Quality Auditor Molding - Fixed Term Contract

West Pharmaceutical Services•Tempe, AZ
•Onsite

About The Position

The Quality Auditor Molding role ensures that in-process and finished products meet customer specifications by providing manufacturing quality inspection services, including quality inspection, quality control, sampling, documentation, and record keeping. Good Documentation Process (GDP) practices are essential for maintaining documentation that supports conformity to specifications and traceability of records. This is an onsite, fixed-term contract projected to last nine months, offering full-time hours, benefits, and training. The schedule is Sunday, Monday, Tuesday, and every other Wednesday, from 5:45 AM to 6:00 PM. No relocation assistance or travel is provided. A $1,000 bonus is offered at 12 and 24 weeks to team members who complete those milestones.

Requirements

  • High school diploma or GED.
  • Acute attention to detail.
  • Basic computer skills.
  • Ability to be aware of relevant standard operating procedures in accordance with company policy.
  • Ability to work independently and as part of a team, with self-motivation, adaptability, and a positive attitude.
  • Willingness to learn new and review existing analytical techniques.
  • Ability to learn, understand, and remember normal tasks.
  • Ability to hear, speak, and understand conversation in English.
  • Ability to work well with others in a variety of situations.
  • Ability to multitask, work under time constraints, solve problems, and prioritize.
  • Ability to read and interpret data, information, and documents.
  • Ability to work under deadlines with constant interruptions.

Nice To Haves

  • One year of manufacturing experience.

Responsibilities

  • Perform sampling, inspections, and testing of in-process and finished goods according to applicable procedures and AQL plans, using visual inspection and calibrated equipment such as CMMs, vision systems, and manual gaging.
  • Release acceptable in-process and finished goods for further processing or shipping, as applicable at the site.
  • Understand and follow applicable ISO standards requirements and good documentation practices.
  • Review inspection records to verify product conformity to specifications and proper documentation practices.
  • Retain finished-product samples and maintain applicable documents for batch records; ensure appropriate batch record disposition, such as filing or scanning.
  • Segregate nonconforming product and handle quarantined product and raw materials as applicable at the site.
  • Escalate out-of-specification events.
  • Perform trace-back investigations of nonconforming raw material and product as directed by the site.
  • Promote and support a Lean environment.
  • Comply with corporate and site-specific regulations, policies, work procedures, instructions, and safety rules.
  • Maintain regular, reliable, punctual, and predictable attendance.
  • Perform other duties as assigned.

Benefits

  • Benefits
  • Training
  • $1,000 bonus at 12 and 24 weeks for those who complete these milestone dates
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service