Walk-In interview's for CMS, GDS, AR&D and Process Engineering
Company: Neuland Laboratories Limited
Experience: 0-3 yrs
Qualification: M.Sc Chemistry / B.E or B.Tech Chemical
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.
Process Engineering:
- Providing inputs / suggestions, continuous discussion on the process for better understanding.
- Understanding the effect of negative experiments on the process, lab validation experiments follow ups
- Consultation of team leader before changing any operation other than BMS during plant validation.
- Informing immediately to team leader in case of any issues during lab / plant validation
- Daily scale-up discussion / updates to team leader
- Preparation of all Technical documents including lab validation data, PED and technical reports during lab validation.
- Selecting the suitable equipments for scale up based on the process requirement.
- Preparation of scale up supporting documents like Equipment comparison data, SAP documents for scale up.
- Keeping track of all the activities in all the shifts during lab and plant validation.
- Handling of all PE lab equipment’s
- Preparation of request for proposal.
Date: 30 October, 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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