Our client is one of the largest medical device companies in the world and has been supporting the vision care industry for decades! They are looking for a new QC Chemist to join their team!

Located in Duluth, GA

*This is a 12 hour shift schedule*
Pay: $25-35/hour DOE
Key Responsibilities:

• Conduct QC testing of raw materials, in-process materials, formulations, and finished products.

• Perform routine and non-routine inspections and generate accurate documentation to support material disposition.

• Maintain laboratory compliance with internal procedures and external regulatory standards.

• Document, review, and approve analytical data and laboratory records in a timely and accurate manner.

• Support laboratory investigations and special analytical/incoming inspection projects as needed.

• Actively participate in continuous improvement initiatives and identify non-value-added activities.

• Execute standard procedures with minimal supervision, including:

  • Sampling and inspecting packaging materials

  • Preparing raw materials for testing

  • Dispositioning materials in SAP and labeling accordingly

• Assist with preparation of quality reports, notifications, and memos with supervisory approval.

• Support non-routine procedures such as protocols, validations, R&R studies, and vendor/site projects.

• Help manage laboratory systems including safety, calibration, documentation, and inventory.

• Stay current on all required training and compliance standards.

• Cross-train and mentor peers within the Analytical and Incoming Inspection labs.

Qualifications:

• Required:

  • Bachelor's Degree in a scientific discipline (Chemistry preferred)

  • 1–2 years of relevant QC experience in a regulated manufacturing or laboratory environment

  • Strong verbal and written communication skills

  • Ability to work independently and as part of a team in a fast-paced setting
  • Proficient in English (written and spoken)

​​​​​​​Preferred Skills & Experience:

• Working knowledge of MS Word and Excel

• Experience with technical writing, root cause analysis, and corrective action reports

• Familiarity with regulatory standards such as ISO 13485, MDSAP, EU MDR/MDD, and GMP

• Proficiency in SAP, MDLIMS, EMPOWER, and TRACKWISE is a plus