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Operator Iii - Tapi

3-5 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Remote 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: Operator III - TAPI
Date: Jan 30, 2025
Location: Gwalior, India, 477117
Company: Teva Pharmaceuticals
Job Id: 60293

Company Overview

TAPI is the leading global supplier of Active Pharmaceutical Ingredients (APIs) with the broadest portfolio in the industry, including over 350 API products. We support 80% of the top 50 global pharmaceutical companies and have been a trusted name in the generic API industry for over 80 years. TAPI’s global presence spans 14 sites, with state-of-the-art production facilities across India, Israel, Mexico, and Europe. Our significant investment in R&D ensures a steady pipeline of products, allowing us to introduce new APIs efficiently.


Job Responsibilities

  • Batch Processing & Production Activities:

    • Carry out dispensing activities following applicable procedures.
    • Record observation of reaction parameters on the batch card as per approved procedures.
    • Fill all batch cards (production cleaning) according to approved instructions.
    • Carry out batch processing including raw material charging, unloading of material, and sampling activities during intermediate production.
  • Equipment and Compliance:

    • Ensure verification of pH meters and weigh balances according to applicable procedures.
    • Maintain work procedures, safety precautions, and comply with cGMP standards.
    • Keep the plant and equipment clean and updated.
  • Documentation and Reporting:

    • Prepare production batch cards, protocols, and other related production documents.
    • Report accidents and irregularities at the work station to the Shift Officer.
    • Ensure ERP operations related to production activities are executed accurately.
  • Coordination & GMP Compliance:

    • Coordinate with QA to ensure online compliance with GMP at the shop floor.
    • Carry out all other production-related activities as advised by the superiors.

Qualifications

  • Education:

    • B.Sc./M.Sc. in Chemistry or a Diploma in Chemical Engineering.
  • Experience:

    • 3-5 years of relevant experience in pharmaceutical or chemical production environments.

If you're a proactive individual with experience in pharmaceutical production and a passion for ensuring quality and compliance, this role offers a great opportunity for you to contribute to a leading company in the API sector.