Entry, Quality Control

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Manufacturing Jobs
1 month
United States
Florida
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ID: 859018
Published 1 month ago by West Pharmaceutical Services
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In Manufacturing Jobs category
Tampa, Florida, United States
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Full job description
Requisition ID: 70202
Date: Jun 18, 2025
Location: St Petersburg, Florida, US
Department: Quality
Description:
Shift Available: 2nd Shift Hours: 1:30PM - +:30PM EST, Monday - Friday
Compensation: Starting at $1+.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/+kg 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. Read more

Published on 2025/09/10. Modified on 2025/09/10.

Description

Full job description
Requisition ID: 70202
Date: Jun 18, 2025
Location: St Petersburg, Florida, US
Department: Quality
Description:
Shift Available: 2nd Shift Hours: 1:30PM - +:30PM EST, Monday - Friday
Compensation: Starting at $1+.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/+kg 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.
West Pharmaceutical Services
West Pharmaceutical Services
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