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.
Post : QA/Analyst
Job Description
• Excellent written and oral communication skills in English
• Clarity in concepts
• Conflict handling and problem solving skills
• Excellent scientific aptitude
• Thorough knowledge on the principles of analytical techniques
• Knowledge on the pharmaceutical industry / regulated research
• Knowledge on Quality Systems (GLP / GMP / GCP) and regulatory requirements (US FDA, OECD, ICH and EMA)
• Preparation / Procession of Samples for Analysis
• Experience in handling HPLC, LC-MS/MS and other analytical equipment
• Experience in handling biological matrix
• Experience in bioanalytical / analytical method development and validation
• Preparation of SOPs, study plan / protocol, study report and other documents
• Calibration of equipment / balance / micropipette
• Good documentation practice and data integrity
• Computerised system validation
• Excellent written and oral communication skills in English
• Clarity in concepts
• Conflict handling and problem solving skills
• Excellent scientific aptitude
• Thorough knowledge on the principles of analytical techniques
• Knowledge on the pharmaceutical industry / regulated research
• Knowledge on Quality Systems (GLP / GMP / GCP) and regulatory requirements (US FDA, OECD, ICH and EMA)
• Preparation / Procession of Samples for Analysis
• Experience in handling HPLC, LC-MS/MS and other analytical equipment
• Experience in handling biological matrix
• Experience in bioanalytical / analytical method development and validation
• Preparation of SOPs, study plan / protocol, study report and other documents
• Calibration of equipment / balance / micropipette
• Good documentation practice and data integrity
• Computerised system validation
Candidate Profile
Area:
Small Molecule Bioanalytical / Analytical / Quality Assurance (GLP)
Education:
• Post graduate degree in Science or Pharmacy
• Preferably with specialization in analytical chemistry/biochemistry
• Good Academic Track record
Area:
Small Molecule Bioanalytical / Analytical / Quality Assurance (GLP)
Education:
• Post graduate degree in Science or Pharmacy
• Preferably with specialization in analytical chemistry/biochemistry
• Good Academic Track record
Additional Information
Qualification : M.Pharm, M.Sc
Location : India
Industry Type : Pharma
Functional Area : QA
End Date : 10th January, 2019
Qualification : M.Pharm, M.Sc
Location : India
Industry Type : Pharma
Functional Area : QA
End Date : 10th January, 2019
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