scientist

Solenis

<div><div>The scientist plays a critical role in delivering innovative and effective water treatment solutions to industrial customers. This role requires a deep understanding of formulation chemistry, raw material evaluation, and analytical result understanding, combined with strong customer-facing skills. The ideal candidate will partner across all levels of the customer interface to identify needs, recommend solutions, and ensure best practices are followed. Sound knowledge of water treatment and familiarity in troubleshooting applications at different industry&rsquo;s is desired</div><div>
Under the technical guidance of team leader capable to perform independently routine scientific / application research tasks using standard techniques, procedures and equipment. Contributes to project experimental plan. Collaborate with business to understand technical challenges and propose tailored water treatment solutions.</div></div>

Scientist

BGIT India Private Limited

SUMMARY/JOB PURPOSE:On a day-to-day basis, scientist is expected to perform a variety of routine and complex analytical experiments using HPLC/UPLC, LC-MS, UV-Vis, FT-IR, Dissolution etc.<ul><li>Operate, maintain, and troubleshoot Agilent LC and MS instruments using Agilent OpenLab and EMPOWER softwares.</li></ul><ul><li>Ability to optimize methods, as well as analyze raw materials, intermediates, drug substance and drug product samples accurately in accordance with established methods.</li></ul>ESSENTIAL DUTIES AND RESPONSIBILITIES:<ul><li>Performing experiments to support drug substance and drug product development and release of finished products.</li></ul><ul><li>Analyze data acquired to draw conclusions based on statistical analysis and established quality control criteria.</li></ul><ul><li>Document work in ELN in compliance with company procedures and Good Documentation Practices.</li></ul><ul><li>Performing duties with commitment to laboratory safety and adherence to best practices is essential.</li></ul><ul><li>Occasionally, coordination with service engineers and company facilities team to schedule maintenance of analytical instrumentation is required.</li></ul>EDUCATION/EXPERIENCE/KNOWLEDGE &amp; SKILLS:<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in chemistry or related field with an emphasis in analytical chemistry.</li></ul><ul><li>One to five years of chromatography experience in pharmaceutical analytical field is required.</li></ul><ul><li>Knowledge and experience in developing and qualifying LC methods utilizing Agilent liquid chromatography instruments is desired.</li></ul>Pay: $65.00 - $70.00 per hourWork Location: In person

Buckeye Global

<div>SUMMARY/JOB PURPOSE:

On a day-to-day basis, scientist is expected to perform a variety of routine and complex analytical experiments using HPLC/UPLC, LC-MS, UV-Vis, FT-IR, Dissolution etc.
<ul><li>Operate, maintain, and troubleshoot Agilent LC and MS instruments using Agilent OpenLab and EMPOWER softwares.</li></ul>
<ul><li>Ability to optimize methods, as well as analyze raw materials, intermediates, drug substance and drug product samples accurately in accordance with established methods.</li></ul>

ESSENTIAL DUTIES AND RESPONSIBILITIES:
<ul><li>Performing experiments to support drug substance and drug product development and release of finished products.</li></ul>
<ul><li>Analyze data acquired to draw conclusions based on statistical analysis and established quality control criteria.</li></ul>
<ul><li>Document work in ELN in compliance with company procedures and Good Documentation Practices.</li></ul>
<ul><li>Performing duties with commitment to laboratory safety and adherence to best practices is essential.</li></ul>
<ul><li>Occasionally, coordination with service engineers and company facilities team to schedule maintenance of analytical instrumentation is required.</li></ul>

EDUCATION/EXPERIENCE/KNOWLEDGE &amp; SKILLS:
<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in chemistry or related field with an emphasis in analytical chemistry.</li></ul>
<ul><li>One to five years of chromatography experience in pharmaceutical analytical field is required.</li></ul>
<ul><li>Knowledge and experience in developing and qualifying LC methods utilizing Agilent liquid chromatography instruments is desired.</li></ul>

Salary info:

$65 - $70 / hr</div>

Lensa

<div>
 Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for LATICRETE. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice.
 
 
 
 Classification
 
 
 
 Salary
 
 
 
 Job Description
 
 
 
 Are you looking for a new challenge? Passionate about innovation? Want to work for a global company that values integrity, teamwork, and loyalty?
 
 
 At LATICRETE International, we aim to be the leading construction brand trusted globally for high-performance tile and stone installation systems and building finishing solutions. We&rsquo;ve been in business for over 65 years , family-owned for three generations , and can be found in over 100 countries . The Hartford Business Journal even named us one of Connecticut&rsquo;s top family-owned companies in 2017!
 
 
 We don't just make innovative, industry-leading products. Our purpose is to improve the built world and the lives of those who build it. We strive to connect with, engage with and improve the lives of our employees, our customers, our partners, and the global communities in which we operate .
 
 
 We are seeking passionate and ambitious employees who want to make a difference not just within our organization, but within their communities , our industry, and the world. If that sounds like you, then what are you waiting for? Join the family and expand your horizons!
 
 
 
 Just Some Of Our Benefits
 
 
 
 <ul>
 <li>
 Medical
 </li>
 <li>
 Dental
 </li>
 <li>
 Vision
 </li>
 <li>
 401k
 </li>
 <li>
 Tuition reimbursement
 </li>
 <li>
 12 paid holidays in addition to paid vacation and sick time
 </li>
 <li>
 Flexible spending
 </li>
 <li>
 Life Insurance, AD&amp;D and Supplemental Insurance
 
 
 </li>
 </ul>
 
 Position Summary
 
 
 
 Under general supervision, the Scientist is responsible for independently formulating and conducting analytical tests in accordance with ANSI, ISO, International standards, ASTM procedures and/or other accepted methods. The Scientist is also responsible for designing complex chemical studies and experiments on organic and/or inorganic compounds for other chemists in the team. This role is also responsible for in-depth analysis of data and accurately reporting results. Scientists will demonstrate technical expertise and techniques in a specific area along with a complete understanding of projects. The scientist also demonstrates competency in planning research projects, production and Quality control. They are expected to train and work with chemists on assigned projects. Scientists are expected to use independent judgment within specific area to determine appropriate approach to project work. Additionally, they must identify new materials and develop quality control tests for new products and maintain working knowledge of all analytical equipment, procedures and techniques.
 
 
 
 Essential Duties And Responsibilities
 
 
 
 Additional duties and responsibilities may be assigned, as necessary.
 
 
 Design, Develop and Validate - (50%)
 
 
 <ul>
 <li>
 Under general supervision, formulate products to meet specified requirements.
 </li>
 <li>
 Devise and conduct experiments to solve increasingly complex problems.
 </li>
 <li>
 Evaluate and suggest new raw materials through increasing communication with raw material suppliers.
 </li>
 <li>
 Review and perform competitive testing and analysis as required.
 </li>
 <li>
 Maintain a clean working laboratory environment as well as properly working equipment. Ensure that all instruments that required periodic calibration and validation requirements do so per laboratory calibration/validation procedures.
 </li>
 <li>
 Comply with all laboratory, company, state and federal safety regulations.
 
 
 </li>
 </ul>
 Provide Product Support - (20%)
 
 
 <ul>
 <li>
 Maintain cooperative, professional attitude with all LATICRETE employees and customers.
 </li>
 <li>
 Support Technical Services requests to evaluate field complaints in specific area.
 </li>
 <li>
 Support Operations in evaluating product inconsistencies &amp; providing disposition
 </li>
 <li>
 Participate in multi-disciplinary teams.
 </li>
 <li>
 Communicate results within R&amp;D, cross-functional departments and Stage Gate Review meetings.
 </li>
 <li>
 Help organize and participate in field trials as required.
 </li>
 <li>
 Interact with end-use customers and contractors to understand product usage, limitations, and needs.
 </li>
 <li>
 Assist and guide the production scale-up of new products developed: Write batching formulas for the production department based upon completed and approved laboratory formulations. Follow process through to full commercialization.
 </li>
 <li>
 Determine Quality Control parameters for product testing. Design Experiments for Chemists, review data and analyze results.
 
 
 </li>
 </ul>
 Data Analysis and Documentation - (10%)
 
 
 <ul>
 <li>
 Responsible for documenting all work via approved methods and sharing developments via occasional technical presentations.
 </li>
 <li>
 Independently process, analyze, and interpret results and data in specific area.
 </li>
 <li>
 Summarize ongoing work and findings to colleagues during department meetings.
 </li>
 <li>
 Document work continuously according to standard practice.
 </li>
 <li>
 Summarize all project work in a formal end report.
 
 
 </li>
 </ul>
 Mentor and Train New and Junior Team Members (20%)
 
 
 <ul>
 <li>
 Write work instructions for R&amp;D related test procedures.
 </li>
 <li>
 Help guide new and junior team members within the lab. Be a resource for escalations and problem solving.
 </li>
 <li>
 Impart Company knowledge of policies and procedures to help them orient to the organization.
 </li>
 <li>
 Consistently uphold Company culture through positive communications, managing conflict and fostering an open and constructive environment.
 
 
 </li>
 </ul>
 
 Required Skills &amp; Qualifications
 
 
 
 To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
 
 
 Education And Experience
 
 
 
 <ul>
 <li>
 BS in Chemistry, Material Science, Polymer Science or relevant Engineering discipline is required.
 </li>
 <li>
 MS a plus.
 </li>
 <li>
 8+ years of construction materials formulation experience with a proven track record of successful New Product Development, Scientific report writing, and skills in mentoring people.
 
 
 </li>
 </ul>
 
 Specialized Skills And Experience
 
 
 
 <ul>
 <li>
 Experience formulating products in a research and development lab environment in a specific area of the construction industry.
 </li>
 <li>
 Experience with Production/Operations, Product Management, QC, ISO processes, Analytical Chemistry, Product Development, Finance, Accounting and Marketing departments.
 </li>
 <li>
 Must be familiar with the process of researching patents, writing invention disclosures, and other publications within the industry.
 </li>
 <li>
 Demonstrated analytical ability in specific area, well organized, detail oriented, and systematic in documenting results.
 </li>
 <li>
 Demonstrated verbal and written communication skills in order to present and write reports.
 </li>
 <li>
 Ability to organize and present results in a clear concise manner.
 </li>
 <li>
 Must be able to analyze data independently and apply some specialized knowledge (e.g. DOE and statistical methods to solve problems).
 </li>
 <li>
 Must be a self-starter and able to multi-task.
 </li>
 <li>
 Computer skills: Intermediate to Advanced knowledge of Microsoft Office 365 (Word, Excel, PowerPoint), Outlook and other specialty software systems as required.
 
 
 </li>
 </ul>
 
 Physical Requirements
 
 
 
 <ul>
 <li>
 Lift: Must be able to lift and/or carry a minimum of 50 pounds.
 </li>
 <li>
 Push/Pull: Must be able to push/pull 50 pounds.
 </li>
 <li>
 Standing: Must be able to stand at least 50% of the day.
 </li>
 <li>
 Sitting: Must be able to sit at least 50% of the day.
 
 
 </li>
 </ul>
 
 Travel
 
 
 
 Domestic travel may be required as needed
 
 
 If you have questions about this posting, please contact support@lensa.com
 
 
</div>

GenScript

<div>
 
 
 About GenScript
 
 
 
 
 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
 
 
 
 GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
 
 
 
 
 About ProBio
 
 
 
 
 ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio&rsquo;s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.&nbsp;
 
 
 
 
 Job Summary:
 
 
 
 We are seeking a detail-oriented and proactive
 
 Analytical Associate Scientist or Scientist
 
 to join our US Protein Department. This role involves performing analytical testing and characterization of protein products to support research, development, and production activities. The ideal candidate will have a strong background in analytical chemistry, biochemistry, or biotechnology, with practical laboratory experience and familiarity with regulatory standards.
 
 
 
 Key Responsibilities:
 
 
 <ol>
 <li>
 Perform routine and non-routine analytical testing on protein samples using techniques such as HPLC, SDS-PAGE, ELISA, UV-Vis spectroscopy, and others as required.
 </li>
 <li>
 Prepare reagents, standards, and samples according to established protocols.
 </li>
 <li>
 Record, analyze, and interpret data with accuracy and integrity; prepare detailed reports and documentation.
 </li>
 <li>
 Maintain and calibrate laboratory instruments and ensure compliance with quality standards and safety regulations.
 </li>
 <li>
 Assist in method development, validation, and troubleshooting of analytical procedures.
 </li>
 <li>
 Collaborate with cross-functional teams to support project timelines and deliverables.
 </li>
 <li>
 Participate in the review and update of SOPs, batch records, and other quality documentation.
 </li>
 <li>
 Support continuous improvement initiatives and additional tasks as assigned by the supervisor.
 </li>
 </ol>
 
 
 Qualifications:
 
 
 <ol>
 <li>
 BS/MS in analytical chemistry, biochemistry, biotechnology, or related with 2+ years of relevant experience in protein purification/characterization.
 </li>
 <li>
 Hands-on experience with analytical instruments such as HPLC, SDS-PAGE, ELISA, UV-Vis, or similar is preferred.
 </li>
 <li>
 Strong attention to detail, organizational skills, and commitment to data integrity.
 </li>
 <li>
 Ability to work independently and collaboratively in a fast-paced team environment.
 </li>
 <li>
 Good communication skills and the ability to clearly document and present data.
 </li>
 <li>
 Experience working in a CRO or CDMO setting is an advantage.
 </li>
 </ol>
 
 &nbsp;
 
 
 
 #GS
 
 
 
 &nbsp;
 
 
 
 GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
 
 
 
 
 GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
 
 
 
 &nbsp;
 
 
 
 
 Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.&nbsp;
 
 
 
</div>

Analytical Associate Scientist/Scientist

CRISPR Therapeutics

<div>Job Description:
Company Overview
Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&amp;D operations based in Boston, Massachusetts and San Francisco, California.
Position Summary
Reporting to the Director of Clinical Development, the Clinical Scientist/Senior Clinical Scientist will provide scientific input to early and later stage clinical development programs.
Responsibilities<ul><li>
Contribute to the scientific development of individual clinical studies in alignment with the clinical development plan, including authoring and reviewing clinical documents (e.g., protocols, investigator brochures, CRFs, ICFs, CSRs)</li><li>
Perform initial review of clinical trial data (safety and efficacy), including assessing for consistency and completeness and providing preliminary assessments and recommendations</li><li>
Contribute to the oversight in collaboration with the clinical development lead during the conduct of the study</li><li>
Assist in communicating a clear overview of trial results</li><li>
Collaborate with internal stakeholders (clinical operations, data management, clinical pharmacology, statistics, safety, commercial, and regulatory affairs) to ensure translation of the clinical protocol into operational deliverables</li><li>
Collaborate with external stakeholders (CROs, investigators and clinical coordinators) to clarify data submissions</li><li>
Review and synthesize scientific literature and competitive intelligence to support study and program strategy</li><li>
Develop scientific and protocol training presentations to support internal and external meetings; e.g., site qualification and initiation, investigator meetings, and training materials</li><li>
Support preparation of scientific material for conference presentations or publications</li><li>
Contribute to the authoring and revision of regulatory submissions</li><li>
Perform analyses and generate scientific slide decks based on clinical, translational and other datasets</li></ul>
Minimum Qualifications<ul><li>
Advanced scientific or clinical degree (eg PhD, PharmD, MPH, etc).</li><li>
Clinical Scientist: 1-3 years/ Senior Clinical Scientist: 4-8+ years of previous experience in clinical or related research</li><li>
Excellent oral and written communication skills and analytical skills</li><li>
Ability to work collaboratively in a fast-paced, team-based matrix environment</li><li>
Familiarity with ICH, GCP, and relevant regulatory requirements, and strong analytical and strategic thinking skills, experience with interacting with medical monitors, development operations (preclinical, clinical operations, regulatory affairs, Quality Assurance) and clinical investigators</li></ul>
Preferred Qualifications<ul><li>
Experience in cellular therapies/CAR-T trials</li><li>
Experience in Phase 1/Phase 2 clinical trials</li></ul>
Competencies<ul><li>
Collaborative &ndash; Openness, one team, positivity</li><li>
Undaunted &ndash; Fearless, can-do attitude, self-starter</li><li>
Results Orientation &ndash; Delivering progress toward our mission; Sense of urgency in solving problems; Attention to details; Practical</li><li>
Entrepreneurial Spirit &ndash; Proactive; Ownership mindset; Thinks outside the box</li></ul>
CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.
Clinical Scientist: Base pay range of $125,000 to $140,000+ bonus, equity and benefits
Senior Clinical Scientist: Base pay range of $150,000 to $170,000+ bonus, equity and benefits
The range provided is CRISPR Therapeutics&rsquo; reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy</div>

Clinical Scientist/ Senior Clinical Scientist

TWIST BIOSCIENCE

<div><h2 class="jobSectionHeader">Scientist/ Sr Scientist / Staff Scientist (DNA Synthesis Process Development) in South San Francisco, CA</h2>
<h3 class="jobSectionHeader">Job Description</h3>

The R&amp;D team at Twist Bioscience is searching for a curious, thoughtful, and driven Scientist with excellent lab hands to help us innovate on our core technology. We are looking for a &quot;Triple Threat&quot; Scientist: someone with strong Molecular Biology skills, a solid grasp of DNA Chemistry, and the ability to code their own data analysis.

Your mission is to close the loop. You will take the DNA from the chip, perform complex enzymology and library preparation, and analyze the sequencing data to prove that our synthesis innovations are working. We are looking for people who have:
<ul>
<li>Excellent Lab Hands. You can handle complex gene assemblies, low-input library preps, and difficult PCRs with precision.</li>
<li>A Chemist's Brain. You aren't just a user; you understand the underlying chemical cycle that created the DNA.</li>
<li>Data fluency. You can look at a raw sequencing dataset and tell a story with data.</li>
</ul>
Job title and compensation will be determined based on several factors, including but not limited to the candidate's years of experience, individual skills, knowledge, and abilities.
<h3 class="jobSectionHeader">
Key Responsibilities:</h3>
<ul><li>Design and execute downstream validation workflows for new synthesis chemistries.</li>
<li>Perform complex nucleic acid enzymology: Utilizes the full range of enzymatic tools (polymerases, ligases, nucleases, kinases) to repair, modify, and assemble DNA from chip to library.</li>
<li>Execute NGS Library Prep: Select and run the appropriate library prep workflows (Illumina/Nanopore) to reveal specific synthesis error modes.</li>
<li>Code your own analysis: Use Python or R to analyze NGS data, generate figures, and correlate biological performance with upstream synthesis conditions.</li>
<li>Troubleshoot synthesis issues by understanding the phosphoramidite cycle and identifying chemical shortcomings.</li>
<li>Move projects forward efficiently and prioritize tasks in accordance with the company's goals.</li>
</ul><h3 class="jobSectionHeader">Qualifications:</h3>
<ul><li>Experience in Molecular Biology, Genomics, Biochemistry, or combination of closely-related field and experience.
<ul><li>Scientist 
Requires a PhD and 0-2 years of previous professional experience; 
or a master's degree and 3-5 years of work experience</li>
<li>Sr Scientist 
Requires a Ph.D. and 2-5 years of professional experience (postdoc may count); 
or a master's degree and 5-7 years of work experience</li>
<li>Staff Scientist 
Requires a Ph.D. and 5-8 years of professional experience (postdoc may count); 
or a master's degree and 7 years of work experience</li>
</ul></li><li>Expert Enzymology: You know anything an enzyme can do on a nucleic acid. Deep hands-on experience with complex manipulations, gene construction, and repair workflows.</li>
<li>Handling Modified Templates: Experience amplifying or manipulating nucleic acids with non-standard modifications (e.g., stability mods, backbone changes, or novel linkers).</li>
<li>DNA Chemistry Literacy: Must understand the fundamentals of the DNA synthesis cycle (coupling, deblocking, oxidation) and how errors arise.</li>
<li>Coded Data Analysis: Proven ability to use Python or R to analyze experimental results (sequencing alignment, error rate calculation, plotting).</li>
<li>Comfortable working in a fast-paced R&amp;D environment.</li>
</ul><h3 class="jobSectionHeader">About Twist Bioscience</h3>

Twist Bioscience synthesizes genes from scratch, known as &quot;writing&quot; DNA. Just as children learn to both read and write, the next phase of development for the genomics revolution is the ability to write DNA.

At Twist Bioscience, we work in service of people who are changing the world for the better. In fields such as health care, agriculture, industrial chemicals and data storage, our unique silicon-based DNA Synthesis Platform provides precision at a scale that is otherwise unavailable to our customers.

Twist Bioscience Corporation is an Equal Opportunity Employer. Twist Bioscience Corporation provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic characteristics, or any other category protected by law.</div>

Scientist/ Sr Scientist / Staff Scientist (DNA Synthesis Process Developme

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