Analytical Chemist II at NEPHRON SC, LLC

West Columbia, South Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

14 Apr, 26

Salary

0.0

Posted On

14 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Skills, Problem-Solving, Attention To Detail, cGMP Regulations, USP Standards, Standard Operating Procedures, Root Cause Analysis, Communication, Continuous Improvement, Data Analysis, Mentoring, Laboratory Testing, HPLC, GC, FT-IR, UV/Vis Spectroscopy, Wet Chemistry

Industry

Pharmaceutical Manufacturing

Description

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. 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.

Responsibilities

Conduct laboratory testing for raw materials, in-process materials, finished products, and stability samples according to approved analytical methods. Mentor and train Chemists while ensuring compliance with laboratory GDP and cGMP requirements.