Analytical Chemist II

Nephron Pharmaceuticals Corporation; West Columbia (SC); On-site; USD 55,000 - 85,000; Full time

Job summary

Nephron Pharmaceuticals Corporation is seeking a Chemist to support quality control testing and R&D activities. The role involves conducting laboratory tests on raw materials, in-process materials, finished products, and stability samples using validated analytical methods.

Ideal candidates hold a BS or MS in Chemistry/ Biochemistry with 2–5 years of pharmaceutical QC/R&D experience and strong analytical skills aligned with cGMP standards. Safety and compliance are essential in daily operations.

Qualifications

• BS or MS in Chemistry, Biochemistry, or related field.
• 2-5 years of pharmaceutical experience preferred.
• Experience with FT-IR, UV/Vis spectroscopy, and wet chemistry techniques required.

Responsibilities

• Conduct routine and complex laboratory testing for raw materials, in-process materials, finished product, and stability samples.
• Perform testing using validated analytical methods and ensure compliance with GDP and cGMP requirements.
• Analyze and interpret data using specifications and test methods.
• Peer review notebooks and verify raw data to support sample release.
• Enter data into reporting systems and release forms accurately.
• Mentor and train chemists to support laboratory operations.
• Troubleshoot equipment and analyses as needed.
• Assist in investigation documentation.

Skills

Analytical thinking

Attention to detail

Communication skills

Problem-solving

Continuous improvement

Team collaboration

Education

BS or MS in Chemistry/Biochemistry or related field

Tools

FT-IR

UV/Vis spectroscopy

HPLC

GC

ICP testing

Job description

Job Purpose:

The purpose of this position is to support quality control testing and research and development activities as needed by conducting laboratory testing for raw materials, in-process materials, finished product, and stability samples in accordance with approved analytical methods.

Essential Duties and Responsibilities:

• Conduct routine and complex laboratory testing for raw materials, in-process materials and samples, finished product samples, and stability samples in accordance with approved analytical methods.
• Conduct and execute laboratory work and testing using best-practice analytical techniques and follow laboratory GDP and cGMP requirements
• Accurately analyze and interpret data using appropriate specifications and test methods.
• Accurately peer review notebooks and verify raw data to support sample release, including data generated in electronic software systems.
• Accurately enter data using appropriate reporting systems and release forms.
• Mentor and train Chemists as needed to support laboratory operations.
• Assist in troubleshooting equipment, analyses, etc.
• Support and contribute to investigation documentation, as needed.

Supplemental Functions:

• Relies on instructions and pre-established guidelines to perform job functions.
• Performs other similar duties as required.
• Works under supervision.

Requirements

Job Specifications and Qualifications:

Knowledge & Skills:

• Strong analytical skills, problem-solving ability, and attention to detail.
• Sound understanding of cGMP regulations pertaining to laboratory controls and thorough knowledge of USP and compendia standards.
• Ability to read, understand, review, and update Standard Operating Procedures, Forms, and Specifications and assist in designing new procedures as necessary independently, subject to management guidance.
• Ability to perform testing and lead root cause analysis for laboratory investigations for OOS and atypical QC test results, subject to management guidance.
• Ability to effectively communicate within Chemistry Laboratory Staff and Management, as well as other departments.
• Acknowledge and identify continuous improvement opportunities in all work activities. Initiate and follow through to implement, track, and achieve on-time completion of testing to support sample release to meet business needs and demands.
• Ability to effectively use a multitude of resources to perform job functions accurately.

Education/Experience:

• BS or MS in Chemistry, Biochemistry, or related field required with 2-5 years of pharmaceutical experience preferred. Experience outside of pharmaceuticals in chemistry quality control or R&D will be considered for the highly qualified candidate.
• Experience with conducting analysis by FT-IR, UV/Vis spectroscopy, and wet chemistry techniques is required.
• Highly skilled in advanced techniques such as HPLC, GC, and ICP testing, needing little or no guidance and supervision.

Working Conditions / Physical Requirements:

• This position requires bending, typing, lifting (up to 40 lbs.), standing, sitting and walking throughout the facility.
• This position encounters the following environmental factors: hazardous materials including HPLC solvents, chemical reagents, acids, and other non-specified hazardous materials that are project specific.
• This position requires safety glasses and other non-specified personal protective equipment to be worn as necessary.