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    Job · 18123013

    Lucent Biotech logo

    F&D Assistant Manager

    Lucent Biotech · Roorkee · onsite · Posted 35d ago

    Undisclosed6–10 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Department: Formulation & Development (F&D)
    Plant: OSD (Oral Solid Dosage)

    Key Responsibilities

    • Handle formulation development activities for OSD products including tablets and capsules.
    • Plan and execute formulation trials, optimization, and scale-up activities.
    • Develop and optimize formulations as per product requirements and regulatory guidelines.
    • Prepare and review BMR/BPR, trial protocols, reports, specifications, and other F&D documents.
    • Coordinate with Production, QA, QC, IPQA, Regulatory Affairs and other departments for product development and technology transfer.
    • Conduct and monitor trials at laboratory, pilot and manufacturing scale.
    • Support troubleshooting of formulation and manufacturing-related issues.
    • Evaluate raw materials and packaging materials for product development.
    • Participate in technology transfer and process validation activities.
    • Ensure proper documentation and compliance with GMP, GLP and applicable regulatory requirements.
    • Review stability data and support stability studies for developed products.
    • Guide and supervise F&D team members and ensure timely completion of assigned activities.

    Required Qualifications

    • B.Pharm M.Pharm in Pharmaceutics or related specialization.
    • 5 to 8 years of relevant experience in Pharmaceutical Formulation & Development, preferably in an OSD manufacturing plant.
    • Strong knowledge of tablets, capsules, granulation, compression and coating processes.
    • Good understanding of GMP, documentation and regulatory requirements.
    • Good analytical, problem-solving and coordination skills.

    Preferred Candidate

    Candidates having experience in OSD formulation development, scale-up, technology transfer and manufacturing plant trials will be preferred.

    Sourced from naukri

    Skills

    QAformulation development activitiesPharmaceutical Formulation & DevelopmentRegulatory AffairsGLPIPQABMR/BPRtrial protocolsGMPQC

    F&D Assistant Manager · waiting for your command