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5.0 - 9.0 years
0 Lacs
vadodara, gujarat
On-site
As a candidate for this role, you should have hands-on work experience in mammalian cell culture, microbial cell culture, and molecular biology. Your experience should include working with therapeutic protein expression and purification using E.coli or yeast expression systems. You should be well-versed in molecular biology techniques such as molecular cloning, primer designing, expression vector generation, characterization, and related molecular biology techniques. Your responsibilities will include: - Experience in generating CHO-based stable monoclonal cell lines for mAb/therapeutic protein production - Proficiency in single cell cloning, fed-batch study, cell bank preparation (RCB, MCB,...
Posted 1 month ago
5.0 - 9.0 years
0 Lacs
dehradun, uttarakhand
On-site
The role at Tata Communications involves managing day-to-day network operations and maintenance in the area of Satellite communications. You will be responsible for handling GCE and RF equipment, including HPA, ACU, LNA, LNB, MODEMS, and UP CONVERTERS. You should be well-versed in satellite-related terms and proficient in customer handling, platform uptime, incident management, problem management, and escalation support. This operational role requires delivering impactful results that directly affect daily operations, including guiding professional or technical staff and ensuring the quality of their work. Your responsibilities will include creating and maintaining the infrastructure essenti...
Posted 3 months ago
2.0 - 4.0 years
0 - 1 Lacs
Hyderabad
Work from Office
We are seeking a dynamic and detail-oriented Analytical Documentation professional with 2-4 Years of experience to join our growing team. This role is critical to ensuring quality and compliance during the pharmaceutical product development lifecycle. Key Responsibilities 1. To Follow the Departmental SOPs. 2. Preparation of Raw materials, In-process and Finished product specifications and standard test procedures. 3. To review/revise/obsolete the Raw materials, In-process and Finished product specifications and standard test procedures as per requirements. 4. Handling of pharmacopeial updations. 5. Preparation of Regulatory assessment documents required for filing Viz., Elemental impurities...
Posted 4 months ago
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