Quality Auditor Molding - Fixed Term Contract

West Pharmaceutical Services, Inc; Tempe (AZ); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

Bonus program

Benefits

Job summary

West Pharmaceutical Services, Inc. in Tempe, AZ seeks a Quality Auditor Molding for a 9-month fixed-term contract. The onsite role focuses on ensuring in-process and finished products meet specifications and GDP integrity.

You will perform sampling, inspection, and documentation per procedures, manage batch records, and support lean initiatives while maintaining traceability and compliance with ISO standards.

Qualifications

• High School Diploma or GED required.
• 1 year manufacturing experience preferred.
• Attention to detail and good documentation practices.

Responsibilities

• Perform sampling, inspections, and testing of in-process and finished goods per procedures and AQL plans.
• Release acceptable in-process and finished goods for processing or shipping.
• Understand and follow ISO standards and GDP documentation requirements.
• Review inspection records to ensure conformance and proper documentation.
• Maintain batch records and disposition documents, filing/scanning as needed.
• Segregate nonconforming product and quarantined materials as applicable.
• Escalate out-of-specification events and perform trace-back investigations as directed.
• Support Lean initiatives and ensure compliance with safety and company policies.
• Exhibit punctual attendance and collaborate with team members.

Skills

Attention to detail

Basic computer skills

SOP awareness

Team player

Self-motivation

Adaptability

Willingness to learn

Education

High School Diploma or GED

Job description

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Title: Quality Auditor Molding - Fixed Term Contract

Requisition ID: 76109

Date: Oct 20, 2026

Location: Tempe, AZ, US, 85288

Department: Quality

Description:

This is an onsite position requiring the team member to be onsite for all scheduled workdays. No relocation assistance is provided for this opportunity.

This Shift is Sunday, Monday, Tuesday every other Saturday 5:45 PM - 6:00 AM

This position is a fixed-term contract projected to last 9 months. The position offers benefits, training, and full time hours.A $1,000 bonus will be offered at 12 & 24 weeks for those that complete these milestone dates.

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

The role is essential in ensuring in-process and finished products meet customer specifications. This role provides total manufacturing quality inspection services including quality inspection, quality control, sampling inspection, documentation and record keeping. Adhering to Good Documentation Process (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.

Essential Duties and 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

Education

• High School Diploma or GED Required.

Work Experience

• 1 year manufacturing experience preferred

Preferred Knowledge, Skills and Abilities

• Must poses 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

Travel Requirements

None: No travel required

Physical Requirements

Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.

Additional Requirements

• 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

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in orderto apply to West, please send an email to [e-mail] . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.

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