Raw Materials Chemist I

LANNETT COMPANY, INC; Seymour (IN); On-site; USD 55,000 - 75,000; Full time

Job summary

LANNETT COMPANY, INC in Seymour, IN is seeking an analytical chemist to perform testing of raw materials, packaging materials and in-process samples for drug products. The role includes documenting results, peer reviewing data, and working within cGMP guidelines in a laboratory setting.

Responsibilities include operating standard lab equipment, performing titrations and Karl Fischer analysis, and maintaining quality notebooks.

Qualifications

• BS Degree in Chemistry or related field required.
• AS Degree in Chemistry or related field with 2+ years pharma experience.
• BS in non-science with 4+ years pharma experience.
• Knowledge of cGMP, USP/NF, and FDA guidelines.
• Experience with analytical methods and lab instrumentation.
• Excellent oral and written communication skills.
• Strong organization and time management.
• Cross-functional teamwork experience.
• Proficiency with Word/Excel; LIMS software familiarity.

Responsibilities

• Perform accurate and timely analysis of raw materials, packaging, or in-process samples per procedures and safety guidelines.
• Test using basic lab equipment (pH, Loss on Drying, Karl Fischer, Residue on Ignition, titrations).
• Document all laboratory testing and maintain notebooks/records clearly.
• Peer review data, reports, and notebooks.
• Assist with other projects and duties as assigned.

Skills

Communication

Organization

Teamwork

Lab procedures

Documentation

Education

BS in Chemistry or related field

AS in Chemistry or related field

BS in non-science field

Tools

LIMS

Microsoft Word

Microsoft Excel

pH meters

Titration

Job description

Description

Job Summary

This position is primarily responsible for the laboratory testing of raw materials and packaging materials or in-process, release and stability samples for commercial drug products.

Responsibilities:

Perform accurate and timely analysis of raw materials and packaging materials or in-process, release and stability samples for drug products according to current analytical procedures, SOPs, laboratory guidelines and safety requirements.

Testing performed to include basic lab equipment and procedures, such as pH, Loss on Drying, Residue on Ignition, Water Content by Karl Fischer, wet chemistry techniques such as titrations.

Document all laboratory testing and maintain accurate and legible notebooks and records.

Peer review of data, reports and notebooks.

Other projects and duties as assigned.

Experience/Education Requirements:

BS Degree in Chemistry or related field

AS Degree in Chemistry or related field and a minimum of 2 years of pharmaceutical experience in a cGMP-regulated environment

BS Degree in non-science field and a minimum of 4 years of pharmaceutical experience in a cGMP-regulated environment

Knowledge of cGMP, USP/NF, and FDA guidelines and regulations

Experience in analytical methods and lab instrumentation (e.g. pH, ovens, titrations)

Excellent oral and written communication skills

Strong organization and time management skills

Demonstrated ability to work as part of a cross-functional team

Working knowledge of Microsoft Word and Excel

Experience with software associated with a Laboratory Information Management System (LIMS)

Work mainly performed in lab

Stand for extended periods of time in a laboratory setting

Wear Personal Protective Equipment (PPE) as needed

Work with hazardous chemicals as needed to complete laboratory testing