Vacancies for Officer / Executive - Analytical Development @ Medreich
Job Description
Candidate should have experience in Method development, Method validation of different pharmaceutical dosage forms.
Hands on experience/ knowledge in handling Analytical work related to DS and DPs in different phases with a proven track record (having worked with Global partners/ International exposure).
Hands on experience in Chromatography (HPLC, UPLC, HSGC), Spectroscopy (FTIR, UV), dissolution apparatus and Particle size measurements. Well versed with 21CFR Part 11 and other global laboratory compliances requirements.
Knowledge in impurity profiling, Forced Degradation studies, Excipient compatibility studies, application of DoE/ QbD concepts in analytical development will be an added advantage.
Good Knowledge of ICH guidelines and different global regulatory authorities requirements related to products and its methods, control strategy towards critical quality attributes.
Ability to interpret the analytical data and draw conclusion based on the scope of the experiments.
KEY Skills: HPLC Method Validation, UV, Dissolution, Apparatus UPLC Method Development FTIR
GPAT passed candidates are preferred.
Click here to apply
Job Description
Candidate should have experience in Method development, Method validation of different pharmaceutical dosage forms.
Hands on experience/ knowledge in handling Analytical work related to DS and DPs in different phases with a proven track record (having worked with Global partners/ International exposure).
Hands on experience in Chromatography (HPLC, UPLC, HSGC), Spectroscopy (FTIR, UV), dissolution apparatus and Particle size measurements. Well versed with 21CFR Part 11 and other global laboratory compliances requirements.
Knowledge in impurity profiling, Forced Degradation studies, Excipient compatibility studies, application of DoE/ QbD concepts in analytical development will be an added advantage.
Good Knowledge of ICH guidelines and different global regulatory authorities requirements related to products and its methods, control strategy towards critical quality attributes.
Ability to interpret the analytical data and draw conclusion based on the scope of the experiments.
KEY Skills: HPLC Method Validation, UV, Dissolution, Apparatus UPLC Method Development FTIR
GPAT passed candidates are preferred.
Click here to apply
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