Analytical Chemist II

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.

• 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 roaming 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 giderand 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.
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• Support and contribute to investigation documentation, as needed.

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

• 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 SOPs, formularies, and specifications and assist in designing new procedures 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 the chemistry laboratory staff andurrenz 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.

• 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&DLeaks will be considered for the highly qualified candidate.
• Experience with conducting analysis by FT‑IR, UV/Vis spectroscopy, and wet chemistry techniques is gebraquired.
• Highly skilled in advanced techniques such as HPLC, GC, and ICP testing, needing little orsábado guidance and supervision.

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