintaining strict adherence to SOP and cGMP requirements and expectations.
Load materials into the machine, operate a manual and/or electric pallet jack, and inspect and clean the assigned machine.
Inspection and packaging of product-filled vials per procedures and batch records.
Performing routine maintenance and cleaning of equipment.
Assist in troubleshooting equipment and system errors as needed (or escalate to management).
Setting up and operating equipment.
Operating a variety of packaging equipment (Assembly, labeler, cartoner, case packer, autoinjector testing, ID testing).
Assisting or participating in other manufacturing operations (e.g., filling support activities).
Internal support operations (e.g. stocking items, tracking inventory, material movement).
Recognizing and reporting malfunctions and making necessary adjustments to equipment.
Training new MPTs on routine tasks.
Required to know, comprehend, and apply packaging configurations, as well as understand, follow and document batch records for the inspection and packaging process.
Reconcile components and products and calculate product exposure to room temperature.

Qualifications:

High school/GED + 1 year of work or military experience or Associate degree
Filling and finishing manufacturing experience. (preferably vial inspection)
Skilled in computer literacy, committed to continuous learning through self-motivation
Effective in collaborative team environments, Machine operations and pharma experience a plus
Prior experience in cGMP environments. (preferred but not required)
Has a track record of being fluent in technology (navigating computer systems and software beyond just Microsoft products) and using those skills in a fast-paced manner.
Night Shift: Onsite 12-hour rotation shift 6:00 PM- 6:30 AM
- Candidate must be willing to work with 12 hours rotational shift with breaks.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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