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West Pharma Technician Quality QC SriCity 
India 
639262642

04.05.2025
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

Graduate in science/Engineering

Work Experience

inimum 1-year experience in QC in any industry

Preferred Knowledge, Skills and Abilities

Ensure that all operations in your area of responsibilities are comply with GMP, GLP, GDP, ISO 9001 & ISO 15378 (as per current version) etc.

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

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

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.