Quality Control Chemist I Position Available In Fulton, Georgia

Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global medical device manufacturer, in Johns Creek, GA. No C2C or Sponsorship is available for this position.

Title:

Quality Control Chemist I Location:

Johns Creek, GA Onsite, Monday to

Friday Contract Duration:

24 months, with likely extension w2

Hourly Rate:

TBD Work Schedule:

12-Hour Shifts Job Description We are seeking a skilled Quality Control Analyst to perform comprehensive quality testing on materials and production samples, ensuring compliance with c

GMP, FDA

regulations, and Corporate Quality policies. This role supports production operations through routine and non-routine incoming inspections, assists in technical problem-solving, and communicates material dispositions to internal and external stakeholders with minimal supervision. Key Responsibilities

• Conduct quality control testing on raw materials, in-process formulations, and finished product samples to support production operations.
• Maintain the Analytical Laboratory in compliance with regulatory standards and site procedures.
• Accurately document and review analytical data and laboratory records in a timely manner.
• Conduct lab investigations and participate in special analytical and incoming inspection projects as assigned.
• Complete ongoing training to stay current with industry best practices and maintain analytical proficiency.
• Engage in continuous improvement initiatives by identifying non-value-added activities and proposing enhancements.
• Execute routine procedures with supervisory guidance, including:
• Obtaining and inspecting packaging material samples.
• Preparing raw material samples for testing and submitting them to designated test areas.
• Managing material disposition in SAP and ensuring proper labeling.
• Prepare reports, emails, and memos for internal and external stakeholders following supervisory approval, including:
• Quality Reports (QR), material disposition notifications, non-conformance reports, and operational memos.
• Assist with non-routine procedures under supervisory direction, including validation studies, protocol execution, R&R studies, and vendor/site support projects.
• Support laboratory system administration, including:
• Lab safety oversight, calibration management, documentation maintenance, data trending, and inventory tracking.
• Maintain compliance with required training on SOPs, GMP, and safety protocols.
• Provide and receive cross-training within the Analytical and Incoming Inspection Laboratory to enhance operational efficiency. Requirements
• Bachelor’s degree in a scientific discipline (Chemistry preferred).
• Fluency in reading, writing, and verbal communication in English.
• 1-2 years of relevant experience in quality control or laboratory operations.
• Availability to work a 12-hour shift schedule.