Teva Pharmaceuticals -Interview for B.Pharm / M.Pharm / Pharm.D / BDS Candidates on 22nd Aug’ 2024 

Teva Pharmaceuticals -Interview for B.Pharm / M.Pharm / Pharm.D / BDS Candidates on 22nd Aug’ 2024 

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Teva Pharmaceuticals is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.

Walk-in Drive for Pharmacovigilance Team @ Teva Pharmaceuticals

  • Experience: 2-6 Years
  • Qualification: B.Pharm / M.Pharm / Pharm.D/BDS
  • Job Location: Bengaluru

Pharmacovigilance Associate |- Literature Review

  1. Relevant experience in Pharmacovigilance including Literature review process in ICSR.
  2. Experience in Patient Safety/ solid knowledge in Pharmacovigilance concepts, regulations & procedures.
  3. Knowledge of database: Embase, Medline, Pubmed, Ovid, etc.
  4. Support PV teams like case processing, training teams, Quality assurance, audits & Inspection etc..

Pharmacovigilance Associate I&II – Patient Safety Operations

  1. Perform the case processing and related activities in alignment with patient Safety Operations.
  2. Extensive knowledge of Medical Terminology, clinical pharmacology, patient treatment, diagnostic investigations & pathology.
  3. Exp in medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in safety database.
  • Day & Date: Thursday, August 22nd 2024
  • Time: 10:00AM-04:00 PM
  • Venue: Teva Pharmaceuticals, Brigade Senate 1, Hebbal Kempapura, Bengaluru – 24

Request to share the relevant profiles by Wednesday, 21st Aug EOD to ankita.sonawane@teva.co.in

Job Category: pharma
Job Type: Full Time
Job Location: Bengaluru

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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