analytical scientist

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
First Shift (Days)<p></p><p><b>
Environmental Conditions</b></p>
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials<p></p><p><b>
Job Description</b></p><p></p><p>
As part of the Thermo Fisher Scientific team, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world&rsquo;s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.</p><p><br>
We are seeking an Analytical Scientist II with exceptional problem-solving skills to join our Research and Development team in High Point, NC, United States. As an Analytical Scientist III, you will have a crucial role in advancing our research initiatives and contributing to the development of innovative scientific solutions.</p><p>
Responsibilities:</p><p>
Conduct cleaning method development and validation for our wide range of products</p><ul><li>Perform routine and investigational testing in accordance with approved methods and specifications, including chemical, physical, and microbiological analyses. Evaluate results, identify trends, and support investigations related to out-of-specification or atypical findings.</li><li>Conduct additional testing as required to support quality investigations, regulatory inquiries, supplier qualification, method validation or verification, stability studies, and risk assessments, including but not limited to impurity, residual solvent, volatile, and trace-level analyses.</li><li>Ensure all testing activities comply with applicable GMP, GLP, and regulatory requirements. Accurately document results, prepare technical summaries, and communicate findings to cross-functional stakeholders. Support continuous improvement initiatives by recommending or implementing enhanced analytical approaches when necessary.</li><li>Collaborate with cross-functional teams to determine project requirements and objectives</li><li>Design and conduct experiments to assess and enhance cleaning procedures</li><li>Analyze samples and interpret data using statistical tools and software</li><li>Prepare and present technical reports and presentations to individuals and groups within and outside the organization</li><li>Ensure compliance with regulatory standards and guidelines</li><li>Contribute to the continuous improvement of analytical methodologies and processes</li><li>Stay updated with industry trends and advancements in analytical techniques</li></ul><p>
Requirements</p><p>
To be successful in this role, you should have:</p><ul><li>A BS degree with 2+ years of relative experience or MS Degree with 1 year experience, a Ph.D. in Analytical Chemistry or a related field</li></ul><p>
&middot;&middot; Proven experience in cleaning method development and validation</p><ul><li>Proficiency in using analytical instruments and software, including but not limited to LC/MS, FTIR and HPLC.</li><li>Strong knowledge of statistical analysis tools and techniques</li><li>Excellent communication and interpersonal skills</li><li>The ability to work independently and as part of a collaborative team</li></ul><p>
What Makes This Opportunity Unique?</p><ul><li>Join a world-class organization at the forefront of scientific innovation</li><li>Work in a pharmaceutical research facility with advanced technology</li><li>Collaborate with a diverse team of experts to solve complex scientific challenges</li><li>Contribute to the development of products that have a meaningful impact on global health and well-being</li><li>Benefit from a competitive compensation package and opportunities for professional growth</li></ul><p>
Equal Opportunity Employer: Thermo Fisher Scientific Inc. is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.</p><p>
Reasonable Accommodation: Thermo Fisher Scientific Inc. is committed to accommodating individuals with disabilities. If you require accommodation due to a disability, please contact us to discuss your needs.</p></div><p></p>

Analytical Scientist II, Cleaning Method Development

Get Offers

<div>
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    Title:
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   Mass Spectomery Scientist (Remote)
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    Engagement:
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   Hourly contract (independent contractor)
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    Location:
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   Remote
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    Compensation:
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   $100 &ndash; $300 per hour
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  <strong>
   Job Summary
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  Join our customer&rsquo;s innovative team as a
  <strong>
   Mass Spectrometry Scientist
  </strong>
  , where you will drive scientific discovery through advanced mass spectrometry techniques in a flexible remote setting. This role offers the opportunity to contribute deep analytical expertise in a collaborative environment while advancing high-impact research initiatives. You will translate complex analytical data into clear, actionable insights for multidisciplinary stakeholders.
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   Key Responsibilities
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   Develop, optimize, and validate mass spectrometry (MS) methods for qualitative and quantitative analysis of complex biological, chemical, or environmental samples.
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   Operate, maintain, calibrate, and troubleshoot mass spectrometry instrumentation and associated laboratory systems.
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   Perform rigorous data interpretation and statistical analysis to ensure scientific accuracy and reproducibility.
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   Collaborate with R&amp;D, quality, regulatory, and cross-functional teams to support project objectives and timelines.
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   Prepare detailed technical documentation, experimental protocols, validation reports, and scientific summaries.
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   Stay current with advancements in MS technologies, ionization techniques, and analytical workflows.
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   Present findings clearly through written reports, publications, and stakeholder presentations.
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   Required Skills and Qualifications
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   Advanced hands-on expertise in mass spectrometry techniques (e.g., LC-MS/MS, GC-MS, MALDI-TOF, HRMS).
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   Strong background in analytical method development, validation, and troubleshooting.
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   Ability to interpret complex datasets with high scientific rigor.
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   Proficiency in MS data processing and analysis software.
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   Excellent written and verbal communication skills with strong attention to detail.
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   Experience working collaboratively in multidisciplinary scientific environments.
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   Ability to manage multiple priorities effectively in a remote work setting.
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   MS or PhD in Chemistry, Biochemistry, Analytical Science, Pharmaceutical Sciences, or a related field.
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   Preferred Qualifications
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   Experience with industry-standard MS software (e.g., Xcalibur, MassLynx, Analyst, or similar platforms).
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   Experience in regulated environments (GLP, GMP, ISO standards).
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   Publication record or conference presentation experience.
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   Background in pharmaceutical, biotech, proteomics, metabolomics, or environmental analysis applications.
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   APPLY NOW !
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Mass Spectomery Scientist (Remote)

United Therapeutics

<div><div>California, US residents <div></div>.</div><div></div><div>
The job details are as follows:</div><div></div><div>
Who We Are</div><div></div><div>
We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.</div><div><br>
United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter&rsquo;s pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF).</div><div><br>
The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.<br>
<br>
Who You Are</div><div>
As an Associate/Research Scientist, Analytical Chemistry, you&rsquo;ll be a critical scientific partner at the intersection of discovery, development, and scale‑up&mdash;helping transform complex chemistry into therapies that can change lives. In this role, you&rsquo;ll work side‑by‑side with synthetic chemists to develop and execute advanced analytical methods, generate high‑quality data, and solve real‑world challenges tied to route selection, impurity control, and process understanding. You&rsquo;ll bring clarity to complexity by interpreting chromatographic data, supporting tech transfer and GMP readiness, and ensuring analytical rigor from early research through manufacturing. If you enjoy being hands‑on in the lab, thinking deeply about data, and collaborating across teams to move innovative science forward, you&rsquo;ll find both purpose and momentum here</div><div></div><div>
The Associate/Research Scientist, Analytical Chemistry supports a team of synthetic chemists by developing and executing various analytical (LC, GC, SFC, KF etc.) methods to solve complex research problems such as route scouting, process understanding, scale-up and impurity isolation/purification. This role also partners with QC, and external vendors to develop robust analytical methods, generate high-quality data, to ensure analytical readiness for scale-up, tech transfer and GMP manufacturing.</div><ul><li>
Collaborate with synthetic chemists to support isolation and characterization of API, impurities, intermediates, and markers using preparative techniques such as prep‑HPLC and SFC while meeting assigned project timelines</li><li>
Execute established analytical methods for chromatographic techniques including LC, GC, and SFC using appropriate detection such as UV, ELSD, CAD, MS, and FID</li><li>
Trend and interpret chromatography data to provide actionable insights including reaction completion, chiral selectivity, impurity profiles, and purge trends, and communicate results clearly to synthetic chemists</li><li>
Analyze samples or materials from vendors according to established or transferred analytical procedures</li><li>
Operate, calibrate, and maintain laboratory instruments and associated computer systems by coordinating with groups such as IT and OT for basic troubleshooting</li><li>
Coordinate vendor service activities including preventive maintenance, repairs, and column selection, and assist with obtaining quotes or making purchases for columns, consumables, and chemicals</li><li>
Author and review technical documentation such as analytical reports, method SOPs, method development summaries, investigations, and data packages for method transfer</li><li>
Contribute to technical documentation such as development summaries, experiment records, method notes, and invention disclosures as needed</li><li>
Ensure data quality and adherence to internal policies and scientific standards</li><li>
Review data packages such as method development reports and protocols from other departments and vendors</li><li>
Utilize scientific literature to support execution of research assignment objectives</li><li>
Drive improvements in analytical throughput and lab efficiency</li><li>
Support safety practices, chemical hygiene, and waste management while applying principles of sustainability</li></ul><div></div><div>
Minimum Requirements</div><div>
Associate Research Scientist, Analytical Chemistry R&amp;D</div><ul><li>
5+ years of relevant chemistry experience in pharmaceutical industry with a Bachelor's degree or 3+ years of relevant chemistry experience in pharmaceutical industry with a Master's degree or 0+ years of relevant chemistry experience in pharmaceutical industry with a PhD</li><li>
Foundational understanding of chromatographic techniques (LC, GC, SFC) and associated detection technologies (UV, ELSD, CAD, MS, FID), sufficient to execute established analytical methods independently</li><li>
Ability to trend and interpret chromatography data to provide actionable insights (reaction completion, chiral selectivity, impurity profiles, purge trends) and communicate results clearly to synthetic chemists</li><li>
Ability to operate, calibrate and maintain various laboratory instruments and related computers by interacting with other departments IT/OT for basic troubleshooting</li><li>
Ability to coordinate vendor service activities (PM visits, repairs, column selection) and assist with obtaining quotes/purchase for columns, consumables, and chemicals</li><li>
Ability to contribute to technical documentation such as development summaries, experiment records, and method notes; contribute to invention disclosures as needed</li><li>
Ability to utilize scientific literature for accomplishing research assignment objectives</li></ul><div></div><div>
Preferred Qualifications</div><ul><li>
Ability to analyze materials from external vendors/CDMOs using transferred procedures; confirm compliance with method requirements and report deviations</li><li>
Ability to ensure data quality and adherence to internal policies and scientific standards</li><li>
Proficient with MS Office, ChemDraw, and SciFinder</li></ul><div></div><div>
Minimum Requirements</div><div>
Research Scientist, Analytical Chemistry R&amp;D</div><ul><li>
8+ years of relevant chemistry experience in pharmaceutical industry with a Bachelor's degree or 6+ years of relevant chemistry experience in pharmaceutical industry with a Master's degree or 2+ years of relevant chemistry experience in pharmaceutical industry with a PhD</li><li>
Experience in independently leading analytical investigations, hands-on experience with HPLC/UPLC/GC method development, troubleshooting and common sample prep techniques</li><li>
Working knowledge of LC&ndash;MS (TOF) for mass-based compound characterization</li><li>
Ability to interpret analytical data in the context of chemical process development</li><li>
Sound knowledge of chromatography software: Waters Empower, Agilent MassHunter, Thermo Scientific Chromeleon and Waters ChromScope</li><li>
Clear technical writing and data storytelling (chromatogram stacking, overlays, etc.)</li><li>
Comfortable in fast-paced R&amp;D environments with shifting priorities</li><li>
Experience with chiral analysis/method development (chiral HPLC and/or SFC) is highly preferred</li></ul><div></div><div>
Preferred Qualifications</div><ul><li>
Doctor of Philosophy (PhD) in chemistry or related discipline</li><li>
Sound knowledge of MS Office, ChemDraw, and SciFinder</li><li>
Experience supporting API process development (route scouting and kilo lab)</li><li>
Experience with CAD detectors and SFC</li><li>
Experience working with external CDMOs and reviewing vendor analytical packages</li><li>
Familiarity with KF, NMR, FTIR</li><li>
Familiarity with regulatory expectations for early to late-stage development (ICH concepts, specs setting and CMC support)</li></ul><div></div><div>
Job Location</div><div>
United Therapeutics requires this candidate to be 100% on-site at our Silver Spring, Maryland location.</div><div></div><div>
The salary range for the Associate Research Scientist position is $96,500 - $130,000 per year and the salary range for the Research Scientist is $111,000 - $150,000 per year. These ranges reflect our good-faith estimate of the compensation for this role at the time of posting. An employee&rsquo;s position within the salary range will be based on factors such as education, qualifications, experience, skills, geographic location, and business needs, as well as other factors permitted by law at the time of posting. This range may be modified in the future based on company and market factors.</div><div></div><div>
At United Therapeutics, our mission and vision are one. We use our enthusiasm, creativity, and persistence to innovate for the unmet medical needs of our patients and to benefit our other stakeholders. We are bold and unconventional. We have fun, we do good.</div><div></div><div>
Eligible employees may participate in the Company&rsquo;s comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off &amp; paid parental leave benefits, disability benefits, and more. For additional information on Company benefits, please visit <div>https://www.unither.com/careers/benefits-and-amenities</div></div><div></div><div>
United Therapeutics Corporation is an Equal Opportunity Employer, including veterans and individuals with disabilities.</div></div><div></div>

Associate Research Scientist/Research Scientist, Analytical Chemistry R&D

<div><p><b>Work Schedule</b></p>
Standard (Mon-Fri)<p></p><p><b>
Environmental Conditions</b></p>
Office<p></p><p><b>
Job Description</b></p><p></p><p>
This is a fully remote role supporting one of our key customers. We welcome applicants from all locations within the US.</p><p>
Must be legally authorized to work in the United States without sponsorship.</p><p>
Must be able to pass a comprehensive background check, which includes a drug screening.</p><p></p><p>
Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission &ndash; to enable our customers to make the world healthier, safer, and cleaner.</p><p>
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.</p><p></p><p>
The Research Scientist acts as the sponsor representative/study monitor for one or more studies and supports the bioanalytical study phases of clinical trials.</p><p></p><p><b>
Key responsibilities:</b></p><ul><li>
Reviews trial related documentation with a link to the GxP vendor (i.e., CTP, SAP, TLF&rsquo;s, CSR, Lab manual)</li><li>
Ensures the bioanalytical vendor receives copies of trial related documentation and relevant amendments (e.g., clinical trial protocol)</li><li>
Reviews and approves study plans of bioanalytical phases of clinical trials</li><li>
Reviews and approves (if applicable) bioanalytical reports</li><li>
Oversees planned and unplanned changes to study plan and vendor procedures are documented according to vendor procedures (e.g., in amendments and deviations) and are shared with the sponsor as stipulated in the quality agreement or communication plan</li><li>
Ensures that the Clinical Trial Team is adequately informed of the project status and that relevant information (e.g., end-of-study timelines and data delivery requirements) from the Clinical Trial Team is conveyed to the project manager and bioanalytical vendor</li><li>
Escalates issues related to timelines, budget or communication to the appropriate stakeholders</li><li>
Manages oversight documentation in eTMF</li><li>
Contributes to interactions with regulatory agencies (if applicable)</li></ul><p></p><p><b>
Education and Experience:</b></p><ul><li><ul><li>PhD in Immunology or Molecular Biology and previous experience in the field of life sciences that provides the knowledge, skills, and abilities to perform the job comparable to 4+ years</li></ul></li><li>
OR</li><li>
Master&rsquo;s Degree and previous experience in the field of life sciences that provides the knowledge, skills, and abilities to perform the job comparable to 6+ years</li><li>
OR</li><li>
Bachelor's Degree and previous experience in the field of life sciences that provides the knowledge, skills, and abilities to perform the job comparable to 8+ years</li></ul><p></p><p>
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</p><p></p><p><b>
Knowledge, Skills and Abilities:</b></p><ul><li>
Experience in managing outsourced activities at external vendors required</li><li>
Strong knowledge of bioanalytical techniques specifically in biologics and antibodies assays required &middot; Experience performing PK and ADA assays required</li><li>
Experience in analyzing human samples in support of clinical trials required</li><li>
Strong understanding of GCP/GCLP guidelines and other current global regulations required</li><li>
Experience with submission documentation and regulatory interactions</li><li>
Experience with clinical immunogenicity data interpretation, writing and reviewing the Integrated Summary of Immunogenicity (ISI) and clinical study report</li><li>
Experience drafting and reviewing bioanalytical modules (2.7.1, 2.7.2) and immunogenicity sections in regulatory documents either independently or collaboration with a medical writer</li></ul><p></p><p>
Working Environment:</p><p>
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:</p><ul><li>
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>
Able to work upright and stationary for typical working hours.</li><li>
Ability to use and learn standard office equipment and technology with proficiency.</li><li>
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul></div><p></p>

Research Scientist PI - Bioanalytical

Uber

<div><b>About the Role
</b><br>
<br>
As an Applied Scientist on the incrementality foundations team within marketing measurement, you will contribute to Uber Marketing Org's commitment to science-backed decision making. This team is responsible for building experiment forms, models, &amp; processes for turning complex hypotheses into reliable, actionable incrementality signals that inform planning, forecasting, and investment decisions across the business. Your work will focus on building robust processes for interpreting measurement data, building foundational models for estimation &amp; inference, and researching experimentation best practices for accurate and complete incrementality measurement. Your work will inform smarter investment and decision-making systems across Uber's Brand and Performance Marketing. This team sits close to production systems, partnering with Product, Engineering, and cross-functional Science teams to ensure incrementality measurement is rigorous, scalable, and decision-ready
<br>
<br>
<b>What the Candidate Will Need / Bonus Points
</b><ul><li>Develop and apply statistical and causal inference models to estimate the incremental impact of marketing across channels, markets, and test designs.
</li><li>Design custom tests &amp; analyze results from complex experiments, including multi-cell, market-level, and longitudinal tests.
</li><li>Contribute to foundational modeling efforts such as hierarchical smoothing, aggregation across tests, and handling of low-signal or sparse data.
</li><li>Assist in research on advanced topics, including learning elasticity with experiments and analyzing event relationships to improve experiment accuracy and interpretation.
</li><li>Partner with Product and Engineering to integrate incrementality models into reporting and decision-making workflows
</li><li>Research and help establish best practices for experiment design, post-analysis interpretation, and measurement tradeoffs.
</li><li>Collaborate with other Applied Science and Data Science teams to align incrementality outputs with broader measurement and investment frameworks.
</li></ul><b>Basic Qualifications
</b><ul><li>Bachelor's degree or higher in a quantitative field such as Statistics, Economics, Mathematics, Computer Science, or a related discipline.
</li><li>2+ years of experience applying statistical and causal inference methods to real-world data in an applied setting.
</li><li>Strong foundation in statistical modeling, hypothesis testing, and experimental design, including A/B testing, incrementality, or quasi-experimental methods.
</li><li>Hands-on experience designing, analyzing, and interpreting experiments, including evaluation of uncertainty, limitations, and tradeoffs.
</li><li>Proficiency in Python or R and SQL for analyzing and modeling large, complex datasets.
</li><li>Experience working with marketing, growth, advertising, or similar business domains where measurement and investment decisions are central.
</li><li>Ability to clearly communicate analytical insights to technical and non-technical stakeholders and collaborate effectively in cross-functional teams.
</li><li>Demonstrated ability to collaborate effectively in cross-functional, fast-moving environments.
</li></ul><b>Preferred Qualifications
</b><ul><li>Bachelor's, Master's or PhD in a quantitative discipline (e.g., Statistics, Economics, Mathematics, Computer Science), or equivalent applied industry experience.
</li><li>Experience with advanced statistical or modeling techniques such as hierarchical / multi-level models, time-series analysis, or meta-analysis.
</li><li>Experience with incrementality testing, geo-experiments, or marketing measurement use cases (e.g., attribution, MMM, or related frameworks).
</li><li>Familiarity with marketing investment concepts such as elasticity, budget allocation, or cross-channel tradeoffs.
</li><li>Experience contributing to shared codebases or production-adjacent analytics systems, including collaboration with Product or Engineering partners.
</li><li>Ability to independently drive scoped projects end-to-end with guidance, and operate effectively in ambiguous or evolving problem spaces.
</li>Curiosity and learning mindset, with demonstrated ability to ramp quickly on new domains, tools, or methodologies.<br>
<li>
</li></ul><br>
<br>
For New York, NY-based roles: The base salary range for this role is USD$161,000 per year - USD$179,000 per year. For San Francisco, CA-based roles: The base salary range for this role is USD$161,000 per year - USD$179,000 per year. For all US locations, you will be eligible to participate in Uber's bonus program, and may be offered an equity award &amp; other types of comp. All full-time employees are eligible to participate in a 401(k) plan. You will also be eligible for various benefits. More details can be found at the following link https://jobs.uber.com/en/benefits.</div>

Applied Scientist, Marketing Measurement

Sandia National Laboratories

<div><div><div><h2 class="jobSectionHeader"><b>About Sandia</b></h2><div><br>
<div><div>
</div><p>Sandia National Laboratories is the nation&rsquo;s premier science and engineering lab for national security and technology innovation, with teams of specialists focused on cutting-edge work in a broad array of areas. Some of the main reasons we love our jobs:</p><ul>
<li>Challenging work with amazing impact that contributes to security, peace, and freedom worldwide</li>
<li>Extraordinary co-workers</li>
<li>Some of the best tools, equipment, and research facilities in the world</li>
<li>Career advancement and enrichment opportunities</li>
<li>Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home)</li>
<li>Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance*</li></ul><p>
World-changing technologies. Life-changing careers. Learn more about Sandia at: http://www.sandia.gov</p><div><ul><li><br>
These benefits vary by job classification.</li></ul></div>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
What Your Job Will Be Like</b></h2>
<div>
<div></div><div><div>We are seeking an Analytical Chemist.</div><div>
</div><div>
On any given day, you may be called on to:</div><ul><li>
Develop new methodologies or tools for measuring gas, liquid, or solid compositions and their impurities</li><li>
Utilize existing tools and technologies in unique ways to solve complex problems</li><li>
Further the understanding of materials aging, decomposition, or interaction with other materials</li><li>
Pursue research funding internally and externally</li><li>
Learn about a variety of processes and products and select appropriate analytical tools to evaluate those processes and products</li><li>
Communicate effectively with internal customers, determine their analytical measurement needs, design protocols and test methods, collect data, and report on results</li><li>
Work collaboratively with other staff, technologists and others both within and external to the Analytical Science &amp; Corrosion department</li><li>
Publish and/or present the results of your work both internally and externally</li></ul><p><br>
This is an outstanding opportunity for a qualified individual to participate in groundbreaking research while contributing to a large variety of problems faced by the national security complex and to bring their skills to bear in solving these problems.</p><p>
Due to the nature of the work, the selected applicant must be able to work onsite.</p><br>
<p></p>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
Salary Range</b></h2><div><br>
<div><div>
</div><p>$117,500 - $235,700</p><ul><li>Salary range is estimated, and actual salary will be determined after consideration of the selected candidate's experience and qualifications, and application of any approved geographic salary differential.</li></ul>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
Qualifications We Require</b></h2>
<div>
<div></div><div><ul><li>A Bachelor's degree in a relevant discipline and five (5) years of directly relevant experience, or an equivalent combination of directly relevant education and engineering or scientific experience that demonstrates the knowledge, skills, and ability to perform independent research and development.</li><li>
Ability to acquire and maintain a DOE Q security clearance</li></ul><p></p>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
Qualifications We Desire</b></h2><div><br>
<div><div>
</div><p>The ideal R&amp;D Material Scientist candidate for Sandia National Laboratories will in addition possess the following:</p><ul><li>
Graduate degree in Materials Science or a highly related field where an independent research project was a graduation requirement (e.g., independent project, thesis, or dissertation).</li><li>
Experience in a research and development environment.</li><li>
Experience with materials characterization techniques.</li><li>
Experience working on teams consisting of multidisciplinary and multi-disciplinary experimentalists, modelers, and theorists with a common goal.</li><li>
Effective interpersonal skills for giving presentations, preparing reports, writing articles, and explaining the important aspects of technical work to customers.</li></ul><p>
The ideal candidate will also have the following:</p><ul><li>
PhD in Chemistry, Materials Science, Chemical Engineering, or closely related science or engineering field, plus 1 or more years of postgraduate experience</li><li>
Solid interpersonal skills as evidenced by a record of publication of results in peer-reviewed journals and presentations at professional technical conferences (A publication list should be included as in your resume)</li><li>
Minimum of 2 years proven experience in a research laboratory</li><li>
Experience with proposing and acquiring funding for original scientific research</li><li>
Research program or expertise that can grow the research portfolio of the department</li><li>
Experience working with highly hazardous chemicals (HF, strong acids, etc.)</li><li>
Experience with inorganic analytical techniques (ICP/MS, ICP/OES, and digestion methods)</li><li>
Experience with separations (gas and liquid) and detectors (mass spectrometry, FID, TCD, UV/VIS)</li><li>
Understanding of and experience with mass spectrometry ionization methods (ESI, APCI, EI, CI, MALDI)</li><li>
Advanced data processing skills with Masslynx and/or Chemstation and/or Masshunter/AMDIS</li><li>
Ability to prioritize tasks and execute multiple projects simultaneously</li><li>
A dedication to quality, safety, collaboration, and teamwork<br>
</li></ul>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>About Our Team</b></h2><div><br>
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</div><p>The reliability of devices, components, and ultimately systems is directly affected by the properties and interactions of their constituent materials. The prime goal of the Analytical Science and Corrosion Department is to ensure that effective materials-related information is provided to customers who design and field high-consequence hardware, such that long-term reliability will be attained. Our department's R&amp;D activities have significant focus on the needs of Sandia's Nuclear Deterrence program customers. We also provide support to customers in other areas including Energy and Environment and National Security Programs. We have expertise in gas/solid interactions, corrosion and electrochemistry, and the aging and mechanical properties of ceramics, glasses and other brittle materials. We provide this expertise and support to our customers during all phases of design, production, storage, use, and retirement.</p>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
Posting Duration</b></h2><div><br>
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</div><p>This posting will be open for application submissions for a minimum of three (3) calendar days, including the 'posting date'. Sandia reserves the right to extend the posting date at any time.</p>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
Security Clearance</b></h2><div><br>
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</div><p>Sandia is required by DOE to conduct a pre-employment drug test and background review that includes checks of personal references, credit, law enforcement records, and employment/education verifications. Applicants for employment need to be able to obtain and maintain a DOE Q-level security clearance, which requires U.S. citizenship. If you hold more than one citizenship (i.e., of the U.S. and another country), your ability to obtain a security clearance may be impacted.</p><p>
Applicants offered employment with Sandia are subject to a federal background investigation to meet the requirements for access to classified information or matter if the duties of the position require a DOE security clearance. Substance abuse or illegal drug use, falsification of information, criminal activity, serious misconduct or other indicators of untrustworthiness can cause a clearance to be denied or terminated by DOE, resulting in the inability to perform the duties assigned and subsequent termination of employment.</p>
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EEO</b></h2><div><br>
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</div><p>All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status and any other protected class under state or federal law.</p>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
NNSA Requirements for MedPEDs</b></h2><div><br>
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</div><p>If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug-releasing pump, hearing aids, or diagnostic equipment and other equipment for measuring, monitoring, and recording body functions such as heartbeat and brain waves, if employed by Sandia National Laboratories you may be required to comply with NNSA security requirements for MedPEDs.</p><p>
If you have a MedPED and you are selected for an on-site interview at Sandia National Laboratories, there may be additional steps necessary to ensure compliance with NNSA security requirements prior to the interview date.</p></div></div></div></div></div>

Senior/Principal R&D S&E, Materials Science - Analytical Chemistry, Onsite

Bristol Myers Squibb

<div><b>Working with Us</b><br>
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.<br>
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Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .<br>
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Our Chemical Process Development group is a team of organic chemists, analytical chemists, and chemical engineers working together to design novel syntheses from raw materials to supply new medicines to patients. Our scientists focus on developing safe, economical, sustainable, and robust processes to support clinical trials and the launch of new medicines across various drug modalities including small molecules, peptides, oligonucleotides, and antibody drug conjugates. The work is driven by innovative science, data-driven decision-making, and collaborative teamwork. The scientific knowledge package from the manufacturing process, design parameters, and control strategies enables regulatory filings to bring these novel medicines to patients worldwide.<br>
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<b>Position Summary:
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This Analytical Development role will be responsible for developing effective collaborations within Chemical Process Development (CPD) project teams consisting of organic chemists, chemical engineers, and analytical scientists to support an increasingly complex portfolio of small molecules and milla-molecular (ADCs, peptides, oligonucleotides) drug candidates.<ul><li>
Accountable for providing fit-for-purpose analytical methods and analyses which provide key insights and process knowledge for scale-up and process optimization studies for projects within the portfolio.</li><li>
Accountable for collaborating within project teams to provide innovative analytical approaches to help solve challenging problems encountered to support route selection and process optimization studies conducted by chemists and chemical engineers.
</li><li>Accountable for developing and transferring methods to other analytical release functions to support the timely release of clinical API batches.</li><li>
Partners with other Analytical Functions within CPD, and across Product Development to evolve, integrate and optimize analytical support to create a world-class analytical function.
</li><li>Successful candidates expected to grow and advance to become either analytical leaders or technical leads for projects within the CPD portfolio.</li></ul><b>
Key Responsibilities:</b><ul><li>
Responsible for willingly and enthusiastically working at the bench to solve analytical challenges encountered within pharmaceutical development. Can be relied upon to work independently to develop and validate methods, as well as investigate and apply innovative separation techniques such as 2DLC or CE. Seeks opportunities to publish/present work externally.</li><li>
Accountable for identifying opportunities and/or implementing solutions to improve monitoring of continuous manufacturing processes, and increasingly applying automation to improve efficiency, productivity, quality or reduce costs.
</li><li>Responsible for actively collaborating with other Key Scientists within the team. Expected to consistently display a can-do attitude and demonstrate the willingness and capability to adapt and grow within a complex and changing environment.
</li><li>Responsible for working with leadership to develop self, share best practices, work effectively to solve pharmaceutical development problems, and continuously learn and improve. Expected to demonstrate capability to advance upon the technical ladder or become an effective analytical lead within project teams.
</li></ul><b>Experience &amp; Qualifications:
</b><ul><li>Ph.D. in analytical or organic chemistry with 0-2 years of experience or M.S. in analytical or organic chemistry with 2-4 years of experience, or B.S. in analytical or organic chemistry 5-7 years of experience; Practical experience directly relevant to the role is critical to success and minimum degree requirements change relative to experience.</li><li>
Experience with chromatographic and/or spectroscopic techniques preferred.</li><li>
Experience with data science, analytical chemistry relevant modeling, AI/ML, &amp;/or programming preferred.
</li><li>Experience in working across matrixed teams highly desirable.</li><li>
Demonstrated commitment to safety.</li><li>
Excellent interpersonal, collaborative, team building, and communication skills to ensure effective collaborations within matrix teams. Demonstrated performance against cooperation principles and enterprise mindset.
</li></ul>If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
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<b>Compensation Overview:</b><br>
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New Brunswick - NJ - US: $99,330 - $120,366<br>
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The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
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Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
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Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
<ul><li><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</li><li>
<b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
</li><li><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
</li></ul><b>Work-life benefits include:
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Paid Time Off
<ul><li>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
</li><li>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
</li></ul>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
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All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.<br>
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<ul><li><b>Eligibility Disclosure: </b>T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
</li></ul><br>
<b>Uniquely Interesting Work, Life-changing Careers</b><br>
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.<br>
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<b>On-site Protocol</b><br>
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BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
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Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
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<b>Supporting People with Disabilities</b><br>
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BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
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<b>Candidate Rights</b><br>
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BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
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<b>Data Protection</b><br>
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We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection .<br>
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Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<br>
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If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
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R1600311 : Scientist, Analytical Development</div>

Scientist, Analytical Development

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