Sign In
 [New User? Sign Up]
Mobile Version

Scientist III Analytical Research and Development

Secunderabad, Telangana
Job Code:
  • Biotechnology & Science
Applying for this job will take you to an external site
  • Shortlist
  • Email Friend
  • Print

Job Details

Roles and ResponsibilitiesMethod development and analysis of samples as per monograph / in-house procedures including reaction monitoring.Prepare development reports for Synthetic Support projects.Involve in project acceptance & approvals.Execute projects per the approved test protocols if assigned.Responsible for preparation of SOPs, protocols, reports, etc.Ensure the projects requirements by coordinating with the Purchasing department.Coordinating with Senior Scientist to complete ARD projects within timelines.Responsible for preparation of the records and documents. Ensure that the calibrations of the equipments are performed as per the schedule.Prepare, execute and complete IQ/OQ/PQ of new instruments.To indent the required glass ware, chemicals and columns for the ARD projects.Maintain GLP & implement safety procedures while working in Lab.Perform other Projects whenever free from ARD activities.Perform other duties as assignedDesired ProfileThe candidate must possess the following experience to be considered for this roleA Masters degree in Organic chemistry / Analytical chemistry with a minimum of 6-8 years of experience in analytical testing and development with focus on process analytical chemistry.Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, FTIR, UV-Visible, wet chemistry, etc.Must be able to communicate effectively with both internal and external customers. Have knowledge on Analytical testing background is a plus and knowledge on pharmacopeial methods, General chapter information, Empower and NuGenesis will be preferred.Working knowledge of computer applications, such as MS Word and MS Excel are required.Excellent technical writing and verbal communication skills are required. Good interpersonal skills and proven ability to function in a team-oriented environment are necessary.Proven self-effectiveness skills are a must. Understanding of GMP / ISO-IEC 17025 Guidelines is a requirement.Exposure to GMP/GLP environment and documentation procedures required.Ability to perform analytical method developments and method validations as and when required.
Degree: M.Sc. (Science)

Additional Degree: B.Sc. (Science)

Experience: 6-8


Goods Manufacturing Practices (GMP) | Pharmaceutical Research
Applying for this job will take you to an external site


© Copyright 2015 Al Nisr Publishing LLC - powered by Gulf News