Pharma Wisdom Jobs
18:42:00
1
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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