pharmaceutical scientist

Medasource

<div>
 
 
 Title:
 
 Associate Scientist I
 
 
 
 Duration:
 
 Contract through June 2026
 
 
 
 Schedule:
 
 M-F 8-5 Onsite
 
 
 
 Occupational Summary
 
 
 
 The Associate Scientist I will support the development, qualification, and execution of analytical methods to
 
 
 enable optimization of processes, formulations and characterization of vaccine products. This incumbent in this
 
 
 position will be involved in pharmaceutical and analytical development for GMP production of vaccine products
 
 
 and therapeutics.
 
 
 
 Work Performed
 
 
 
 &bull; Perform pharmaceutical development and successful GMP release including:
 
 
 o Analytical development
 
 
 o Develop product specific release and characterization methods
 
 
 &bull; Quality methods for product release and complete comprehensive characterization of clinical lots
 
 
 &bull; Complete GMP testing in line with OCH and regulatory guidance
 
 
 &bull; Formulation development - developing formulations to stabilize vaccine products
 
 
 &bull; Employ analytical characterization tools to inform product formulation design
 
 
 &bull; Lead formulation &amp; filling of vaccine products including tech transfer &amp; production under GMP
 
 
 conditions
 
 
 &bull; Execute and document development and GMP actitivites in compliance with regulatory requirements
 
 
 &bull; Collaborate closely with other development teams to provide support for development activities and will
 
 
 work diligently with other development functions to understand how the production process changes
 
 
 impact product quality
 
 
 &bull; Compile data and perform analysis and interpretation and draw conclusions regarding progress and
 
 
 results of work, utilizing the data in appropriate decision making; summarize date, present results and
 
 
 propose next steps to advance development
 
 
 &bull; Write and review development reports; writes procols for tech transfer and SOPs for GMP production,
 
 
 and present data to project teams and larger settings
 
 
 
 Required Qualifications
 
 
 
 &bull; Knowledge and hands on classwork with analytical methods and/or product formulation
 
 
 &bull; Hands on experience with specific analytical methods (HPLC, immunoassays, biochemical methods),
 
 
 molecular or pharmaceutical product formulation (buffer &amp; excipient screening, thermal stability
 
 
 evaluation, biophysical methods) is preferred.
 
 
 &bull; GMP experience huge plus
 
 
 &bull; Must have the ability to work independently with guidance from senior scientists/managers
 
 
 &bull; Demonstrated ability in solving moderately complex analytical problems with guidance from senior
 
 
 development scientists
 
 
 &bull; Strong oral and written communication skills
 
</div>

Associate Scientist

HEOR Scientist - Pneumococcal Vaccines Location: RemoteContract Type: TemporaryRate: £650-800 per day approx. (Umbrella) SRG are supporting a leading global pharmaceutical company with their search for an HEOR Scientist supporting Pneumococcal Vaccines. This will be an initial 9 month contract and the role is predominantly remote based. Reporting to the Global RWE & Health Outcomes Research Lead, you'll play a key role in designing and delivering impactful real-world evidence (RWE) studies that inform strategic decisions and support global market access. Key Responsibilities <ul> <li>Design and execute multiple RWE studies, managing timelines, deliverables, and budgets.</li><li>Ensure quality and compliance across study documentation including protocols, analysis plans, and publications.</li><li>Translate strategic evidence needs into innovative study concepts and protocols.</li><li>Advise internal and external stakeholders on scientific design and data sources.</li><li>Build strong cross-functional relationships across medical, market access, and commercial teams.</li><li>Engage with external thought leaders to ensure robust and credible research approaches.</li></ul> Requirements & Experience <ul> <li>MSc or equivalent in health economics, epidemiology, pharmacy, or life sciences.</li><li>1-3 years' experience in the pharmaceutical industry, ideally within a multinational setting.</li><li>Proven ability to manage projects and budgets in a matrix environment.</li><li>Experience with RWE study designs and HTA/reimbursement evidence generation.</li><li>Experience with Pneumococcal Vaccines would be a major advantage - Vaccines in general or Immunology also useful experience</li><li>Strong communication skills to translate complex data for diverse audiences.</li><li>Knowledge of global healthcare systems and payer decision-making processes.</li></ul> Preferred: PhD/PharmD, launch experience, and direct payer engagement. To Apply If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

HEOR Scientist - Vaccines

Merck

<div>Job Description
Our company's Pharmaceutical Sciences organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, developing and scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing facilities, our Scientists use cutting edge science to transform drug delivery and manufacturing technology to positively impact patients.
The successful candidate will be a passionate Scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new chemical entities as part of a matrix team from initial first in human formulations (suspensions, solutions, capsules, tablets) through final market formulation definition and manufacturing process robustness assessment. 
Additional responsibilities are as follows:<ul><li>
Develops and applies basic principles and scientific concepts to execute work in a laboratory or pilot plant environment to advance new solid oral drug products.</li><li>
Capability to support manufacturing operations in non-GMP and GMP environments.</li><li>
Executes routine experiments and data interpretation with appropriate technical guidance.</li><li>
Ability to operate and trouble shoot equipment and processes.</li><li>
Capable of learning practical laboratory/pilot plant skills and fundamental scientific principles to utilize as part of their daily responsibilities.</li><li>
Can understand overall project timelines to manage prioritization of individual contributor deliverables with appropriate supervision.</li><li>
Works well with others in collaborative team environments.</li><li>
Builds awareness of relevant new and current technologies to grow as a pharmaceutical scientist.</li></ul>
Education Minimum Requirement:<ul><li>
B.S. or M.S. degree in Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences or related discipline (expected no later than June 2026).</li></ul>
Required Experience and Skills:<ul><li>
Ability to learn and apply new scientific principles to execution of daily responsibilities</li><li>
Demonstrated ability to collate and conduct basic data analysis</li><li>
Prior experience with Microsoft Office</li><li>
Strong verbal and written communication skills</li></ul>
Preferred Experience and Skills:<ul><li>
Prior experience in a laboratory environment</li><li>
Prior experience with statistical software (JMP, Minitab) and numerical analysis software (Matlab)</li><li>
Strong mechanical aptitude</li><li>
Passion to learn and develop as a pharmaceutical scientist</li></ul>
 *Shift assignments may vary at company&rsquo;s discretion.* 
#eligibleforerp PSCS
Required Skills:
Accountability, Accountability, Analytical Thinking, Animal Vaccination, Biochemical Analysis, Biomedical Engineering, Chemical Engineering, Clinical Manufacturing, Creativity, Data Analysis, Dosage Forms, Econometric Software, Evaluating New Technologies, GMP Compliance, Machine Learning (ML), Manufacturing Operations, Manufacturing Support, Medical Knowledge, Microsoft Office, Patent Analysis, Pharmaceutical Production, Pharmaceutical Sciences, Pharmacology, Product Development, SAS System {+ 5 more}
Preferred Skills: 
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another&rsquo;s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as &ldquo;remote&rdquo;.
The salary range for this role is
$70,500.00 - $110,900.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee&rsquo;s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully 
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
Domestic
VISA Sponsorship:
Yes
Travel Requirements:
10%
Flexible Work Arrangements:
Not Applicable
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
No
Job Posting End Date:
11/20/2025<ul><li>A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. 
</li></ul> 
Requisition ID:R373158</div>

Associate Scientist, Research Pharmacy

CPS, Inc.

<div>
 The Formulation Scientist will join the R&amp;D Group in Utah, reporting to the Director of R&amp;D. The role focuses on application development of Nutraceutical oral dosage forms including hands on experience in product development, physical properties, analytical testing, technical support, and primarily for the pharmaceutical and nutraceutical markets.
 
 
 The Formulation Scientist applies formulation science knowledge to oral solid dosage forms, collaborating with marketing, sales, manufacturing, supply chain, quality, analytical labs, and other R&amp;D groups. Responsibilities include generating scientific data across lab, pilot plant, and commercial scales, becoming an in-house expert on customer usage of company products. The role involves project management, report writing, and data presentation, balancing customer-facing and laboratory-focused tasks. Travel to customer locations for visits and scale-up trials is required. The working environment spans office, laboratory, pilot production, and manufacturing setting, with occasional domestic and international travel.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Execute application development projects for customers in the nutraceutical market.
 </li>
 <li>
 Identify gaps in the company product line and generate new product ideas.
 </li>
 <li>
 Collaborate with R&amp;D team members on new product development.
 </li>
 <li>
 Validate company products through qualitative and analytical evaluations.
 </li>
 <li>
 Contribute to customer formula development programs, showcasing company ingredients in various product categories.
 </li>
 <li>
 Assess competitive product lines.
 </li>
 <li>
 Stay current with new technologies and developments.
 </li>
 <li>
 Perform tests on new samples produced in the pilot plant, comparing actual results to predictions.
 </li>
 <li>
 Source equipment and ingredients for laboratory projects.
 </li>
 <li>
 Maintain accurate R&amp;D files, project files, and lab notebooks.
 </li>
 <li>
 Perform other duties as assigned.
 </li>
 <li>
 If you&rsquo;d like to hear more about this opportunity and others we are currently working on, please contact Sam Kovacevic at skova@cps4jobs.com.
 
 
 </li>
 </ul>
 JO: 135.25KK
 
 
 Salary
 
 
 $110,000
 
 
 Benefits Available
 
 
</div>

Formulation Scientist (Nutraceuticals)

Curia

<div>Research Scientist I; Medicinal Chemistry in Buffalo, NY
Build your future at Curia, where our work has the power to save lives.
The Research Scientist I is an integral part of the Curia team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. The Research Scientist is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry.
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers&rsquo; therapies from curiosity to cure and ultimately to improve patients&rsquo; lives.
We proudly offer
<ul><li>Generous benefit options (eligible first day of employment)
</li><li>Paid training, vacation and holidays (vacation accrual begins on first day of employment)
</li><li>Career advancement opportunities
</li><li>Education reimbursement
</li><li>401K program with matching contributions
</li><li>Learning platform
</li><li>And more!
</li></ul>Responsibilities
<ul><li>Synthesize compounds efficiently using literature or in-house notebook procedures.
</li><li>Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques.
</li><li>Analyze and identify compounds using a good range of modern separation and spectroscopic techniques. This will include interpretation of TLC, HPLC, polarimetry, IR, and NMR spectra of moderate complexity.
</li><li>Organize work time so that several reactions are run concurrently. Use time efficiently to produce target compounds and perform other tasks.
</li><li>Manage workload and time to enable the incumbent to perform multiple projects effectively, and ensure all necessary paperwork is completed on a timely basis.
</li><li>Conduct laboratory operations in a safe manner. Maintain familiarity with the Chemical Hygiene Plan. Exhibit safety awareness and safe work practices.
</li></ul>Qualifications
<ul><li>Bachelor&rsquo;s or Master&rsquo;s Degree with major in chemistry or equivalent industrial/scientific experience
</li><li>0-5 years of industry experience in the medicinal chemistry field
</li></ul>Preferred
<ul><li>The capability to modify reaction conditions in order to improve yields (design of new or alternate reaction sequences is not a normal expectation, but will enhance the performance evaluation of the scientist).
</li><li>The ability to conduct literature searches for specific target compounds, structures related to the target compound, or to determine specific conditions for compounds and reactions.
</li></ul>Pay Range : $60,046/yr.
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-KD1</div>

Research Scientist I, Medicinal Chemistry

Julphar

<div></div><div><div><div><div><div>At Julphar, we are on a journey of culture transformation &amp; our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.
Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.
<h3 class="jobSectionHeader">
Job Overview</h3>

The Senior Research Scientist 2 will play a key role in the formulation development of pharmaceutical products for regulated markets. This position involves hands-on R&amp;D activities, cross-functional collaboration, and end-to-end project management from literature review to technology transfer.

<h3 class="jobSectionHeader">Key Responsibilities</h3>
<ul>
<li>Conduct comprehensive literature surveys and patent searches; prepare Prototype Formulation Reports.
</li>
<li>Identify reference products and coordinate procurement activities.
</li>
<li>Develop Quality Target Product Profiles (QTPP) based on literature and reference product characterization.
</li>
<li>Finalize API and excipient sources for new product development.
</li>
<li>Execute pre-formulation studies and drug&ndash;excipient compatibility assessments.
</li>
<li>Drive process optimization and reformulation activities with thorough documentation and closure.
</li>
<li>Prepare regulatory dossiers and support CTD documentation for submissions.
</li>
<li>Design and execute pharmaceutical experiments using Quality by Design (QbD) principles.
</li>
<li>Review analytical development data and compile comprehensive product development reports.
</li>
<li>Support batch manufacturing for process optimization, regulatory submissions, and bioequivalence (BE) studies.
</li>
<li>Assist with pilot and scale-up batches, including documentation and technology transfer to production.
</li>
<li>Develop and maintain R&amp;D SOPs in line with cGMP and GDP standards.
</li>
<li>Submit periodic project reports to management for review and alignment.
</li>
<li>Collaborate with departments including Analytical R&amp;D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs to ensure project timelines are met.
</li>
<li>Handle Technology Transfer Out and Contract Manufacturing for assigned projects.
</li>
<li>Oversee and manage eQMS activities related to R&amp;D.
</li>
</ul><h3 class="jobSectionHeader">Core Competencies</h3>
<ul>
<li>Strong result and process orientation with a proactive, responsible approach.
</li>
<li>High level of accountability, ownership, and attention to detail.
</li>
<li>Demonstrated cost-consciousness in R&amp;D operations.
</li>
<li>Effective team collaboration, time, and task management.
</li>
<li>Excellent written and verbal communication in English.
</li>
<li>Highly disciplined, motivated, and organized.
</li>
</ul><h3 class="jobSectionHeader">Educational Qualifications</h3>
<ul>
<li>Master&rsquo;s degree in Pharmacy (preferred) or Bachelor&rsquo;s degree in Pharmacy.
</li>
</ul><h3 class="jobSectionHeader">Experience &amp; Functional Knowledge</h3>
<ul>
<li>Minimum 8 years of hands-on experience in Formulation Development for regulated markets.
</li>
<li>Proven experience in addressing regulatory queries for agencies such as US-FDA, EU, Canada, UAE, Jordan, and KSA.
</li>
<li>Strong background in developing and handling multiple dosage forms, particularly Biosimilars and Injectables.
</li>
<li>Expertise in Technology Transfer and Contract Manufacturing processes.
</li>
</ul>We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar</div></div></div></div></div>

Senior Research Scientist 1- Formulation

Baxter International Inc.

<div>
 
 
 This is where&nbsp;
 
 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.&nbsp;
 
 
 
 Baxter Pharmaceuticals R&amp;D is seeking a highly motivated scientist with proven expertise in liquid chromatography and mass spectrometry to join its Characterization team.&nbsp; As a key contributor within the Pharmaceuticals Global Business Unit, the successful candidate will oversee and apply state-of-the-art technologies in LC-MS and GC-MS in support of new and existing pharmaceutical products.&nbsp; The scientist in this role will support Nitrosamine studies using mass spectrometry-based approaches to identify nitrosamines, potential leachables nitrosamines from container extracts and develop and validate LC/MS methods to quantify nitrosamines in finished drug product solutions.&nbsp; The candidate is expected to work independently in the laboratory, to direct studies, conduct independent experiments, and generate and interpret data to solve challenging analytical problems.
 
 
 
 
 &nbsp;
 
 
 
 What you'll be doing
 
 <ul>
 <li>
 Perform chemical extractions of container closure systems and drug product solutions in the laboratory.
 
 </li>
 <li>
 Apply state-of-the-art mass spectrometry-based approaches to solve challenging problems.&nbsp; Develop and validate novel mass spectrometry-based analytical methods.
 
 </li>
 <li>
 Independently plan, execute, and manage projects/programs that both span multiple disciplines and utilize established methods, techniques, or approaches.
 
 </li>
 <li>
 Approve technical feasibility of complex design concepts within area of expertise; advise management regarding appropriate action.
 
 </li>
 <li>
 Interpret data, evaluate analytical results, identify trends/exceptions relative to product requirements, definitions, and/or project goals.
 
 </li>
 <li>
 Reach conclusions based on research analysis and incorporate recommendations into larger projects. &nbsp;
 
 </li>
 <li>
 Share research outcomes and methodology with team members and other divisional personnel.
 
 </li>
 <li>
 Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development to ensure compliance in all research, data collection, and reporting activities.
 
 </li>
 <li>
 Maintain an in-depth knowledge and understanding of GxP and related regulations and guidance.&nbsp; Be able to provide expert insights into such regulations so as to facilitate efficient product registration.&nbsp; Be an active participant in the generation, review, adoption, and interpretation of such regulations.
 
 
 
 </li>
 </ul>
 &nbsp;
 
 
 What you'll bring
 
 <ul>
 <li>
 Master's degree with at least 10-14 years, or PhD with 6-7 years in relevant discipline required.
 
 </li>
 <li>
 Must have formal training in mass spectrometry.&nbsp; Must be skilled in carrying out sophisticated mass spectrometric experiments, such as accurate mass and MS/MS, and in the interpretation of mass spectrometric data.
 
 </li>
 <li>
 Must have good knowledge of organic chemistry and other analytical disciplines, such as chromatography, NMR, IR, etc. Possess skills or demonstrated scientific background for the development of the necessary skills, for the elucidation of unknown compound structure using a multidisciplinary approach.
 
 </li>
 <li>
 Experience in Nitrosamine (must), E&amp;L testing (optional) /study design, environmental chemistry testing, and/or trace organic analysis preferred.
 
 </li>
 <li>
 Experience with complex method development and validation, particularly for quantitative LC/MS methods, preferred.
 
 </li>
 <li>
 Must be able to able to carry out strategy and vision set by upper management and be able to communicate the vision to more junior associates.
 
 </li>
 <li>
 Ability to make routine, and some less routine, decisions independently.
 
 </li>
 <li>
 Can effectively communicate with internal and external partners.
 
 </li>
 <li>
 Experience working in a regulated pharmaceutical environment (e.g., cGXP) preferred.
 
 </li>
 <li>
 Ability to learn quickly and to tackle problems in a timely manner using analytical chemistry skills.
 
 
 
 </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>

Research Scientist I, R&D - CRT

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