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.