Quality Auditor Molding - Fixed Term Contract

West Pharmaceutical Services•Tempe, AZ
•Onsite

About The Position

The Quality Auditor Molding role provides manufacturing quality inspection services to ensure that in-process and finished products meet customer specifications. The work includes inspection, quality control, sampling, testing, documentation, and record keeping. The position requires adherence to Good Documentation Process (GDP) to ensure conformity to specifications and traceability of records. This is an onsite, fixed-term contract projected to last nine months, with full-time hours. The shift is Sunday, Monday, Tuesday, and every other Saturday from 5:45 PM to 6:00 AM. Benefits and training are offered. A $1,000 bonus is offered at 12 and 24 weeks to team members who complete those milestone dates. No relocation assistance is provided.

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 to the site.
  • Understand and follow applicable ISO standards 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 to form batch records; ensure appropriate disposition of batch records, such as filing or scanning.
  • Segregate nonconforming product and handle quarantined product and raw materials, as applicable to the site.
  • Escalate out-of-specification events.
  • Perform trace-back investigations of nonconforming raw materials and products 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 are offered.
  • Training is offered.
  • $1,000 bonus at 12 and 24 weeks for those who complete those milestone dates.
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