Research Scientist I

• 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.
• May act as a study director for studies, supervisor for testing exceptions and owner for laboratory investigation. Independently evaluate results and impact to studies/laboratory.
• May provide training and supervision to junior members within the laboratory. Routinely provide advice and assistance to team members regarding unique problems.
• Perform review of test data, which includes overall documentation practices. Perform review functions in LIMS or other computerized systems. 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.
• Influence program, project and/or functional leadership and cross-functional teams.
• Proposes and drives solutions to complex technical problems in area of expertise. Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot instrumentation.

• Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with at least 5+ years' experience or 3+ years' experience with a Masters degree.
• Analytical chemistry instrumentation experience (e.g. HPLC, UPLC, pH, KF, etc) and MS experience is preferred.
• Must have HPLC/UPLC/UHPLC experience in a regulated environment and strong technical problem-solving skills.

• Experience with Biosimilars and associated analytical techniques is desired
• Electronic Lab Notebook experience is preferred.
• Pharmaceutical GMP laboratory experience is desired.
• Empower experience required. Custom fields experience is desired.
• Stability study execution and/or method validation experience is desired.
• Must demonstrate effectiveness in ability to train others, leadership, organization, teamwork/interpersonal skills, results orientation, and task completion.
• Must be able to handle multiple tasks concurrently and in a timely fashion.
• Possess relevant laboratory/technical, writing, and computer skills.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $96,000 - $132,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.