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Quality Control Inspector

West Pharmaceutical Services
Jersey Shore, Pennsylvania, US, United Statesfull_timeVerifiedPosted 24 Feb 2025

About the role

 

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

Jn this role, you will work as a team member to monitor and maintain Quality product/standards throughout the plant operating with a 24/7 two-week rotating schedule.

Essential Duties and Responsibilities

This is a 12 hour- 3rd shift schedule- D shift

  • Perform Inspection compliance with a variety of Quality concepts, practices, AQL sampling plans for attribute and dimensional testing
  • Approve in-process production functions, incoming materials and finished product specifications
  • Maintain Hold status of non-conforming materials
  • Document and input data results into Quality database
  • Operate measurement equipment by following operating instructions
  • Properly clean assigned workstations
  • Regular attendance is necessary
  • Perform daily audits of the Manufacture process
  • Other duties as assigned

Preferred Knowledge, Skills and Abilities

  • Functional understanding of cGMPs
  • Basic computer skills (Excel and SAP experience preferred)
  • Willing and able to work as a team to make general decisions within authorized responsibility
  • Willing and able to work overtime within the department as necessary or advised
  • Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
  • Support and contribute in Lean Sigma programs and activities towards delivery of the set target
  • Able to comply with the company’s safety policy at all times
  • Able to comply with the company’s quality policy at all times.

Education

  • High school diploma or equivalent
  • At least 1 year of related experience in support of manufacturing processes/procedures

Additional Responsibilities

  • Ability to learn, understand, and remember normal tasks.
  • Ability to hear, speak, and understand conversation in English in a normal tone of voice.
  • Ability to see and read letters, numbers, characters, or symbols and identify colors.

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Company

West Pharmaceutical Services

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