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West Pharma Quality Assurance Technician 
United States, Pennsylvania, Williamsport 
264325663

Yesterday

Training for this position will be Monday - Friday Day shift. In Fourth Quarter of 2025, or First Quarter 2026 this position will change to a 2-2-3-2 12 hour night shift schedule.

Schedule-12 hour night shift 5:45p-6am

In this role, you will perform a variety of tasks and conducts test procedures in regard to the quality process, ensuring that the pre-determined high standards of quality are achieved and maintained.

Essential Duties and Responsibilities
  • Review and approval of metrology reports, where appropriate, for batch release and validation purposes
  • New product validation, analysis and reporting.
  • Quality support to Engineering and Production Departments.
  • Establish and maintain documentation in line with West Williamsport and West Pharmaceutical Services Quality Systems.
  • Liaise with customers and suppliers on new and existing projects.
  • Receiving and inspection of incoming goods and materials.
  • Ensure that all parts/ materials, which require incoming inspection, conform to all requirements and applicable drawings and specifications.
  • Maintain good communications both internally and externally.
  • Ensures that all metrology equipment is correctly calibrated.
  • Assists shift personnel with quality issues and/or measurement techniques.
  • Assists in problem resolution with customers.
  • Perform periodic audits as requested and completes necessary documentation.
  • Archives quality records, samples and log procedures.
  • Makes periodic clean-out of records and samples exceeding minimum retention requirements as per West procedures.
  • Batch paperwork review and final decision to release product for shipment.
Additional Responsibilities
  • Provide a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
  • Maintain a clean, orderly, and safe workstation and environment at all times.
  • Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
  • Exhibit regular, reliable, and punctual attendance.
  • Perform other duties as assigned based on business needs.
  • Keep current with new GMP compliance guidance and internal QA procedures
  • Support new GMP compliance guidance and Data Integrity initiatives
Education
  • High School Diploma or GED Required.
  • Preferred Associates degree in Metrology or QA; or 3 years’ on the job experience in a plastics manufacturing environment
Work Experience
  • 3 years of job-related experience; in QA/QC and the use of measuring equipment.
Preferred Knowledge, Skills and Abilities
  • Able to be aware of all relevant standard operating procedures as per Company policy
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target
  • 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
  • Meet individual and departmental goals as required
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
  • Ability to learn, understand, and remember normal tasks.
  • Ability to hear, speak, and understand conversation in English in a normal tone of voice.
  • Must maintain the ability to work well with others in a variety of situations.
  • 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