Title: Technician, Quality,QC, SriCity

Requisition ID: 69347

Date: Apr 25, 2025

Location:

IN

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

In this role you will be responsible for performing inspection of incoming materials/components, semi-finished goods and finished products as per procedure

Essential Duties and Responsibilities

Perform inspection of incoming materials/components, semi-finished goods and finished products as per procedure.
Maintenance of stock control samples and records.
Ensure all QC equipment’s and measuring tools used are calibrated.
Perform routine calibration of QC Equipment.
Responsible to operate in close co-ordination with production functions for testing and analysis.
Preparing and maintaining necessary QC SOI and upgrading same time to time
Ensure all QC related records are maintained as per GMP, GLP, GDP requirements.
Release acceptable finished goods product for further processing.
Perform review of inspection records to assure product conforms to specifications and proper documentation practices.
Maintain all applicable documents to form batch records
Perform approval of rework and sorted product
Print documents from Master Control
Manage documents related to the Quality System
Segregate nonconforming product
Handle quarantined product and raw materials
Generate rejection and deviation reports
Perform trace back investigation of nonconforming raw material and product.
Any other Duties assigned by supervisor.

Additional Responsibilities

Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude
Willingness to learn new and review new analytical techniques
Must be able to multi-task, work under time constraints, problem solve, and prioritize.
Read and interpret data, information and documents
Work under deadlines with constant interruptions

Education

Graduate in science/Engineering

Work Experience

Minimum 1-year experience in QC in any industry

Preferred Knowledge, Skills and Abilities

Quality: The job holder is aware of his/her special responsibility for quality and conducts his/her activities in accordance with the Company quality policy at all times. Ensure that all operations in your area of responsibilities are comply with GMP, GLP, GDP, ISO 9001 & ISO 15378 (as per current version) etc.

SOI: The job holder of all relevant SOPs as per Company as they are related to the position covered by this Job Description.

Safety: The job holder is aware of his/her special responsibility towards health and safety in accordance with the company’s safety policy at all times.

Lean: Support and contribute actively in Lean sigma programs and activities towards delivery of the set target

License and Certifications

Travel Requirements

10%: Up to 26 business days per year

Physical Requirements

Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.

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. 