Neuland Laboratories Limited - Walk-In Interviews on 7th Jan' 2021 - PHARMA WISDOM

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Tuesday, 5 January 2021

Neuland Laboratories Limited - Walk-In Interviews on 7th Jan' 2021

 

Walk-In interview's for API & CMS

Roles and Responsibilities

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.
  • 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.

API:

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 GDS.
  • 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 GDS from lab scale to commercial Scale.

Date: 7th January, 2021

Time: 9.30 AM - 2.00 PM

Venue:

Neuland Laboratories Limited

R&D Centre, Survey No: 474, 347, 490/2,

 Veerabhadraswamy Temple Road,, Jinnaram,,

Bonthapally Village, Telangana 502313


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