JT988 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN at Quality Consulting Group

New Albany, Ohio, United States -

Full Time

Start Date

Immediate

Expiry Date

27 Jun, 26

Salary

0.0

Posted On

29 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Standard Operating Procedure Adherence, Product Inspection, Packaging, Equipment Maintenance, Equipment Operation, Manufacturing Support, Inventory Tracking, Material Movement, Malfunction Recognition, Equipment Adjustment, Training, Batch Record Documentation, Component Reconciliation, Temperature Calculation, GMP Knowledge, Teamwork

Industry

Outsourcing and Offshoring Consulting

Description

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). Inspection and packaging of product-filled vials per procedures and batch records. Performing routine maintenance and cleaning of equipment. Setting up and operating equipment. 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. 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 No prior manufacturing or pharmaceutical experience is required, but it would be considered a plus. Experience in filling and finishing manufacturing (preferably vial inspection) Basic GMP knowledge Equipment operation knowledge Teamwork and communication skills Able to stand for extended periods of time Able to occasionally lift up to 50lbs Shift: 1st and 2nd starting at 6:00am - 6:30pm 3 days week 1: Mon, Thurs, Friday 4 days week 2: Tues, Wed, Sat, Sun Able to work on weekends 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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Responsibilities

The role involves routinely performing moderately-complex to complex manufacturing processes, including the inspection and packaging of product-filled vials according to Standard Operating Procedures and batch records. Responsibilities also include performing routine equipment maintenance, setup, operation, and assisting with other manufacturing support activities.