Openings for B.sc/M.sc Chemistry, B.pharma/ M.pharma Candidates as Research Associate/ Scientist posts @ Syngene
Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC. Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.
Job Title : Sr. Research Associate/ Associate Scientist/research Scientist
No of openings : 10
Qualification : B.sc/M.sc Chemistry, B.pharma/ M.pharma
Experience : 2-7 years
Job Description :
Ability to work in coordination with various department to drive the projects
Execute analytical programs in support of formulation development with a high degree of independence
Develop, modify and validate analytical methods to support the formulation needs and regulatory filings using various instrumental techniques.
Extract target analytes from sample matrices using various extraction techniques, such as liquid-liquid, reflux and SPE
Perform stability studies on experimental formulations and finished dosage forms
Method and knowledge transfer to QC in order to smooth running of validation and GMP activities
Troubleshoot dosage forms stability using advanced physico-chemical methods of analysis, determine degradation pathways and elucidate structure of degradation products
Design and conduct in vitro drug release testing of solid and semi-solid formulations including various dissolution techniques
Identify and implement new technologies to enhance the analytical capabilities of the department
Click here to apply
Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC. Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.
Job Title : Sr. Research Associate/ Associate Scientist/research Scientist
No of openings : 10
Qualification : B.sc/M.sc Chemistry, B.pharma/ M.pharma
Experience : 2-7 years
Job Description :
Ability to work in coordination with various department to drive the projects
Execute analytical programs in support of formulation development with a high degree of independence
Develop, modify and validate analytical methods to support the formulation needs and regulatory filings using various instrumental techniques.
Extract target analytes from sample matrices using various extraction techniques, such as liquid-liquid, reflux and SPE
Perform stability studies on experimental formulations and finished dosage forms
Method and knowledge transfer to QC in order to smooth running of validation and GMP activities
Troubleshoot dosage forms stability using advanced physico-chemical methods of analysis, determine degradation pathways and elucidate structure of degradation products
Design and conduct in vitro drug release testing of solid and semi-solid formulations including various dissolution techniques
Identify and implement new technologies to enhance the analytical capabilities of the department
Click here to apply
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