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Central Islip

    Manufacturing Operator - Central Islip, United States - Unizon Technology LLC

    Unizon Technology LLC
    Unizon Technology LLC Central Islip, United States

    2 weeks ago

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    Description

    Job Description

    Job Description

    Job Summary

    This position is a Manufacturing Operator assigned to support Granulation, Blending, Compression, Coating, and Encapsulation. This is an hourly laborer and individual contributor role that will report to a Front-Line Supervisor. This position may be based at the Company's manufacturing units in Hauppauge or Central Islip, New York.

    There are two shifts available:

    1st Shift 07:00 am pm

    2nd Shift 03:00 pm - 11:30 pm

    Candidate must be working in a Pharma Manufacturing unit as a Manufacturing Operator supporting the below skills

    Granulation, Blending

    Compression

    Encapsulation

    Please confirm and mention what shift is preferred.

    Job Responsibilities:

    • Person must be able to know how to operate pharmaceutical production machinery independently.
    • Execute procedures for manufacturing processes in accordance with batch manufacturing record (BMR) and Standard Operating Procedures (SOP) requirements.
    • Perform machine changeovers, cleaning and set up as per SOPs. Ensure the proper area & equipment cleanliness and setup in stipulated time.
    • Prepare a room and equipment for line clearance, replace room filters, Ensure verification and calibration of balance/scale and check pressure differential for the rooms.
    • Ensure line clearance before initiating manufacturing activities in each area.
    • Receive/transfer material from/to dispensing/manufacturing storage and check dispensed materials/final mix blend/compressed tablets and labeling as per BMR.
    • Wear appropriate personal protective equipment (PPE) as stated in the SOP/BMR before initiating process.
    • Able to operate applicable equipment independently as per area of operation.
    • Troubleshoot and make appropriate adjustments to equipment to maintain product/BMR specifications.
    • Ensure adherence to quality standards during all stages of the manufacturing process.
    • Complete manufacturing documents on time, ensuring accuracy and completeness.
    • Responsible for training on all relevant SOPs and always maintain compliance with related SOPs and current Good Manufacturing Practices (cGMP) in the manufacturing process.
    • Perform duties through the proper, safe use of equipment, according to Health & Safety procedures and Equipment Manuals.
    • Flexible to work extended hours, to achieve manufacturing schedule when needed.
    • Should maintain discipline and comply with company policies and procedures.
    • Should perform entire duties as communicated time to time by department management/designee.

    Minimum Requirements:

    • Solid mechanical aptitude and troubleshooting skills.
    • Minimum of 2 years of experience working in industrial environments such as pharmaceutical manufacturing and related settings.
    • Must have excellent communication skills.
    • Must be able to clearly communicate in English (verbally and in writing).
    • Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors.
    • Must be able to work different shifts as per organizational requirement and should be flexible for working additional hours such as overtime and weekends.

    Physical Requirements

    • Should not have any restriction to work with powder containing active pharmaceutical ingredients.
    • This position requires the ability to do heavy lifting / bending frequently.
    • Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift to 35 pounds.
    • Must be able to move pallets/equipment weighing about 200 – 300 kgs using suitable moving equipment like pallet jacks.
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