Executive - Analytical Method Validation (Dilution/Infusion Study, QC) - Ahmedabad

The position involves analysis related to the qualification of instruments and equipment, as well as standards. It requires knowledge of chemical analysis, LIMS/QMS systems, and current pharmaceutical guidelines. The job also involves troubleshooting analytical problems and maint ...

Analysis related to qualification of Instrument/Equipment and Standards. Qualification of Standards and Instruments. · ...

Analisis relacionado a la calificacion de instrumentos/ equipamiento y estandares; conocimiento y habilidades en instrumentos sofisticados como UV etc. · ...

The MD/MV group develops and validates assay methods for drug analysis in biological fluids using LC/MS/MS. · Evaluate precision accuracy stability of drug/metabolite in biological fluid after extraction. · ...

+ Proven Experience of working in GMP/GLP and scientific environment. · + Basic knowledge of Spectroscopic and Biophysical techniques, · Peptide chemistry, peptide and peptide characterization (Expertise in any one of the subject). · Experience in related compound method developm ...

We are looking for an experienced Analytical Development professional to join our lab. · ...

The role involves leading method development and validation of analytical methods for raw materials, intermediates and final APIs. · ...

We are pleased to invite experienced professionals for Walk-In Interviews at Intas Pharmaceuticals Ltd. · ...

The Assistant Manager will provide technical inputs for physicochemical analytical methodologies for monoclonal antibodies (mAbs) and deliver robust analytical methods that can be easily validated. · ...

The role involves supporting the analytical lifecycle of biosimilar products in the MSAT-ADL laboratory. · Develop and validate analytical methods for biologics, biosimilars, and upstream processing. · Transfer methods from research to manufacturing scale-up. · ...

The incumbent will be responsible for method development validation and routine bioanalysis of drugs and their metabolites in biological matrices using LC/MS/MS. · Perform sample extraction using wet chemistry techniques as per study protocols and SOPs. · Handle centrifugation ev ...

Perform Quality review of bioanalytical data, including chromatograms, calibration curves and final reports. · ...

Conduct NPD and process optimization. · Maintain documentation and coordinate with QA, · QC and production. ...

We are seeking an Assistant Manager to provide technical inputs for physicochemical analytical methodologies for monoclonal antibodies (mAbs). The successful candidate will be responsible for delivering robust analytical methods that are easily validatable. · ...

+This is a job description. · +Develop analytical methods for OSD products using techniques such as UV, FTIR, Dissolution, HPLC, GC, Ion Chromatography Wet Analysis etc. · Conduct method validation studies to ensure compliance with regulatory requirements. · Collaborate with cros ...

The job description is as below: · Performing Bacterial Endotoxin Tests (BET): Utilizing the Limulus Amebocyte Lysate assay to detect and quantify endotoxins in raw materials, in-process samples, and finished products. · ...

The Jr. Auditor will be responsible for planning and executing audits on conduct, compliance verification and corrective actions. · The role also involves conducting system and vendor audits, · reviewing SOPs and quality assurance documents, · and assisting with sponsor/client au ...

Perform analysis of raw in process finished goods operate GC HPLC UV KF IR maintain records follow GLP SOPs support method validation ensure ISO regulatory compliance coordinate with QA production for batch release · ...

In your new role you will participate and contribute to requirements elicitation and definition phase of the project. · ...

Manage the activities of the quality control laboratory to ensure timely delivery of materials for use in production and releases of finished products from the laboratory as committed. · ...