Neuland Laboratories Limited - Walk-In Interviews on 11th Dec' 2020 - PHARMA WISDOM

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Tuesday, 8 December 2020

Neuland Laboratories Limited - Walk-In Interviews on 11th Dec' 2020


Walk-In interview's For CMS & API-Peptide @ Neuland R&D Centre


Roles and Responsibilities

  • 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.
  • Synthesis of new / existing molecules by employing different methods. Key Involvement in the process development scale-up by Optimization of reaction conditions / manufacturing process and validation.
  • Planning and execution of projects to ensure timely delivery.
  • Aware of in-house SOPs, scale-up records and implementation.
  • Route scouting, chemistry evaluation, process development, optimization and validation of new drugs and intermediates.
  • Route scouting and evaluation of the chemistry for ongoing research projects to produce effective solutions.
  • Monitoring the daily research activities, and give effective solutions.
  • Creating Safety awareness among the teams and implementing safe practices both in lab and plant scale. Ensuring EHS procedures are adhered to and to promote good practice.


Roles and Responsibilities

  • 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.
  • Planning and monitoring of daily lab experiments.
  • Evaluation of lab experiment results along with team.
  • Lead and guide team/s on day to day activities.
  • Reading and evaluation of patents and literature and support IP for preparing IP reports and AR&D for analytical method development.
  • Preparation of specification for RMs, intermediates and API.
  • To ensure the good laboratory practices in the lab.
  • Maintenance of documents like patents, literature, analytical reports.
  • Discussion with analytical chemists and DQA on analytical results and specifications.
  • Generation of complete data at lab scale to support DMF filing (like PDR, impurity profiling, stability).
  • Playing key role during the scale up at plant, coordination with manufacturing, T.T and quality.
  • Responsible for end to end synthesis of an API from lab scale to commercial Scale.
  • Reading and evaluation of Patents and Literature for Solid Phase Peptide Synthesis of Peptides.

Perform Manual Solid Phase Peptide Synthesis of Peptides on Medium scale, commercial scale (1 to 10 g , 100 g and 1kg final product) with minimal or no supervision.

Desired Candidate Profile

Candidate should have MSc organic Chemistry with 2-5 Years of relevant experience in Crams/ CRO and Peptides-API

Date & Time: 11th December , 9.30 AM - 2.00 PM


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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