Are you passionate about analytical science and biological standards? Here’s an exciting opportunity to make a global impact with one of the most prestigious scientific organizations—The U.S. Pharmacopeial Convention (USP) is hiring for the role of Senior Scientist I – Bioanalytical at their Hyderabad facility.
About USP
The U.S. Pharmacopeial Convention (USP) is a globally recognized nonprofit scientific organization that develops and sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements. USP’s standards are enforceable in the U.S. by the FDA and used in over 140 countries, playing a critical role in ensuring safe and high-quality medicines globally.
Position Overview
- Job Title: Senior Scientist I – Bioanalytical
- Location: Hyderabad, India
- Job Category: Chemistry & Scientific Standards
- Job Type: Full-Time
- Requisition ID: SENIO002768
This is a hands-on, individual contributor role involving execution and contribution to bioanalytical projects, standard development, and characterization of biological products like proteins, enzymes, mAbs, vaccines, peptides, and raw materials.
Key Responsibilities
- Conduct analytical testing using HPLC/UPLC, Capillary Electrophoresis, Mass Spectrometry, SEC-MALS, Circular Dichroism, and other high-end techniques.
- Perform complex analyses like Intact Mass, Peptide Mapping, Glycan Profiling, HCP, Impurity Profiling, and PTM Analysis.
- Contribute to Compendial and R&D projects and new initiatives.
- Coordinate with global cross-functional teams and align with biologics strategy.
- Mentor junior scientists and ensure compliance with ISO 9001, ISO 17025, and QMS standards.
- Write and review project reports, SOPs, and documentation with adherence to cGMP/cGLP standards.
Who Can Apply?
Minimum Qualifications:
- Ph.D. in Biochemistry/Analytical Chemistry/Biological Sciences with 7–10 years of relevant post-doctoral experience
OR - M.Sc./M.Tech./M.Pharm. with 11–13 years of experience in Analytical R&D or QC in the Biopharmaceutical industry
Must-Have Skills:
- Experience in method development, validation, and tech transfer for biomolecules.
- Hands-on expertise in analyzing peptides, mAbs, CGT, and Vaccines.
- Strong knowledge of biopharmaceutical reference standards.
- Prior experience in QMS, cGMP/cGLP environments, and strong technical troubleshooting skills.
Preferred Skills
- Technical writing and documentation in a regulated environment.
- Experience working with reference standards and collaborative testing.
- Excellent communication and presentation skills.
- Proficiency in handling analytical instruments and troubleshooting.
Why Join USP?
By joining USP, you’ll be contributing directly to improving global health through rigorous scientific standards. You’ll work alongside top scientists and engage in meaningful projects that protect public health worldwide. USP also supports continuous professional growth through a people-first and equity-driven culture.
Apply Now and Be a Part of USP’s Mission to Improve Global Health Through Science!
🔗 Visit USP Careers to apply (Search by Req ID: SENIO002768)
