
Quality Technician
1 day ago
Select how often (in days) to receive an alert:
Title: Quality Technician - Shift Role (FTC)
Requisition ID: 68306
Date: Apr 17, 2025
Location:
Dublin, Leinster, IE
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
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.
Retain sample of finished products and maintain all applicable documents to form batch records and ensure appropriate batch records disposition (i.e. filing, scanning etc.) as necessary.
Print documents from Master Control, shopfloor or other software program and manage 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.
Promote and support a Lean environment.
Conform with and abide by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
Exhibit regular, reliable, punctual and predictable attendance.
Other duties as assigned.
Education
High School Diploma preferred.
Work Experience
1 to 3 years manufacturing experience required.
Preferred Knowledge, Skills and Abilities
Must possess 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 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 order to apply to West, please send an email to ****** .
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 and/or a pre-employment drug screening.
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