Analytical Chemist I at NEPHRON SC, LLC

West Columbia, South Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

15 Sep, 26

Salary

0.0

Posted On

17 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Chemistry, cGMP, USP Standards, FT-IR, UV/Vis Spectroscopy, Wet Chemistry, HPLC, GC, Data Analysis, GDP, Laboratory Investigations, OOS Testing, SOP Documentation, Quality Control, Peer Review, Problem Solving

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 routine 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 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. 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. An understanding of cGMP regulations pertaining to laboratory controls and knowledge of USP standards. Ability to read, understand, review, and update Standard Operating Procedures, Forms, and Specifications and assist in designing new procedures as necessary under management guidance. Ability to perform testing for laboratory investigations for OOS and atypical QC test results under management guidance. Ability to effectively communicate within Chemistry Laboratory Staff and Management. Acknowledge and identify continuous improvement opportunities in all work activities. 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 0-3 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. Experience in more advanced techniques such as HPLC and GC is preferred. 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

Perform routine quality control testing on raw materials, in-process materials, and finished products using approved analytical methods. Ensure compliance with GDP and cGMP requirements while accurately documenting and interpreting laboratory data.