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<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a scientist with strong organizational skills, excellent oral and written communication, and keen attention to detail. The ideal candidate will support the development, optimization, and qualification of analytical methods in a compliance-based environment. This role involves method development, process support, documentation, and potential technology transfer, along with some analytical testing. The ability to work independently and collaboratively, along with self-motivation, adaptability, and a positive attitude, is essential.
Responsibilities Include:&nbsp;
<ul>
<li>Contributing as part of a small team of scientists towards the development/optimization, and qualification of analytical methods to be used in support of biological therapeutic product release and characterization testing in a compliance-based environment</li>
<li>90% Method development,&nbsp;qualification, and process supporting related work, as well as associated protocol/report documentation and presentations;
<ul>
<li>May include technology transfer activities, regulatory support, and possible project team participation</li>
</ul>
</li>
<li>10% Analytical testing
<ul>
<li>Liquid Chromatography&nbsp;and Plate-Based&nbsp;</li>
</ul>
</li>
<li>Independently executes method development for: elucidation and monitoring of functional properties of protein therapeutics and the quantitation of process- and product-related impurities</li>
</ul>
Qualifications 
The Ideal Candidate will Have:&nbsp;
<ul>
<li>Experience in high throughput technologies and automated liquid handling systems – TECAN, Hamilton, etc.&nbsp;</li>
<li>Experience working in a GMP/GLP environment&nbsp;</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives</li>
<li>Understands and applies advanced scientific principles, theories, concepts, practices, and standards to process and product development</li>
</ul>
Minimum Qualifications:&nbsp;
<ul>
<li>BS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>2 years of demonstrated work experience with cell-based assays</li>
</ul>
</li>
<li>Or MS in&nbsp;Cell and Molecular Biology, Biochemistry, or Pharmaceutical concentration
<ul>
<li>6 months of Demonstrated experience with cell-based assays&nbsp;</li>
</ul>
</li>
<li>Experience with&nbsp;experience working with sterile cell culture and execution of cell-based and plate-based immunological methods such as Bioassay, ELISA, Octet protein binding assays, Host Cell Protein assays, Activity and Binding assays</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with the Region Recruiter</li>
<li>45-60 Minute Virtual Interview with the Manager and/or Group Leader</li>
<li>30 Minute Virtual Meeting with the Site Director&nbsp;</li>
</ul>
Additional Details:&nbsp;
The position is full-time, Monday-Friday from 8 am-5 pm. Candidates living within a commutable distance of Lexington, Massachusettes, and the surrounding areas are encouraged to apply.&nbsp;&nbsp;
<ul>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioassay Scientist

<h3>Job Description</h3>
Job DescriptionThe McAlister Lab at the College of the Holy Cross seeks a full-time research associate/ technician for an NSF-funded project studying the reproductive energetics of facultative symbiosis in the temperate coral Astrangia poculata. The position provides an excellent opportunity to continue developing scientific research and communication skills while co-mentoring a passionate group of undergraduate students. Techniques used for this project will include colorimetric assays of biochemical content in eggs and larvae, optode-based respirometry of larvae and adult colonies, PAM measurements of photosynthetic efficiency, quantification of lipid amount and type in eggs and larvae using IATROSCAN, field collection of adult colonies using SCUBA, light microscopy, digital photography and image analysis, and saltwater aquarium maintenance. Learn more about the McAlister Lab here: <a href="https://sites.google.com/holycross.edu/mcalisterlab/home&nbsp;&nbsp;&amp;nbsp" target="_blank">https://sites.google.com/holycross.edu/mcalisterlab/home&nbsp;&nbsp;&amp;nbsp</a>;Major Areas of ResponsibilityThe research associate/technician will work in association with the PI and a team of undergraduate students based at Holy Cross, and a PhD student and postdoc based in a collaborator’s lab at Tufts University. The research associate/technician will have the opportunity to work independently on a research project, expected to lead to authorship in peer-reviewed publication(s), will maintain the lab equipment and supplies daily, and will assist in training undergraduate students.&nbsp;&nbsp;Minimum QualificationsThe position requires a master’s degree in marine biology or a related field (or a bachelor’s and 2 years of post-bachelor’s work experience), experience working with marine invertebrates, open water SCUBA certification (and the possession or ability to obtain AAUS Scientific Diver certification). The candidate is expected to have a genuine interest in mentoring undergraduate students. Candidate should possess good interpersonal, organizational and communication skills, a strong work ethic and a high motivation to learn.&nbsp;The position is a three-year&nbsp;NSF-funded project / appointment with benefits, pending continuation of funding, with the possibility of renewal.&nbsp; Interested candidates should submit a CV and cover letter (including a list of two references).&nbsp;&nbsp;&nbsp;&nbsp;DisclaimerThe description above represents the most significant duties of this position but does not exclude other occasional work assignments not mentioned, the inclusion of which would be in conformity with the factor degrees assigned.&nbsp;Additional information:This is a full time exempt level position. The College is committed to providing competitive market pay for its employees.&nbsp; The College also offers a competitive benefits package for full-time staff, including:
<ul>
<li>10% College contribution to the 403(b) Retirement Plan (1 year wait waiver available)</li>
<li>Condensed summer 4-day work week</li>
<li>Tuition &amp; Education benefits</li>
<li>Wellness programs &amp; ongoing Training and Development opportunities</li>
<li>Generous paid time off</li>
</ul>
The College is an Equal Employment Opportunity Employer and complies with all Federal and Massachusetts laws concerning Equal Opportunity and Affirmative Action in the workplace.To review our Employee Benefit Options, please go to:&nbsp;<a href="https://www.holycross.edu/human-resources/benefits" target="_blank">https://www.holycross.edu/human-resources/benefits</a> APPLICATION INSTRUCTIONS:In your cover letter please address how your work might support the College's mission as a Jesuit, undergraduate liberal arts college (see&nbsp;<a href="http://www.holycross.edu/mission" target="_blank">http://www.holycross.edu/mission</a>) and its core commitment to justice and&nbsp;inclusive excellence. Please provide examples of any past work that illuminate your commitments in these areas.Review of applications will begin as received and continue until the position has been filled.The College also provides reasonable accommodations to qualified individuals with disabilities during the hiring process in compliance with law. Please contact Merrilee Grenier, Senior Associate Director of Employee Relations and Legal Compliance, for questions or to request an accommodation via email at&nbsp;<a href="mailto:mgrenier@holycross.edu" target="_blank">mgrenier@holycross.edu</a>, or by calling 508-793-3957.&nbsp;&nbsp;

Research Associate / Technician (Environmental Studies)

<h3>Job Description</h3>
Job Description
We are looking for&nbsp;Research Associate&nbsp;for our client in&nbsp;Cambridge, MA&nbsp;
Job Title:&nbsp;Research Associate
Job Location:&nbsp;Cambridge, MA&nbsp;
Job Type:&nbsp;Contract Job Description:
Pay Range: $30hr&nbsp;- $32hr
Responsibilities:
<ul>
<li>Key responsibilities include operation, maintenance, and troubleshooting of latest generation Phenocycler Fusion and Visium; preparation of samples and reagents; and assistance in assay development and optimization.</li>
<li>Operate and maintain the instruments.</li>
<li>Prepare and manage reagents.&nbsp;</li>
<li>Perform reagent validation.&nbsp;</li>
<li>Prepare slides for analysis.</li>
<li>Maintain an accurate record of samples, reagents.&nbsp;</li>
<li>Maintain and organize the inventory.</li>
<li>Perform routine data transferring.</li>
<li>Assist in the development of new reagents.</li>
</ul>
Qualifications And Experience:
<ul>
<li>Bachelor's degree in biological sciences, engineering, chemistry, physics, math, computer sciences, or related fields.</li>
<li>Prior experience with spatial technologies or pathology/histology/IHC is preferred but not required, as training will be provided.</li>
<li>Ideal candidates will be quick learners and comfortable with new technologies and have excellent hands-on and organizational skills, with attention to detail and quality.</li>
<li>Skills for effective and timely communication with colleagues.</li>
<li>A 3-5 years of lab related experience preferred.</li>
</ul>
Working Conditions:
<ul>
<li>Contingent worker will be primarily in a laboratory environment and may work with hazardous materials, including tissue and blood samples.</li>
</ul>
Company Descriptionvisit our career site to see all open positions @ <a href="http://jobs.cynetsystems.com" target="_blank">http://jobs.cynetsystems.com</a> 
<h3>Company Description</h3>
visit our career site to see all open positions @ <a href="http://jobs.cynetsystems.com" target="_blank">http://jobs.cynetsystems.com</a>

Research Associate

<h3>Job Description</h3>
Job Description
Intro:&nbsp;&nbsp;
Reimagine what a health and wellness agency can be. At Fingerpaint Group, we’re built differently—independent by nature and driven by empathy. Here, your individuality fuels innovation, and your talent finds its spark. With a powerhouse team spanning the U.S. and Europe, we’ve breathed life into over 200 brands, crafting experiences that resonate and inspire. This is where creativity flows effortlessly—where bold ideas flourish, collaboration ignites, and extraordinary happens every day. &nbsp;
&nbsp; Objectives of This Role:&nbsp;&nbsp;
Are you hungry to help push the boundaries of what’s possible in medicine? Come join our team in translating the latest scientific discoveries into compelling brand strategies, provider education, and patient care. At Fingerpaint, we focus on infusing science into all aspects of a unified brand-building process to drive commercial and medical communication strategies. The senior director, scientific strategy will need to utilize all of their capabilities as a scientist and a person, tapping into both their scientific thinking and creative core. Our ideal partner is a deep and dynamic thinker who can read beyond the data to create focused scientific concepts, push past observations to insights, and help guide our teams forward in strategic development. The senior director is the scientific lead for multiple brands and will own approach and finalization of deliverables, leading client relationship and interactions while learning to support scope of work development, design workstreams.
&nbsp; Duties and Responsibilities:&nbsp;
<ul>
<li>Partner across the disciplines of strategy to drive brand building, unbranded initiatives, and communication planning&nbsp;</li>
<li>Foster authentic and effective relationships with client brand and medical teams, as well as other relevant medical personnel (eg, key opinion leaders, MSLs, etc)&nbsp;</li>
<li>Partner on development and execution of strategic workshops, inclusive of development of workshop agenda, framework, content and shared meeting leadership, and breakout group facilitation&nbsp;</li>
<li>On-site congress and advisory board coverage and generation of an accurate and comprehensive output report complete with perceptions, barriers, opportunities, and Fingerpaint recommendations&nbsp;&nbsp;</li>
<li>Run client workshops and advisory boards independently&nbsp;</li>
<li>Actively participate in development of and attendance at new business pitches&nbsp;&nbsp;</li>
<li>Maintain status as being highly informed and knowledgeable across brands&nbsp;&nbsp;</li>
<li>Independently create and guide a scientific concept and brand advantage&nbsp;&nbsp;</li>
<li>Partner with medical affairs, HEOR, and/or clinical development to propose novel approaches to evidence generation&nbsp;&nbsp;</li>
<li>Elevate the quality or increase efficiency of existing projects and propose novel ideas for Fingerpaint services or deliverables&nbsp;</li>
<li>Make recommendations about brand coverage and staffing based on in-depth brand understanding of workload fluctuations&nbsp;&nbsp;</li>
<li>Partner in annual scope development and review&nbsp;</li>
<li>Develop meaningful and productive lead client relationships (medical and commercial)&nbsp;</li>
</ul>
Job Requirements:&nbsp;&nbsp;
<ul>
<li>Relevant degree (PhD preferred)&nbsp;</li>
<li>Minimum of 6 years of experience in the pharmaceutical industry and/or pharmaceutical marketing&nbsp;</li>
<li>Experience developing medical communications programs preferred&nbsp;</li>
<li>Is effective in a variety of formal presentation settings—one-on-one, small/large groups, with peers, subordinates, and bosses— both inside and outside the organization&nbsp;</li>
<li>Proficiency in Microsoft PowerPoint, Word, and Adobe&nbsp;</li>
<li>Constant curiosity with the passion to explore and create&nbsp;</li>
</ul>

Director, Scientific Strategy

<h3>Job Description</h3>
Job Description
Position Summary:
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for a Research Associate/Senior Research Associate in Cellular Analytical Development to join efforts in developing test methods for the company’s novel TCR-engineered T cell therapy products. This newly created role will reside within the Process and Analytical Sciences department and will report to the Associate Director of Cellular Analytical Development. Key activities will include the development and execution of analytical methods to support cellular process development and the tech transfer of in-process, release, and stability-indicating assay methods to QC, amongst others.
The ideal candidate will have essential knowledge in analytical method development and testing for cell and gene therapies including cell culture and nucleic acid analysis. Experiences with SOP documentation and statistical analysis are highly preferred. The ideal candidate will be self-motivated, capable of thriving in a fast-paced and agile environment, a team player with the ability to foster productive relationships with internal colleagues and external partners.
Responsibilities:
<ul>
<li>Participate in the development, optimization, and qualification of analytical methods for TCR-engineered T cell processes and products.</li>
<li>Work closely with Process Development team, perform timely in-process sample testing, generate reports to provide information for optimization.</li>
<li>Contribute to tech transfer of optimized / qualified methods to QC and assist quality in developing testing strategies and validation efforts.</li>
<li>Authorize and review technical documentation including SOPs, method development reports and meeting presentations.</li>
<li>Maintain a detailed electronic laboratory notebook and present findings to the team, department, and company, as appropriate.</li>
</ul>
Requirements:
<ul>
<li>Research Associate: BS with 0-3+ years of relevant experience</li>
<li>Senior Research Associate: BS with 3-5+ years of relevant experience, or MS with 0-2 years of experience.</li>
<li>Degree emphasis in immunology, cell biology, molecular biology, biochemistry, or related field is preferred. </li>
<li>Experiences on mammalian cell culture and ddPCR are required; prior experiences with cell-based potency assays and method qualification are plus for consideration.</li>
<li>Scientific creativity, critical thinking, ability to innovate, and analytical problem solving.</li>
<li>Excellent communication skills (both written and oral) are critical.</li>
<li>Experience drafting SOPs and testing documentation as well as supporting documentation for regulatory filings is strongly desired.</li>
</ul>
About TScan:
TScan Therapeutics is a fully integrated, next-generation TCR-T cell therapy company. Founded in 2018, TScan’s platform was developed by Stephen Elledge, Ph.D., and Tomasz Kula, Ph.D., at Brigham and Women’s Hospital and Harvard Medical School. TScan’s transformative platform enables rapid discovery of TCRs and targets for engineered T cell therapy. This technology is extremely versatile and is applicable across multiple therapeutic areas beyond cancers, including autoimmune disorders and infectious diseases.
Do YOU have the anatomy of a TScanner? 
Our talented, compassionate, and intelligent team is what makes TScan a Top Place to Work (as ranked by The Boston Globe). Our state-of-the-art offices with over 70,000 square feet of premium lab space, including an internal GMP manufacturing suite, are an environment that supports innovation, camaraderie, and professionalism. We are passionate, fun, flexible, and team oriented. Sound like you? Apply today.
EEO Statement
TScan is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, citizenship status, sexual orientation, gender identity or expression, or any other characteristic identified by federal, state, or local laws where we operate. TScan provides reasonable accommodations to qualified applicants and employees with disabilities. To begin an interactive dialogue with TScan regarding a reasonable accommodation in connection with the hiring process and/or to perform the responsibilities of the position for which the applicant has applied, please contact the recruiter.
Recruitment &amp; Staffing Agencies
TScan Therapeutics does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics’ internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of TScan Therapeutics, and TScan Therapeutics will not owe any referral or other fees with respect thereto.

Research Associate/Sr. Research Associate, Analytical Development

<h3>Job Description</h3>
Job Description
We are seeking a Principal Associate Scientist with a strong background in analytical chemistry to support non-GMP testing activities. The ideal candidate will perform both chromatographic and non-chromatographic analytical methods and contribute to documentation, data mining, and troubleshooting efforts. This role requires a detail-oriented and collaborative individual committed to high-quality work and timely execution.
Key Responsibilities
<ul>
<li> Perform non-GMP analytical testing using: </li>
<ul>
<li> Non-chromatographic techniques: Stand-alone UV assay, pH, osmolality, moisture, and thermal melting temperature determination using UV </li>
<li> Chromatographic techniques: Reverse phase and ion exchange chromatography </li>
</ul>
<li> Document all analytical results in electronic laboratory notebooks (ELN) </li>
<li> Generate and/or review: </li>
<ul>
<li> Certificates of Testing </li>
<li> Protocols </li>
<li> Technical reports </li>
</ul>
<li> Conduct data mining activities and summarize historical/relevant analytical data </li>
<li> Provide support in troubleshooting analytical issues as needed </li>
<li> Coordinate aliquoting and shipping of samples and materials </li>
</ul>
Skills &amp; Attributes
<ul>
<li> Strong focus on accuracy and timeliness ("Right First-Time" mindset) </li>
<li> Excellent organizational skills </li>
<li> Effective communication and collaboration with internal stakeholders </li>
<li> Experience with core analytical instrumentation and a solid understanding of analytical chemistry principles </li>
<li> Ability to commit to the full duration of the assignment </li>
</ul>
Requirements
Education &amp; Experience
<ul>
<li> Bachelor’s degree in a scientific discipline (preferably Chemistry) </li>
<li> 3–5 years of industry experience in analytical testing and documentation evelopment (e.g., HPLC, LC-MS, spectrophotometry).</li>
</ul>

Principal Associate Scientist

<h3>Job Description</h3>
Outlier helps the worlds most innovative companies improve their AI models by providing human feedback.&nbsp;Are you an experienced&nbsp;Expert&nbsp;who would like to lend your expertise to train AI models?

About the opportunity:&nbsp;

<ul>
<li>Outlier is looking for talented &nbsp;Chemistry Experts to help train generative artificial intelligence models</li>
<li>This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you</li>
</ul>
You may contribute your expertise by

<ul>
<li>Assessing the factuality and relevance of domain-specific text produced by AI models</li>
<li>Crafting and answering questions related to Chemistry</li>
<li>Evaluating and ranking domain-specific responses generated by AI models</li>
</ul>
Examples of desirable expertise:

<ul>
<li>A bachelor's or higher degree in &nbsp;Chemistry or a related subject</li>
<li>Experience working as a Chemistry&nbsp;professional</li>
<li>Ability to write clearly about concepts related to &nbsp;Chemistry in fluent English</li>
</ul>

Payment:
<ul>
<li>Currently, pay rates for core project work by Chemistry&nbsp;experts range from $30 to $50 per hour USD.&nbsp;</li>
</ul>

<ul>
<li>Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.&nbsp;</li>
</ul>

Chemistry Expertise Sought for AI Training (Part time work from home)

<h3>Job Description</h3>
Outlier helps the worlds most innovative companies improve their AI models by providing human feedback. Are you an experienced&nbsp;Math Expert&nbsp;who would like to lend your expertise to train AI models?

About the opportunity:&nbsp;
<ul>
<li>Outlier is looking for talented Math Experts to help train generative artificial intelligence models</li>
<li>This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you</li>
</ul>
 
You may contribute your expertise by
<ul>
<li>Assessing the factuality and relevance of domain-specific text produced by AI models</li>
<li>Crafting and answering questions related to Math</li>
<li>Evaluating and ranking domain-specific responses generated by AI models</li>
</ul>
Examples of desirable expertise:
<ul>
<li>A bachelor's or higher degree in Math or a related subject</li>
<li>Experience working as a Math professional or in a highly technical/analytical field</li>
<li>Ability to write clearly about concepts related to Math in fluent English</li>
</ul>
 
Payment:
<ul>
<li>Currently, pay rates for core project work by Math experts range from $30 to $50 USD per hour</li>
<li>UK: Estimated 22-37 per hour</li>
<li>Canada: Estimated $40-67 CAD per hour</li>
<li>Australia:&nbsp;Estimated $43-73 AUD per hour</li>
<li>Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.</li>
</ul>

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