at Baxter Healthcare Corporation in Round Lake, Illinois, United States
Job 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.
Your Role at Baxter
This is where your work saves lives.
The research we do and the products we develop improve outcomes for patients around the world. As a Manager of Research at Baxter, your work contributes directly to making a significant impact on others. We collaborate cross-functionally and lead by influence. As a key part of projects, our research and development team is responsible for delivering results to drive decisions and ensure safety of our existing and new products. We work on products that make a meaningful difference in others' lives. When you join Baxter, you'll use your analytical approach to identify risks and opportunities for innovation. Agile and willing to take action, you stay calm under pressure!
Your Team
While everyone at Baxter has a shared passion for our mission, the R&D teams play a meaningful role in our ability to save and sustain lives. Scientists and engineers in R&D work together to develop, test, sustain, and launch products that improve patient care. As a Research Associate III, you will be responsible for performing analytical testing with minimal assistance, demonstrating technical knowledge to troubleshoot problems and handle non-routine situations, assisting and mentor other team members, and embracing accountability for deliverables and leading team discussions/initiatives. While you will primarily support stability testing, you may also support new product development and/or sustaining product initiatives.
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.
What you'll be doing
Design and coordinate cGMP stability studies. Participate in the development of stability study protocols for new pharmaceutical products with speed, accuracy, and consistency to meet project timelines.
Coordinate activities of internal and external laboratories. Monitor stability study progress to ensure timely and effective completion.
Support Regulatory submissions by authoring and reviewing CTD sections for global dossiers.
Participate on project teams and/or interact with various functions within Baxter to provide technical support and assistance. Proactively provide guidance regarding study set-up specifications, processes and timelines.
Maintain knowledge of relevant Quality System Regulations, high level of expertise in current regulatory requirements and technical issues as related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities. Active participation in the generation, review, adoption and interpretation of such regulations.
Aid in exploring innovative approaches to processes and technologies. Responsible for identifying improvements in metrics and lead process improvements.
Maintain and own internal documents (protocols, reports, change control, presentations, etc.). Author, review, and revise Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet evolving requirements.
What you'll bring
Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with at least 10 years of experience or 5 years of experience with Masters.
Strong interpersonal skills and great attention to detail are necessary. Must be a strong team player with good problem solving, and excellent verbal and written communication skills. Must have the ability to encourage teamwork and drive decisions.
Must be able to handle multiple projects concurrently. Have knowledge of FDA Regulations and experience in the application of Good... For full info follow application link.
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
