Analytical Services Chemist III

LANNETT COMPANY, INC; Seymour (IN); On-site; USD 65,000 - 95,000; Full time

Job summary

LANNETT COMPANY, INC in Indiana is seeking a chemist to perform and supervise laboratory testing of raw materials, in-process and finished drug products for development and release under cGMP.

You will develop and validate analytical methods (HPLC, GC, dissolution) per ICH/FDA/USP and train team members on instruments, ensuring accurate documentation and regulatory compliance.

Qualifications

• BS degree in Chemistry or related field; 4–8 years pharma QA analysis in cGMP lab.
• Experience with analytical instrumentation and method validation per ICH/FDA.
• Strong written and oral communication; ability to work in cross-functional teams.

Responsibilities

• Perform routine and non-routine physical and chemical tests on materials and products.
• Conduct tests with pH, Loss on Drying, Karl Fischer, HPLC, GC, dissolution.
• Develop analytical methods for test according to ICH/FDA/USP; transfer methods.
• Validate cleaning validation methods and test cleaning validation samples.
• Document results and maintain notebooks; peer review data.
• Provide progress updates; comply with regulatory requirements.
• Train team members on instruments and methods.
• Mentor junior chemists; support instrument purchases.

Skills

Pharma lab exp

cGMP knowledge

Analytical methods

HPLC/GC/Dissolution

Method development

ICH validation

Communication skills

Organizational skills

Cross-functional teamwork

LIMS/CDS experience

MS Office basics

Education

BS in Chemistry or related

Job description

Description

Summary

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

Requirements

Experience

• BS Degree in Chemistry or related field and 4 – 8 years of pharmaceutical product analysis experience in a cGMP-regulated lab environment

Skills

• 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)