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 in-process and finished products meet customer specifications. The position includes quality inspection and control, sampling inspection, testing, documentation, and record keeping. Following Good Documentation Process (GDP) is essential to maintain required documentation and ensure conformity to specifications and record traceability. This is an onsite, fixed-term contract projected to last 9 months, with full-time hours. The schedule is Wednesday, Thursday, Friday, and every other Saturday, from 5:45 AM to 6:00 PM. The position offers benefits and training, as well as a $1,000 bonus at 12 and 24 weeks for team members who complete those milestones. No relocation assistance is provided.

Requirements

  • High school diploma or GED.
  • Acute attention to detail.
  • Basic computer skills.
  • Ability to be aware of applicable 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 and review analytical techniques.
  • Ability to learn, understand, and remember normal tasks.
  • Ability to hear, speak, and understand conversation in English in a normal tone of voice.
  • 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.
  • Ability to exert light force up to 20 lbs/9 kg frequently, and/or a negligible amount of force frequently or constantly to move objects.

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 a laser micrometer and optical comparator.
  • Release acceptable in-process and finished goods for further processing or shipment, as applicable to the site.
  • Understand and follow applicable ISO standards requirements.
  • Review inspection records to verify product conformity and proper documentation practices.
  • Retain finished-product samples and maintain documents for batch records, ensuring appropriate disposition such as filing or scanning.
  • Print and manage Quality System documents from Master Control, shopfloor, or other software programs.
  • Segregate nonconforming products and handle quarantined products and raw materials, as applicable to the site.
  • Generate rejection and deviation reports as directed by the site.
  • 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 these milestone dates.
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