Bliss GVS Pharma Ltd -Interview For Quality Assurance / Production on 21 Jan 2024

Bliss GVS Pharma Ltd -Interview For Quality Assurance / Production on 21 Jan 2024

Bliss GVS Pharma Ltd., a renowned pioneer in suppositories and pessaries, stands as a global leader in healthcare innovation. Expanding its horizons, the company is now at the forefront of revolutionizing oral solids, dry powders, semi-solids, suspensions, and syrups. Our cutting-edge facility in Palghar East (Vevoor) is a testament to our commitment to excellence. As we continue to push the boundaries of pharmaceutical advancements, we invite dynamic individuals to join our team and contribute to shaping the future of healthcare. Seize the opportunity to be part of our state-of-the-art facility and embark on a rewarding journey with a trailblazing industry leader.

  • Department: QA / Production
  • Position: Operator/Operator/Officer
  • Qualification: ITI/B.Sc./ D.Pharm/M.Sc./B.Pharm /M.Pharm
  • Experience: 2 to 6 Years
  • updated resume
  • 3 passport size photograph
  • last three months’ salary slip
  • latest increment letter copy
  • Date : 21 Jan 2024
  • Time: 9 AM to 6 PM
  • Venue: Hotel Woodlands, National Highway No.8, near Tejpal Motors, Balitha, Vapi, Gujarat 396191

Incase you are not able to attend the walk-in you can send your CV to hr1500@blissgvs.com
or call on 074988 57057

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

Apply for this position

Allowed Type(s): .rtf

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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