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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