Home / Job / Neuland Laboratories -Walk-In Interviews for CMS/ GDS/ AR&D & Process Engineering On 30th Oct’ 2020

Neuland Laboratories -Walk-In Interviews for CMS/ GDS/ AR&D & Process Engineering On 30th Oct’ 2020

Neuland Laboratories -Walk-In Interviews for CMS/ GDS/ AR&D & Process Engineering On 30th Oct’ 2020

Job Description

♦CMS:

Process development for new drugs & intermediates. Responsible for literature survey and its analysis to plan a non-infringing, scalable and economic route; patent analysis preferred.

♦GDS:

Responsible for day to day LAB activities.

Collection and evaluation of literature.

Design of ROS for target molecules.

Evaluation of costing and scalability of processes.

♦AR&D: 

Actively involving analytical method development and validation in corresponding tech like HPLC / GC / ICP-MS / other techs.

Preparation of technical report and submitted to reviewer for review and incorporate the comments provided by reviewer/ approver if any.

♦Process Engineering: 

Providing inputs/ suggestions, continuous discussion on the process for better understanding.

Understanding the effect of negative experiments on the process, lab validation experiments follow ups.

Consultation of team leader before changing any operation other than BMS during plant validation.

Post Name: CMS/ GDS/ AR&D & Process Engineering

Qualification: B.Tech/ B.E. in Chemical, MS/ M.Sc (Science) in Chemical

Experience: 0-3 years

Location: Hyderabad

Contact Details

Company: Neuland Laboratories Limited

Time And Venue Details:

 Walk-In On 30th October from 9:30 AM to 2:00 PM at Neuland Laboratories Limited R&D Centre, Survey No: 474, 347, 490/2, Veerabhadraswamy Temple Road,, Jinnaram,, Bonthapally Village, Telangana 502313, Contact – Gurrala Neha/ T. Krishna Rao ( 08458672651 )

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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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