Last Updated on May 30, 2023 by The Health Master
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Post: Senior Scientist I – Bioanalytical
Job Description
тАв Aligns with USPтАЩs mission, goals, and objectives and complies with USPтАЩs guidelines and other requirements.
тАв Demonstrates analytical chromatography (HPLC/UPLC/Ion-chromatography), capillary electrophoresis, SEC-MALS, circular dichroism, and mass spectrometry laboratory skills and hands-on expertise.
тАв Perform Intact Mass, Peptide mapping, Glycan profiling, HMW & LMW, HCP, Impurity Profiling studies & PTM analysis
тАв 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.
тАв Evaluates and analyzes scientific reports, applies personal experience, academic training, and technical insights to troubleshoot and solve problems in the laboratory within the scope.
тАв Performs administrative responsibilities, mentors and trains team member/members as assigned.
тАв Actively engages in project coordination with cross-functional/global teams and aligns with Global Biologics objectives.
тАв Prepares and reviews project reports, SOPs, and other documents to ensure compliance to USPтАЩs Quality Management System and contribute in ISO 9001 and ISO 17025 audits
тАв Assists and recommends improvements in laboratory/project management methods and processes.
тАв Performs other duties as assigned.
Candidate Profile
тАв 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.
тАв 8-12 years of industry experience working in Analytical R&D and QC department of Biopharmaceutical industry.
тАв Experience in method development, validation and technology transfer and analytical characterization for biomolecules.
тАв 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.
тАв 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.
тАв Previous experience working in biopharma cGLP/cGMP/QMS environment with practical experience in good documentation practices would be an advantage.
тАв 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 Type: Pharma / Healthcare / Clinical research
Functional Area: Bioanalytical
End Date: 30th December, 2022
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