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3.0 - 7.0 years
0 Lacs
karnataka
On-site
As a Process Engineer at Shriyata Lifetech Private Limited, you will play a crucial role in designing and optimizing cutting-edge processes in the Pharmaceutical or Biopharmaceutical industry. Your responsibilities will involve: - Designing, developing, and optimizing processes for pharmaceutical and biopharmaceutical production. - Collaborating with R&D, manufacturing, and quality teams to ensure process efficiency and regulatory compliance. - Troubleshooting process-related challenges and implementing effective solutions. - Preparing and reviewing process documentation, SOPs, and technical reports. - Supporting scale-up activities and technology transfer from lab to commercial production. ...
Posted 1 month ago
0.0 - 4.0 years
0 Lacs
noida, uttar pradesh
On-site
As an ideal candidate for this position, you will be responsible for assisting in the development and testing of new plastic materials and formulations. This will involve conducting lab-scale trials and providing support for scale-up activities in production. Your role will also include supporting quality control by analyzing material properties such as tensile strength, melt flow index, and hardness. In addition, you will collaborate with cross-functional teams on product development and technical evaluations. Your contribution will be crucial in troubleshooting processing or material-related issues. It is essential to maintain accurate technical documentation and lab records to ensure the ...
Posted 1 month ago
2.0 - 6.0 years
0 Lacs
ahmedabad, gujarat
On-site
As a Formulation Development Scientist, you will be responsible for the following: - Conducting formulation development for oral solid dosage forms such as tablets and capsules. - Executing method development, method validation, and technology transfer activities. - Compiling and reviewing development protocols, reports, and other technical documents. - Coordinating with cross-functional teams (QA, QC, RA, Production) to ensure successful project execution. - Ensuring compliance with regulatory guidelines from ICH, WHO, USFDA, etc. - Maintaining accurate records and documentation as per cGMP requirements. Key Skills Required: - Sound knowledge of pre-formulation and formulation techniques. -...
Posted 2 months ago
3.0 - 7.0 years
0 Lacs
rudrapur, uttarakhand
On-site
As a Research Associate at Naari Pharma, you will play a crucial role in the execution of formulation development activities for solid dosage forms across regulated and semi-regulated markets. Your responsibilities will include conducting literature search and pre-formulation studies, evaluating innovator/RLD products, executing R&D trial batches and scale-up activities, and preparing stability batches. You will also be responsible for documentation tasks such as preparing Master Formula Cards, Product Development Reports, and Stability Protocols, as well as supporting regulatory submissions. You will work closely with cross-functional teams to monitor scale-up and exhibit batches, troublesh...
Posted 3 months ago
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