Executive - QC (Chemical Analysis) Panacea Biotec
Panacea Biotec
Office Location
Full Time
Experience: 2 - 2 years required
Pay:
Salary Information not included
Type: Full Time
Location: Baddi
Skills: hplc, GC, Chemical Analysis, Sampling, Documentation, Stability studies, Validation, Instrument Calibration, cGLP, Chemical management
About Panacea Biotec
Panacea Biotec is a research-based health management company involved in research, manufacturing and marketing of high-quality, affordable pharmaceutical, vaccines and herbal products. The product portfolio includes highly innovative prescription products in important therapeutic areas like pain management, diabetes, cardiovascular, renal disease management, osteoporosis, gastro-intestinal care products and vaccines.
Panacea Biotec is committed towards disease prevention by introducing Innovative Vaccines that helps to reduce child mortality. Our portfolio consists of worlds first fully liquid Hexavalent vaccine i.e. EasySix (DTwP-Hib-HepB-IPV), the world’s first fully-liquid Pentavalent vaccine i.e. Easyfive-TT (DTwP-Hib-HepB), Oral Polio vaccines (like bOPV, tOPV, mOPV), etc. We have a high-impact pipeline of vaccines including Pneumococcal conjugate vaccines (PCV), tetravalent dengue vaccine, etc. We have supplied 10+ billion immunizations of Polio vaccines in last 20 years, 150+ million immunizations of Novel Innovative fully liquid wP-based vaccines like the wP-Hexavalent vaccine (DTwP-Hib-HepB-IPV). And are a trusted partner for WHO, GAVI and UN Agencies with track-record of sustainable supplies for UNICEF, PAHO, and National Immunization Programs.
Job Description
Department: Quality Control Educational Qualification : M. Sc. Chemistry Designation: Executive - Chemical Analysis (RM, FG, Stability and PM) Job Title : Executive Quality Control Job Summary: Analysis, sampling and documentation in chemical section Reporting To : (Designation) Section Manager Job Responsibilities Analysis of finished product, stability, raw material, in-process, packing material and validation samples as per respective STPs. (HPLC & GC technique) Sampling of raw material and packing material. Charging of samples for stability studies at different stability conditions and withdrawal of stability samples at different time intervals as per respective protocol. Monitoring of stability chambers for temperature and humidity. Preparation of stability summary reports. Chemical and column management as per defined procedure. Qualification of working standards & volumetric solutions. Calibration of instruments as per schedule. To maintain cGLP in Quality Control laboratory. To execute any other work assigned by HOD/ section manager.,