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Oper I, Packing

0-2 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: Operator I, Packing
Location: Ahmedabad, Gujarat, India
Job Category: Manufacturing
Date Posted: 04/14/2025


Company Overview:

At Baxter, we are deeply committed to our mission of saving and sustaining lives. For over 85 years, our products and therapies have positively impacted patients worldwide, found in hospitals, clinics, and homes. By joining Baxter, you will be contributing to meaningful work that improves healthcare outcomes globally.

Together, we create a positive and inspiring environment where we help each other succeed. Join us and be a part of a mission that accelerates your purpose while improving lives.


Key Responsibilities & Authorities:

  • Safety:

    • Ensure a safe working environment in the VIT/Packing area, with no safety-related incidents.

    • Ensure all personnel wear appropriate PPE while operating or maintaining machines.

    • Report any safety concerns promptly to supervisors.

  • Quality:

    • Perform regular cleaning and lubrication of machines.

    • Ensure smooth operation of machines according to standards.

    • Ensure packing activities are performed as per Standard Operating Procedures (SOP) and Batch Packing Record (BPR).

    • Verify packing material status labels to avoid mix-ups.

    • Ensure packing activities begin only after receiving line clearance.

    • Handle packing rejections as per SOP and resolve any issues immediately.

    • Regularly engage with workers to ensure productivity and quality standards are met, reinforcing Good Manufacturing Practices (GMP).

    • Ensure no machine resumes operation after breakdown or maintenance without clearance from Quality Assurance (QA).

    • Provide training to personnel for critical operations, including visual inspection and labeling.

  • Supply:

    • Ensure timely machine startup and challenging tests.

    • Replace change parts and trial machines within required timelines.

    • Ensure the availability of properly labeled packaging material.

    • Prevent the destruction of good containers as rejection.

    • Maintain change parts in good condition, checking periodically.

    • Monitor and take action to maintain productivity according to defined norms.

  • People:

    • Attend monthly ACE (Achieving Continuous Excellence) checks with the respective department head.

    • Report maintenance needs or parts requirements to the technical department in advance.

    • Communicate any abnormalities related to packing materials, non-conformities, or delayed start-ups to the Department Head before initiating packing activities.