The candidate will supervise the team of eight members and provide the guidance.
The candidate is expected to work with cross functions like Upstream, Downstream & clone development team.
The candidate is expected to develop HPLC based methods for protein and peptide products.
The candidate is expected to design and implement integrated strategies, linking appropriate analytical tools, to perform a qualitative and quantitative assessment of product related variants and impurities. Develop and apply novel sample preparation with emphasis on RP-HPLC, SEC-HPLC, CEX-HPLC..etc
Responsible for designing advance workflows to measure & characterize process related impurities at different stages of product development such as Host cell protein (HCPs), Host Cell DNA (HCD) & Leachable.
The candidate is expected to qualify the methods for intended purpose for all pipeline products.
Responsible for routine in process sample analysis.
Responsible for preparation and review of method development reports (MDRs) and analytical test procedures (ATPs).
Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations.
Responsible for managing the regulatory queries.
The candidate is expected to draft the technical content for regulatory dossier.
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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