Tatva Chintan Pharma-Interview on 29th August 2024 

Tatva Chintan Pharma-Interview on 29th August 2024 

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Tatva Chintan Pharma Chem Limited is conducting a walk-in interview for multiple positions across our Ankleshwar and Dahej plants. We are seeking talented individuals with experience in chemical/API industries to join our dynamic team.

Position Openings:

  1. Plant Operator – Production (Ankleshwar/Dahej)
    • Qualifications: ITI-AOCP/Diploma in Chemical Engineering
    • Experience: 3 to 6 years in SSR/GLR/Distillation Column/Pilot plant operation in Chemical/API Industries
  2. Officer – Production (Ankleshwar/Dahej)
    • Qualifications: B.Sc/M.Sc in Chemistry/BE in Chemical Engineering
    • Experience: 3 to 5 years in handling Chemical/API Plant Operation
    • Skills: Knowledge of IMS, GMP, & Computer Proficiency
  3. Store Officer (Dahej)
    • Qualifications: Graduate
    • Experience: 3 to 5 years in Chemical/API industries handling RM, FG, Engineering & Packing
    • Preferred Skills: Knowledge of SAP & Diploma in Material Management
  4. Store Operator (Dahej)
    • Qualifications: ITI-AOCP
    • Experience: 3 to 6 years in Chemical/API industries handling RM, FG, Engineering & Packing
    • Skills: Knowledge of operation of stacker, tanker Loading/Unloading
  • Date: 29th August 2024 (Thursday)
  • Time: 10:00 AM to 4:00 PM
  • Venue: Tatva Chintan Pharma Chem Limited, Plot No. 502/17, Ramdev Chokdi, GIDC, Ankleshwar, Gujarat, India
Job Category: pharma
Job Type: Full Time
Job Location: Ankleshwar Gujarat

Apply for this position

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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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