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Quality Technician Molding


Job Location:

Phoenix, AZ - USA

Monthly Salary: Not provided by the employer
Posted: 21 August 2026 (12 hours ago)
Application Deadline: 18 November 2026
Vacancies: 1 Vacancy

Job Summary

At West were 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 Wests indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future

Theres 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

In this role you assist the Quality Auditors Batch Record Reviewers Engineering and Operations with daily duties including inspection batch records document and record control and shipping requirements.

Essential Duties and Responsibilities
  • Point of QA contact in the WEST location. Organize the QA lab work loads and drive performance across the 4 QA lab shifts.
  • Perform and oversee component or product inspection sampling analyses following standard methods and procedures and approval/release.
  • Write review and revise procedures work instructions and any related forms for specific job-related activities.
  • Conducts review of batch documentation for GMP Compliance. Works with production personnel to resolve GMP discrepancies. Establishes/updates files/data summaries for batch documentation.
  • Works with databases to collect information and data pertaining to batch documentation.
  • Performs QA release of finished product for acceptable materials.
  • Assist with the disposition of Nonconforming material in the Bond Room and dispositions nonconformance material per procedures and MRB reviews.
  • Train existing QAs and Quality Techs to the material review process for business continuity provide continued training as required.
  • Updates internal and external customer with daily lot release updates.
  • Performs other duties as assigned by the Quality Supervisor or Manager.

Additional Responsibilities
  • Proficiency with PC and Microsoft Office; Knowledge of QMS Master Control MeasurLink and other Quality systems is preferred.
  • Must be able to prioritize and perform position responsibilities accurately and meet required deadlines
  • Strong attention to detail; Strong problem identification/analysis and solving skills with hands-on approach
  • Excellent verbal and written communication skills; Maintain an organized and clean quality Lab.
  • Ability to multi-task and prioritize in a fast-paced environment; Ability to interface with all personnel levels
  • Motivated self-starter with ability to work independently on multiple assignments in a team environment
Education

High School Diploma or GED Required

Work Experience
  • 3 years of experience in manufacturing environment.
Preferred Knowledge Skills and Abilities
  • Able to be aware of all relevant standard operating procedures as per Company policy
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target
  • 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
  • Meet individual and departmental goals as required
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
Shift

Monday Friday 7:00 AM - 4:30 PM

West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe treated fairly valued and respected. We do not discriminate on the basis of race religion color national origin gender sex gender identity sexual orientation age marital status veteran status disability status or other applicable legally protected characteristics. Where permitted by law employment with West Pharmaceutical Services Inc. or any of its subsidiary or affiliate companies is contingent upon the satisfactory completion of post-offer background screening.

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Required Experience:

IC


About Company

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West Pharmaceutical Services, Inc. is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products.

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