Entry, Quality Control

Shift Available: 2nd Shift Hours: 1:30PM - 9:30PM EST, Monday - Friday

Compensation: Starting at $19.06/hour + $1.00/shift differential

Start Date: July 17th, 2025

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 to include laser micrometer, optical comparator and other equipment as applicable

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

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

Print documents from Master Control, shopfloor or other software program and manages documents related to the Quality System

Segregate nonconforming product and handle quarantined product and raw materials as applicable by site

Generate rejection and deviation reports as directed by site

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

Additional Responsibilities

Education

High School Diploma required

Work Experience

No min required 1 to 3 years manufacturing experience required

Preferred Knowledge, Skills and Abilities

Must poses an acute attention to detail

Basic computer skills

License and Certifications

Travel Requirements

None: No travel required

Physical Requirements

Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.

Additional Requirements

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 and/or drug screening.