Analytical Chemist II

Bureau Veritas•Indianapolis, IN

5d•$28 - $31•Onsite

About The Position

The Analytical Chemist is responsible for supporting the oligonucleotide analysis portfolio and delivering analytical quality management. This role will utilize a variety of analytical instruments including AKTA, LC-MS, HPLC/UPLC, LTQ, QDA, CAD, Circular Dichroism, Karl Fischer titration, UV-vis/Fluorescence spectrophotometer, TFF, thermal cycler, Nanodrop, SoloVPE, along with automation integration systems on a routine basis.

Requirements

Bachelor's Degree in Chemistry and Analytical Chemistry or closely related fields
Minimum of three (3) years of experience
Strong laboratory skills and experience with analytical instrumentation such as AKTA, Agilent LC-MS and UPLC, Vanquish LTQ, Water’s QDA, etc.
Experience in developing new chromatographic methods (IEX/RP-HPLC, SPE, LC-MS).
Pay attention to details, conduct thorough quality checks throughout the experiment, and proactively identify any inconsistencies as well as implementing corrective actions.
Strong attention to details, organizational skills
Strong written and oral communication skills
Confident, execution-focused, and team oriented with a desire to thrive in a fast-paced growing environment
Written and verbal communication skills including the ability to communicate effectively in a group setting, with colleagues and clients
Ability to perform multiple tasks
Ability to organize and prioritize workload to meet or exceed deadlines
Individual and Team work ethic
Proficiency with Windows, Word & Excel & PowerPoint
Positive attitude, self-motivated, high level of engagement
Champions company values including team engagement

Nice To Haves

An equivalent combination of education and experience may be accepted in lieu of above.

Responsibilities

Perform chemical stability and accelerated stability evaluation of samples over an extended period using established procedures.
Perform precise and accurate sample preparation, including weighing, diluting, extracting, and purifying samples for various analytical techniques.
Develop, validate, and document standard operating procedures for sample handling, ensuring consistency and repeatability in all preparation activities.
Maintain detailed records and logs of all sample preparation steps, calculations and observations, supporting data integrity and traceability.
Collect, record and organize experimental data, conduct basic analyses to interpret results and support ongoing laboratory research.
Develop, adapt and improve laboratory protocols, including but not limited to sample preparation, mobile phase preparation, sample quality control, chemical stability and accelerated stability evaluation, to support consistent and reliable qualification and quantitation of target analytes.
Use of general laboratory equipment including but not limited to single/multichannel pipettors, centrifuges, incubators, biological safety cabinets, and analytical balances.
Follow instruction and perform instrumental analysis on instruments including but not limited to AKTA, LC-MS, HPLC/UPLC, LTQ, QDA, CAD, Circular Dichroism, Karl Fischer titration, UV-vis/ Fluorescence spectrophotometers, thermal cycler, Nanodrop, SoloVPE instruments, etc. Provide basic troubleshooting to mentioned instrument.
Work closely with members of the RNAi chemistry team to understand and validate requirements for oligonucleotide analytical control.
Hands-on and independent lab experience with concentration calculation and unit conversion, buffer preparation, solution preparation, separation, quantification of DNA/RNA, oligonucleotides, etc.
Detailed record keeping of daily experiments in ELNs.
General lab maintenance and Inventory management.
Coordinate with third-party vendors to schedule PM, provide assistance for onsite engineers and follow up with the updates.
Follow the guidelines set forth with clients and Company Quality, Health, Safety, Security and Environmental policies and procedures.
Comply with clients’ and Company management systems in accordance with appropriate regulatory agencies.
Perform other essential tasks projects and responsibilities as required.
Follows guidelines set forth by clients and in the company Quality, Health, Safety and Environmental policies and procedures.
Other duties as defined by Manager, department needs and workload.