Senior Scientist I, Documentary Standards US Pharmacopeia

7.0 - 13.0 years

0 Lacs

hyderabad, telangana

On-site

Role Overview: You will be working as a Sr. Scientist I in the India Biologics department at USP, in a hands-on, non-supervisory role. Your main responsibility will be to collaborate in the development of reference standards for biotechnology pharmaceutical products. You will also be involved in supporting the suitability program by preparing and reviewing testing protocols, providing technical assistance to testing labs, and reviewing analytical data to confirm the continued suitability of USP Reference Standards. Key Responsibilities: - Maintain smooth collaboration with key stakeholders to develop reference standards for biotechnology pharmaceutical products - Draft protocols, reports, an...

Posted 1 week ago

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Associate Scientist II, Analytical Development for Characterization Viltis

1.0 - 6.0 years

0 Lacs

karnataka

On-site

As a member of the Analytical Development team at our clinical-stage vaccine innovation company, your primary responsibility will be to support the developmental activities in the laboratory. You will have the opportunity to assist in the design, execution, and interpretation of experiments to analyze drug substances and intermediates, including proteins and carbohydrates. Your key responsibilities will include: - Performing microplate assays, including enzymatic assays - Utilizing HPLC techniques, especially SEC and RP-HPLC with experience in Chemstation - Working with CE and iCIEF, especially with Protein Simple or PA-800 systems - Assisting in analytical method development of new assays -...

Posted 2 months ago

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Senior Scientist I, Documentary Standards (Reviewer) US Pharmacopeia

7.0 - 13.0 years

0 Lacs

hyderabad, telangana

On-site

You will be joining USP's Global Biologics department as a Sr. Scientist - I (RSS-Review), where you will play a crucial role in supporting the development of USP documentary standards and reference standards for biological products. In this hands-on, non-supervisory position, you will be responsible for ensuring the accuracy, clarity, and compliance of scientific documents, managing the reference standard stability program, and driving continuous process improvements. Your primary responsibilities will include performing technical and quality reviews of documents, developing and reviewing SOPs and training materials, assisting in investigations of quality-related issues, and collaborating w...

Posted 4 months ago

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