*RandD Chemist I - Weekend Shift (Fri.-Sun. - 7:00amto7:00pm *andMon. -8:00am to 12:00pm)

[**Corporate Statement

Nephron Pharmaceuticals Corporation is a privately owned global leader in the manufacturing of generic drug products, over-the-counter (OTC) drug products and medical devices. Nephrons products are sterile, preservative and additive free and proudly made in the USA! We are headquartered in West Columbia, South Carolina, with additional distribution centers in Kentucky and Arizona. Our location provides the ability to develop new devices and medications including respiratory therapies, ophthalmics, and injectables, for in-house or contract manufacturing opportunities. The facility utilizes completely automated manufacturing, packaging, and distribution systems, in addition to high volume and redundant utility systems, to ensure production system availability. Nephron specializes in Blow-Fill-Seal (BFS)manufacturing, a niche technology that allows a vial of medication to be formed, filled and sealed in a continuous process, in a sterile, enclosed environment and without human intervention.

[As an industry leader in product safety and quality, Nephron produces a variety of inhalation solutions, and has distributed over 1 billion doses of respiratory medication per year since 2009. Nephron is currently working on research and development projects that include over 50 new products. The companys longstanding relationships with major drug wholesalers allow us to distribute our products to retail pharmacies, mail order pharmacies, hospitals, home care companies, and long term care facilities. Nephron has a sales force that covers all fifty states and Puerto Rico, with additional sales channels throughout South America, the Middle East, and Europe. Nephron exists to provide top-quality, affordable medications to everyone.

[* Position Summary:]{open="" sans",sans-serif"=""}]{open="" sans",sans-serif"=""}]{open="" sans",sans-serif"=""}*

• Perform research and development projects for established products and new products including but not limited to analytical test method validation/transfer/verifi cation, deformulation, procedures, investigations, and other non-specified projects or initiatives.
• Plans, organizes, and manages resources on projects to assure technical quality and schedule adherence
• Performs other duties as assigned or apparent

[*Primary Accountabilities: *]{open="" sans",sans-serif"=""}

Capable of working in a GMP environment and responsible for generating GMP data.

Capable of working with different analytical techniques including but not limited to HPLC, UPLC, GC, Automatic Titrator, IR, DSC, ICP, and Mass Spectrometry.

Responsible for performing different analytical tests for RandD and QC as needed.

Responsible for executing research and development projects for established products and new product development with respect to formulation, laboratory investigations, and early process development.

Responsible for evaluating new raw materials and components for quality and safety prior to implementation into exhibit batches and GMP production.

Responsible for conducting the development and validation of analytical methods for pharmaceutical ingredients and dosage forms, including establishment of specifications.

Assist in drafting RandD and QC protocols and report.