• Production Operator

    West Pharmaceutical Services (Williamsport, PA)


    Production Operator

    Requisition ID:

    71780

    Date:

    Dec 2, 2025

    Location:

    Williamsport, Pennsylvania, US

    Department:

    Operations

    Description:

    Job Summary

    In this role, you will be responsible for the production of components that meet or exceed pre-determined specifications. Responsible for inspection, packaging, labelling and completion of documentation necessary to provide quality, production and traceability records in accordance with Quality Systems ISO 9001/ ISO 13485.

    Essential Duties and Responsibilities

    + Ensures the quality of the parts produced by inspecting parts visually, ensures relevant documentation is recorded and signed off in real time.

    + Maintaining accuracy of batch documentation at all times and ensuring that it is filled in and right first time.

    + Completing measurements as required by the work instructions, reviewing measurement results and alerting appropriate personnel of any deviations from the customer specification or part print.

    + Packages the parts according to customer specification and indicates the status of the part (accept/reject) according to proper procedure and specifications.

    + Places finished product in correct location.

    + Understands and safely operates all equipment.

    + Reports and/or corrects unsafe working conditions.

    + Performs secondary operations as necessary to meet customer specifications.

    + Performs general cleaning of machines and ancillary equipment.

    + Verifies the labels for correct part and lot numbers.

    + Maintains proper level of packaging supplies at each machine.

    + Maintains work areas in a clean and orderly manner by practicing good housekeeping.

    + Define machine status on OEE System in order to determine machine downtime and run time.

    + Compliance to all site Environmental, Health and Safety requirements, training and regulations.

    + Compliance to all local site company policies, procedures and corporate policies.

    + Support and contribute to Lean Sigma programs and activities towards delivery of the set target.

    + Act in accordance with the company’s guiding principles and adherence to the corporate Code of Conduct.

    + Performs additional duties at the request of the direct supervisor.

    + Maintains methods/procedures and all supporting documentation to meet the requirements of Quality Systems ISO 13485:2016.

    + Other duties as assigned.

    Additional Responsibilities

    Education

    + High School Diploma or GED preferred

    Work Experience

    + Previous production work experience would be an advantage.

    + Knowledge of Good Manufacturing Practices (GMP) requirements would be an advantage.

    Preferred Knowledge, Skills and Abilities

    + Must have good verbal reasoning, numerate ability and mechanical aptitude skills.

    + Must have good communication skills, both written and oral.

    + Must have good organizational skills.

    + Must be able to work in a team environment.

    + Basic knowledge and understanding of a computer.

    + Must be willing to work in a controlled environment, which involves the wearing of a gown, cap and relevant personal protective equipment.

     

    License and Certifications

    Travel Requirements

    5%: Up to 13 business days per year

    Physical Requirements

    Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.

    Additional Requirements