Quality Control Compounding Inspector

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Founded in 2010 and based in the Austin area, Goodkind is a leading manufacturer of clean and green personal care and beauty products. Goodkind specializes in natural deodorant, skincare, and facial care products. The company has a wealth of experience in the formulation of these products and can develop according to a variety of guidelines from consumer organizations such as Ecocert to EWG, to retailers such as Credo or Sephora.

Goodkind is a certified B Corporation. As such, we balance purpose and profit, considering the impact of decisions across associates, customers, suppliers, community, and the environment. Goodkind believes by following this central multi-stakeholder approach, we are creating optimal value for each stakeholder while leaving the world a better place.

Reporting to the Quality Control Manager, the Quality Control Compounding Inspector is responsible for verifying and validating raw materials, compounding processes, industrial cleaning processes and quality control processes.

• Follow all safety guidelines and be an integral part of the safety of the workplace by participating in all safety initiatives.
• Wear all appropriate PPE when working with the chemicals and equipment required for weighing and batching.
• Verify formula  SKU Master.
• Equipment Verification/Validation Logs.
• Verify raw materials against FBS and PI’s before addition - lot code, quantity/.
• Monitor and record in-process parameters such as temperature, mixing time, mixing speeds, order of additions, homogeneity.
• Ensure adherence to all documented processes.
• Conduct in-process sampling for appearance, odor, and penetration.
• Verify bulk download processes and procedures.
• Perform visual inspections of material and processes.
• Sock Filter verification for particle size adherence to protocol.
• Verify Holding Temperatures.
• Verify Proper Mixing in staging pots.
• Verification of Tank Tag information/Verify that the holding pots are properly marked with the appropriate tank tags.
• Cleaning Validation (Perform swabbing for ATP/Micro and other cleaning validation activities).
• Report deviations immediately and coordinate with compounding, QC, or production for corrective actions.
• Support compliance for all CGMP and GDocP guidelines.

• High School diploma or equivalent, Bachelor’s Degree in a science preferred.
• Excellent English (written and verbal communication).
• Ability to stand for a significant portion of the shift.
• Ability to lift up 50 lbs regularly through the shift.
• Must be willing to work overtime and/or weekend work as required by management or the production schedule.
• Must be able to perform fundamental mathematical calculations.
  
  Availability to be onsite daily with reliable attendance during work hours; must be available/reachable during off hours in case of emergency.
• Consistently meet individual and team goals daily.
• Ability to work cross-functionally across the organization, maintaining a positive and professional attitude.

Entry level

Full-time

Quality Assurance

Personal Care Product Manufacturing

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