About Company:
Provis Biolabs is a fast-growing biotechnology company specializing in animal-origin-free bioreagents for global pharmaceutical and biopharmaceutical applications. Founded in 2019, we have commercialized 10 products and continue to expand our robust pipeline. Our mission is to address unmet needs in life sciences research and therapeutic development by delivering high-quality and reliable solutions. Backed by WHO-GMP, GLP, ISO 9001:2015, Halal and Kosher certifications, we offer end-to-end capabilities spanning R&D to GMP manufacturing. Leveraging our state-of-the-art fermentation facility, we provide scalable production solutions to partners worldwide. Our expertise covers critical areas such as vaccines and biologics, monoclonal antibodies (mAbs), cell culture and cell and gene therapy products, ensuring versatile support for diverse industry demands. Provis Biolabs serves as a Contract Development and Manufacturing Organization (CDMO), offering specialized fermentation-based development and manufacturing services. We guide partners through every stage—from clone development and strain engineering to process optimization, scale-up and commercial manufacturing. Provis Biolabs is poised to be a global leader in the life sciences industry by delivering superior quality products and solutions to improve health and environment through sustainable means.
Website
http://provisbiolabs.com
Vacancy Details:
Job Description:
Greetings from Provis!
We are hiring for the following posts
1.Quality Control (QC) Analyst – CRO AR&D/Peptides
Experience: 1-3 years
Qualification:- M. Sc(chemistry, Analytical chemistry, Biotechnology) or B. Pharm -M. Pharm
key Responsibilities:
1.Perform routine HPLC, UPLC, MS, FTIR, UV, and Karl Fischer Analysis for peptide products.
2.Prepare, review, and maintain QC documentation, including analytical reports, COAS, and validation protocols.
3.Follow ICH, GMP, and regulatory guidelines for analytical method validation and quality control.
4.Ensure compliance with CRO-Specific quality requirements in peptide synthesis projects.
2.Data & Quality Assurance (DQA) Executive
Experience: 1-3 years
Qualification:- M. Sc (Analytical chemistry, Biotechnology) or B. Pharm/M. Pharm
Key Responsibilities
1.Review and ensure data integrity and accuracy of HPLC, UPLC, MS, and NMR Analytical results.
2.Implement and maintain Good Documentation Practices(GDP) in peptide analytical workflows.
3.Perform quality audits, risk assessments, and deviation investigations for QC/analytical department.
4.Support laboratory audits and data compliance inspections.
Location: Hyderabad & Jadcherla
Send CV and Cover Letter to careers@provisibiolabs.com
