senior analytical chemist

Eurofins

<div><b>Company Description</b><p><br>
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.</p><p>
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.</p><b><br>
Job Description</b><p><br>
The Senior Chemist is responsible for maintaining instrumentation; tuning and calibrating instrument daily; analyzing quality control and client samples; reviewing and assembling data in an efficient manner with a high degree of quality; evaluating current organizational and analytical systems; diagnosing complex problems and offering solutions with a high degree of independence; suggesting and implementing improvements to maximize quality and productivity; acting as technical resource for internal problems and projects; assisting in &ldquo;brainstorming&rdquo; client problems and projects; training new employees in all aspects of instrumentation; researching new and emerging technologies</p><p><b>
Essential Duties and Responsibilities:</b></p><ul><li>
Applies GMP/GLP in all areas of responsibility, as appropriate</li><li>
Demonstrates and promotes the company vision</li><li>
Regular attendance and punctuality</li><li>
Perform routine and advanced maintenance on the instrumentation</li><li>
Tune and calibrate instrumentation</li><li>
Analyze samples and associated QC</li><li>
Review, work up, and assemble all supporting data</li><li>
Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department</li><li>
Perform additional responsibilities (i.e., audit, verification, etc.) with minimal supervision</li><li>
Evaluate current analytical system performance and recommend corrective action to enhance efficiency and productivity</li><li>
Train other departmental analysts in procedures related to operations listed in the above</li><li>
Search technical literature for scientific information relative to improving analytical or operational performance</li><li>
Understand and use LIMS</li><li>
Make working calibration standards</li><li>
Use word processor on PC</li><li>
Additional duties as assigned</li></ul><br>
<b>
Qualifications</b><p><b><br>
Basic Minimum Qualifications:</b></p><ul><li>
Bachelor's degree in Biology, Chemistry, or related field</li><li>
At least 5 years of relevant experience</li><li>
Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.</li><li>
Authorization to work in the United States without restriction or sponsorship</li></ul><p><b>
Ideal candidates will have:</b></p><ul><li>
Significant previous experience with Wet Chemistry</li><li>
Exceptional technical skills, including logical thinking and deductive reasoning</li><li>
High accuracy in recording and transcribing data</li><li>
Good written and oral communication skills</li><li>
Willingness to learn new methods and techniques</li><li>
Willingness to follow instructions and comply with company policies</li><li>
Consciousness of, and a positive attitude toward, quality control and safety procedures</li><li>
Good understanding of chemical principles</li><li>
Accurate management of numbers, both by hand and using a calculator</li><li>
Ability to set up and perform non-routine standardized tests with minimal supervision</li><li>
Demonstrated versatility, flexibility, and efficiency</li><li>
Effective use of time while managing multiple priorities</li><li>
Self-motivated to improve technical skills and operations</li><li>
Superior leadership, organizational, and communication skills</li><li>
Ability to lead a project to a satisfactory conclusion on time</li><li>
Ability to consult with clients on work performed for them</li></ul><br>
<b>
Additional Information</b><p><br>
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.</p><ul><li><i>The benefits package offered will vary based on the employee&rsquo;s full-time or part-time regular status.</i></li></ul><p><b>
We support your development! </b>Do you feel you don&rsquo;t match 100% of the requirements? Don&rsquo;t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.</p><p><b>
We embrace diversity!</b> Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.</p><p><b>
Sustainability matters to us!</b> At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in &ldquo;Testing for Life,&rdquo; our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins&rsquo; commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same&mdash;serving as a true ESG Enabler.</p><p>
Find out more in our career page: https://careers.eurofins.com/</p><p><i>
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
</i></p><p><i>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralized and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
</i></p><p><i>In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.</i></p><p>
All your information will be kept confidential according to EEO guidelines.</p><div></div><p><b>
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.</b></p></div>

Senior Chemist - Instrumental Wet Chemistry - Environment Testing

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>
<div><div>
</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>
<div><div>
</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>
<div><div>
</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>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>
EEO</b></h2><div><br>
<div><div>
</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>
<div><div>
</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

GRANULES

<div>Description:<p><br>
<br>
<b>Analytical QA Associate </b>is responsible of providing analytical data review of QA Documents, support the development to ensure compliance with cGMP, FDA, Internal Policies, Procedures and Specifications. Responsible for the safe and efficient execution of job duties.<b>Principle Accountabilities</b></p><h5 class="jobSectionHeader"><b><i>
JOB DUTIES &amp; RESPONSIBILITIES</i></b></h5><ul><li>
Part of analytical data review team according to the priorities.</li><li>
Perform Data Review of Raw Material, Finished Product, Packaging Materials, In-Process, Finished Product, outside testing data, water testing data, Stability Samples, cleaning validation, swab analysis, equipment calibrations, IQ, OQ, PQ, Method Validations, Verifications of Drug Substance and Drug Product and cleaning methods (Electronic data, Notebooks, logbooks, Reports, and electronic sign off's) and notify Laboratory management or designee for any deviations, Out of Trend, extraneous peaks or out of specification result</li><li>
Perform product review for analytical data.</li><li>
Responsible for ensuring and performing Data review of Analytical R&amp;D, FDA deficiencies, PDR reports, ANDA submission data related to analytical area.</li><li>
Ensure logbook is up to date of all instruments in quality control or analytical laboratory.</li><li>
Standard and accurate usage logbooks (USP, In-house, secondary, any other pharmacopoeia) and column logbooks.</li><li>
Review the data to comply with Laboratory Procedures, Test method, Protocols, GLP, GDP and cGMP and work with Laboratory personnel for any corrections and promote cGMP culture.</li><li>
Responsible to ensure the documentation is completed, any discrepancy found during the review shall be corrected before data sign-off.</li><li>
Any additional activity as assigned by the Supervisor.</li></ul><p><b>
Management Responsibility Reports to</b>AQA Manager/Associate Manager <b>Internal/External Contacts</b>NA<b>Knowledge &amp; Skills</b></p><ul><li>
Knowledge of 21CFR, ICH, USP and other applicable regulatory requirements and standards.</li><li>
Manage and host Regulatory inspections.</li><li>
Ability to maintain integrity and honesty at all times.</li><li>
Ability to communicate and lead with transparency.</li><li>
Lead department for optimal performance and set course for future improvements.</li><li>
Accountable for performance and results of department.</li></ul><p><b>
Experience &amp; Education</b></p><ul><li>
Requires minimum BA/BS in Pharmacy, Biochemistry, Chemistry or related field with 3+ years of experience in the biotech or pharmaceutical industry. Management experience in Quality Control required and MS/MA preferable.</li></ul><p><b>
Physical Requirements/Working Environment</b>NA<b>Travel </b>Minimal<b>Disclaimer</b>The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.</p>
Requirements:
<p><b>
Required Qualifications:</b></p><ul><li>
Quality assurance within Pharmaceutical Industry: 2 years highly preferred</li><li>
Manufacturing: 2 years (Preferred)</li><li>
Document management: 2 years (Preferred)</li></ul><p><b>
Knowledge &amp; Skills</b></p><ul><li>
cGMP compliance within the pharmaceutical manufacturing industry.</li><li>
Writing and maintaining cGMP documentation.</li><li>
Analyze data/information and resolve complex issues.</li><li>
Verbal and written communication skills.</li><li>
Work and communicate with cross-functional teams.</li><li>
Multiple priorities and re-prioritize tasks.</li></ul><p><b>
Experience &amp; Education</b></p><ul><li>
At least 2 -3 years of experience in a quality assurance role in a cGMP-regulated environment.</li><li>
A college Degree preferably in sciences (i.e., Biology, Chemistry etc.), or related discipline</li></ul></div>

Analytical Quality Assurance Associate/ Bio Chemist

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

Noblis

<div>Responsibilities:
<ul><li><i>This job posting is for upcoming opportunities.</i></li></ul><div></div><div><br>
We are seeking a Senior Program Analyst - Chemical and Biological Weapons Elimination with extensive expertise with the Deputy Assistant Secretary of War for Threat Reduction and Arms Control (DASW(TRAC)) Chemical and Biological Weapons Elimination (CBWE) Division within the Washington Headquarters Services in Falls Church, VA to join our team.</div><div></div><div><b><br>
Responsibilities:</b></div><ul><li>
Support work to enable development of integrated and enduring capability to destroy chemical and biological weapons within U.S. and abroad.</li><li>
Provide evaluation of threats, identification of gaps and potential solutions, and development of investment strategy ensuring long-term access to innovative technical solutions, trained operators, and ability to execute required support functions.</li><li>
Support management of requirements collection, validation, and prioritization to inform PPBE process.</li><li>
Evaluate, integrate, and synchronize DoD's capabilities to address current and future foreign chemical and biological weapons and materials of concern to potentially eliminate threats.</li><li>
Review and provide technical and analytical assessments on integration of U.S. material solutions and overall capabilities to eliminate foreign chemical and biological weapons and materials of concern.</li><li>
Assist in facilitating/coordinating all research, engagements, strategies, and reviews to ensure effective and efficient execution of foreign chemical and biological elimination tasks.</li><li>
Assist in maintaining resource investment strategy to inform senior OSD leadership decisions on material investments and ensure DoD is optimally positioned to address current and future threats.</li></ul>
Required Qualifications:
<div>
Master's degree in relevant area.</div><ul><li>
5 years of DoD experience in project management, requirements development, technology evaluation, and acquisition management.</li><li>
Familiar with CBWE mission space.</li><li>
US. Citizen.</li><li>
Active Secret security clearance.</li></ul>
Desired Qualifications:
<ul><li>Technical background in chemical or biological sciences.</li><li>
Experience with international CBWE programs and partnerships.</li><li>
Knowledge of Chemical Weapons Convention (CWC) and Biological Weapons Convention (BWC).</li><li>
Experience with technology assessment and evaluation.</li><li>
Understanding of nonproliferation and counterproliferation strategies.</li><li>
Strong technical writing and briefing skills.</li></ul>
Overview:
<div><b>
Overview</b></div><div>
Noblis and our wholly owned subsidiaries, Noblis ESI and Noblis MSD, take on some of the nation&rsquo;s toughest challenges, delivering advanced solutions to our customers&rsquo; most critical missions. We bring together leading scientific, engineering, and management expertise in a culture grounded in objectivity and collaboration, ensuring our work creates lasting impact across federal missions.</div><div></div><div><br>
We work with a broad range of government agencies in the defense, intelligence, and federal civilian sectors. Learn more and find opportunities at careers.noblis.org</div><div></div><div><b><br>
Why Work at Noblis</b></div><div></div><div><br>
At Noblis, we share a passion for excellence and innovation, and we create an environment where people can do meaningful work while maintaining the balance that keeps them energized and fulfilled. We seek out individuals with a natural curiosity and desire to collaborate and learn. We believe our people are our greatest strength, and we consistently seek exceptionally skilled, mission‑driven professionals who care deeply about doing work that enriches lives and makes our nation safer.</div><div></div><div><br>
Noblis has earned numerous workplace awards for our culture, our commitment to employee well‑being, and our dedication to meaningful, impactful work. We also maintain a drug‑free workplace.</div><div></div><div><i><br>
Remote/hybrid status is subject to change based on Noblis and/or government requirements.</i></div>
Commitment to Non-Discrimination:
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All qualified applicants will receive consideration for employment without regard to race, color, ethnicity, sex, age, national origin, religion, physical or mental disability, pregnancy/childbirth and related medical conditions, veteran or military status, or any other characteristics protected by applicable federal, state, or local law.</div><div></div><div><br>
If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact us.</div><div>
EEO is the Law | E-Verify | Right to Work</div><br>
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Total Rewards:
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At Noblis we recognize and reward your contributions, provide you with growth opportunities, and support your total well-being. Our offerings include health, life, disability, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, and work-life programs. Our award programs acknowledge employees for exceptional performance and superior demonstration of our service standards. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in our benefit programs. Other offerings may be provided for employees not within this category. We encourage you to learn more about our total benefits by visiting the Benefits page on our Careers site.</div><div></div><div><br>
Compensation at Noblis is determined by various factors, including but not limited to, the combination of education, certifications, knowledge, skills, competencies, and experience, internal and external equity, location, clearance level, as well as contract-specific affordability, organizational requirements and applicable employment laws. The projected compensation range for this position is based on full time status. For part time or on-call staff, compensation is proportionately adjusted based on hours worked. While monetary compensation is important, it's just one component of Noblis&rsquo; total compensation package.</div><br>
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Posted Salary Range: USD $86,800.00 - USD $135,625.00 /Yr.</div>

Senior Program Analyst - Chemical and Biological Weapons Elimination (CBWE)

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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<b>Position Summary</b>
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Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.<br>
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<b>Duties/Responsibilities</b>
<ul><li>Perform method transfer/validation and routine testing of in-process, final product, and stability samples.</li><li>
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.</li><li>
Perform data verification, data review and review of GMP documentation for general and complex methods.</li><li>
Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.</li><li>
Train and mentor others on QC test methods, processes and procedures.</li><li>
Perform other tasks as assigned.</li><li>
Perform other tasks as assigned.</li></ul>
<b>Qualifications</b>
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Specific Knowledge, Skills, Abilities :<ul><li>
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.</li><li>
Demonstrated technical writing skills.</li><li>
High problem-solving ability/mentality, technically adept and logical.</li><li>
Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs.</li><li>
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.</li><li>
Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred.</li></ul>
Education/Experience/ Licenses/Certifications :<ul><li>
Bachelor's degree or equivalent required, preferably in science. Netherlands: Bachelor's degree / HLO in (bioanalytical) science required.</li><li>
4+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.</li><li>
Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).</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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Summit West - NJ - US: $82,220 - $99,632<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.
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<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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R1599973 : Senior Specialist, QC Analytical, Cell Therapy</div>

Senior Specialist, QC Analytical, Cell Therapy

Capacity Chemical

<p>Job Description</p><p>The Quality Control Chemist at Capacity Chemical LLC will play a key role in ensuring the chemical integrity, consistency, and safety of agricultural chemical products through all stages of blending, dilution, and packaging. The Chemist will perform analytical testing, monitor quality control protocols, and ensure compliance with regulatory and customer specifications. This</p><p>role directly supports production, safety, and regulatory teams and helps maintain product quality and operational efficiency.</p><p>Core Job Duties and Responsibilities</p><ul><li>Conduct physical and chemical testing of raw materials, in-process blends, and finished agricultural chemical products</li><li>Verify and validate the concentration, purity, pH, specific gravity, and other critical parameters of chemical blends, dilutions, and packaged goods</li><li>Perform Quality Control checks on all production batches</li><li>Troubleshoot and maintain laboratory instrumentation</li><li>Support regulatory compliance efforts</li><li>Collaborate with production teams to identify and resolve any product quality issues during formulation, dilution, or packaging processes</li><li>Ensure safe handling and disposal of hazardous chemicals in accordance with federal and state safety and environmental regulations</li><li>Assist in the development and revision of quality procedures, test methods, and safety protocols to reflect evolving regulatory standards and company requirements</li><li>Participate in internal audits, quality improvement initiatives, and training of junior lab staff or new hires as directed.</li></ul><p>Required Knowledge and Skills</p><p>The position requires a Bachelor&rsquo;s degree in Chemistry, Biochemistry or a closely related field. Through academic coursework and laboratory training, the candidate must possess the following</p><p>knowledge and skills:</p><ul><li>Proficiency in general, organic, analytical, and physical chemistry, with laboratory techniques such as titration, spectroscopy, chromatography, and pH measurement.</li><li>Ability to conduct chemical testing of raw materials and finished products, validate results, and troubleshoot standard laboratory instrumentation.</li><li>Knowledge of laboratory safety protocols, hazardous chemical handling, and environmental compliance procedures.</li><li>Competence in documenting test results, preparing reports, and maintaining accurate laboratory records.</li><li>Ability to collaborate in laboratory and team-based environments and communicate findings clearly.</li><li>Familiarity with quality control principles, regulatory standards, and good laboratory practices (GLP).</li></ul><p>Pay: $25.00 - $35.00 per hour</p><p>Work Location: In person</p>

Quality Control Chemist

Search 10000+ Senior analytical chemist jobs near you this March. New roles added regularly across leading industries. Apply today.