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Manufacturing Associate

GQR

Roswell (GA)

On-site

USD 35,000 - 50,000

Full time

Today
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Job summary

A leading company in pharmaceutical manufacturing is seeking a Manufacturing Associate in Roswell, GA. The role involves various manufacturing activities, including inventory control, data entry, and compliance with FDA regulations. Ideal candidates will have a high school diploma and relevant experience in manufacturing or quality roles. Join a dynamic team dedicated to maintaining high standards in a regulated environment.

Qualifications

  • 2+ years of experience in manufacturing and/or quality roles preferred.
  • Experience in regulated environments preferred.

Responsibilities

  • Issue, track, and review Manufacturing Work Order documentation.
  • Manufacture and assemble products according to approved operating procedures.
  • Perform environmental monitoring and data review.

Skills

Inventory Control
Environmental Monitoring
Data Entry

Education

High School diploma

Job description

Job Title: Manufacturing Associate

Note: This role requires experience working in pharmaceutical manufacturing.

This position involves experience in Receiving, Receiving Inspection, Shipping, Inventory Control, Manufacturing activities, environmental monitoring, and maintenance. The individual will perform routine data entry in the MRP database, LHR releases, preparation of shipping documentation, and more.

Responsibilities:
  1. Issue, track, and review Manufacturing Work Order (LHR) documentation for accuracy and component/product traceability.
  2. Manufacture and assemble products according to approved operating procedures.
  3. Perform label printing, initial packaging, and final packaging as needed to support operations.
  4. Prepare product samples for sterilization and lot release testing.
  5. Perform self-inspections on all assembly work to ensure adherence to workmanship standards.
  6. Maintain a clean and organized workstation.
  7. Follow all corporate, safety, and production operating procedures.
  8. Perform environmental monitoring, including viable and non-viable particulate counting, surface microbial testing, and review of data for each test cycle.
Inventory, Receiving, & Distribution:
  1. Process incoming receiving and inventory transactions in the MRP system.
  2. Handle transactions and documentation related to product returns.
  3. Perform periodic cycle counts to monitor inventory levels and report balances for financial reconciliation.
  4. Prepare shipments with proper documentation in compliance with procedures and export requirements.
  5. Prepare and review inspection documentation and conduct inspections as needed.
Qualifications:

High School diploma or equivalent (entry-level position).

2+ years of experience in manufacturing and/or quality roles (production, packaging, labeling, shipping, critical systems, etc.) preferred.

Experience in regulated environments preferred, with compliance to specifications, procedures, FDA QSR’s (21 CFR 820), and ISO 13485.

Additional Information:
  • Seniority level: Associate
  • Employment type: Full-time
  • Job function: Manufacturing
  • Industries: Pharmaceutical Manufacturing and Biotechnology Research

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