Pharmaceutical Process Operator

Piramal Enterprises Ltd
  • Hicksville, NY
    16 days ago

    Job 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

    Pharmaceutical Process Operator

    Job Description

    Job Summary:

    Piramal Pharma Solutions - Morpeth is seeking a dedicated Pharmaceutical Process Operator to execute and monitor manufacturing processes for pharmaceutical products, ensuring adherence to quality standards and safety protocols.

    Job Responsibilities:

    • Operate, monitor, and troubleshoot production equipment according to Standard Operating Procedures (SOPs) and batch records.
    • Perform in-process checks and document all manufacturing activities accurately and thoroughly.
    • Clean and sanitize production equipment and facilities in compliance with Good Manufacturing Practices (GMP).
    • Identify and report equipment malfunctions, deviations, and quality issues to supervisors.
    • Follow all safety regulations and participate in safety training programs.
    • Collaborate with team members to optimize production efficiency and quality.
    • Maintain a clean and organized work environment.

    Job Qualifications:

    • Some experience in a pharmaceutical manufacturing environment, or a related regulated industry is preferable but not required.
    • Familiarity with GMP and other regulatory guidelines.
    • Ability to read and interpret technical documents, including SOPs and batch records.
    • Strong attention to detail and accuracy in documentation.
    • Basic mathematical skills for calculations and measurements.
    • Excellent communication and teamwork skills.
    • Proficiency in basic computer applications.

    Good Manufacturing Practices (GMP), Standard Operating Procedure (SOP)

    Numbers & Facts

    LocationHicksville, NY

    Skills

    • Antibodiesunmatched
    • Application Programming Interface (API)unmatched
    • Biotech and Pharmaceuticalunmatched
    • Check Processingunmatched
    • Clinical Trialunmatched
    • Communication Skillsunmatched
    • Computer Skillsunmatched
    • Contract Manufacturingunmatched
    • Detail Orientedunmatched
    • Documentationunmatched
    • Dosage Formsunmatched
    • Drug Developmentunmatched
    • Drug Discoveryunmatched
    • Drug Manufacturingunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • Identify Issuesunmatched
    • Maintain Complianceunmatched
    • Manufacturingunmatched
    • Manufacturing/Industrial Processesunmatched
    • Mathematicsunmatched
    • Medical Productsunmatched
    • Network Integrationunmatched
    • Organizational Skillsunmatched
    • Production Controlunmatched
    • Quality Managementunmatched
    • Quality Metricsunmatched
    • Regulationsunmatched
    • Safety Trainingunmatched
    • Safety/Work Safetyunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Team Playerunmatched
    • Technical Writingunmatched
    • Training Programunmatched

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