Neuland Laboratories Ltd Interview For CDS/ CMS/ AR&D/ Peptides

Neuland Laboratories Ltd Interview For CDS/ CMS/ AR&D/ Peptides

 Exp. :- 04 – 05 year

Job Locations:- Hyderabad

Job description

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.

Time and Venue

18th 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 )