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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
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.
Prepares and reviews SOPs.
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
Required Experience
Master s degree in pharmacy or Analytical chemistry.
Minimum 5 to 7 years of relevant laboratory experience.
Prior experience in a high volume pharmaceutical manufacturing QC laboratory or contract pharmaceutical analytical testing laboratory.
Keyskills :
presentation skillspharmaceutical industrydiabetesfilingfile managementproject directioncontinuous improvement facilitationapifinancial justificationiso 17025pharmaceutical manufacturingcommunication skillsmusic makingtechnical supportprojec