Quality Control Inspector II

Cohere Beauty Omaha IncPhoenix, AZ
10hOnsite

About The Position

Cohere Beauty is a diverse team of strategic collaborators, product innovators, R and D formulators, and manufacturing professionals. Built on beauty and rooted in quality, our promise is to collaborate, co-innovate, co-develop, and co-manufacture. Promoting diversity and sustainability through our facilities and supply chains, Cohere Beauty’s approach to social, safety, and environmental responsibility is grounded in a commitment to our employees, customers, and the communities where we live and work. At Cohere Beauty, we’re here for what’s next. Job Summary    The Quality Control Inspector is responsible for applying quality control principles to ensure products meet regulatory, client, and company standards.

Requirements

  • High School diploma or equivalent.
  • Strong telephone skills and telephone etiquette.
  • Strong MS Office Skills.
  • Excellent organizational skills.
  • Clear and concise communication skills to employees.
  • Ability to read, write, and speak English competently.
  • Ability to work on-site.
  • Ability to maintain regular, reliable, and predictable attendance.

Nice To Haves

  • Spanish a plus

Responsibilities

  • Monitor the quality of the product in process on lines; including fill weights, torque values, housekeeping status, line GMP compliance, and line start-up approvals.
  • Inspect incoming components, raw materials, in-process bulk, and finished products against company specifications.
  • Investigate discrepancies in documentation and fill out paperwork for batch records.
  • Perform line checks, evaluating at a minimum applicable product weight, product concentration levels, component weights, and accuracy of silk-screened components.
  • Verify correct components and accuracy of identification.
  • Do daily scale checks and set scales for accurate bottle weights.
  • Audit finished goods.
  • Evaluate the cleanliness of the lines.
  • Perform random line checks, documenting findings.
  • Review batch records for errors.
  • Perform and/or assist with GMP inspections and documentation of them.
  • Assist as needed in training employees.
  • Communicate needed corrections, major defects, and potential and actual need for line shutdown to appropriate management personnel.
  • Monitor and record reject deviations and investigations.
  • Ensure proper use of QC communication such as status stickers and placards.
  • Assist with writing Standard Operating Procedures (SOPs), and upkeep of the SOP book.
  • Develop/document processes for new procedures.
  • Communicate effectively with others.
  • Perform work onsite.
  • Perform other duties as assigned.
  • Perform at an experienced and functional level therefore requiring limited supervision.
  • Engage in Professional Development Activities.
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