6

HPLC Job Vacancies in Hyderabad

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  • 2 - 5 yrs
  • Hyderabad
Tablets Capsules Sterile Injections Pellets Dry & Liquid Syrups Ointments Lyophilized Powder For Injection HPLC Polarimeter
Exposure of analysis for Finished product, stability samples, raw material, Handling of HPLC, Dissolution, AASHandling of shop floor QMS Documents and GLP compliances.
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Quality Control Manager

Kreative Organics Private Limited

Quality Control HPLC Quality Analysis Methode Validation Method Development GMP CGMP GC Analysis Empower3 Walk in
Plan and manage all activities of Laboratory (analysis, chemical management, calibrations, standards management, investigations, incidents or out of specifications, method optimizations, validations .Manpower Planning ,Preferred candidate profile Having 2 to 3 Years of experience as a manager(Only Male).
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Quality Control Chemist

Gpt Pharmaceuticals Private Limited

  • 0 - 4 yrs
  • 3.0 Lac/Yr
  • Nacharam Hyderabad
Experience in HPLC QC Chemist
We are looking for 04 Quality Control Chemist Posts in Nacharam, Hyderabad, Telangana,Experience in HPLC, with deep knowledge in Experience in HPLC and Required Educational Qualification is : B.Sc, M.Sc
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Quality Control Analyst

Bhagyavati Placement & Services

Microsoft Office Pharma Quality Control HPLC Quality Analysis
Quality Control Analyst RoleWe are seeking a Quality Control Analyst to ensure the consistent quality of our production output. In this role, you will conduct laboratory tests on incoming raw materials, in-process production samples, and final products before distribution. You will analyse data to ensure product specifications are met and perform peer reviews of other analyses. As part of this role, you will also review current GMP documentation relating to testing methods and regulations and implement ways that we can update or improve our processes. Applicants should have a bachelors degree in chemistry, biochemistry, or another biological sciences field.Quality Control Analyst DutiesPerform QC testing on raw materials, in-process items, and final productsAssess data to make sure product specifications are metReview good manufacturing practise documentation, including test methods and protocolsPerform review of test data and analysisMaintain inventory of testing suppliesSupport process improvementMaintain laboratory equipmentQuality Control Analyst RequirementsBachelors degree in chemistry, biochemistry, or another biological sciences fieldMasters degree a plusAnalytical skillsFamiliarity with Industry standards and regulationsClinical laboratory experience preferred
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Research & Development Chemist

UMED PHARMA LABS PVT LTD

  • 2 - 4 yrs
  • 2.8 Lac/Yr
  • Sultanpur Hyderabad
HPLC XRD GC Analysis
Perform analysis as per the procedures/monographs Perform the analysis independently on techniques: GC and HPLC Techniques. Perform the routine calibration of analytical balance and GC. Experience on method development and validation by HPLC / GC / XRD
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QC Analyst

Issar pharmaceuticals private limited

  • 3 - 5 yrs
  • 6.5 Lac/Yr
  • Greater Hyderabad
Complete Knowledge Of Operation Good Documentation QC Chemist QC Analyst Documentation Analyst HPLC LCMS
The candidate should have complete Knowledge of operation and familiarity of various instruments including HPLC, LCMS, GC, and TOC with Good documentation and timely analysis and recording of stability data.
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Quality Control Analyst

Kreative Organics Private Limited

  • 3 - 6 yrs
  • 5.0 Lac/Yr
  • Hyderabad
Pharma Quality Control HPLC Quality Analysis Empower Software Method Development Pharma Quality Walk in
1. To ensure compliance with Good laboratory practices and Good manufacturing practices.2. Should be follow laboratory safety personal protective equipments while handling analysis.3. Based on work allocation analysis should be perform and same day document completion.4. All the analysis of raw materials, in-process, intermediate, stability, Recovery solvents, R&Dsamples and finished product HPLC and GC analysis as per procedure.5. All working standards HPLC and GC related analysis planned as per schedule date.6. Working standard should be use by ensuring validity of standard within the period.7. Chemist should be ensuring before using the instrument status and calibration of instrumentand earlier analysis results should be ensure.8. Chemist should be ensure before starting analysis availability of standards, chemicals andglasswares etc.,9. Analyst should follow good laboratory practices laid down in the quality control laboratory.10. Analyst should follow after completion of chromatography analysis ensure the results anddiscard the solutions if results within the specification.11. Analyst once started the sequence set of sample loading same day next day need to processyesterday samples then only go for new work.12. Analyst should process the samples contemporaneously if any abnormal results observedinform immediately senior supervisor/reviewer/designee then only next decision to be taken.13. Analyst is responsible for analysis and documentation and sample disposition.14. Analyst is responsible for laboratory cleaning, instrument cleaning and maintenance in goodcondition.15. Results are reported as per rounding of the SOP.16. Equipments calibration shall be performed as per internal calibration master schedule.17. After usage of the working standards and reference standards it shall be kept in designatedplace.18. Monitoring the daily room temperature and its recording as per procedure.
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