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Job Details


Quality Control Chemist I



Full Time

On Site


Wilson, North Carolina, United States

Job Description

With 53 manufacturing sites across the globe, our aspiration is to become the top manufacturer of innovative and generic medicines in the industry!

Novartis is seeking a Quality Control Chemist I to join their manufacturing site in Wilson, NC. In this role you will support operations by providing analytical testing for materials and productions, including data analysis and reporting.

Primary Responsibilities:
• Understands the basic test in Laboratory (e.g. pH, KF, titration, std preparation, etc).
• Conducts all testing in compliance with cGMP, SOP’s, and established policies.
• Follows schedule and task assigned by your supervisor, to support the plan.
• Conducts analytical testing for Materials and Products.
• Completes on time all Laboratory task as part of routine processes.
• Meets productivity, quality and teamwork metrics for level.
• Identifies suspect data and works with others to complete an investigation.
• Initiates a Triage, when necessary.
• Manages own development plan to ensure all needed training for the role is completed.
• Maintains proper documentation of laboratory data and follow GMP's documentation practice.
• Complies with safety requirements and assumes responsibility for themselves and others and the work environment.
• Adheres to all applicable procedures, cGMPs, company policies and any other quality or regulatory requirements. (For example: OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.).
• Performs other duties as assigned and be multitasking.