Scientific Research Associate II (Chemist)

Job Details

Immediate opportunity for a Scientific Research Associate II with experience running LCMS or related instrumentation (HPLC/UPLC). This position is responsible for analytical testing, validation/verification, and/or transfer of test method supporting Pharmaceuticals parenteral products. Work will primarily support new product development and sustaining product initiatives and will conduct research and design experiments with minimal assistance.

Schedule/Shift: 1st shift, Mon.-Fri.

Position Type: Contract positions for 8 mos. (through 12/31/24) with potential to extend.

Essential Duties and Responsibilities:

• Conduct critical chemical, and physical analyses on finished product stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or department projects. Work under minimum supervision.
• Perform review of test data, which includes overall documentation practices.
• Use sophisticated laboratory instrumentation and computer systems to collect and record data (LCMS system).
• Perform advanced chemical assays requiring precise analytical skills and understanding of chemistry principles.
• Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules
• Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.
• Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support.
• Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot basic instrument problems

Qualifications:

• Bachelor s degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with analytical chemistry laboratory coursework and at least one (1) to two (2) years of experience OR advanced degree in Chemistry
• Analytical chemistry instrumentation experience (e.g. HPLC, UPLC, UHPLC, Mass Spectrometry)
• Pharmaceutical GMP laboratory experience is desired
• Residue analysis experience by LC-MS/MS is desired
• Must have good oral and written communication skills, strong analytical skills and be detail oriented.
• Proficient in advanced wet chemistry, volumetric preparation techniques and instrumental methods of analysis
• Must demonstrate effectiveness in organization, teamwork/interpersonal skills, results orientation, and task completion
• Must be able to handle multiple tasks concurrently and in a timely fashion
• Possess writing and computer skills
• Must communicate effectively with managers, peers, and subordinates.
• Interpret available information and make recommendation to resolve technical challenges

Physical Requirements:

• Must be able to hand write and use computers for the majority of the work day
• Must be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testing
• May require standing for extended periods
• Must be able to lift up to 10 pounds routinely
• This work is subject to hazards including exposure to chemicals, drug products.

 Randstad Life Sciences US

 05/12/2024

 Round Lake,IL