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Adl Officer

Lifecare Nuero Products Ltd

  • 1 - 5 yrs
  • 5.5 Lac/Yr
  • Baddi Solan
Analytical Validation Method Calibration Of Instruments GLP GDP Compliance in Analytical Laboratory
must have knowledge to perform analysis of Development, Routine and stability sample.
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  • 2 - 7 yrs
  • Vadodara
GLP Method Validation Analytical Method Development Instrument Calibration
Job Responsibility: 1. To ensure that GLPs followed in the laboratory. 2. To establish, develop, validate testing Procedures. 3. To Prepare protocols, reports and monitor samples of Method validation andMethod Development. To perform the calibration of instrument/equipment. To ensure that instruments andequipment are calibrated as per given schedule and records are maintained accordingly. To perform analysis for Raw material, finish products and stability samples. To ensure that samples are analysed in time and results are conveyed todepartment head or reviewer as per requirement and as per the procedure. To maintain documentation for Regulatory Submission Maintaining of SOP as per regulatory requirements and periodically reviewed. To ensure all record are maintained as per the procedures. Any other work assigned by the superiors. To prepare Method of analysis (MOA) and Specification and any otherdocuments of new drug product. To perform Method transfer to Q.C Department.Qualification :B. Pharm / M. PharmExperience : 2-3 YearsJob Location :Vadodara
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  • 3 - 4 yrs
  • 4.0 Lac/Yr
  • Navsari
Analytical Method Development Pharmaceutiocal Production Walk in
JOB Profile - ADL (Analytical & Development Officer)Our Client . is looking for profiles to fill the position of Chemist (Analytical Development), contributing to the accomplishment of the Analytical development function objectives. The position will report to Quality Control and Analytical Development Manager. The role would be involved not limited to below mentioned areas:1. Execute Analytical Method Development activities of drug products.2. Execution of Analytical Method validation activities for drug products as per the regulatory requirements.3. Trouble shooting related to Testing methods, Stability studies, test results and designing of additional experimentations as necessary.4. Preparation and review of Specifications, Method of analysis procedures and Analytical development reports.5. To identify, develop and qualify/validate methodology suitable for the product. 6. Preparation of analytical technical documents for dossier / Technology transfer executions / Regulatory submissions of projects.7. Assessment & coordination on regulatory deficiencies. 8. Assisting with analytical requirements in finalization of project costings.9. Any other specific functional activities defined on case to case basis
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