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Section Lead

10-15 years
Not Disclosed
10 April 16, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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: Section Lead
Location: Ahmedabad, Gujarat, India
Job Category: Manufacturing
Date Posted: 04/10/2025


Company Overview:

At Baxter, we are dedicated to saving and sustaining lives. For over 85 years, our products and therapies have positively impacted patients worldwide, found in hospitals, clinics, and homes. Joining Baxter means contributing to meaningful work that improves healthcare outcomes for millions of people.

Together, we create a supportive environment where success and inspiration thrive. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.


Key Selection Criteria (Education & Experience):

  • Educational Qualification:
    Bachelor's or Master’s in Pharmacy or equivalent.

  • Experience Range:
    10-15 years of experience in manufacturing, preferably in a similar role.


Key Responsibilities & Authorities:

  • Safety & Compliance:

    • Ensure adherence to Baxter’s safety policies and guidelines.

    • Ensure employees raise safety hazards and wear appropriate PPE during operations and maintenance.

  • Production & cGMP Adherence:

    • Ensure staff behavior in clean rooms and production areas aligns with Current Good Manufacturing Practices (cGMP) norms.

  • Supply & Equipment Management:

    • Oversee supply of raw materials, components, and equipment for production, ensuring equipment is operational.

  • Performance Improvement:

    • Maintain and enhance departmental performance to meet regulatory, customer, and internal quality standards.

  • Continuous Improvement:

    • Participate in and drive continuous improvement initiatives within the manufacturing facility.

  • Production Supervision:

    • Supervise daily production output and ensure adherence to quality parameters.

    • Contribute to monthly production planning and manage production output within acceptable yield criteria.

  • Maintenance Coordination:

    • Work with the Engineering department on plant-related breakdowns and preventive maintenance.

  • Training & Development:

    • Identify team training needs and ensure skill upgrades and awareness on cGMP norms.

  • Discrepancy Investigation:

    • Lead investigations into discrepancies, errors, complaints, and failures, ensuring actions are documented and corrective measures are taken.

  • Breakdown Analysis:

    • Perform breakdown analysis and develop action plans to minimize downtime, in consultation with the Engineering Manager.

  • Shift Communication:

    • Communicate production issues to shift personnel and ensure resolutions are tracked.

  • Packing Oversight:

    • Ensure packing activities comply with SOPs and Batch Packing Records, ensuring timely packing of goods.