Quality Auditor Molding - Fixed Term Contract

West Pharmaceutical Services•Rockford, 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 work includes quality inspection and control, sampling inspection, testing, documentation, and record keeping. The role requires adherence to Good Documentation Process (GDP) to maintain documentation that demonstrates conformity to specifications and traceability of records. This is an onsite, fixed-term contract projected to last 9 months, with full-time hours and a shift of Sunday, Monday, Tuesday, and every other Wednesday, from 5:45 AM to 6:00 PM. Benefits and training are offered. A $1,000 bonus is offered at 12 and 24 weeks for team members who complete those milestones. No relocation assistance is provided. No travel is required.

Requirements

  • High school diploma or GED.
  • Acute attention to detail.
  • Basic computer skills.
  • Ability to learn and follow 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 and review 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

  • Sample, inspect, and test 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.
  • Understand and follow applicable ISO standards and good documentation practices.
  • Review inspection records to verify product conformance and proper documentation.
  • Retain finished-product samples, maintain applicable documents for batch records, and ensure appropriate batch-record disposition, such as filing or scanning.
  • Segregate nonconforming product and handle quarantined product and raw materials as applicable by 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.
  • Follow 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.
  • A $1,000 bonus is offered at 12 and 24 weeks to those who complete these milestone dates.
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