Home / Job / Neuland Laboratories Limited – Walk-In Interviews on 7th Jan’ 2021

Neuland Laboratories Limited – Walk-In Interviews on 7th Jan’ 2021

Neuland Laboratories Limited – Walk-In Interviews on 7th Jan’ 2021

Walk-In interview’s for API & CMS

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.

API:

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.

Date: 7th January, 2021

Time: 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

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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