Research associate - chromatography
at Baxter
Braine-l'Alleud, Wallonie, Belgium -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 31 Jan, 2025 | Not Specified | 01 Nov, 2024 | 5 year(s) or above | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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.
Join Baxter, a global leader in healthcare solutions, as a Research Scientist in Gas and Liquid Chromatography. Contribute to our mission of saving and sustaining lives through the development of essential medical products.
Responsibilities:
As a Research Scientist in Gas and Liquid Chromatography at Baxter, you will collect information required for the analytical target profile from project stakeholders, propose and test candidate analytical techniques, and develop robust and efficient analytical methods using modern and state-of-the-art statistical approaches. You will collect data from development, make decisions and propose solutions based on obtained results, and prepare support and present development status in technical team review meetings.
You will assure that complex technical data are reported with scientific excellence and communicate the outcome of the analytical activity conducted to team, supervisor, and customer. You will understand and master all regulations requirements pertaining to analytical method performance and contribute to analytical method validation/co-validation/transfer both internally and with CRO.
You will design complex study designs and write associated Quality documents (protocols, reports, procedures), document results in laboratory notebooks according to established GDP procedures, and advise supervision and customer when facing issues and propose options to meet timelines or define new timelines when facing issues. You will mentor junior team members on method development and validation aspects, participate in method comparability/equivalence studies to enable the continuation of the analytical method lifecycle, and effectively coordinate and track the progress of multiple analytical related projects and activities.
You will interact with cross-functional teams of analytical experts, internally and externally, and effectively communicate risks, issues, and opportunities to supervisor and customer.
Finally you will collaborate on investigations of complex analytical issues, demonstrating critical thinking skills to find solutions for the business above functional considerations, lead by exemplifying the Baxter Culture Levers (Collaboration, Courage, Simplicity, Speed) and enforce to quality system requirements and general and specific environmental, health, and safety guidelines.
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Braine-l'Alleud, Belgium