QC Chemicals Executive

1 week ago

Vadodara, India Job Excel Full time
Ensuringthe quality and compliance of our pharmaceutical products includingthose in formulation through rigorous chemical analysis andtesting. You will be responsible for overseeing and executingquality control activities related to the chemical aspects ofproduct manufacturing ensuring adherence to regulatory standardsand companypolicies.

Performinga wide range of chemical tests and analyses on raw materialsintermediates finished products and formulation samples usingvarious analytical techniques such as HPLC GC FTIR UVVisspectroscopy and wet chemistrymethods.

Toimprove analytical techniques enhance sensitivity and reduceanalysis time and costs with a focus on formulationtesting.

Ensureall quality control activities comply with current GoodManufacturing Practice (cGMP) Good Laboratory Practice (GLP) andother relevant regulatory standards including those applicable toformulationtesting.

Maintainaccurate and complete documentation of all testing proceduresresults and records in compliance with regulatory requirements andcompany policies particularly for formulationsamples.

Requirements

Previousexperience working in a pharmaceutical quality control environmentis essential with a strong background in chemical analysis andtestingtechniques.

Proficiencyin operating and troubleshooting analytical instruments andequipment with handson experience in HPLC GC FTIR UVVisspectroscopy and other relevanttechnologies.

Knowledgeof analytical chemistry principles including qualitative andquantitative analysis formulation analysis separation techniquesand spectroscopicmethods.

Familiaritywith laboratory information management systems (LIMS) data analysissoftware and electronic laboratory notebooks (ELN) isbeneficial.

Understandingof current Good Manufacturing Practice (cGMP) Good LaboratoryPractice (GLP) International Council for Harmonization (ICH)guidelines and other relevant regulatoryrequirements

Stronganalytical and problemsolving abilities the ability to maintainaccurate and complete records of testing procedures results anddocumentation in compliance with regulatory standards and companypolicies.

Excellentverbal and written communication skills to convey technicalinformation effectively collaborate with crossfunctionalteams.

Previous experience working in a pharmaceutical quality controlenvironment is essential, with a strong background in chemicalanalysis and testing techniques. Proficiency in operating andtroubleshooting analytical instruments and equipment, with hands-onexperience in HPLC, GC, FTIR, UV-Vis spectroscopy, and otherrelevant technologies. Knowledge of analytical chemistryprinciples, including qualitative and quantitative analysis,formulation analysis, separation techniques, and spectroscopicmethods. Familiarity with laboratory information management systems(LIMS), data analysis software, and electronic laboratory notebooks(ELN) is beneficial. Understanding of current Good ManufacturingPractice (cGMP), Good Laboratory Practice (GLP), InternationalCouncil for Harmonization (ICH) guidelines, and other relevantregulatory requirements Strong analytical and problem-solvingabilities, the ability to maintain accurate and complete records oftesting procedures, results, and documentation in compliance withregulatory standards and company policies. Excellent verbal andwritten communication skills to convey technical informationeffectively, collaborate with cross-functional teams.

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