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<h3>Job Description</h3>
Job Description
The Research Associate (RA) is a key member of the R&amp;D team, supporting important research projects and ongoing scientific activities. The RA brings 3-5 years of experience at a life sciences company, academic or medical research organization and is comfortable working in a fast-paced environment. The RA plays an important role assisting the CSO and other team members' conduct of the Company's clinical studies, technical validations, and scientific initiatives associated with CND's suite of neurodiagnostic products and services. The RA helps define research plans in collaboration with team members and performs secondary research on assigned topics. The RA provides key facts and figures for peer-reviewed publications and helps review and ensure all data is accurate and checked. The individual is a strong collaborator and is comfortable interfacing across multiple departments and communicating effectively with various team members. The RA has excellent attention to detail and provides effective written summaries of complex information. The individual also offers key insights on analyses and has experience discussing methods and conclusions with senior leaders in the organization.
Job Responsibilities:
Research Design and Execution
<ul>
<li>Contribute to the design and implementation of research projects </li>
<li>Conduct literature reviews to identify relevant research and methodologies</li>
<li>Support the development of research protocols and procedures </li>
<li>Help collect, analyze, and interpret data from various sources </li>
<li>Maintain accurate records of research activities and data </li>
</ul>
Data Analysis and Reporting
<ul>
<li>Support statistical analyses and other data analysis techniques</li>
<li>Develop figures for effective display of information</li>
<li>Help prepare reports, posters, presentations, and publications summarizing research findings </li>
<li>Aid in publication of manuscripts, abstracts and protocols</li>
</ul>
Collaboration and Communication
<ul>
<li>Work collaboratively with project teams, principal investigators(PIs), other researchers, and team members</li>
<li>Communicate research progress and findings effectively, both orally and in writing </li>
<li>Assist with grant writing and securing funding for research projects </li>
</ul>
Other Duties
<ul>
<li>Play a key role in maintaining the Company's scientific publications library and providing summaries of specific publications when needed</li>
<li>Stay current with advancements in the field and communicate to Company leaders</li>
<li>Assist with laboratory or field research activities when requested</li>
<li>Help manage research budgets and resources Perform literature searches as required and communicate relevant publications and findings to the research team.</li>
<li>Review agendas and abstracts from upcoming or previous scientific meetings and share relevant insights with the research team.</li>
<li>Contribute to additional activities, as needed, that support the goals of the research or study team</li>
<li>Perform other duties as assigned.</li>
</ul>
Knowledge, Skills &amp; Experience:
<ul>
<li>Experience in a research lab focused on innovative scientific advancements</li>
<li>Familiarity with moderately complex statistical methods that apply to applicable clinical studies</li>
<li>Ability to effectively manage multiple tasks and projects</li>
<li>Proficiency in relevant software, statistical packages, and laboratory techniques </li>
<li>Strong analytical and problem-solving skills are essential</li>
<li>Excellent written and verbal communication skills are necessary for effective collaboration and reporting </li>
<li>Strong organizational and time-management skills are needed to manage multiple projects and deadlines.</li>
<li>Ability to work effectively in a team environment.</li>
</ul>
Education, Certifications &amp; Licensures:
<ul>
<li>Master's degree or Ph.D is neuroscience required</li>
</ul>
Other:
<ul>
<li>This position is based in our Boston office (Coolidge Corner, Brookline) and is expected to be in-office at least 3-4 days/week.</li>
</ul>

Research Associate

<h3>Job Description</h3>
Job DescriptionThe Company We are Alloy Therapeutics—a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. MAY THE BEST DRUG WIN. Alloy is headquartered in Waltham, MA with additional labs in Cambridge, UK; Basel, Switzerland, and Athens, GA. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. This is an on-site and full-time position in Waltham, MA. At Alloy, we have an ethos of “Mentorship-By-Apprenticeship” in all of our positions.&nbsp;&nbsp;We strive to have workers in the office when needed to interact organically and face-to-face.&nbsp;&nbsp;Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year.&nbsp;&nbsp;We respect and value our colleagues for their hard work that requires them to be in the lab every day.&nbsp;&nbsp;We ask our people who have more flexible accommodations, like this position, to appreciate their colleagues who have less flexibility.&nbsp;&nbsp;We are all one team! The Team&nbsp; Alloy RNA Medicines group developed the AntiClastic platform, a novel oligonucleotide technology with a broad range of applications spanning the fields of antisense therapeutics to immunomodulating oligonucleotides. The team works closely with external drug discovery partners to accelerate the development of innovative AntiClastic RNA medicines. The Role&nbsp; As a Scientist, you will work within the RNA Medicine team in Waltham, MA. You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. This role will have an autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy.&nbsp; How You’ll Drive Impact&nbsp;
<ul>
<li>Innovate: Develop novel assays to elucidate the mechanism of action of novel ASO formats.</li>
<li>Deliver: Design, execute, analyze, and interpret in vitro and in vivo experiments. Generate robust, high-quality data.</li>
<li>Collaborate: Work closely with internal/external partners on drug discovery projects to ensure studies are executed to meet scientific goals and timelines.</li>
</ul>
Principal Responsibilities&nbsp;
<ul>
<li>Design and execute several molecular biology and protein techniques including, but not limited to, nucleic acid isolation, RT-qPCR, western blots and ELISA.</li>
<li>Culture various cell types including established cell lines, primary cells and iPSCs.</li>
<li>Perform a range of cell-based assays, including those utilizing microscopy and plate readers for fluorescence/luminescence detection.</li>
<li>Process mouse tissue for nucleotide extraction and downstream analysis.&nbsp;</li>
<li>Operate high-throughput tools, including 96 channel electronic pipets to streamline and enhance experimental workflows.</li>
<li>Analyze data using GraphPad software and prepare presentation-ready images to effectively communicate experimental findings.</li>
<li>Maintain comprehensive and accurate records of all experiments using the Benchling electronic notebook, ensuring meticulous documentation and data integrity.</li>
</ul>
Qualifications
<ul>
<li>PhD degree in Biology or related science with 1 to 3 years of additional experience in biotech/pharma.</li>
<li>Knowledge of antisense oligonucleotide modalities and their mechanism of action. Previous Experience working with ASOs is highly desirable</li>
<li>Experience designing and running molecular biology, protein and cell-based assays.&nbsp;</li>
</ul>
Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation
<ul>
<li>Competitive base and equity compensation commensurate with level of experience and independence</li>
<li>401(k) company match</li>
</ul>
Health &amp; Family
<ul>
<li>Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered</li>
<li>Company-paid disability (STD, LTD) and life insurance</li>
<li>Paid parental leave</li>
<li>Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)</li>
</ul>
Unique Perks
<ul>
<li>Unlimited PTO (paid time off) and flexible schedules</li>
<li>Annual stipend for continuing education with commitment to your career through individualized professional development plan</li>
<li>Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness</li>
</ul>
Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated annual base salary range is $100,000 - $125,000 with the final offer based on factors like your experience, skills, and alignment with our needs.
Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines.
We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help.
Alloy Therapeutics is an equal opportunity employer.&nbsp; All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status.&nbsp; If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at <a href="mailto:recruiting@alloytx.com" target="_blank">recruiting@alloytx.com</a>.&nbsp; We will make every effort to respond to your request for disability assistance as soon as possible. &nbsp;
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Scientist, Genetic Medicines

<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 
Purpose:
The Associate QC Scientist performs laboratory testing within a fast-paced GMP environment in support of one or more of the following areas: raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab investigation reports.
Responsibilities:
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for the department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>2+ years of related work experience in a GMP and Quality Control environment (with knowledge of/experience with techniques such as Infrared (IR), FTIR, UV-vis, SoloVPE, Truscan)</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" 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>

Associate Scientist, Quality Control

<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 
The Associate QC Scientist performs laboratory testing within a fast-paced GMP environment in support of one or more of the following areas: raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab investigation reports.
The work schedule and hours for this position are Sunday through Wednesday, 4:00pm to 2:30am.
Responsibilities:
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for the department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>2+ years of related work experience</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" 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>

Associate Scientist, Quality Control (2nd shift, Sun-Wed, 4pm-2:30am)

<h3>Job Description</h3>
Job DescriptionR&amp;D Chemist External ID # 8035 Marlborough, MA- ONSITE 12 month W2 contract (with potential to extend or transition to perm) Pay rate: $33-38/hr - Depending on Education and Experience Summary: We have an exciting opportunity within the Advanced Circuit and Packaging (ACP) business for a R&amp;D Chemist, located in Marlborough, MA. The position in the R&amp;D Development group of ACP will focus on the development, optimization and commercialization of new products in a broad range including metal plating, photoresists and dielectric materials in the semiconductor industry.&nbsp; &nbsp; Key areas of focus will include: organic synthesis, formulation and filtration, analytical characterization (GPC, HPLC, SEM, Particle measurements, etc.), electrochemical analysis (CVS, Electroplating, Titration, etc.) and cleanroom &amp; fab activities. &nbsp; Responsibilities: 
<ul>
<li>Adept at hands-on lab work, creative thinking, problem solving in a unique and fast-paced laboratory environment.</li>
<li>Hands-on work in the lab for organic &amp; polymer synthesis, purification, filtration, ion exchange and analytical characterization to support raw material supply and process development on the scale from 100 mL to 20 L.</li>
<li>Support polymer synthesis in lab-scale to kilo-lab and pilot-scale.</li>
<li>Develop and execute analytical methods to characterize raw materials and products.</li>
<li>Support development of new formulations used in electroplating and Polymeric / Dielectric products for the microelectronics industry.</li>
<li>Prepare lab-scale lacquer and formulation of products to support timely customer sampling.</li>
</ul>
&nbsp; Techniques/Skills: 
<ul>
<li>Analytical techniques include CVS, HPLC, UPLC, GPC, % solids, titrations, potentiostatic measurements, surface tension, cloud point, densitometer, and rheometer.</li>
<li>Assume responsibility for execution of cleanroom workflows such as laminations, coatings, lithography and cure techniques, as well as thermal and mechanical analysis.</li>
<li>Support Quality and Manufacturing for root cause investigations and customer complaints.</li>
<li>Strict adherence to enhanced safety protocols and ability to work safely and participate in all group safety activities.</li>
<li>Proper documentation including new methods, method validation, batch data, management of change, etc. Qualifications</li>
</ul>
Required Qualifications 
<ul>
<li>B.S. or Associate degree in Chemistry, Chemical Engineering, Materials Science or relevant fields with industrial lab experience.</li>
<li>Hands on organic synthesis experience to support polymer synthesis and development</li>
<li>Hands-on industrial experience in semiconductor fab or similar environment and familiarity with material characterization, wafer-level metrology and/or thin film analysis</li>
</ul>
&nbsp; What’s In It For You? We welcome you to be a part of one of the largest global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. 
<ul>
<li>Medical, Dental &amp; Vision Benefits</li>
<li>401K Retirement Saving Plan</li>
<li>Life &amp; Disability Insurance</li>
<li>Direct Deposit &amp; weekly ePayroll</li>
<li>Employee Discount Programs</li>
<li>Referral Bonus Programs</li>
</ul>
&nbsp; &nbsp; Estimated Min Rate: $34.00 Estimated Max Rate: $38.00 Note: Any pay ranges displayed are estimations.&nbsp; Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description.&nbsp; All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit&nbsp;<a href="https://www.yoh.com/applicants-with-disabilities&amp;nbsp" target="_blank">https://www.yoh.com/applicants-with-disabilities&amp;nbsp</a>;to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.&nbsp; All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.Company DescriptionFounded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day &amp; Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations. Company Website: <a href="https://www.yoh.com/" target="_blank">https://www.yoh.com/</a> 
<h3>Company Description</h3>
Founded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day &amp; Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations.\r\nCompany Website: <a href="https://www.yoh.com/" target="_blank">https://www.yoh.com/</a>

R&D Chemist

<h3>Job Description</h3>
Outlier helps the worlds most innovative companies improve their AI models by providing human feedback. Are you an experienced Geography 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;Geography expert 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 Geography</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;Geography or a related subject</li>
<li>Experience working as a Geography&nbsp;professional</li>
<li>Ability to write clearly about concepts related to &nbsp;Geography&nbsp;in fluent English</li>
</ul>

Payment:
<ul>
<li>Currently, pay rates for core project work by Geography&nbsp;experts range from $20 to $40 per hour USD.&nbsp;</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>

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

<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’re looking for a detail-oriented and motivated individual to join our team.&nbsp;In this role, you’ll execute routine testing using gel electrophoresis, HPLC, and compendial methods.&nbsp;This is a great opportunity for someone with strong analytical skills and a passion for lab-based work in a collaborative, client-focused environment. Responsibilities include:&nbsp;
<ul>
<li>Execute testing of assigned analysis type for routine sample submissions using gel electrophoresis, HPLC, and compendial methods</li>
<li>Identify and help to resolve equipment and basic test method issues</li>
<li>Develop expertise to serve as a backup executor of a limited number of other analysis types (other test methods)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li>
<li>Provide feedback to client on the performance of existing assays / test methods</li>
</ul>
Qualifications 
<ul>
<li>BS in science (chemistry, pharmacy, or equivalent life sciences degree)
<ul>
<li>1+ years of directly related experience</li>
</ul>
</li>
<li>Prior knowledge and lab experience with HPLC instrumentation and data processing&nbsp;</li>
<li>Prior knowledge and lab experience with&nbsp;compendial analysis</li>
<li>Prior knowledge and lab experience with LC-UV and Empower skills&nbsp;is required</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
</ul>
Additional Details:&nbsp;
The position is full-time and permanent,&nbsp;Monday-Friday, 8 am-5 pm,&nbsp;with overtime as needed.&nbsp;Candidates living near or in&nbsp;Cambridge, MA,&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>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 holidays</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 clients’ 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.

Associate Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
<ul>
<li>Katalyst Healthcares &amp; Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.</li>
<li>We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.</li>
</ul>
Job Description 
Job Description:
<ul>
<li>Impeccable lab practices, including aseptic cell line/primary cell maintenance and stimulation. Self-motivated with excellent attention to detail.</li>
<li>Demonstrated ability to optimize cell culture conditions, phenotypical assays, Western Blot, migration/contraction assays (fibroblasts), viability assays, qPCR, ELISA/multiplex protein assays, and flow cytometry.</li>
<li>Experience with human cell types relevant to tissue homeostasis such as fibroblast, epithelial cells, and macrophages.</li>
<li>Familiar with complex in vitro models such as co-culture, tissue explants, Transwells, organoids, 3D/microfluidic/chip systems a plus.</li>
<li>Ability to analyze, plot, interpret, and present data in team meetings.</li>
<li>-Aptitude to communicate in a virtual environment and a hybrid office/virtual setting</li>
<li>Proficient at maintaining accurate and well-organized records and laboratory electronic notebooks.</li>
</ul>
Requirements:
<ul>
<li>5 + years hands-on academia/industry experience.</li>
<li>BS/MS degree in Biology, Biochemistry, Immunology, Bioengineering/Biomedical engineering, or Medical/Pharmaceutical sciences.</li>
<li>Primary cell culture and stimulation.</li>
<li>Molecular biology techniques (e.g. ELISA, qPCR, RNAseq, Western Blot, flow cytometry).</li>
<li>Pharmacological treatment with small/large molecules and siRNAs.</li>
<li>Data analysis including statistics.</li>
</ul>
Additional Information 
All your information will be kept confidential according to EEO guidelines.

Biologist III

<h3>Job Description</h3>
Job DescriptionDescription:
The Wildlife Service Technician is responsible for providing wildlife control services to residential and commercial customers, ensuring safety, professionalism, and high-quality work. This role includes conducting property inspections, exclusion and repair work, safely handling wildlife, and resolving various wildlife-related issues. The position requires working both indoors and outdoors in various weather conditions and involves using power tools and ladders. Technicians must possThe Wildless strong problem-solving skills, excellent communication, and the ability to work independently and efficiently.
 
Essential Job Functions:
1. Conduct thorough inspections of residential and commercial properties to assess wildlife activity and potential entry points.
 
2. Diagnose and determine appropriate wildlife control strategies based on the type of animal, damage caused, and customer needs.
 
3. Implement humane wildlife control techniques, including safe capture, removal and at times termination of nuisance animals.
 
4. Utilize traps and other wildlife control equipment to capture and relocate animals, ensuring compliance with local wildlife laws and regulations.
 
5. Perform exclusion work by sealing entry points to prevent wildlife from re-entering properties. This includes minor carpentry and repair tasks such as installing screens, sealing gaps, and repairing damaged areas.
 
6. Use ladders to access rooftops and hard-to-reach areas, ensuring proper installation of exclusion materials.
 
7. Safely operate power tools such as drills, saws, and other equipment to complete exclusion work efficiently and effectively.
 
8. Meet with customers to assess their wildlife issues, explain the services to be provided, and answer any questions or concerns they may have.
 
9. Provide clear communication and set proper expectations regarding the wildlife control process and timeline.
 
10. Maintain a professional and courteous demeanor while interacting with customers on-site, ensuring customer satisfaction.
 
11. Obtain and maintain required state wildlife certifications to ensure legal compliance in all services provided.
 
12. Adhere to all local, state, and federal regulations regarding wildlife control, safety procedures, and environmental protections.
 
13. Accurately document customer interactions, services performed, and materials used for each job.
 
14. Maintain clear, up-to-date records in company systems, ensuring accurate billing and service history tracking.
 
15. Report any safety concerns, equipment issues, or wildlife control challenges to management in a timely manner.
 
16. Work closely with the Wildlife Supervisor and other technicians to share knowledge and best practices.
 
17. Assist other team members as needed on larger or more complex wildlife control projects.
 
18. Ensure consistent communication with the office staff and management to keep everyone informed of job status and any changes.
 
19. Maintain company-provided vehicle in clean and proper working order, ensuring it is stocked with necessary tools and materials for wildlife control.
 
20. Perform routine checks and maintenance of wildlife control equipment to ensure safe and effective operation.
 
21. Support other areas of the business as needed, including cross-training in other pest control services.
 
22. Participate in team meetings and training sessions to stay current on best practices and industry regulations.
Requirements:
1. Must be at least 18 years of age.
2. Valid driver's license with a clean driving record.
3. High school diploma or equivalent.
4. At least 2+ years of experience in carpentry, construction, or a related field.
5. Experience working with ladders and on rooftops .
6. Pre-employment background check required.
7. Hunting experience or familiarity with wildlife handling is required.
 
Physical Requirements:
While performing the duties of this job, the employee is frequently required to stand, walk, sit, climb, bend, kneel, and crawl within tight spaces. Specific hearing and vision abilities required include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The employee must occasionally lift and move up to 50 pounds. Technicians must be comfortable using ladders up to 40 feet tall and operating power tools such as drills and saws independently. Additional role related tasks may be added to ensure HR alignment with business needs with/without notice, per HR Directors discretion
 
Other Duties:
This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the Team Member for this job. Duties, responsibilities, and activities may change at any time to ensure Human Resources consistent alignment with Pest-End business needs, with or without notice, per Director of Human Resources professional discretion.
 
Pest-End Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, or any other characteristic protected by law.

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