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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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