field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionAbout Us and the Role:
At BlueShift, we aim to remove gigatons of CO2 from the ocean and atmosphere and extract valuable critical minerals from industrial waste. BlueShift unlocks rapid scalability by integrating proprietary membrane-free electrochemical technology from the University of Michigan and University of Massachusetts Amherst with additive manufacturing and existing infrastructure.
As an entry-level chemist or intern, you will run experiments to support the prototyping and scaling up of our carbon removal and mineral extraction processes. You will also practice characterization techniques of the intermediates and products we produce. The candidate is expected to value working in a fast-paced, entrepreneurial, and collaborative environment with a small and agile team. This position will report to the Chief of Science and Operations. Qualifications
<ul>
<li>B.S. or soon to have B.S. in chemistry or chemical engineering</li>
<li>Experience and comfortability in a wet lab setting and familiar with chemical safety and waste procedures</li>
<li>Experience preparing solutions, reagents, and running multi-step chemical processes to produce a product</li>
<li>Organized and ability to follow procedures closely, with careful notetaking</li>
<li>Practice with characterization techniques such as FTIR, UV-vis, and potentially XRD</li>
<li>Great to Have: experience with carbon mineralization, electrochemistry (running potentiostats / galvanostats, electroplating), solvent extraction, environmental chemistry, designing experiments </li>
</ul>
Please tailor your resume to your position and address the following in your cover letter: 
What attracted to you to this position and why do you believe you're a good fit for BlueShift?
What experience do you have related to the qualifications above (specific projects, skills learned, coursework)
What is your experience (not required) or interest in working at a startup?
BlueShift Carbon, Inc is an equal opportunity employer.

Entry Level Chemist or Chemical Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 128,000-190,000 DOE 
General Summary
We are seeking a highly motivated and proactive chemist to join our growing medicinal chemistry/bioconjugation drug discovery team. In this laboratory-based position, the successful candidate will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of ADC drug discovery projects. The successful candidate will be skilled in the art of organic synthesis and familiar with modern synthetic methods, analytical data interpretation, troubleshooting reactions, and purifications. The candidate will also demonstrate aptitude for learning new therapy areas as Orum expands its pipeline.
 
Principle Duties and Responsibilities
<ul>
<li> Design, synthesize, and characterize novel drug-like molecules utilizing medicinal chemistry knowledge and an understanding of ADME, pharmacokinetics, optimal physicochemical properties, and AI/ML predictive tools.</li>
<li> Design and synthesize novel conditional release linkers and payload-linker combinations for bioconjugation chemistry.</li>
<li> Support our internal and external synthetic chemistry teams in troubleshooting and proposing alternative synthetic routes.</li>
<li> Apply structure-based drug design and computational and modeling approaches to prioritize syntheses. </li>
<li> Analyze screening data, elucidate structure activity relationships using multi-parameter analysis, perform literature reviews, design, propose, and implement medicinal chemistry plans, and coordinate chemistry and biology data to drive the SAR optimization cycle toward project goals.</li>
<li> Support the project team efforts on compound progression, nominate/ prioritize lead compounds for in vitro and in vivo biological and ADME assessment.</li>
<li> Contribute to the chemistry and bioconjugation team organization, productivity, and expertise through collaboration and generation and exchange of innovative ideas.</li>
<li> Present scientific updates and effectively communicate research findings in internal and external collaborators project team meetings and contribute to strategic R&amp;D decisions.</li>
<li> Contribute to the development of intellectual property and assist in patent drafting and/ or scientific publications.</li>
<li> Maintain proper electronic notebook and sample management record keeping.</li>
<li> Maintain and promote a culture of safe laboratory practices and laboratory citizenship.</li>
<li> Contribute to the build-out and upkeep of an expanding laboratory through maintaining shared equipment, assisting with general laboratory housekeeping, and developing processes for improving workflow efficiency.</li>
<li> Mentor and support junior team members.</li>
</ul>
Skills, Abilities &amp; Competencies
<ul>
<li> Experience in the biopharmaceutical industry.</li>
<li> Strong track record of achievement in the synthesis of complex molecules and/or synthetic route optimizations, with deep knowledge of modern synthetic &amp; analytical techniques. </li>
<li> Proven track record of scientific contributions including peer reviewed publications, patents and/or presentations.</li>
<li> Experience with the selection and application of appropriate purification techniques (flash chromatography, HPLC, SFC, etc.), QC and structural elucidation methods (LC/MS, NMR, etc.).</li>
<li> Some experience with computational chemistry methods is preferred.</li>
<li> Experience with design and synthesis of conditional release linkers and/or prodrugs is preferred.</li>
<li> Current knowledge of the key Medicinal Chemistry principles and physicochemical properties of drug-like matter, and a strong understanding of biology, pharmacology, drug metabolism, and pharmacokinetics</li>
<li> Experience with various small molecules drug discovery modalities such as small molecule inhibitors, PPI inducers including PROTACs and MGs, etc. Familiarity with antibody drug conjugates is a plus.</li>
<li> Strong problem-solving skills and the ability to effectively collaborate in a highly matrixed environment.</li>
<li> Collaborative team player with strong communication and time-management skills, the ability to handle multiple projects simultaneously, and the ability to effectively collaborate with a global multidisciplinary team.</li>
<li> Strong work ethic and ability to work independently with minimal supervision.</li>
</ul>
Education- Ph.D. or equivalent degree in organic/medicinal chemistry or a related field with minimum 2 years' industrial experience, MS degree with 8 years', or BS degree with 11 years' 
Orum offers a Core benefits program which includes: medical, dental, short and long term disability, life insurance and a 401k.
*U.S. citizens and those authorized to work in the U.S. (green card) are encouraged to apply. We are unable to sponsor at this time.
*Candidate must be able to pass a background investigation.
*Only local residents to the Boston area will be considered.
*Unable to work with 3rd party candidates or agencies.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily within the context of the representative work environment and physical demands described above. Likewise, qualifications listed are representative of the knowledge, skills, and abilities required to perform the positions essential functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Orum Therapeutics is an Equal Opportunity Employer (EOE).

Medicinal Chemist

<h3>Job Description</h3>
Job DescriptionDescriptionPerforms routine chemical productions and process developments based on provided work instructions and training in a safe and high-quality manner. Works collaboratively with internal laboratory production colleagues, R&amp;D, operations, and quality during directed development efforts. Key Responsibilities
<ul>
<li>Performs and completes routine chemical production based on written procedures or direct instruction within expected timelines.</li>
<li>Ability to set up all required equipment for production of products and other related activities.</li>
<li>Evaluates his/her projects/production (e.g. in process parameters and quality control measures) and offers suggestions for improvements.&nbsp;</li>
<li>Capable of running routine in-process control tests based upon written and direct instructions.</li>
<li>Responsible for maintaining a clear and detailed lab notebook and production records.</li>
<li>Responsible for maintaining neat, clean and safe work area.</li>
<li>Performs other duties of similar complexity as directed.</li>
</ul>
 Skills, Knowledge and ExpertiseMinimum Qualifications:
<ul>
<li>Associate degree in chemistry or engineering with 5+ years of relevant experience.</li>
<li>Proficiency in general inorganic and organic chemistry.</li>
<li>Demonstrated experience in laboratory chemical processes and techniques.</li>
<li>Experience working with products that may pose special hazards, such as air-sensitive, moisture-sensitive, pyrophoric, high-energy, toxic, high-potency, etc., as well as synthetic organic, organometallic, or inorganic chemistries and associated equipment and techniques (e.g., glove boxes, Schlenk techniques).</li>
<li>Strong organizational, problem-solving, and analytical skills.</li>
<li>Self-starter with the ability to manage priorities and workflow.</li>
<li>Capacity to work independently and handle multiple projects while meeting deadlines.</li>
<li>Strong interpersonal skills.</li>
<li>Proficient in collaboration tools such as Teams, Salesforce, SharePoint, and Electronic notebooks.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Bachelor's degree in chemistry or engineering with 0-2+ years of relevant experience.</li>
</ul>
 Benefits 
<ul>
<li>Medical, Dental, Vision - effective day one of employment.</li>
<li>401(k) with company match with immediate vesting - effective first of the month, following date of hire.
<ul>
<li>First 3% is matched dollar-for-dollar.&nbsp;</li>
<li>Second 3% is matched at 70 cents on the dollar.&nbsp;</li>
</ul>
</li>
<li>3 Weeks' Vacation.</li>
<li>12 Paid Holidays.</li>
<li>Basic Life, AD&amp;D, STD, and LTD provided at no cost to employee.</li>
</ul>

Production Chemist

<h3>Job Description</h3>
Job Description
 
Position Summary
Perform all activities associated with Quality Control release testing for starting materials and drug product disposition. Provide the organization with technical expertise in analytical instrumentation and chemistry laboratory experiment design. Utilize your experience with technology transfer and a knowledge of cGMP/ICH/FDA/EU regulations 
Duties and Responsibilities
 
<ul>
<li>Work as part of a cross-functional team to perform QC activities for technology transfer of manufacturing and testing processes to external CMO/CTOs</li>
<li>Perform release and stability testing for starting materials and drug product</li>
<li>Perform data review, analysis, identification of trends, and complex problem solving</li>
<li>Perform assay troubleshooting and identify and implement improvements to existing assays</li>
<li>Write and review QC SOPs and qualification/validation protocols and reports, as needed</li>
<li>Prepare, execute, and review deviations, change controls, CAPAs, OOT/OOS</li>
<li>Ensure all products are QC tested in a timely fashion to meet customer demand</li>
<li>Ensure Standard Operating Procedures are in place for all testing procedures and supporting procedures</li>
<li>Ensure lab is properly equipped and supplied</li>
<li>Identify and implement process/procedural improvements related to QC functions to improve efficiencies and effectiveness</li>
<li>Collect and prepare data for metric reporting to management, such as Key Quality Indicators (KQI)</li>
<li>Maintain control and confidentiality of documents and information </li>
<li>Ability to work unscheduled and overtime hours as needed</li>
<li>Other duties as assigned</li>
</ul>
Regulatory Responsibilities 
<ul>
<li>Ensure testing is in compliance with all applicable Regulatory requirements </li>
<li>Ensure accurate and timely date submission for Regulatory Authority</li>
<li>To meet Regulatory requirements and standards set internally and those by Corporate Global Quality</li>
<li>Responsible for the compliance to USDA rules and regulations and to internal standards</li>
<li>Conduct business in a responsible manner that complies with all state, FDA, OSHA and HIPAA regulations, or otherwise as applicable</li>
</ul>
Supervisory Responsibilities
Provide leadership in daily operations and have employees incorporate compliance practices into their daily routines 
Experience
Two to four (2-4) years experience in QC GMP environment, or related education 
Education
Bachelor’s degree in a Biological or related sciences 
Knowledge, Skills &amp; Abilities
<ul>
<li>Experience in analytical chemistry and familiarity with Quality Control functions </li>
<li>Experience related to Quality Assurance/Quality Systems with exposure to GMP environment</li>
<li>Experience with technology transfer</li>
<li>Strong technical knowledge and skill base. Experience with wet chemistry and analytical chemistry. </li>
<li>Leadership skills and demonstrated ability to work in a productive and collaborative cross-functional manner</li>
<li>Knowledge of cGMP/ICH/FDA/EU regulations</li>
<li>Proficiency in Microsoft Office Suite applications of intermediate to advanced level </li>
<li>Superb written and oral communication skills</li>
<li>“Do-what-it-takes” attitude</li>
<li>Excellent organizational skills, sufficient to multi-task in an extremely fast-paced environment with changing priorities</li>
<li>Satisfactory audio-visual acuity</li>
<li>Ability to read and write English</li>
<li>Able to travel to customers and/or other contractual facilities as needed.</li>
</ul>
Physical Requirements

<ul>
<li>Ability to sit for prolonged periods of time</li>
<li>Ability to stand for prolonged periods of time</li>
<li>Ability to lift up to 10lbs</li>
</ul>
Perform all activities associated with Quality Control release testing for starting materials and drug product disposition. Provide the organization with technical expertise in analytical instrumentation and chemistry laboratory experiment design. Utilize your experience with technology transfer and a knowledge of cGMP/ICH/FDA/EU regulations

QC Chemist I

<h3>Job Description</h3>
Job Description
Background: Tri- K is one of leading suppliers of natural actives such as proteins, peptides and a comprehensive cosmetic ingredients portfolio to the personal care industry. It has an R&amp;D center with state-of-the-art equipment and testing facilities. To strengthen its innovation capabilities and improve customer connectivity, the R&amp;D organization focuses on developing new innovative ideas, products, and formulations with proven efficacy. This senior level R&amp;D position is part of the manufacturing organization based in Derry, NH
Summary: 
We are seeking a highly motivated and experienced protein chemist to join our team. The ideal candidate should have a PhD in protein chemistry, biochemistry, or a related field, or have at least 3 years of experience in protein characterization, purification, and analysis.
Essential Duties and Responsibilities include the following. Other duties may be assigned. 
<ul>
<li>Develop and optimize protein purification protocols.</li>
<li>Characterize and analyze proteins and peptides using techniques such as HPLC, SDS-PAGE, and mass spectrometry.</li>
<li>Perform chemical reactions to implement protein modification. </li>
<li>Conduct protein stability studies and develop formulations to improve protein stability.</li>
<li>Collaborate with other scientists to develop new protein-based cosmetic ingredients and products.</li>
<li>Maintain and troubleshoot laboratory equipment.</li>
<li>Write technical reports and present findings to internal and external stakeholders.</li>
</ul>
<ul>
<li>Search and evaluate published literature to understand hair and skin substrates, new protein technologies and new methodologies.</li>
</ul>
<ul>
<li>Research the latest market trends, customer needs, and competitor positioning.</li>
<li>Provide guidance to the Technical Services Team in addressing customer inquiries in a direct and succinct manner.</li>
<li>Collaborate with the Sales, Marketing and Business Managers, to ensure effective marketing claims, and to ensure continued positive client relationships and to build relationships with new clients.</li>
</ul>
<ul>
<li>Investigate possibilities and benefits of line extensions and functional blends surpassing industry standards. </li>
<li>Research the feasibility of combining proteins with other chemistries and technology promoting synergistic effects.</li>
<li>Research prior patents to allow for “freedom to operate”. </li>
</ul>
<ul>
<li>Explore new partnerships and collaborations with academia. </li>
</ul>
Required Skills and Competencies
Strong Technical Background in Protein/Peptide Chemistry is required. The incumbent must have a strong understanding of protein/peptide behavior to modify, identify and purify the active proteins/peptides from a complex natural source. He/She should be open to new challenges and be able to implement creative and innovative approaches. 
Competencies
To perform the job successfully, an individual should demonstrate the following competencies:
<ul>
<li>Strong knowledge of protein chemistry and biochemistry</li>
<li>Experience with protein purification techniques such as chromatography and ultrafiltration</li>
<li>Experience with protein analysis techniques such as HPLC, SDS-PAGE, and mass spectrometry</li>
<li>Strong problem-solving and analytical skills</li>
<li>Excellent communication and interpersonal skills</li>
<li>Ability to work independently and in a team environment.</li>
<li>Strong technical, and strategic acumen. </li>
<li>Exceptional verbal, written communication, and presentation skills</li>
<li>Comfort &amp; capability to work effectively in a collaborative cross-functional organization.</li>
<li>Analytical, and Problem-Solving skills to find effective solutions and overcome challenges. </li>
<li>Project Management - Develop project plans; Complete projects on time and budget. </li>
<li>Strong time management and prioritization skills. </li>
<li>Innovation - Develop and present innovative approaches and ideas. </li>
</ul>
Qualifications:
The requirements listed below are representative of the knowledge, skill, and/or ability required.
Education/Experience:
PhD in protein chemistry, biochemistry, or a related field. Or have at least 3 years of experience in protein characterization, purification, and analysis.
Scientific Language Ability:
Ability to read, analyze, and interpret scientific periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, and customers.
Analytical skills: 
Ability to solve practical problems and deal with numerous assumptions and variables in situations where only limited standardization exists. Knowledge of MS Suite and other PC tools is essential.
Physical Demands:
This position requires working at the Derry, NH R&amp;D center 5 days a week, unless travelling to attend trade shows or visit other Tri-K sites. 
Travel Requirements:
10% travel including domestic/international with overnight stays to drive business development efforts.

Senior Protein Chemist

<h3>Job Description</h3>
Job Description
*** Candidates must be authorized to work in the U.S. without current or future visa sponsorship. Sponsorship is not available for this position.
Are you a creative and results-driven lead chemist with a passion for developing innovative polymer formulations? Do you thrive in a fast-paced environment, collaborating with R&amp;D, production, and customers to deliver high-performance plastic solutions? If so, we want to hear from you!
Why Join?
<ul>
<li>Be part of a rapidly growing and innovative plastics manufacturer.</li>
<li>Work on cutting-edge polymer formulations with industry-leading experts.</li>
<li>Opportunity to make a direct impact on product development and customer success.</li>
<li>Collaborative, fast-paced, and dynamic work environment.</li>
</ul>
Key Responsibilities:
<ul>
<li>Develop and optimize polymer formulations to meet customer requirements and improve first-pass acceptance rates.</li>
<li>Manage multiple customer sample requests and ensure timely delivery within R&amp;D lead times.</li>
<li>Collaborate with operations and manufacturing to scale up new products and optimize production processes.</li>
<li>Provide technical support to sales teams and customers, including product recommendations and troubleshooting.</li>
<li>Maintain R&amp;D records, formulations, and testing data while ensuring compliance with quality and environmental standards.</li>
</ul>
What You Bring:
5+ years of hands-on experience in plastic development, including formulation, processing, and performance optimization. PVC experience preferred. And the ability to take on progressively challenging responsibilities.
BS in Chemistry, Materials Science, or Chemical Engineering preferred but not required.
Strong understanding of polymer properties, processing, and application performance.
Ready to innovate and drive the future of polymer materials? 
EOE

Senior Research and Development Chemist

<h3>Job Description</h3>
Job DescriptionDescription
We are seeking a passionate PhD-level synthetic chemist to drive the discovery of small molecules for next-generation 3D printing resins. Similar to a drug discovery role, this position involves rapid exploration of chemical space through organic synthesis to develop structure-property relationships. However, our feedback loops take only days rather than months or years, and the structure-property relationships involve diverse photochemistry. This role is particularly appealing to synthetic chemists with a passion for physical organic chemistry. Our process uses a small amount of each lead candidate, so synthetic creativity is not limited by the scalability concerns that usually narrow the available chemical space in materials applications.
Responsibilities:
<ul>
<li>Design, refine, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates. </li>
<li>Characterize lead candidates via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry. </li>
<li>Contribute to the development of high-throughput analytical capabilities, small molecule databases, and virtual libraries. </li>
<li>Work closely with analytical chemists and chemical engineers to establish structure-property relationships in formulations containing lead candidates.</li>
</ul>
Minimum Qualifications:
<ul>
<li>PhD in Organic Chemistry or BS in Chemistry and 5+ years of experience in a small molecule discovery role. </li>
<li>Candidates should have strong expertise in both synthetic and physical organic chemistry, demonstrated through publications and other activities.</li>
<li>Significant experience designing and executing multi-step synthetic routes.</li>
<li>Extensive experience with modern computing and data analysis tools relevant to synthetic chemistry. </li>
<li>Excellent communication, organizational, and time management skills. </li>
<li>Demonstrated ability to independently drive an idea from conception to project completion. </li>
<li>Evidence of strong collaboration and teamwork talents/skills. </li>
<li>Strong publication record, both as lead author and as contributor to other projects.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Expertise in photochemistry and/or radical chemistry. </li>
<li>Experience with synthesis of heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics. Experience with cheminformatics and/or computational chemistry tools (e.g. DFT) relevant to the production of structure-property relationships.</li>
</ul>
Additional Information:
<ul>
<li>Travel: Occasional travel may be required from time to time </li>
<li>Location: Boston, Massachusetts </li>
</ul>
 We value diversity in our company and are an Equal Opportunity Employer.

Senior Chemist

<h3>Job Description</h3>
Job Description
Summary: The Quality Control (QC) Chemist is responsible for performing complex chemical and physical analyses of raw materials, in-process samples, and finished products to ensure compliance with quality standards and regulatory requirements. This role involves method development and validation, data analysis, troubleshooting, and collaboration with cross-functional teams to support manufacturing processes.
 Essential Duties and Responsibilities include the following. Other duties may be assigned.
<ul>
<li>Analytical Testing:
<ul>
<li>Perform complex chemical and physical analyses using advanced laboratory techniques and instrumentation.</li>
<li>Develop, validate, and implement new analytical methods as needed.</li>
</ul>
</li>
<li>Data Analysis and Reporting:
<ul>
<li>Interpret analytical data to assess product quality and identify trends or anomalies.</li>
<li>Prepare detailed reports and documentation in compliance with regulatory standards.</li>
</ul>
</li>
<li>Method Development and Validation:
<ul>
<li>Develop and validate analytical methods to support new product development and process improvements.</li>
<li>Ensure methods are robust, reproducible, and compliant with industry standards.</li>
</ul>
</li>
<li>Troubleshooting and Problem-Solving:
<ul>
<li>Investigate and resolve analytical issues, non-conformances, and out-of-specification results.</li>
<li>Collaborate with production and quality teams to implement corrective actions.</li>
</ul>
</li>
<li>Compliance and Documentation:
<ul>
<li>Ensure all laboratory activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other regulatory requirements.</li>
<li>Maintain accurate and complete records of all analyses, calibrations, and maintenance activities.</li>
</ul>
</li>
</ul>
Location:
Must be commutable within 25 miles of Derry, NH. Local applicants considered only.
Education/Experience:
Bachelor's degree from four-year college or university, preferably in Microbiology, Chemistry, Biology or a related field. Experience with microbiology is preferred. Four plus years of laboratory experience, including internships or academic lab work; or equivalent combination of education and experience is a plus. Basic understanding of chemical analysis techniques and laboratory equipment is also preferred.
Language Ability:
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.
Qualifications:
<ul>
<li>Proficiency in advanced analytical techniques and instrumentation (e.g., HPLC, GC, FTIR, UV-Vis).</li>
<li>Strong problem-solving and troubleshooting abilities.</li>
<li>Excellent attention to detail and organizational skills.</li>
<li>Effective communication and interpersonal skills.</li>
<li>Ability to work independently and as part of a team</li>
</ul>

Senior Chemist - Quality Control

<h3>Job Description</h3>
Job Description
The Uban Environmental Chemist provides expert advice and technical support in the assessment, management, and mitigation of chemical-related environmental issues. This role involves conducting detailed environmental studies, interpreting data, and developing strategies to address chemical contamination in water and wastewater. The consultant works closely with clients from various sectors, including industrial, governmental, and non-profit organizations, to ensure compliance with environmental regulations and to promote sustainable practices.
Key Responsibilities:
<ol>
<li>MassDEP Certified Laboratory Supervisor</li>
</ol>
<ul>
<li>Supervisor laboratory operations in compliance with the MassDEP requirements</li>
<li>Ensure all reporting and data analysis in complete.</li>
<li>Maintain all QA/QC procedures.</li>
</ul>
 
<ol>
<li>Environmental NPDES Monitoring:</li>
</ol>
<ul>
<li>Conduct chemical analyses of environmental samples (water).</li>
<li>Identify and quantify contaminants and assess their potential impacts on the environment and human health.</li>
<li>Design and implement field samplingprograms and laboratory tests.</li>
</ul>
 
<ol>
<li>Data Analysis and Interpretation:</li>
</ol>
<ul>
<li>Analyze complex chemical data using advanced statistical and modeling techniques.</li>
<li>Interpret findings and prepare detailed technical reports, including risk assessments and environmental impact statements.</li>
</ul>
 
<ol>
<li>Regulatory Compliance:</li>
</ol>
<ul>
<li>Advise clients on compliance with local, state, and federal environmental regulations.</li>
<li>Assist in obtaining necessary permits and approvals for projects involving chemical usage or remediation.</li>
<li>Stay updated on changes in environmental laws and standards.</li>
</ul>
 
<ol>
<li>Consultation and Client Interaction:</li>
</ol>
<ul>
<li>Provide expert advice and solutions to clients on chemical management and environmental issues.</li>
<li>Prepare and deliver presentations and reports to clients, regulatory agencies, and other stakeholders.</li>
<li>Facilitate workshops and training sessions on environmental chemistry topics.</li>
</ul>
 
<ol>
<li>Sustainability and Environmental Management:</li>
</ol>
<ul>
<li>Promote sustainable chemical practices and processes in client operations.</li>
<li>Evaluate and recommend improvements to reduce environmental footprints and enhance sustainability.</li>
<li>Support the development of corporate environmental policies and strategies.</li>
</ul>
 
Qualifications:
<ul>
<li>Education:</li>
<ul>
<li>Bachelor’s degree in Environmental Chemistry, Chemistry, Environmental Science, or a related field.</li>
</ul>
<li>Experience:</li>
<ul>
<li>Minimum of 3-5 years of experience in environmental chemistry, environmental consulting, or a related field.</li>
<li>Proven track record in environmental assessments, data analysis, and regulatory compliance.</li>
</ul>
<li>Skills:</li>
<ul>
<li>Proficiency in chemical analysis techniques and laboratory instrumentation.</li>
<li>Strong understanding of environmental regulations and standards (e.g., EPA, OSHA).</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Effective communication and presentation skills.</li>
<li>Project management experience is a plus.</li>
</ul>
</ul>
Working Conditions:
<ul>
<li>Combination of office, laboratory, and field work.</li>
<li>May require travel to client sites.</li>
<li>Ability to work in various environmental conditions and handle hazardous materials safely.</li>
</ul>

Urban Environmental Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
AbbVie Analytical Research &amp; Development (Analytical R&amp;D) is a global analytical scientific organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products.  Our scope includes AbbVie's diverse pipeline of innovative small molecule medicines and spans from the selection of Discovery candidate molecules through Early-Stage Clinical Development.  We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines.  Careers in AbbVie Analytical R&amp;D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies.  We are looking for diverse candidates with strong scientific and leadership experience to join the AbbVie Analytical R&amp;D team and can offer exciting and rewarding career opportunities for these candidates.&nbsp;
Position Description:&nbsp;
For the&nbsp;Principal Research Scientist I position, we are seeking a highly motivated, experienced analytical scientist to be a Analytical Project Leader in New Chemical Entities (NCEs) drug substance and drug product in both preclinical and clinical programs.&nbsp; The candidate should have extensive expertise within an R&amp;D environment with a fit for purpose mind set.&nbsp; Familiarity with solid oral dosage forms including nanoparticles, amorphous systems and lipids is expected. &nbsp;Experience with lipid nanoparticles is a plus.&nbsp;
He/she should be able to conceive, execute and communicate novel multi-disciplinary research or development strategies that achieve project and strategic goals. Serve as a analytical project leader and contribute scientific insights on discovery programs with candidate compounds moving to clinical.
He/she must foster productive collaborations within the global Analytical R&amp;D organization and with R&amp;D cross-functional partners such as Discovery, Pre-Clinical Safety, Process Chemistry, Process Engineering, Molecular Profiling and Drug Delivery, Drug Product Development, and Quality Assurance and CMC-Regulatory. &nbsp;
Qualifications 
<ul>
<li>Bachelors, Masters, or Ph.D. in Analytical Chemistry typically with a minimum of 14 (BS), 12 (MS), or 6 (Ph.D.) years related industry experience.</li>
<li>Strong technical background in analytical chemistry, excellent analytical problem-solving skills. Capable of independently developing and troubleshooting analytical methods.</li>
<li>Experience with analytical approaches toward physicochemical characterization of pharmaceutical dosage forms (i.e. HPLC, UPLC, MS, DSC, TGA, DVS, PXRD, dissolution)</li>
<li>Knowledge of preclinical and clinical formulation development principles relevant to lipid nanoparticle (LNP) formulations - demonstrated industry experience strongly preferred.</li>
<li>Working knowledge of typical formulation approaches and routes of administration (i.e. IV, SC, IP, PO) across multiple species.</li>
<li>Familiarity with the role that physicochemical properties play in drug delivery and formulation design.</li>
<li>Demonstrate creative 'out of the box' thinking to solve difficult problems</li>
<li>Self-motivated, hard-working, detail-oriented individual able to work in a fast-paced team environment.</li>
<li>High-quality written and oral communication skills and ability to interact effectively with interdisciplinary scientists and engineers.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>​This is an on-site opportunity located at AbbVie Bioresearch Center (ABC) in Worcester, MA.&nbsp;</li>
<li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​</li>
<li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</li>
<li>This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​</li>
<li>This job is eligible to participate in our long-term incentive&nbsp;programs​</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.&nbsp; It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html&amp;nbsp" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>;
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

166 Science Jobs