Mankind’s state of the art R&D Center is located in Manesar and administered by more than 350 leading scientists from diverse fields, with a prime focus on promoting innovation, knowledge and leading-edge skills. The development capabilities include New Drug Discovery and Research (NDD) Active Pharmaceutical Ingredients (APIs) Formulations and Development (F&D) Analytical Research and Development (ARD) Clinical Research & Biopharmaceutics Regulatory Affairs & Biotechnology and Intellectual Property Management.
Mankind Pharma Recruiting For Following:
- Qualification: M.Pharm
- Experience : 08-12+years
- Department: R&D Form Dev – Injectable / Parental
- Role: Research Associate
- Job Location: Gurgaon/Gurugram( Manesar ), Manesar
Related Jobs: MSN Laboratories – Walk-Ins for B.Sc, M.Sc, B.Pharm, B.Tech, B.Com, ITI, Diploma Candidates in Production / QC / Warehouse / TSD on 15th July’ 2023
Job Description:
- Supervise the lab experiments/compatibility/QbD studies activities, to provide the technical inputs to finalize the formulation and manufacturing process. To evaluate the Q1/Q2/Q3 assessment.
- To do literature review regarding the developmental products, key information of the RLD, SBOA information search, review of patent landscape about the projects.
- To review the lab notebooks online, maintain the lab do the document lab scale activities in Lab, note book and maintain relevant documentation online.
- To compile and review lab scale batches stability data for insight for the development activity.
- To coordinate with cross functional team including analytical, packaging, regulatory, intellectual property departments and productions departments.
- To involve in the filter validation and external lab studies like D-value study, to send the samples, review the protocols and reports. API & Excipients vendor’s finalization, Container and closures finalization.
- To involve SAP, QMS, technology transfer related activities.
- To involve trial, scale-up and submission batch executions in production site.
- To prepare product specifications as per ICH/USP monographs/regulatory guidance documents. Preparation of justifications for specifications.
- To prepare product trial batch documents, risk assessment reports, sampling plan and technology transfer documents, stability protocols and product development report for submission.
- Compilation of the stability and development studies data, presentation and scientific discussion of the data with seniors and management, planning of new trials based on the outcome of compiled data.
- Response to the regulatory regarding the query raised for the formulation and process with sound scientific justification.
- To intimation of shortage raw materials, lab wares, spare parts of lab equipment’s etc.
- Excellent written and verbal communication and presentation skills
- Excellent people skills
Required Qualification and Industrial Experience : M Pharmacy from reputed university
You can also mail your CVs to careers.rnd@mankindpharma.com
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