Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Operator Iii - Tapi

Teva Pharmaceuticals
Teva Pharmaceuticals
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.