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    Supervisor, Production - Encapsulation

    Teva Pharmaceuticals
    4-7 years
    Not Disclosed
    Goa India
    10 Feb. 12, 2025
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Title: Supervisor, Production - Encapsulation

    Location: Goa, India, 403722
    Company: Teva Pharmaceuticals
    Job ID: 60659
    Date Posted: February 7, 2025

    WHO WE ARE

    At Teva Pharmaceuticals, we are committed to making good health more affordable and accessible, helping millions of people around the world enjoy healthier lives. As the world’s leading manufacturer of generic medicines, we are proud to produce many products on the World Health Organization’s Essential Medicines List. Today, over 200 million people globally rely on our medicines every day. Join us to be a part of a mission-driven company, making a difference across nearly 60 countries.

    KEY RESPONSIBILITIES

    As a Supervisor, Production - Encapsulation at Teva, you will be responsible for overseeing the Encapsulation area within the Production Department. Your key responsibilities include:

    • Supervision and Upkeep of Encapsulation Area: Supervise and maintain the encapsulation section in the production area to ensure smooth operations.
    • SOP & Documentation Review: Prepare, review, and ensure compliance with Standard Operating Procedures (SOPs) and other manufacturing documentation.
    • SAP R/3 System Management: Handle manufacturing-related transactions in the SAP R/3 system.
    • Investigation of Deviations: Prepare and review investigations related to deviations, Out-of-Specifications (OOS), Out-of-Trend (OOT), market complaints, and exception reports.
    • Quality Management System: Initiate, review, and assess the impact of Quality Management Systems during investigations, such as Change Controls, CAPAs, and Risk Assessments.
    • Equipment Qualification: Sign documents related to equipment qualifications as a business owner.
    • Calibration and Maintenance: Review and ensure compliance, calibration, and preventive maintenance of encapsulation machines in the production area.
    • Glorya EDMS Activities: Perform tasks related to the Glorya EDMS system.
    • Batch Manufacturing: Perform and review batch manufacturing activities according to Batch Manufacturing Record (BMR) instructions.
    • Production Planning and Execution: Handle daily production planning and execution in alignment with the production schedule.
    • Coordination with Cross-functional Teams: Collaborate with other departments for smooth execution of production processes.
    • Material Storage Management: Manage material storage areas to ensure proper handling and compliance.
    • Compliance with cGMP: Ensure adherence to current Good Manufacturing Practices (cGMP) in all production activities.
    • Training & Development: Train and develop staff, ensuring they meet identified training needs for effective execution.
    • Safety & Work Culture: Promote a disciplined work culture and enforce safety precautions within the production area.
    • Inspection Readiness: Manage and ensure the readiness for regulatory inspections and ensure compliance during internal and external audits.
    • Continuous Improvement: Identify and implement improvement projects on the shop floor and adopt best practices in production processes.
    • Data Integrity Compliance: Ensure compliance with data integrity standards as per laid down procedures.

    QUALIFICATIONS & EXPERIENCE

    • Education:
      • B.Pharm / M.Pharm
    • Experience:
      • 4-7 years of experience specifically in the encapsulation process within pharmaceutical production.

    WORKING AT TEVA

    Teva Pharmaceuticals is committed to fostering an inclusive and diverse workplace and ensuring equal employment opportunities for all individuals. We adhere to a global policy that supports employment decisions made without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity, ancestry, veteran status, national or ethnic origin, or any other legally recognized status protected by law. We also provide reasonable accommodations during the recruitment process as needed.

    How to Apply:
    If you're ready to take the next step in your career and be part of a mission-driven company, apply today for the Supervisor, Production - Encapsulation position in Goa, India.

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    Warsaw |

    Remote :

    Remote - Africa | Remote | Bishop | Remote - South America (Latin Americal) | French | Switzerland | Melbourne | Nairobi | Hammond | Blue Bell | Minnesota | Faridabad | Remote, USA | Remote - Middle East | Zaragoza | Slovakia | Bountiful | Tulsa | Ireland | Riga | Leinster | Springville | Belgium | Thailand | Manipal | McFarland | Green Way | Hungary | Lousiana | Xzagreb | Victoria | Lenexa | Castlebar | Medan | Texas | Remote - Europe |

    Bucharest :

    Bucharest |

    Makkah :

    Jeddah | Rabigh | Riyadh | Khulais | Najran | King Abdullah Economic City |

    Nišava District :

    Niš |

    Singapore :

    Singapore |

    South Africa :

    Midrand | South Africa |

    Brazil :

    Sao paulo | Brazil |

    South America :

    Peru | Argentina |

    Catalonia :

    Barcelona |

    Madrid :

    Madrid |

    Sweden :

    Sweden |

    Taipei :

    Taipei |

    Williamson :

    Brentwood |

    Republic of Thailand :

    Bangkok |

    Kyiv Oblast :

    Kyiv |

    Dubai :

    Dubai |

    Hà Nội :

    Hà Nội | Hanoi |

    Ho Chi Minh :

    Ho Chi Minh City |