Operator II- Granulation

Piramal Pharma

  • Sellersville, Pennsylvania
  • 30+ days ago

    Highlights

    This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle.

    Numbers & Facts

    LocationSellersville, Pennsylvania
    Websitepiramalpharmasolutions.com

    Description

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    Division

    Piramal Pharma Solutions

    Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.  

    This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  

    Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

    For more details, please visit : www.piramalpharmasolutions.com

    Job Title

    Operator II- Granulation

    Job Description

    The Manufacturing Operator II – Granulation is responsible for operating, cleaning, disassembling, and reassembling granulation equipment in accordance with applicable cGMPs and SOPs. Equipment may include low and high shear mixers, mills, and fluid bed dryers. In this role, the incumbent may rotate to other Manufacturing or Packaging departments based on business needs.

    Essential Duties & Responsibilities:

    • Operate, set up, disassemble, clean, and reassemble granulation equipment.
    • Ensure equipment and work areas are cleaned between batches to prevent cross-contamination and maintain GMP compliance.
    •  Monitor process parameters to ensure consistency and product quality - Perform visual inspections to identify defects or irregularities.
    • Read, review, and train on SOPs using internal systems.
    •  Complete documentation and support production metrics as required.
    • Build effective working relationships across teams.
    • Work independently or collaboratively in a team environment.
    • Follow all Safety, Health, and Environmental policies and procedures.
    • Perform other duties as assigned based on business needs.

    Experience & Qualifications:

    • High school diploma or GED required.
    • Equivalent education, training, or experience will be considered.
    • 3–5 years of experience in a pharmaceutical, chemical, biochemical, or food manufacturing environment preferred.
    • Experience working in a cGMP-regulated environment.

    Physical Requirements:

    • Ability to lift up to 40 lbs. and occasionally move drums weighing up to 300 lbs.
    • Ability to work safely with heavy equipment.
    •  Regularly stand, walk, sit, and use hands to handle equipment and tools.
    • Good vision, hearing, and communication abilities required.
    •  May be required to wear Personal Protective Equipment (PPE).
    • Must not be allergic to chemicals or bio substances found in production environments.

    Shift Details:

    • 3rd Shift: 11:00 PM – 9:00 AM - Schedule: Monday – Thursday (4 x 10-hour shifts)

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