Bharat Parenterals – Walk-In-Interview for Production / Quality Assurance / Regulatory Affairs / F&D / PPIC / Store / Admin / Art Work / Civil / Export / Liaison Departments on 26th & 27th Aug’ 2023 

Bharat Parenterals – Walk-In-Interview for Production / Quality Assurance / Regulatory Affairs / F&D / PPIC / Store / Admin / Art Work / Civil / Export / Liaison Departments on 26th & 27th Aug’ 2023 

 

 

Bharat Parenterals Limited is conducting Walk In Interview for Multiple Positions in Production / Quality Assurance / Regulatory Affairs / F&D / PPIC / Store / Admin / Art Work / Civil / Export / Liaison  Departments on 26th & 27th Aug’ 2023 (Saturday & Sunday) at Vadodara.

JOB DESCRIPTION:

1) Department: Production / Quality Assurance / Regulatory Affairs / F&D / PPIC / Store / Admin / Art Work / Civil / Export / Liaison

  • Position: Executive/ Sr. Officer / Officer / Jr. Officer
  • Qualification: B.Sc / M.Sc / B.Pharm/ M Pharm / MBA / Any Graduation / ITI / Diploma
  • Experience: 01 – 10 yrs
  • No. of Vacancy: 31
  • Job Location: Vadodara
  • Date & Day: 26th & 27th Aug’ 2023 (Saturday & Sunday)
  • Time: 09:00 AM To 5:00PM
  • Venue: 144-A, Village; Haripura, Ta: Savli, Jarod Samlaya Road, Vadodara-Gujarat 391520
  • Email ID: neha.thakkar@bplindia.insaroj.tiwari@bplindia.in

Note: 

  • Only Male & Experience Candidates have to share their profile to specific mail id mentioning the specific job code in the subject line.
  • Candidate should be ready to come in shift if required.
  • Candidate must be ready to sign long term association agreement with incentive scheme for 02 or 03 years.
Job Category: pharma
Job Type: Full Time
Job Location: vadodara

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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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