Analytical Services Chemist III

Lannett Company, Inc.; Seymour (IN); Sur place; USD 75 000 - 110 000; Plein temps

Résumé du poste

Lannett Company, Inc. in the United States seeks an analytical chemist to perform laboratory testing of raw materials, in-process and finished products in a cGMP environment.

You will evaluate new materials, assist method transfers, and develop and validate analytical procedures. Responsibilities include pH, moisture (loss on drying), water content (Karl Fischer), assay/impurities by HPLC, dissolution, residual solvents by GC, and various wet chemistries.

Qualifications

• BS degree in Chemistry or a related field.
• 4–8 years of pharmaceutical product analysis experience in a cGMP-regulated lab.
• Masters degree preferred.
• Experience with cGMP, USP/NF, and FDA guidelines.
• Expertise with analytical methods and lab instrumentation (e.g. HPLC, GC, dissolution, wet chemistry).

Responsabilités

• Perform routine and non-routine physical and chemical tests and assays on raw materials, API’s, in-process, finished products, experimental batches and associated stability studies
• Testing performed to include basic and complex lab equipment and procedures, such as pH, Loss on Drying, Residue on Ignition, Water Content by Karl Fischer, Assay/Impurities by HPLC, Dissolution, Residual Solvents by GC, and wet chemistry techniques such as titrations and sample derivatizations
• Conduct analytical research and develop analytical methods to test pharmaceutical products for conformance to established specifications with some supervision.
• Develop and validate analytical test methods for assay, dissolution, preservatives in drug products according to ICH/FDA/USP requirements with minimal to no supervision.
• Develop and validate test methods for residual solvents and impurities/degradation products in drug substances/excipients/drug products according to ICH/FDA/USP requirements under some supervision
• Develop and validate analytical Cleaning Validation methods and perform testing of cleaning validation samples and generate analytical report with minimum supervision.
• Multi-task by working on several simultaneous projects. Develop project timelines.
• Document all laboratory testing and maintain accurate and legible notebooks and records
• Perform peer review on other analysts’ data.
• Provide regular update progress reports of projects
• Comply with all relevant regulatory requirements
• At all times strive to maintain the self-esteem of individual team members and the professionalism of the group as a whole
• Perform laboratory troubleshooting, propose solutions and implement
• Other projects and duties as required or assigned
• Provide technical input for purchase of new/updated laboratory instruments and software systems
• Train other laboratory chemists on analytical instrumentation and methods.
• Mentor/Train team members on new/revised skills and testing procedures

Connaissances

Analytical testing

Method development

Validation

Regulatory compliance

Team collaboration

Formation

BS Degree in Chemistry or related field

Masters Degree preferred

Outils

HPLC

GC

Dissolution

Karl Fischer

Description du poste

This position is primarily responsible for the laboratory testing of raw materials, packaging materials, in-process, release and stability samples for developmental and pre-commercial drug products, including the evaluation of new raw materials, new packaging materials, reference standard qualifications, method transfers, and develop and validate methods within the framework of cGMP compliance guidelines.

Responsibilities:

• Perform routine and non-routine physical and chemical tests and assays on raw materials, API’s, in-process, finished products, experimental batches and associated stability studies
• Testing performed to include basic and complex lab equipment and procedures, such as pH, Loss on Drying, Residue on Ignition, Water Content by Karl Fischer, Assay/Impurities by HPLC, Dissolution, Residual Solvents by GC, and wet chemistry techniques such as titrations and sample derivatizations
• Conduct analytical research and develop analytical methods to test pharmaceutical products for conformance to established specifications with some supervision.
• Develop and validate analytical test methods for assay, dissolution, preservatives in drug products according to ICH/FDA/USP requirements with minimal to no supervision.
• Develop and validate test methods for residual solvents and impurities/degradation products in drug substances/excipients/drug products according to ICH/FDA/USP requirements under some supervision
• Develop and validate analytical Cleaning Validation methods and perform testing of cleaning validation samples and generate analytical report with minimum supervision.
• Multi-task by working on several simultaneous projects. Develop project timelines.
• Document all laboratory testing and maintain accurate and legible notebooks and records
• Perform peer review on other analysts’ data.
• Provide regular update progress reports of projects
• Comply with all relevant regulatory requirements
• At all times strive to maintain the self-esteem of individual team members and the professionalism of the group as a whole
• Perform laboratory troubleshooting, propose solutions and implement
• Other projects and duties as required or assigned
• Provide technical input for purchase of new/updated laboratory instruments and software systems
• Train other laboratory chemists on analytical instrumentation and methods.
• Mentor/Train team members on new/revised skills and testing procedures

Education/Qualifications:

• BS Degree in Chemistry or related field and 4 – 8 years of pharmaceutical product analysis experience in a cGMP-regulated lab environment
• Masters Degree preferred
• Experience working in the pharmaceutical industry and/or analytical laboratory
• Knowledge of cGMP, USP/NF, and FDA guidelines and regulations
• Expertise in analytical methods and lab instrumentation (e.g. HPLC, GC, dissolution, wet chemistry)
• Demonstrated ability to perform method development and validation in accordance with ICH regulations with minimal supervision
• Excellent oral and written communication skills
• Strong organization, time management, leadership and troubleshooting skills
• Demonstrated ability to work as part of a cross-functional team
• Basic knowledge in Microsoft Word and Excel
• Experience with software associated with a Laboratory Information Management System (LIMS) and a Chromatography Data System (CDS)