Manager - Analytical Development
Talentmate
India
18th September 2025
2509-5643-117
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.
Job Details
| Role Level: | Mid-Level | Work Type: | Full-Time |
|---|---|---|---|
| Country: | India | City: | Vadodara ,Gujarat |
| Company Website: | http://www.sunpharma.com | Job Function: | Analyst |
| Company Industry/ Sector: |
Pharmaceutical Manufacturing | ||
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