Research Associate II at Baxter
Round Lake, Illinois, USA -
Full Time


Start Date

Immediate

Expiry Date

05 Aug, 25

Salary

80000.0

Posted On

06 May, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Sponsorship, Market Data, Legal Requirements, Chemicals, Materials

Industry

Pharmaceuticals

Description

THIS IS WHERE YOU SAVE AND SUSTAIN LIVES

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission.

PHYSICAL ACTIVITIES AND 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, and bacteria. This includes Penicillin, Cephalosporin, their related products and/or materials.
  • The individual must not be allergic to Penicillin, Cephalosporin, or their related products and/or materials.
    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 $80,000 - $110,000 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.
Responsibilities

WHAT YOU’LL BE DOING

  • 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 investigations. 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.
  • Use sophisticated laboratory instrumentation and computer systems to collect and record data.
  • May be required to be a system owner or conduct validations.
  • 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.
  • Support project teams and lead initiatives. Embrace accountability for critical decisions and deliverables within area of responsibility.
  • 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.
Loading...