Manager, Research
Overview
This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives.
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Support for Parents
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Continuing Education/ Professional Development
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Employee Heath & Well-Being Benefits
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Paid Time Off
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2 Days a Year to Volunteer
Success Profile
What makes a successful Research and Development team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.
- Courage
- Action Oriented
- Collaborates
- Cultivates Innovation
- Manages Ambiguity
- Drives Results
Manager, Research
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.
Your Role at Baxter
This is where your work saves lives.
Join Baxter as a Manager of Research and contribute to groundbreaking advancements in healthcare! In this role, you'll lead a team of researchers, design and coordinate cGMP stability studies, and collaborate cross-functionally to drive decisions and ensure the safety of our products. Your work will directly impact patients worldwide, making a meaningful difference in their lives.
What you'll be doing::
Managing a team of researchers
Designing and coordinating cGMP stability studies
Coordinating activities of internal and external laboratories
Supporting regulatory submissions by authoring and reviewing CTD sections for global dossiers
Participating on project teams and providing technical support and assistance
Maintaining knowledge of relevant Quality System Regulations and ensuring compliance in all research activities
Exploring innovative approaches to processes and technologies, and identifying improvements in metrics and leading process improvements
Maintaining and owning internal documents, authoring, reviewing, and revising Standard Operating Procedures (SOPs)
What you'll bring:
Bachelor's degree in a relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with 8+ years of experience or 5+ years of experience with a Master's degree
Experience managing or leading a team of researchers
Experience designing and coordinating cGMP stability studies
Strong interpersonal skills, attention to detail, and excellent verbal and written communication skills
Ability to handle multiple projects concurrently and knowledge of FDA Regulations
Experience in the application of Good Manufacturing Practices and familiarity with Laboratory Information Management Systems (LIMS) and statistical tools used for evaluating data trending.
Join us at Baxter and make a significant impact on the lives of patients around the world!
Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.
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 our employees, and we strive to be more transparent with our pay practices. To that end, this position has a base salary range of $120,000 to $165,000 plus an annual incentive bonus. The above range represents the expected base salary range for this position. The actual salary may vary based upon several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location.
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Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
EEO is the Law
EEO is the law - Poster Supplement
Pay Transparency Policy
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
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