Qureos Mentor

Baxter

<div>This is where your work makes a difference.
At Baxter, we believe every person&mdash;regardless of who they are or where they are from&mdash;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&mdash;you will find purpose and pride.
Sat&#305;&#351; temsilcisi kendi sorumlu&#287;undaki &uuml;nite veya b&ouml;lgedeki b&uuml;t&uuml;n sat&#305;&#351; hedeflerinden ve sonu&ccedil;lar&#305;ndan sorumludur, bunlara ula&#351;&#305;rken &#351;irketin de&#287;erleri ile hareket edecektir.
Hedefler ve sonu&ccedil;lar k&#305;sm&#305;nda cirolar, karl&#305;l&#305;k rakamlar&#305;, sat&#305;&#351;&#305;n d&ouml;n&uuml;&#351; h&#305;z&#305;, adet, &ouml;deme vadesi gibi parametrelerden sorumludur.
Tak&#305;m &ccedil;al&#305;&#351;mas&#305;na uygun davran&#305;&#351;lar sergiler ve &uuml;r&uuml;n bilgiseviyesini artt&#305;rmak i&ccedil;in e&#287;itim kaynaklar&#305;n&#305; etkili kullan&#305;r.
Ameliyathanede &uuml;r&uuml;n uygulama deste&#287;i verir, sa&#287;l&#305;k profesiyonellerine periyodik olarak &uuml;r&uuml;n haz&#305;rl&#305;k ve uygulama e&#287;itimleri verir.
Sa&#287;lik bakanl&#305;&#287;&#305; taraf&#305;ndan onayl&#305; SDE, KDE ve &Uuml;TS belgeleri olmal&#305;d&#305;r.<h3 class="jobSectionHeader">
ESSENTIAL DUTIES AND RESPONSIBILITIES (TEMEL G&Ouml;REV VE SORUMLULUKLAR)</h3><ul><li>
Advanced Surgery i&#351; plan&#305;nda yer alan ve b&ouml;lgesel/&uuml;nite seviyesindeki t&uuml;m y&#305;ll&#305;k ve &ccedil;eyrek d&ouml;nem hedeflerin ger&ccedil;ekle&#351;tirilmesinden sorumludur.</li><li>
B&ouml;lgesel olarak y&#305;ll&#305;k ve uzun d&ouml;nemli pazarlama politika ve stratejilerinin olu&#351;turulmas&#305;na katk&#305;da bulunur. B&ouml;lge pazar&#305;n&#305; b&uuml;y&uuml;tmeye y&ouml;nelik faaliyetler ger&ccedil;ekle&#351;tirir.</li><li>
B&ouml;lgedeki pazarlama ve sat&#305;&#351; faaliyetlerini Sat&#305;&#351; M&uuml;d&uuml;r&uuml;'ne rapor ederek etkin olarak uygular.</li><li>
B&ouml;lgesinde bulunan &uuml;nitelerde ihaleleri takip eder, merkeze bildirir ve &#351;irketimizin i&#351;tiraki i&ccedil;in gerekli deste&#287;i verir, &ouml;deme s&uuml;re&ccedil;lerinin takip eder.</li><li>
&Uuml;r&uuml;nlerle ilgili bireysel e&#287;itim ihtiyac&#305;n&#305; kar&#351;&#305;layacak d&ouml;k&uuml;manlar&#305; &#351;irket i&ccedil;i kaynaklardan temin eder, ihtiyaca y&ouml;nelik olarak tak&#305;m arkada&#351;lar&#305;yla payla&#351;&#305;r.</li><li>
Sat&#305;&#351; karl&#305;l&#305;k ve pazar pay&#305; hedeflerinin ger&ccedil;ekle&#351;tirilmesini sa&#287;lamak amac&#305;yla pazarlama planlar&#305; do&#287;rultusunda strateji ve taktikleri uygulamak, sorumlu oldu&#287;u &uuml;nite sat&#305;&#351; hedeflerine ula&#351;mak, sat&#305;&#351; tahmini, sat&#305;&#351; ve tan&#305;t&#305;m b&uuml;t&ccedil;esi, pazar ve rakip faaliyetleri konusunda Sat&#305;&#351; ve Pazarlama M&uuml;d&uuml;r&uuml;'ne geribildirimde bulunur.</li><li>
Sat&#305;&#351; ve Pazarlama M&uuml;d&uuml;r&uuml;, ilgili &Uuml;r&uuml;n M&uuml;d&uuml;r&uuml; ve Medikal M&uuml;d&uuml;r ile koordineli &ccedil;al&#305;&#351;arak m&uuml;&#351;terilere teknik/klinik/bilimsel destek sa&#287;lar. Ameliyathanede &uuml;r&uuml;nlerin uygulamal&#305; olarak e&#287;itimini verir ve sa&#287;l&#305;k profesiyonellerinin do&#287;ru bir &#351;ekilde &uuml;r&uuml;nlerimizi uygulamas&#305;ndan sorumludur.</li><li>
Kurulu&#351;umuzun ortak de&#287;erleri do&#287;rultusunda m&uuml;&#351;terilere kaliteli ve &uuml;st&uuml;n hizmet sunmak ve m&uuml;&#351;teri &#351;ikayetlerini asgariye indirir.</li><li>
Sorumlu oldu&#287;u &uuml;nitelerde,Sat&#305;&#351; M&uuml;d&uuml;r&uuml; ile koordineli olarak Fikir Liderleri ile olan ili&#351;kileri y&uuml;r&uuml;t&uuml;r.</li><li>
Merkezde y&uuml;r&uuml;t&uuml;len pazarlama planlar&#305; ya da spesifik pazarlama projelerinin b&ouml;lge temsilcisi olur, kendi sahas&#305;nda gerekli durumlarda, ihtiyaca ve &ccedil;&ouml;z&uuml;me y&ouml;nelik projeler &uuml;retir, konu ile ilgili sahada ara&#351;t&#305;rma yapar ve ilgili &#304;&#351; Birim M&uuml;d&uuml;r&uuml;, &Uuml;r&uuml;n M&uuml;d&uuml;r&uuml;&rsquo;ne girdi sa&#287;lar.</li><li>
&#350;irketin M&uuml;&#351;teri Boost vb. Gibi m&uuml;&#351;teri ili&#351;kileri sistemlerini kullan&#305;r ve i&ccedil;erik sa&#287;lar.</li></ul><h3 class="jobSectionHeader"> 
JOB REQUIREMENTS (N&#304;TEL&#304;KLER)</h3><ul><li>
&Uuml;niversitelerin ilgili b&ouml;l&uuml;mlerinden mezun</li><li>
&#304;yi derecede &#304;ngilizce bilgisi</li><li>
En az 4 y&#305;l sat&#305;&#351; tecr&uuml;besi (tercihen ila&ccedil;, sa&#287;l&#305;k ve medikal cihaz sekt&ouml;r&uuml;)</li><li>
Tak&#305;m &ccedil;al&#305;&#351;mas&#305;na uyumlu ve farkl&#305; g&ouml;revleri &uuml;stlenebilen</li><li>
G&uuml;&ccedil;l&uuml; ileti&#351;im ve sunum becerilerine sonu&ccedil; odakl&#305; m&uuml;zakere yetene&#287;ine sahip,analitik d&uuml;&#351;&uuml;nme yetene&#287;ine sahip olmak</li><li>
Seyahat engel durumu bulunmayan</li><li>
MS Office programlar&#305;na hakim</li><li>
Aktif olarak ara&ccedil; kullanmak</li></ul>
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 
 
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.</div>

Sales Representative-Ankara

<div>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&mdash;where your purpose accelerates our mission. 
At Baxter, we are driven by our mission to save and sustain lives. Our portfolio of essential medical products touches millions of lives every day across hospitals and healthcare systems worldwide. As we grow in the dynamic META region, we are looking for a strategic and collaborative leader to help shape healthcare policy, improve patient access, and drive sustainable reimbursement models across diverse healthcare systems. 
The META Government Affairs &amp; Reimbursement Head will lead and execute public affairs, health policy, and reimbursement strategies across the Middle East and Africa. This role is critical in shaping an enabling policy environment, fostering strong relationships with government stakeholders, and ensuring patient access to Baxter&rsquo;s innovative therapies and technologies. 
Essential duties and responsibilities 
Government Affairs &amp; Policy Advocacy<div><ul><li> 
Develop and execute a cohesive government affairs strategy for the META region aligned with global and regional business objectives.</li><li>Establish and maintain trusted relationships with key policymakers, regulatory authorities, health ministries, and trade associations.</li><li>Monitor and influence public policy developments affecting the healthcare, medtech, and reimbursement landscape.</li><li>Lead Baxter&rsquo;s representation in policy dialogues, multi-stakeholder forums, and public-private partnerships.</li></ul> 

Reimbursement &amp; Market Access</div><div><ul><li> 
Collaborate cross-functionally with regional market access, pricing, medical, and commercial teams to develop and implement reimbursement strategies.</li><li>Drive evidence generation and health economics initiatives to support the value proposition of Baxter&rsquo;s products.</li><li>Work with local teams to shape payer engagement, funding pathways, and successful health technology assessments (HTA) or reimbursement submissions.</li><li>Identify and pursue innovative access solutions tailored to each country&rsquo;s healthcare financing model.</li></ul></div> 
Strategic Leadership &amp; Alignment<div><ul><li> 
Serve as a trusted advisor to the META leadership team on public affairs and market access matters.</li><li>Lead a team of market access/government affairs professionals in select META countries.</li><li>Build internal capabilities and ensure best practices are shared across the region.</li><li>Collaborate with related counterparts to align strategies and ensure cohesive execution.</li></ul></div> 
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 
 
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.</div>

META Government Affairs and Reimbursement Senior Manager

<div>This is where your work makes a difference.
At Baxter, we believe every person&mdash;regardless of who they are or where they are from&mdash;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&mdash;you will find purpose and pride.
Summary:
This Research Associate-I position will act as a formulation scientist in the development of new or support of existing products. This position will also provide support for formulation/stability testing with Baxter external partners.
Essential Duties and Responsibilities:
Product Development:<ul><li>
To conduct development trials as per requirement.</li><li>
To compile &amp; evaluate the development &amp; stability data.</li><li>
To ensure development trails to be performed as per Quality by Design (QBD) approach.</li><li>
To prepare the technical documents e.g., Master Formula Record (MFR), Product Development Report (PDR), Product Development Lifecycle Management (PDLM) documents, Protocols &amp; Reports.</li><li>
To provide required information for meetings with cross functional teams like Analytical, Regulatory, PSM, Product Quality, manufacturing, Contract Manufacturing Organization (CMO), Project management for on time project delivery.</li><li>
To provide required information for meetings with Contract Manufacturing Organizations (CMO), Contract Research Organizations (CRO) &amp; contract Labs for on time project delivery.</li><li>
To support the execution of stability batches in Baxter sites &amp; CMOs.</li><li>
To support process validation and commercial batches.</li><li>
To provide support for successful technology transfer of drug products at manufacturing plant &amp; Contract Manufacturing Sites.</li><li>
To review engineering batch &amp; stability batch documents.</li><li>
To collect the Stability batch data and review for trending and conduct review of artworks.</li><li>
To support sub-department manager to review the technology transfer documents for products developed by CRO &amp; assess the documents which are in-line with QBD based approach &amp; as per current regulatory requirement.</li><li>
To perform the required activities for remediation projects to fulfill the regulatory commitments for Out of Specification or Project Change Control Notes or Corrective and Preventive Action or product nature and criticality.</li><li>
To perform the required activities to fulfil the regulatory submission &amp; query requirements.</li><li>
To prepare the reports to be provided for regulatory response.</li><li>
To handle trouble shooting during exhibit and commercial batches with an ability to investigate any Out of Specification (OOS) or Out of Trend (OOT) results.</li><li>
To interact with the plant team and impart new product introduction prior to start of production.</li><li>
To support External and Internal regulatory audits with respect to Manufacturing Process.</li><li>
To support market complaint related activities.</li><li>
To possess and be updated on product submission and knowledge in regulatory market, current guidelines i.e. ICH (International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use), US-FDA (United States Food and Drug Administration), MHRA (Medicines and Healthcare products Regulatory Agency), EMEA (European Medicines Agency) etc.</li><li>
To identify &amp; make available the necessary required resources or infrastructure or instruments to carry-out the day-to-day functions and ensure entire documentation related to formulation development &amp; execution of batch.</li><li>
To assist Sub-department Manager &amp; Department Head in investigation for complaints and deviations. To analyze investigation, to suggest any further actions required, to conclude root cause and to seek approval of Corrective and Preventive Action (CAPA) from Department Head.</li><li>
To prepare change control and ensure timely closure of the same.</li><li>
To ensure compliance related to Lab equipment, instruments, documentation &amp; warehouse.</li><li>
To prepare and update SOPs and send for further review of Sub-department Manager &amp; approval of Department Head.</li><li>
To document experiments in Electronic Lab Notebook (ELN).</li><li>
To identify &amp; request for New Equipment's or instruments for projects in upcoming portfolio &amp; continuous improvement of Development Lab.</li><li>
To adopt &amp; follow the Global Quality procedures.</li><li>
To identify the safety hazards &amp; perform the Hazard Identification Risk Assessment (HIRA) in coordinates with EHS (Environmental health and safety) practices at place.</li></ul>
Administrative:<ul><li>
To work collaboratively in cross-functional teams.</li><li>
To liaise with customers, staff and suppliers for material procurement or query related or any other work.</li><li>
To review the entries in logbooks.</li><li>
In the absence of Executive, Sub-department Manager will ensure these roles and responsibilities.</li></ul>
Authorities for rejections or approval:<ul><li>
To hold the projects due to lack of resources as per guidance by Sub-department Manager.</li><li>
To take decision for non-compliance results as per guidance of Sub-department Manager.</li></ul>
Communication to the management / superiors:<ul><li>
To communicate with sourcing team if any information requires from suppliers.</li><li>
To communicate with cross functional team if any information required for product development.</li><li>
To communicate about any failure or abnormal notification or non-compliance results to Sub-department Manager &amp; Department Head for their attention and seeking for the solution.</li><li>
To communicate project related issues to Sub-department Manager and implement action plan under the guidance of Sub-department Manager.</li></ul>
Qualifications:<ul><li>
M.S. (Pharm.)/M. Pharm/PhD in Pharmaceutics</li><li>
1 - 8 Years of experience in formulation &amp; development of injectable drug products.</li></ul><ul><li>
Writing and computer skills relevant to recording original data as well as creating protocols, reports, and presentations to communicate with partners and team members.</li><li>
The ability to energetically attack a problem and synthesize the results into a clear and logical summary in a timely manner is critical.</li><li>
Subject matter expertise in areas associated with modern formulation instrumentation. Ability to learn and master new development strategies and develop new methods where appropriate.</li><li>
Communication skills to build relationships across functional and geographical boundaries and present technical concepts to technical and non-technical teams.</li><li>
Comfort with risk and ambiguity, ability to negotiate critical timelines for analysis in emergency situations.</li></ul><ul><li>
Personal responsibility and independent ownership of analysis and results.</li><li>
Preferred to have experience with leading large projects and formulation development and technology transfer.</li><li>
A good understanding of ICH and cGxP practice.</li><li>
Experience in working in global cross-functional teams and project management is a plus.</li><li>
Quality oriented.</li><li>
Ability to adapt to changes and to work in a team environment as well as delegate effectively to junior team members.</li></ul>
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 
 
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.</div>

Associate Scientist I, R&D - F&D

<div>This is where your work makes a difference.
At Baxter, we believe every person&mdash;regardless of who they are or where they are from&mdash;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&mdash;you will find purpose and pride.
Summary:
Support the Extractables and Leachables scientific excellence of the Ahmedabad R&amp;D. As a scientist on this team, use state-of-the-art technology (LC-MS, GC-MS, GC, UV, LC, IC, ICP-MS, ICP-OES) to solve complex analytical problems &amp; investigations, including Structure Elucidation. Ensure technical capabilities and expertise are aligned with business needs to sustain products, support development of new products, contribute to investigations, and drive specific innovation initiatives to position the organization for the future. Collaborate with Team Lead and global subject matter experts to meet the needs of partners across Baxter&rsquo;s Global Business Units. Ensure Quality culture and compliance is embedded in the team and lab. Build a professional network within the business unit, across units and outside of Baxter.
Essential Duties and Responsibilities:<ul><li>
The Research Associate I is responsible for contributing to all phases of Extractable &amp; Leachable studies carried out IH and at CROs. This would include study design as sample preparation, analysis, and data interpretation.</li><li>
Independently or with support of sub department manager, author and contribute to the experimental protocols, process and interpret data, author technical reports in English.</li><li>
Ensure technical output of the team is of the highest quality, scientifically sound and appropriately addresses the business need.</li><li>
Ensure compliance in all research, data collection and reporting activities.</li><li>
Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.</li><li>
Support the build out of the R&amp;D- E&amp;L laboratory.</li><li>
Develop and enhance technical capability through training and on job experience.</li><li>
Ensure laboratory is equipped with instrumentation that is qualified to appropriate standards, maintained in a functional state and aligns with the business needs.</li><li>
Key contributor during experimental study designs, execution and review/approval at IH &amp; CROs study.</li><li>
Competent in interpreting complex analytical data and presenting in a form that is suitable for a wide-ranging audience</li><li>
Collaborate with a multidisciplinary team of subject matter experts to generate innovative solutions to complex problems through the use of multiple disciplines and technical principles.</li><li>
Create innovative products/processes/methods through novel combinations of expertise within the organization.</li><li>
Contribute to the long-term scientific strategy of the department.</li><li>
Track/monitor the regional external regulatory environment in the areas of Extractables &amp; Leachables, Elemental Impurities, and Structure Elucidation. Write technical reports and documenting development work.</li></ul>
Qualifications:<ul><li>
Must be well-versed in analytical chemistry, spectroscopy, and impurity quantitation and characterization, structure elucidation and possess knowledge in related disciplines. Must be able to critically analyze complex data.</li><li>
Experience in at least one of either LC-MS, HRMS, GC-MS or ICP-MS.</li><li>
Experienced in Analytical development and validation.</li><li>
Demonstrates ability to critically interpret chromatographic and complex spectroscopic data.</li><li>
Competent in operating and troubleshooting chromatographic and spectroscopic instrumentation.</li><li>
Strong organizational &amp; time management skills.</li><li>
Effective communication &amp; fluency in English oral and written skills.</li><li>
Technical, managerial, leadership, project management and strategic strengths are all important for this role.</li><li>
Knowledge of GMP and regulatory guidelines.</li><li>
Capable of analyzing and innovatively solving complex problems.</li></ul>
Education and/or Experience:<ul><li>
Educational Qualification: Master&rsquo;s in pharmacy / Chemistry or Ph.D. in chemistry related field</li></ul>
Experience range (desirable): Between 6-8 years.
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 
 
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.</div>

Assoc Scientist I

<div>This is where your work makes a difference.
At Baxter, we believe every person&mdash;regardless of who they are or where they are from&mdash;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&mdash;you will find purpose and pride.
Summary:
Support the Extractables and Leachables scientific excellence of the Ahmedabad R&amp;D. As a scientist on this team, use state-of-the-art technology (LC-MS, GC-MS, GC, UV, LC, IC, ICP-MS, ICP-OES) to solve complex analytical problems &amp; investigations, including Structure Elucidation. Ensure technical capabilities and expertise are aligned with business needs to sustain products, support development of new products, contribute to investigations, and drive specific innovation initiatives to position the organization for the future. Collaborate with Team Lead and global subject matter experts to meet the needs of partners across Baxter&rsquo;s Global Business Units. Ensure Quality culture and compliance is embedded in the team and lab. Build a professional network within the business unit, across units and outside of Baxter.
Essential Duties and Responsibilities:<ul><li>
The Research Associate II is responsible for contributing to all phases of Extractable &amp; Leachable studies carried out IH and at CROs. This would include study design as sample preparation, analysis, and data interpretation.</li><li>
Independently or with support of sub department manager, author and contribute to the experimental protocols, process and interpret data, author technical reports in English.</li><li>
Ensure technical output of the team is of the highest quality, scientifically sound and appropriately addresses the business need.</li><li>
Ensure compliance in all research, data collection and reporting activities.</li><li>
Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.</li><li>
Support the build out of the R&amp;D- E&amp;L laboratory.</li><li>
Develop and enhance technical capability through training and on job experience.</li><li>
Ensure laboratory is equipped with instrumentation that is qualified to appropriate standards, maintained in a functional state and aligns with the business needs.</li><li>
Key contributor during experimental study designs, execution and review/approval at IH &amp; CROs study.</li><li>
Competent in interpreting complex analytical data and presenting in a form that is suitable for a wide-ranging audience</li><li>
Collaborate with a multidisciplinary team of subject matter experts to generate innovative solutions to complex problems through the use of multiple disciplines and technical principles.</li><li>
Create innovative products/processes/methods through novel combinations of expertise within the organization.</li><li>
Contribute to the long-term scientific strategy of the department.</li><li>
Track/monitor the regional external regulatory environment in the areas of Extractables &amp; Leachables, Elemental Impurities, and Structure Elucidation. Write technical reports and documenting development work.</li></ul>
Qualifications:<ul><li>
Must be well-versed in analytical chemistry, spectroscopy, and impurity quantitation and characterization, structure elucidation and possess knowledge in related disciplines. Must be able to critically analyze complex data.</li><li>
Experience in at least one of either LC-MS, HRMS, GC-MS or ICP-MS.</li><li>
Experienced in Analytical development and validation.</li><li>
Demonstrates ability to critically interpret chromatographic and complex spectroscopic data.</li><li>
Competent in operating and troubleshooting chromatographic and spectroscopic 
instrumentation.</li><li>
Strong organizational &amp; time management skills.</li><li>
Effective communication &amp; fluency in English oral and written skills.</li><li>
Technical, managerial, leadership, project management and strategic strengths are all important for this role.</li><li>
Knowledge of GMP and regulatory guidelines.</li><li>
Capable of analyzing and innovatively solving complex problems.</li></ul>
Education and/or Experience:<ul><li>
Educational Qualification: Master&rsquo;s in pharmacy / Chemistry or Ph.D. in chemistry related field</li><li>
Experience range (desirable): Between 8 -12 years.</li></ul>
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 
 
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.</div>

Assoc Scientist II