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.
Date & Time: 18th December , 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
Contact - Gurrala Neha/ T. Krishna Rao ( 08458672651 )
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