Zydus – interview for (USP/DSP/QMS) Production department for on 09th June 2024, Sunday

Zydus – interview for (USP/DSP/QMS) Production department for on 09th June 2024, Sunday

Zydus - interview

Inviting candidates for a walk-in interview for (USP/DSP/QMS) Production department for Zydus Biologics (Zydus Biotech Park) on 09th June 2024, Sunday from 9:00 am to 4:00pm

(The interviews will take place at Navi Mumbai)

WALK-IN INTERVIEW AT NAVI MUMBAI

We are hiring for Zydus Biologics

Drug Substance Production: Executive / Senior Executive / Assistant Manager

USP Production

  • SS bioreactors
  • CIP, FIT, PHT & SIP
  • Media / feed preparation
  • Centrifuge operation
  • Manufacturing monoclonal antibodies & bio- therapeutic proteins.

DSP Production

  • Recombinant product purification
  • TFF
  • Chromatography
  • Virus filtration
  • CIP & SIP
  • Buffer preparation activities

QMS Production

  • Risk assessment
  • Root cause analysis for deviations,
  • OOT. OOS & QMS document via Trackwise
  • Reducing human errors
  • Reviewing cGMP & equipment qualifications

Job location: Ahmedabad, Gujarat

Experience: 2-10 Years

Educational Qualification: M.Sc./B. Tech / B.E/ M. Tech (Biotechnology)

Date: 9th June, 2024 (Sunday)

Time: 9 am to 4 pm

Venue: Zydus Takeda Healthcare Pvt. Ltd.
C 4. MIDC, Village Pawane, Thane Belapur Road Navi Mumbai 400703, Phone – 022 68375200.

Apply through link : https://zydusgroup.darwinbox.in/ms/candidate/careers/a659cde6b9d29c/custom_source/Walk%20In%20at%20Navi%20Mumbai%20for%20production%20dept

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

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

Check Also

Automatic Ink Jet Sticker Label Overprinting Machine  

Operation, Cleaning, And Overprinting of Automatic Ink Jet Sticker Label Overprinting Machine  Objective: To lay …