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    Glenmark Careers Hiring Now: Officer- Solid Dosage Role for B.Pharm, M.Pharm Graduates

    Glenmark Pharmaceuticals hiring Jr Officer Role | B Pharm & M Pharm Graduates Eligible

    Looking for a Pharma Job with one of India’s leading pharmaceutical companies? Glenmark Careers brings an excellent opportunity for professionals seeking growth in pharmaceutical manufacturing. Glenmark Pharmaceuticals is hiring for multiple positions at its USFDA-approved manufacturing plant in Indore. Candidates with B.Pharm, M.Pharm, Diploma, or ITI qualifications and 1–7 years of experience can apply for Junior Officer, Officer, and Senior Officer roles across Solid Dosage, Semi Solid Dosage, Engineering, and Warehouse departments.

    • Position: Officer, Jr Officer, Sr Officer
    • Location: Indore

    About the Company

    Glenmark Pharmaceuticals is one of India’s leading global pharmaceutical companies, recognized for its high-quality formulations, APIs, and innovative healthcare solutions. Through Glenmark Careers, the company offers excellent opportunities for professionals looking to build a successful Pharma Job in a USFDA-approved manufacturing environment.

    Job Description

    Glenmark Pharmaceuticals is hiring for its USFDA-approved manufacturing plant in Indore, Madhya Pradesh. The company has announced multiple Pharma Job openings across Solid Dosage, Semi-Solid Dosage, Engineering, and Warehouse functions. This is an excellent opportunity to build a career with a leading pharmaceutical company operating a world-class USFDA-approved manufacturing facility.

    Key Responsibilities

    • Perform manufacturing and operational activities in the assigned department.
    • Execute production processes in Solid Dosage or Semi-Solid Dosage manufacturing as applicable.
    • Support engineering activities to ensure smooth operation and maintenance of manufacturing equipment.
    • Handle warehouse operations, including material receipt, storage, dispensing, and dispatch as per company procedures.
    • Follow Good Manufacturing Practices (GMP) and comply with USFDA quality standards.
    • Maintain accurate documentation and records as per regulatory requirements.
    • Coordinate with cross-functional teams to achieve daily production targets.
    • Ensure adherence to safety, quality, and compliance guidelines at all times.
    • Contribute to continuous improvement initiatives to enhance operational efficiency.
    • Perform responsibilities assigned by the reporting manager in accordance with departmental requirements.

    Qualifications

    • B.Pharm / M.Pharm
    • Experience:1 to 7 years

    Contact Information

    CLICK HERE FOR ORIGINAL NOTIFICATION

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