Junior Executive, Quality Control Pelltech Healthcare

1.0 - 5.0 years

0 Lacs

palghar, maharashtra

On-site

As a Quality Control Analyst, your role involves analyzing Vendor Approval samples, preparing and standardizing solutions, and implementing GLP/GMP requirements. You will be responsible for analyzing Raw Materials, Finished Products, Stability samples, and Packing materials while ensuring compliance with cGMP requirements. Additionally, you will review laboratory chemicals, calibrate instruments like HPLC, UV, IR, Dissolution, KF Potentiometer, and perform Working standard qualification. Maintenance of Stability Incubators and reviewing analytical data, calibration data, and qualification data are also part of your key responsibilities. Qualifications required for this position include a min...

Posted 4 weeks ago

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Junior Executive, Quality Control Pelltech Healthcare

1.0 - 5.0 years

0 Lacs

palghar, maharashtra

On-site

You will be responsible for analyzing Vendor Approval samples and preparing Standardization of Solutions as needed. You will also need to implement GLP/GMP requirements and analyze Raw Materials, Finished Products, Stability samples, and Packing materials. Ensuring samples and related documentation meet cGMP requirements is crucial. Additionally, you will need to oversee the analysis of Raw Materials, Finished Products, and Stability Samples from outside commercial labs. Reviewing laboratory chemicals, calibrating instruments such as HPLC, UV, IR, Dissolution, KF Potentiometer, and performing Working standard qualification are part of your duties. Maintenance of Stability Incubators, loading...

Posted 3 months ago

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Junior Executive, R&D-Analytical Development Laboratory (ADL) Pelltech Healthcare

1.0 - 5.0 years

0 Lacs

palghar, maharashtra

On-site

As a skilled Analytical Chemist, you will be responsible for various tasks related to method development, validation, and query response for finished products. Your duties will include preparing analytical method development reports, Certificates of Analysis (COA), and performing analysis of in-process samples, finished goods, and stability samples in accordance with cGMP requirements. It will be your responsibility to monitor the general laboratory and ensure its maintenance as needed. Your role will involve routine analysis and stability testing of finished products for parameters such as assay, related substances, dissolution, residual solvent, etc. Additionally, you will be required to r...

Posted 3 months ago

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