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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