Assoc Scientist II

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

Purpose of the job: We now have a vacancy for an analytical scientist with proven expertise in chromatographic and mass spectroscopic techniques, applied within a highly regulated environment. The successful candidate will have the responsibility of oversight of project related activity, managing key stakeholders and collaborating with a multidisciplinary team of subject matter experts to develop, execute and summarize the E&L strategy within global regulatory dossiers for Baxter’s Pharma Injectables Business. The data generated plays a pivotal role in demonstrating the safety of the materials used to manufacture, package and deliver drug products within the Baxter’s Pharma injectables portfolio. It will be a hybrid role with majority of desk work and some lab work.

Job Description:

• Execution of a diverse range of E&L projects of high complexity for Baxter’s Pharma Injectables segment 

• Application of practical and theoretical expertise in chromatographic (GC and LC), spectroscopic and mass spectrometry techniques  

• Development and execution of non-routine experimental protocols 

• Interface with internal partners to interpret complex analytical data; including quantitation, structural elucidation and toxicological assessment 

• Authoring/Reviewing of a variety of technical reports, protocols, and regulatory dossiers 

• Data management and organization 

• End-to-end E&L ownership of injectable projects from feasibility to approval stage. 

Skill Set and Qualifications:

Key candidate should have good learning agility, good scientific understanding and communication, responsible and ready to step out of comfort zone to get things completed on time 

• Hands-on Experience in Protocol & report writing  

• Good technical and scientific writing skills 

• Good understanding of Chromatographic Analytical principles and GC-MS/LC-MS/ICP-MS instrumentation principles   

• Experience/understanding in E&L Studies, preferably of Injectables  

• Good learning agility 

• Self-initiative to complete tasks within the stipulated time by being resourceful and proactive in collaboration with CFTs.    

• Good organization and Planning skills   

• Qualification – M.S/M.Pharm/P.hd with approximate 5-8 Years of relevant experience  

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.

Reasonable Accommodations

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