Govt Job: For Senior Scientist at USP – United States Pharmacopeia

Last date : 30th December 2022

Picture: Piaxabay

Last Updated on December 2, 2022 by The Health Master

United States Pharmacopeia (USP) is proud to be an equal opportunity/affirmative action employer.

Employment selection and related decisions are made without regard to sex, gender identity, race, age, disability, religion, national origin, color, veteran status or any other protected class.

We are committed to working with and providing reasonable accommodation to individuals with disabilities.

Post: Senior Scientist I – Bioanalytical

Picture: Pixabay

Job Description
• Aligns with USP’s mission, goals, and objectives and complies with USP’s guidelines and other requirements.

• Demonstrates analytical chromatography (HPLC/UPLC/Ion-chromatography), capillary electrophoresis, SEC-MALS, circular dichroism, and mass spectrometry laboratory skills and hands-on expertise.

• Perform Intact Mass, Peptide mapping, Glycan profiling, HMW & LMW, HCP, Impurity Profiling studies & PTM analysis

• Plans and executes Compendial and R&D projects besides contributing in the new initiatives viz., proof of concept studies in Biologics for product classes such as proteins, enzymes, vaccines, monoclonal antibodies, peptides, antibiotics, and any other biological products as assigned.

• Evaluates and analyzes scientific reports, applies personal experience, academic training, and technical insights to troubleshoot and solve problems in the laboratory within the scope.

• Performs administrative responsibilities, mentors and trains team member/members as assigned.

• Actively engages in project coordination with cross-functional/global teams and aligns with Global Biologics objectives.

• Prepares and reviews project reports, SOPs, and other documents to ensure compliance to USP’s Quality Management System and contribute in ISO 9001 and ISO 17025 audits

• Assists and recommends improvements in laboratory/project management methods and processes.

• Performs other duties as assigned.

Candidate Profile
• M.Sc. (Biochemistry / Biotechnology) / M.Tech (Biotechnology / Bioprocess Engineering) / M.Pharm with practical hands-on experience on advanced techniques such as Mass Spectrometry, Capillary Electrophoresis, SEC-MALS, Circular-dichroism, Chromatography & Biochemical or Enzymatic Assays.

•  8-12 years of industry experience working in Analytical R&D and QC department of Biopharmaceutical industry.

•  Experience in method development, validation and technology transfer and analytical characterization for biomolecules.

• Knowledge of reference standards development and collaboration related to biopharmaceutical products (mAb, Peptide, Vaccine etc).

Experience with reference materials manufacturing and development is a plus.

• The candidate should be well-versed with operation and troubleshooting of all instruments used in performing the above-mentioned analytical techniques and should have sound knowledge of QMS systems.

• Previous experience working in biopharma cGLP/cGMP/QMS environment with practical experience in good documentation practices would be an advantage.

• The candidate should have strong competencies in technical writing, communication, and presentation skills.

Additional Information
Experience: 8-12 years
Qualification: M.Sc, M.Pharm, M.Tech

Location: Hyderabad
Industry TypePharma / Healthcare / Clinical research

Functional Area: Bioanalytical
End Date: 30th December, 2022

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