Quality Auditor - Fixed Term Contract

West Pharmaceutical Services • Phoenix, AZ

1d • Onsite

About The Position

In this role you will be responsible to independently provide analytical review of the data generated for internal and external customers as well as supporting post-production related Quality activities such as finished batch release, including sterilization, packaging specifics, work order approval and support additional quality department activities. This position also requires maintaining knowledge of the current local and/or International regulations/guidelines/policies applicable to West's products and services.

Requirements

• High School Diploma or GED Required.
• 1 year of experience required.
• Must possess an acute attention to detail.
• Basic computer skills.
• Able to be aware of all relevant standard operating procedures as per Company policy.
• Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude.
• Willingness to learn new and review new analytical techniques.
• Ability to learn, understand, and remember normal tasks.
• Ability to hear, speak, and understand conversation in English.
• Must maintain the ability to work well with others in a variety of situations.
• Must be able to multi-task, work under time constraints, problem solve, and prioritize.
• Read and interpret data, information and documents.
• Work under deadlines with constant interruptions.

Responsibilities

• Perform sampling, inspections, and testing of in-process and finished goods products per applicable procedures and AQL plans, utilizing both visual means as well as calibrated test equipment that includes CMMs, Vision Systems, and manual gaging.
• Release acceptable in-process and finished goods product for further processing and/or shipping as applicable per site.
• Understand and follow applicable ISO standards requirements and follow good documentation practices.
• Perform review of inspection records to assure product conforms to specifications and proper documentation practices.
• Retains sample of finished products and maintains all applicable documents to form batch records and ensures appropriate batch records disposition (i.e. filing, scanning etc.) as necessary.
• Segregate nonconforming product and handle quarantined product and raw materials as applicable by site.
• Escalate "out of specification" events.
• Perform trace back investigation of nonconforming raw material and product as directed by site.
• Promotes and supports a Lean environment.
• Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
• Exhibits regular, reliable, punctual and predictable attendance.
• Other duties as assigned.

Benefits

• benefits
• training
• A $1,000 bonus will be offered at 12 & 24 weeks for those that complete these milestone dates.
• opportunities for lifelong learning, growth and development
• benefit programs
• empower the physical, mental, emotional and financial health of our team members and their families
• giving back to help those in need in the communities where we live and work
• creating a healthier environment and planet through our sustainability efforts

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED