Granules India Limited – Walk-In Interviews for ITI, Diploma Candidates in Production / Quality Control Departments on 4th Aug’ 2023

Granules India Limited – Walk-In Interviews for ITI, Diploma Candidates in Production / Quality Control Departments on 4th Aug’ 2023

Granules India Limited is conducting Walk-in Drive for Experienced B.Sc, M.Sc, B.Pharm, M.Pharm, ITI, Diploma candidates in Production / Quality Control department on 4th August’ 2023 at Gagillapur Unit, Hyderabad.

Department: Quality Control

Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm

Experience: 2-6 yrs

Should be willing to work in shifts.

Spot Offers will be given to selected candidates(subject to above mentioned photocopies submission)

Latest Resume

Current Increment Letter

All Educational Certificates

Aadhar & PAN CardContact no: 08418696400/08418696401

 

  • Department: Production
  • Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm, ITI, Diploma
  • Experience: 2-6 yrs
  • Should be willing to work in shifts.
  • Spot Offers will be given to selected candidates(subject to above mentioned photocopies submission)Mandatory Document Photocopies to carry:
    • Latest Resume
    • Current Increment Letter
    • All Educational Certificates
    • Aadhar & PAN Card
    Walk-In Date: 04 August, 2023
    Time: 10.00 AM – 04.00 PM
    Venue: Granules India Limited, Gagillapur Village, Dundigal-Gandimaisamma Mandal,
    Medchal-Malkhajgiri District – 500 043,
    Telangana, India
Job Category: pharma
Job Type: Full Time
Job Location: , Dundigal-Gandimaisamma Mandal

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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