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Quality Inspector

Job in Kinston, Lenoir County, North Carolina, 28504, USA
Listing for: West Pharmaceutical Services, Inc
Full Time position
Listed on 2026-06-21
Job specializations:
  • Quality Assurance - QA/QC
    Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 40000 - 60000 USD Yearly USD 40000.00 60000.00 YEAR
Job Description & How to Apply Below

Title:

Quality Inspector

Requisition

Date:
May 29, 2026

Location:

Kinston, NC, US, 28504

Department:
Quality

Description:

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

This role is essential in ensuring customer specifications and timelines are met and is accountable for in‑process quality control services and support. The Quality Specialist role will be responsible for materials acceptance activities, provide additional quality inspection, quality control testing, sampling inspection and documentation control activities within the Quality team. Adhering to Good Documentation Process (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.

The Quality Specialist will handle projects and tasks in support of product development and will play an active role to ensure products meet quality standards consistent with internal procedures and acceptance criteria, while meeting company and regulatory requirements.

Shift: Days and Nights (12‑hr on 2, 2, 3 rotation)

Essential Duties and Responsibilities
  • Provide guidance on documentation structures and format to ensure compliance to procedures, relevant regulations and standards.
  • Manage and maintain traceable, accountable, password protected, documentation system in compliance with Corporate guidelines.
  • Inspects in-process production by confirming specifications, conducting Visual, Dimensional and Functional tests, and communicating required adjustments to required personnel. May lead the process for raw materials acceptance activities including issuance of Certificate of Compliance.
  • Support batch release by completing batch card review and provide quality document control oversight on documentation and reports.
  • Approve batch records against approved specifications, quality standards, company procedures and regulatory filings for release of product to market.
  • Collaborate with teams on the development of product development DHF documents, specifically in regard to facilitating document control activities.
  • Contribute to and support the development of product development QMS procedures and work instructions.
  • Calibrates all equipment gauges, measuring devices, weighing devices and hand‑held gauging devices.
  • Identify, define, monitor, track, and report on documentation metrics (e.g., documentation release rates, documentation rejection rates, etc.).
  • Responsible for identification, front line management and appropriate escalation of major and critical incidents.
  • Generate associated OOS/Deviation/Non‑Conformances.
  • Work collaboratively with internal customers to refine and optimize analysis and reporting criteria as well as manage expectations around analysis delivery timelines and output capabilities.
  • Leading the process of the approval of all graphic and label related raw material.
  • Establish routine communication strategies for project tracking and prioritization.
  • Drive continuous quality improvement efforts to reduce scrap, cycle times, improve efficiency, and eliminate waste.
  • Responsible for conducting Production floor GEMBA walks.
  • Compliance to all Environmental, Health and Safety regulations.
  • Compliance to all company policies, procedures, and…
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