r&d scientist

PepsiCo

<div>
 
 Overview
 
 
 
 <ul>
 <li>
 There is an internal slated candidate being considered for this position. However, all qualified candidates are encouraged to apply.
 
 
 </li>
 </ul>
 The role will lead the technical aspects and implementation of medium to high complexity R&amp;D enabled productivity and sustainability projects for the Grains Platform
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Leverage expertise inside and outside of the organization to deliver product and process development and innovation.
 </li>
 <li>
 Develop, plan, conduct, and coordinate product development initiatives to use experimental design and data interpretation tools to make technically sound recommendations to business.
 </li>
 <li>
 Engage with Middle East Foods Business Unit Global Procurement &amp; Supply Chain to support and manage technical aspects of productivity agendas of Grains Portfolio
 </li>
 <li>
 Develop product against consumer and business KPIs by leveraging available resources including R&amp;D Laboratory tools, bench top, factory equipment, pilot plants, supplier&rsquo;s technical assets.
 </li>
 <li>
 Coordinate samples requirements with manufacturing plants, global R&amp;D function etc. for NPD, internal screening, bench taste, sensory test, consumer test, shelf life stability, sales samples, scale-up trials, and other needs.
 </li>
 <li>
 Develop &amp; review FC, business P&amp;L and finalize product and ingredient specifications with PQP guardrails.
 </li>
 <li>
 Develop an understanding and demonstrate the application of consumer product testing; sensory and analytical etc. to deliver superior products to the market and establish product intelligence. Actively participate in marketing research programs including focus groups and other consumer research formats.
 </li>
 <li>
 Lead Technical Stage Gate and related work for his/her project and ensure timely completion of all TSG stages and its deliverables.
 </li>
 <li>
 Develop project briefs/Global Innovation Briefs (GIB) and seek R&amp;D and other cross functional alignment (especially Marketing and Supply Chain).
 </li>
 <li>
 Lead exploration of new ingredients, formulation and process technologies and leverage expertise inside and outside the organization to deliver new product and process development.
 </li>
 <li>
 Represent R&amp;D on multi-functional business teams and Influence others through strong communication &amp; interpersonal skills.
 </li>
 <li>
 Develop project briefs/Global Innovation Briefs (GIB) and seek R&amp;D and other cross functional alignment (especially Marketing and Supply Chain).
 </li>
 <li>
 Lead exploration of new ingredients, formulation and process technologies and leverage expertise inside and outside the organization to deliver new product and process development.
 </li>
 <li>
 To plan, organize and run raw material qualification programs.
 </li>
 <li>
 Drive global knowledge growth and thought leadership in emerging process technologies and imbed cross functionally.
 </li>
 <li>
 Drive CAST implementation through leadership of training programs.
 </li>
 <li>
 Work closely with Regulatory to ensure legal compliance
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Graduation degree in Food Science /Engineering (Chemical/industrial) / Food &amp; Nutrition/Pharma
 </li>
 <li>
 Must have FMCG experience of &gt;3 years.
 </li>
 <li>
 Food Science or Engineering related discipline.
 </li>
 <li>
 Good understanding / appreciation of the broader business environment and application of technical and commercial knowledge during project execution.
 </li>
 <li>
 Excellent interpersonal skills with ability to communicate and negotiate effectively across all levels and all functions of the organisation.
 </li>
 <li>
 Good presentation skills (written &amp; verbal).
 </li>
 <li>
 Strong analytical skills &ndash; ability to interpret complex data and distil into useful and actionable information.
 </li>
 <li>
 Ability to explain complex technical issues / solutions to a non-technical audience.
 </li>
 <li>
 Strives for high standards, seeks innovative solutions, drives continuous improvement of products, processes or methods and demonstrates a high degree of intellectual curiosity.
 </li>
 <li>
 Passion for creativity and innovation within a commercially driven environment.
 </li>
 <li>
 Cultural sensitivity / flexibility in responding to diverse teams and environments.
 </li>
 <li>
 Self-starter and motivator.
 </li>
 </ul>
</div>

R&D Associate Scientist

H.B. Fuller

<div>
 
 As the largest pureplay adhesives company in the world, H.B. Fuller&rsquo;s (NYSE: FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day. Founded in 1887, with 2024 revenue of $3.6 billion, our mission to Connect What Matters is brought to life by more than 7,500 global team members who collaborate with customers across more than 30 market segments in over 140 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets. Learn more at www.hbfuller.com.
 
 
 
 
 
 
 
 
 
 Job Title: Scientist II
 
 
 
 
 
 
 
 Location: Ras Al Khaimah
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Position Overview
 
 
 
 
 
 
 
 
 
 
 
 
 The Scientist II supports Research &amp; Development and Technical Service activities for strategic business markets within the BAS Business Line. This role is responsible to spearhead laboratory experimentation, advanced application testing, rigorous documentation, in-depth product evaluation, and seamless technology transfer to accelerate market impact.
 
 
 
 
 
 
 
 
 This position is required to support ongoing R&amp;D projects, product development, and lab testing critical to the BAS business. It ensures timely innovation, raw material evaluation, and technical support essential for customer and plant needs.
 
 
 
 
 
 
 
 
 
 
 
 
 PRIMARY DUTIES
 
 
 
 
 
 <ul>
 <li>
 Design and execute advanced lab experiments to innovate and optimize product performance.
 </li>
 <li>
 &middot;Conduct rigorous application testing tailored to real-world construction demands.
 </li>
 <li>
 Author precise technical documentation, reports, and protocols to support regulatory compliance and knowledge transfer.
 </li>
 <li>
 Perform in-depth product evaluations, including stability, efficacy, and scalability assessments.
 </li>
 <li>
 Collaborate cross-functionally to facilitate seamless technology transfer from lab to production scale.
 </li>
 <li>
 Provide technical expertise to internal teams and external customers, resolving complex challenges in strategic markets.
 </li>
 </ul>
 
 
 
 
 
 Critical Qualifications &amp; Expectations
 
 
 
 
 
 
 <ul>
 <li>
 
 Proven Product Development Leadership
 
 : Demonstrated success in construction segment product innovation&mdash;from ideation and formulation to commercialization and scale-up. Track record of delivering high-impact, market-ready solutions.
 </li>
 </ul>
 
 
 
 <ul>
 <li>
 
 Regional Expertise
 
 : Currently based in the ME region (strongly preferred) to leverage local market insights, foster agile partnerships, and drive region-specific strategies.
 </li>
 </ul>
 
 
 
 <ul>
 <li>
 
 Technical Mastery
 
 : Comprehensive command of solvent-based products and formulations.
 </li>
 <li>
 Extensive hands-on exposure to waterproofing coatings and sealants, with deep knowledge of PU (polyurethane), MS Polymer, and Silicone technologies.
 </li>
 </ul>
 
 
 
 <ul>
 <li>
 
 Industry Acumen
 
 : Solid understanding of construction sector dynamics, including regulatory landscapes, customer needs, and competitive trends.
 </li>
 </ul>
 
 
 
 <ul>
 <li>
 
 Relevant Experience
 
 : 5+ years in R&amp;D, product development, or technical service within adhesives, coatings, or sealants&mdash;ideally in construction applications.
 </li>
 </ul>
 
 
 
 
 
 Minimum Qualifications
 
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in chemistry with
 
 5+ years
 
 of relevant experience, OR
 </li>
 <li>
 Master&rsquo;s degree in chemistry with
 
 2+ years
 
 of experience, OR
 </li>
 <li>
 Associate degree in chemical technology with
 
 4+ years
 
 of industrial lab/application experience.
 </li>
 <li>
 Familiarity with laboratory testing methods, equipment, and adhesives‑related processes.
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 
 
 
 
 <ul>
 <li>
 Experience with Solvent based, Water based Emulsions, Rubbers, Polyurethane, Acrylic, Elastomeric Polymers and related chemistries
 </li>
 <li>
 Knowledge of quality systems, product development processes, and adhesives performance testing.
 </li>
 <li>
 Ability to prepare clear, concise technical reports and customer‑ready presentations.
 </li>
 <li>
 Strong communication skills in English (verbal and written).
 </li>
 </ul>
 
 
 
 
 
 
 
 
 Key Competencies
 
 
 
 
 
 <ul>
 <li>
 
 Adaptability:
 
 Thrives in a dynamic, fast‑paced environment with changing priorities.
 </li>
 <li>
 
 Collaboration:
 
 Works effectively across teams, prioritizing shared goals.
 </li>
 <li>
 
 Customer Focus:
 
 Delivers value through technical expertise and service excellence.
 </li>
 <li>
 
 Accountability:
 
 Takes ownership, ensures accuracy, and delivers high‑quality output.
 </li>
 <li>
 
 Operational Discipline:
 
 Follows SOPs and ensures compliance with safety and quality systems.
 </li>
 <li>
 
 Self‑Management:
 
 Performs tasks with minimal supervision while actively seeking growth.
 </li>
 </ul>
 
 
 
 
 
 Work Environment
 
 
 
 
 
 
 This role operates within an R&amp;D laboratory and technical center environment, requiring adherence to all safety and operational protocols.
 
 
 
 
 
 
 H.B. Fuller is an Equal Employment Opportunity employer and proud to have created a collaborative culture where employees around the world are seen, heard, and respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, or marital status or status as a protected veteran, or any other legally protected classification.
 
 
 
 
 
 
 
 H.B. Fuller does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with H.B. Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate. Without a signed service agreement, H.B. Fuller shall not be obligated for payment of any fee or compensation.
 
 
 
 
 
</div>

Scientist II

<div>
 As the largest pureplay adhesives company in the world, H.B. Fuller&rsquo;s (NYSE: FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day. Founded in 1887, with 2024 revenue of $3.6 billion, our mission to Connect What Matters is brought to life by more than 7,500 global team members who collaborate with customers across more than 30 market segments in over 140 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets. Learn more at www.hbfuller.com.
 
 
 
 Job Title: Scientist II
 
 
 Location: Ras Al Khaimah
 
 
 
 
 Position Overview
 
 
 
 The Scientist II supports Research &amp; Development and Technical Service activities for strategic business markets within the BAS Business Line. This role is responsible to spearhead laboratory experimentation, advanced application testing, rigorous documentation, in-depth product evaluation, and seamless technology transfer to accelerate market impact.
 
 
 This position is required to support ongoing R&amp;D projects, product development, and lab testing critical to the BAS business. It ensures timely innovation, raw material evaluation, and technical support essential for customer and plant needs.
 
 
 
 Primary Duties
 
 
 
 <ul>
 <li>
 Design and execute advanced lab experiments to innovate and optimize product performance.
 </li>
 <li>
 </li>
 <li>
 Conduct rigorous application testing tailored to real-world construction demands.
 </li>
 <li>
 Author precise technical documentation, reports, and protocols to support regulatory compliance and knowledge transfer.
 </li>
 <li>
 Perform in-depth product evaluations, including stability, efficacy, and scalability assessments.
 </li>
 <li>
 Collaborate cross-functionally to facilitate seamless technology transfer from lab to production scale.
 </li>
 <li>
 Provide technical expertise to internal teams and external customers, resolving complex challenges in strategic markets.
 
 
 
 </li>
 </ul>
 
 Critical Qualifications &amp; Expectations
 
 
 
 <ul>
 <li>
 Proven Product Development Leadership: Demonstrated success in construction segment product innovation&mdash;from ideation and formulation to commercialization and scale-up. Track record of delivering high-impact, market-ready solutions.
 </li>
 <li>
 Regional Expertise: Currently based in the ME region (strongly preferred) to leverage local market insights, foster agile partnerships, and drive region-specific strategies.
 </li>
 <li>
 Technical Mastery: Comprehensive command of solvent-based products and formulations.
 </li>
 <li>
 Extensive hands-on exposure to waterproofing coatings and sealants, with deep knowledge of PU (polyurethane), MS Polymer, and Silicone technologies.
 </li>
 <li>
 Industry Acumen: Solid understanding of construction sector dynamics, including regulatory landscapes, customer needs, and competitive trends.
 </li>
 <li>
 Relevant Experience: 5+ years in R&amp;D, product development, or technical service within adhesives, coatings, or sealants&mdash;ideally in construction applications.
 
 
 
 </li>
 </ul>
 
 Minimum Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in chemistry with 5+ years of relevant experience, OR
 </li>
 <li>
 Master&rsquo;s degree in chemistry with 2+ years of experience, OR
 </li>
 <li>
 Associate degree in chemical technology with 4+ years of industrial lab/application experience.
 </li>
 <li>
 Familiarity with laboratory testing methods, equipment, and adhesives‑related processes.
 
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 Experience with Solvent based, Water based Emulsions, Rubbers, Polyurethane, Acrylic, Elastomeric Polymers and related chemistries
 </li>
 <li>
 Knowledge of quality systems, product development processes, and adhesives performance testing.
 </li>
 <li>
 Ability to prepare clear, concise technical reports and customer‑ready presentations.
 </li>
 <li>
 Strong communication skills in English (verbal and written).
 
 
 
 </li>
 </ul>
 
 Key Competencies
 
 
 
 <ul>
 <li>
 Adaptability: Thrives in a dynamic, fast‑paced environment with changing priorities.
 </li>
 <li>
 Collaboration: Works effectively across teams, prioritizing shared goals.
 </li>
 <li>
 Customer Focus: Delivers value through technical expertise and service excellence.
 </li>
 <li>
 Accountability: Takes ownership, ensures accuracy, and delivers high‑quality output.
 </li>
 <li>
 Operational Discipline: Follows SOPs and ensures compliance with safety and quality systems.
 </li>
 <li>
 Self‑Management: Performs tasks with minimal supervision while actively seeking growth.
 
 
 
 </li>
 </ul>
 
 Work Environment
 
 
 
 This role operates within an R&amp;D laboratory and technical center environment, requiring adherence to all safety and operational protocols.
 
 
 
 H.B. Fuller is an Equal Employment Opportunity employer and proud to have created a collaborative culture where employees around the world are seen, heard, and respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, or marital status or status as a protected veteran, or any other legally protected classification.
 
 
 
 
 H.B. Fuller does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with H.B. Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate. Without a signed service agreement, H.B. Fuller shall not be obligated for payment of any fee or compensation.
 
</div>

Baylor Miraca Genetics Laboratories LLC

<div>We are seeking a highly motivated Scientist III to join our Assay R&amp;D team developing next‑generation clinical assays for rare disease diagnostics. In this role, you will design and optimize cutting‑edge DNA and RNA sequencing&ndash;based assays using a variety of input materials, including blood, saliva, and buccal swabs.

This position is ideal for an accomplished scientist with expertise in molecular biology, sequencing technologies, and clinical assay development who thrives in a fast‑paced, innovation‑driven environment.

Key Responsibilities
<ul>
<li>Lead the design, development, and optimization of sequencing-based clinical assays for rare disease detection.</li>
<li>Develop end-to-end workflows utilizing multiple sample types, including blood, saliva, and buccal swabs.</li>
<li>Design and execute experiments, analyze data, and interpret results to guide assay performance improvements.</li>
<li>Define assay performance metrics and collaborate with validation teams on verification and validation studies.</li>
<li>Work cross-functionally with bioinformatics, automation, validation, and clinical teams for successful assay transfer.</li>
<li>Maintain accurate experimental documentation in compliance with quality and regulatory standards.</li>
<li>Present scientific findings and contribute to reports and/or publications.</li>
<li>Stay current with emerging technologies and scientific trends to support innovation.</li>
</ul>
Required Qualifications
<ul>
<li>Ph.D. in molecular biology, biochemistry, genetics, or related field.</li>
<li>3+ years of hands-on experience in sequencing workflows and assay development, ideally in a clinical or diagnostic lab.</li>
<li>Expertise working with diverse sample types including blood, saliva, and buccal swabs.</li>
<li>Strong proficiency in molecular biology techniques (PCR, qPCR, NGS, nucleic acid extraction).</li>
<li>Experience with NGS data analysis tools and pipelines.</li>
<li>Excellent problem‑solving skills, attention to detail, and communication abilities.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience transferring R&amp;D assays into clinical or production operations.</li>
<li>Familiarity with regulated environments such as CLIA or CAP.</li>
<li>Experience with automated liquid handling systems.</li>
</ul>
Ability to rapidly learn and apply new technologies.

EEO Statement:

 Baylor Genetics is proud to be an equal opportunity employer dedicated to building an inclusive and diverse workforce. We do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, gender identity, veteran status, disability, genetic information, pregnancy, childbirth, or related medical conditions, or any other status protected under applicable federal, state, or local law.

Note to Recruiters:

We value building direct relationships with our candidates and prefer to manage our hiring process internally. While we occasionally partner with select recruitment agencies for specialized roles, we do not accept unsolicited resumes from recruiters or agencies without a written agreement executed by the authorized signatory for Baylor Genetics (&quot;Agreement&quot;). Any resumes submitted to Baylor Genetics in the absence of an Agreement executed by Baylor Genetics' authorized signatory, will be considered the property of Baylor Genetics, and Baylor Genetics will not be obligated to pay any associated recruitment fees.</div>

Research & Development Scientist III - Clinical Assay Development (Rare Disease Diagnostics)

Julphar

<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.
 
 
 
 Roles And Responsibilities
 
 
 
 <ul>
 <li>
 Conduct literature surveys, patent searches, and prepare Prototype Formulation Reports.
 </li>
 <li>
 Identify reference products and initiate procurement processes.
 </li>
 <li>
 Develop Quality Target Product Profiles (QTPP) based on literature insights and reference product characterization.
 </li>
 <li>
 Development of Injectable dosage forms; Biologics/Biosimilar products- upstream &amp; downstream, for regulated markets.
 </li>
 <li>
 Identify and finalize API and excipient sources for new product development.
 </li>
 <li>
 Perform and conclude pre-formulation and drug&ndash;excipient compatibility studies for assigned projects.
 </li>
 <li>
 Contribute to product process optimization and reformulation activities, including report preparation and closure.
 </li>
 <li>
 Prepare registration dossiers for submission and support CTD/dossier documentation requirements.
 </li>
 <li>
 Plan, design, and execute pharmaceutical experiments using the QbD (Quality by Design) approach.
 </li>
 <li>
 Review analytical development data and systematically compile product-related data.
 </li>
 <li>
 Support manufacturing of batches for process optimization, submission, and bioequivalence (BE) studies.
 </li>
 <li>
 Assist in pilot and scale-up batch manufacturing, with necessary documentation, and facilitate technology transfer to production.
 </li>
 <li>
 Develop and maintain R&amp;D-related SOPs in compliance with cGMP and GDP principles.
 </li>
 <li>
 Prepare and submit periodic project reports to management.
 </li>
 <li>
 Collaborate cross-functionally with Analytical R&amp;D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs to ensure timely project completion.
 </li>
 <li>
 Handle Technology Transfer out/Contract Manufacturing activities for assigned projects
 </li>
 <li>
 Experience in packaging development and life cycle management
 
 
 </li>
 </ul>
 
 Qualification/Functional Knowledge
 
 
 
 
 Education:
 
 Master&rsquo;s degree in Pharmacy/ Master&rsquo;s degree in Biotechnology
 
 
 
 Experience
 
 
 
 <ul>
 <li>
 Minimum 8 years of extensive experience of working in Formulation Development of Injectable dosage forms; Biologics/Biosimilar products- upstream &amp; downstream, for regulated markets.
 </li>
 <li>
 Significant exposure in addressing regulatory queries for US-FDA, EU, Canada, UAE, KSA and other stringent regulatory markets.
 </li>
 <li>
 Past experience of handling different dosage forms in R&amp;D i.e. injectables, Biosimilars, Biologics etc.
 
 
 </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>

Sr. Research Scientist 2

<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.

Roles and Responsibilities 
<ul>
<li>Conduct literature surveys, patent searches, and prepare Prototype Formulation Reports.</li>
<li>Identify reference products and initiate procurement processes.</li>
<li>Develop Quality Target Product Profiles (QTPP) based on literature insights and reference product characterization.</li>
<li>Development of Injectable dosage forms; Biologics/Biosimilar products- upstream &amp; downstream, for regulated markets.</li>
<li>Identify and finalize API and excipient sources for new product development.</li>
<li>Perform and conclude pre-formulation and drug&ndash;excipient compatibility studies for assigned projects.</li>
<li>Contribute to product process optimization and reformulation activities, including report preparation and closure.</li>
<li>Prepare registration dossiers for submission and support CTD/dossier documentation requirements.</li>
<li>Plan, design, and execute pharmaceutical experiments using the QbD (Quality by Design) approach.</li>
<li>Review analytical development data and systematically compile product-related data.</li>
<li>Support manufacturing of batches for process optimization, submission, and bioequivalence (BE) studies.</li>
<li>Assist in pilot and scale-up batch manufacturing, with necessary documentation, and facilitate technology transfer to production.</li>
<li>Develop and maintain R&amp;D-related SOPs in compliance with cGMP and GDP principles.</li>
<li>Prepare and submit periodic project reports to management.</li>
<li>Collaborate cross-functionally with Analytical R&amp;D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs to ensure timely project completion.</li>
<li>Handle Technology Transfer out/Contract Manufacturing activities for assigned projects</li>
<li>Experience in packaging development and life cycle management</li>
</ul>
Qualification/Functional Knowledge

Education: Master&rsquo;s degree in Pharmacy/ Master&rsquo;s degree in Biotechnology

Experience:
<ul>
<li>Minimum 8 years of extensive experience of working in Formulation Development of Injectable dosage forms; Biologics/Biosimilar products- upstream &amp; downstream, for regulated markets.</li>
<li>Significant exposure in addressing regulatory queries for US-FDA, EU, Canada, UAE, KSA and other stringent regulatory markets.</li>
<li>Past experience of handling different dosage forms in R&amp;D i.e. injectables, Biosimilars, Biologics etc.</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>

Confidential Government

<div>
 
 
 Job Responsibilities:
 
 
 
 
 
 <ul>
 <li>
 Deep knowledge of Carbon capture and utilization.
 </li>
 <li>
 Experience in gas separation technologies (membranes, adsorption, absorption, cryogenics).
 </li>
 <li>
 Materials synthesis and characterization (e.g., MOFs, zeolites, porous polymers, nanomaterials).
 </li>
 <li>
 Technical Skills: CO₂ capture and conversion pathways (amine scrubbing, MOFs, electrochemical/photocatalytic reduction, etc.)
 </li>
 <li>
 Catalysis and reactor design.
 </li>
 <li>
 Data analytics for process optimization.
 </li>
 <li>
 Tools: simulation, programming and characterization.
 </li>
 <li>
 Skills: Scientific curiosity and innovation mindset, communication and strong teamwork and interdisciplinary collaboration.
 </li>
 <li>
 Hands-on experience working on a pilot or demonstration project for carbon capture or utilization.
 </li>
 <li>
 Experience collaborating with R&amp;D partners.
 </li>
 <li>
 Peer-reviewed publications or patents in CO₂ capture or conversion technologies.
 </li>
 <li>
 Proven success in scaling lab-based research to field or industrial applications.
 </li>
 <li>
 Technically driven and innovation-oriented.
 </li>
 <li>
 Skilled in experimental design and hypothesis testing.
 </li>
 </ul>
 
 
 
 
 
 Qualifications and Experience
 
 
 
 
 
 <ul>
 <li>
 PhD degree, in the field.
 </li>
 <li>
 Master's degree and 4 + years of relevant experience.
 </li>
 <li>
 Bachelor's degree and 6 + years of relevant experience.
 </li>
 </ul>
</div>

Senior Researcher

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Research & Development Scientist III - Clinical Assay Development (Rare Disease Diagnostics)

Sr. Research Scientist 2

Sr. Research Scientist 2

Senior Researcher