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Operator Iii - Tapi

5+ years
Not Disclosed
10 June 4, 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

 

Operator III – TAPI

Date Posted: May 29, 2025
Location: Gwalior, India, 477117
Company: Teva Pharmaceuticals
Job ID: 61734


Who We Are

Teva Active Pharmaceutical Ingredients (TAPI) is the world’s top supplier of high-quality APIs with a portfolio of over 350 products. Serving 80% of the top 50 pharmaceutical companies globally, TAPI brings 80+ years of trusted manufacturing and scientific excellence to the generics industry. With more than 4,000 professionals across 14 global sites, we drive API innovation and exceptional customer service.


How You’ll Spend Your Day

  • Execute dispensing operations and follow all applicable SOPs

  • Record reaction parameters and observations in batch cards

  • Fill and maintain batch and cleaning documentation per compliance standards

  • Verify and ensure proper calibration of pH meters and balances

  • Adhere to cGMP, safety protocols, and plant SOPs

  • Maintain equipment hygiene and plant housekeeping standards

  • Report incidents and irregularities to shift officers

  • Carry out raw material charging, sampling, and unloading during batch processing

  • Operate ERP systems for production-related transactions

  • Collaborate with QA for ongoing GMP compliance

  • Support other production activities as instructed by supervisors


Your Experience and Qualifications

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

  • Experience: Minimum 5+ years in pharmaceutical manufacturing

  • Strong knowledge of GMP, documentation practices, and production protocols

  • Familiarity with regulated environment and ERP operations preferred