Neuland Laboratories Limited - Walk-In Interview's for CMS / GDS / AR&D / Peptides on 18th Dec' 2020

Walk-In Interview's for CMS / GDS / AR&D and Peptides @ Neuland Laboratories Limited

Experience: 4-5 yrs

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.

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.
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.

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.
Review the instrument calibration report and take necessary action suggested by HOD.
Interacting with CRD about the daily activities and DQA for any documentation activities.
Provide technical support to juniors as on required.
Providing COA for complete analysis in different techniques like HPLC /GC / Other Techs.

Peptides:

Literature search and collection of MSDS.
Discuss work plan with group leader and assign work to the team member.
Work plan needs discuss with AR&D and other CFT Members to complete the tasks.
Review outcome of experiments with group leader.
Documentation of lab experiments, experimental results and interpretation of spectral data.
Support to manufacturing team during execution of Projects.
Maintenance of documents like patents, literature, analytical reports.
Discussion with analytical chemists and DQA on analytical results and methods.
To account for chemical usage and availability of raw materials
Ensure maintenance of good laboratory practices.
Preparation of documents like feasibility optimization & Process development reports.
Ensure lab safety.
Preparation of customer report & Reviewed with group leader.