About the role
Tentamus India (formerly Megsan Labs) is a US-FDA Inspected, ISO 17025 accredited, FSSAI approved and DCGI (Drug Controller General of India -Indian FDA) approved laboratory, which provides analytical testing services to food, pharmaceutical and related companies. The services comprise elemental impurity studies, E&L studies, method development & validation and microbiological testing.Analyses
- Chemical Analyses
- Microbiological Testing
- Molecular Biological Analysis
- Residue Analysis
- Pharmaceutical
- Food
- Medical Devices
Job Responsibilities :
- Hands on experience in HPLC/GC including method development, routine analysis and method validations along with good documentation practices.
- Responsible to perform the Analytical method validation, method verification and method transfer activities.
- Capable of handling standard chromatographic reports, validation/verification's, stability design matrix-protocols &reports
- Good Exposure on GDP,GLP, ALCOA+ Guidance
- Exposed to various regulatory Audits like USFDA,MHRA,TGA,ANVISA
- Coordinating with cross functional team to address the QMS related to Log events
- To be good at communication skills and writing skills
Qualification :
- UG: B. Pharma in Pharmacy
- PG: MS/ M.Sc (Science) in Chemistry, M. Pharma in Any Specialization
- Hands on experience in HPLC/GC/LC-MS/GC-MS including method development routine analysis and method validations along with good documentation practices