Job Description

• To work as per cGMP and ensure its compliance as per current guideline and SOPs.

• Responsible to align with organization goal and other responsibilities assigned by reporting authority.

• Responsible to perform the calibration of instrument and to maintain instrument/equipment as per SOPs.

• Responsible to follow safety precaution as per laboratory procedure.

• Responsible for method development studies of Drug Substance, Drug Product & In process Materials related to Peptides.

• Responsible for method Validation studies of Drug Substance, Drug Product & In process Materials related to Peptides.

• Responsible for analysis of routine samples and stability studies of Drug Product & In process Material Drug Substance, Drug Product & In process Materials related to Peptides.

• Responsible to prepare Study Protocol and Study Reports.

• Responsible for analysis of Oligonucleotides (DNA & RNA molecules) of single strand (Sense and Antisense) and Duplexes molecules.

• Responsible for Development of IEX and Ion Pair method for Sense and Antisense to separate charge variants in DNA and RNA molecules

• Responsible for Development of SEC method to separate size variants in DNA and RNA molecules.

• Responsible for Isolation of Peptide molecules from impurities by PREP HPLC.