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Scientist II , Verification Programs

1.00 to 2.00 Years   Hyderabad   23 Sep, 2020
United States Pharmacopeia-India (P) Limited
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

This is a key hands-on, non-supervisory position. In this role, the Scientist performs the required analytical tests of Dietary supplements samples using appropriate methods. The Scientist will contribute to the scientific expertise and work ethic of the laboratory through a broad range of technical support and knowledge. The Scientist has mastered many common techniques in the laboratory and is able to contribute his/her own observations and input to difficult projects. The incumbent will provide technical assistance to the Verification Program by performing analytical tests and preparing summary reports. Roles and Responsibilities:

  • Executes the Verification projects by performing individual analytical tests allotted by the Group Leader.
  • Completes the projects as per the project timelines and priorities.
  • Demonstrates solid scientific approach to analysis in the laboratory.
  • Routinely applies personal experience, academic training, and technical insights including emerging sciences to solve complex technical problems within the laboratory;
  • Compiles project reports and responds QA observations.
  • Executes all testing and analysis of data with excellence and essentially no errors;
  • Demonstrates a strong desire to continue learning and grow personal capability;
  • Pursues, recommends, and implements new approaches or processes to improve laboratory operations;
  • Positively influences project direction by ensuring own work is congruent with overall direction of laboratory projects;
  • Assists with other testing programs and housekeeping duties in the laboratory as needed.
  • Ensures the implementation of GLP, safety systems in labs.
  • Ensures the calibration of the equipment as per the schedule.
  • Indents chemicals, columns, Glassware, etc. and procures them by coordinating with lab operations and purchase department in advance keeping in mind the project deadlines.
  • Ensures and follows USP mission, policies and procedures.
  • Maintains good relationship with QA, HR, Purchase, accounting, IT and other dept.
  • Preparation and planning for ISO-9001 & ISO- 17025 certification/recertification by participating actively and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner.
  • Supports collaborative testing, GPH, RSL and other departmental teams in terms of project testing, review, execution and approval whenever needed.
Required Skills Proven track record of consistently delivering projects on time and with high quality. Proficient with pharmaceutical testing requirements and test protocols involving compendial methods for reference materials (USP, FCC, NF, etc.). Expert in Chromatographic analysis, especially in HPLC and troubleshooting, proficient in other related analytical instrumentation (Titrations, IR, KF, UV, Thermal, Elemental analysis etc.), Takes personal responsibility for delivery of projects to customers. Ability to embrace and lead change. Extremely adaptable. Excellent communication skills, both written and verbal. Having knowledge of Empower software, ELN, ERP, QR coding system are added advantages. Prior experience in a high volume pharmaceutical manufacturing QC laboratory or contract pharmaceutical analytical laboratory testing organization is a plus. Required Experience Ph.D. in Chemistry with 1-2 years or Master degree in Chemistry with 3-5 years of relevant laboratory experience.,

Keyskills :
project reportstechnical supportdocumentationapicalibrationmusic makingiso 9001hplccontinuous improvement facilitationdelivering projects on timedelivery of projectsresearch

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