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<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.

Wildlife Service Technician

<h3>Job Description</h3>
About Outlier
Outlier is the worlds leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities.
 
We are looking for advanced Biology experts to teach AI how to interpret and solve complex problems by:
<ul>
<li>Evaluate AI-generated content for factual accuracy and relevance in Biology</li>
<li>Develop and answer Biology-related questions to refine AI understanding.</li>
<li>Assess and rank AI responses based on scientific rigor.</li>
</ul>
Required expertise and qualifications:
<ul>
<li>Education: Masters degree or higher (PhD preferred) in Biology or a related field (can be currently enrolled)</li>
<li>Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&amp;D contributions</li>
<li>English Proficiency: Ability to read and write with minimal errors</li>
<li>Bonus Skills: AI model training experience is not required but helpful</li>
</ul>

Payment:
<ul>
<li>Currently, pay rates for core project work by Biology&nbsp;experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below)</li>
<li>Opportunities for higher-paying research projects based on performance.</li>
</ul>

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;

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

<h3>Job Description</h3>
Job Description
Responsibilities:
<ul>
<li>
We are seeking a highly motivated contractor/Scientist III to join the Tissue Homeostasis team.
</li>
<li>
Work with the company's Disease Discovery Teams (DDTs) and Genomics Research Center (GRC) team members to design and execute in vitro cell biology and mechanism of action experiments to advance target validation and assay platform development efforts in using immune cells and stromal cells.
</li>
<li>
Perform mammalian cell culture of primary and transformed cells.
</li>
<li>
Develop immune-stromal cell co-culture systems (e.g. Myeloid cells-fibroblast) to dissect signal transduction in cell-cell interactions with disease relevant cues
</li>
<li>
Perform qPCR analysis, flow cytometry, and Western Blotting analysis.
</li>
<li>
Perform cell-based assay with human primary cells and human cell lines (AlphaLISA, ELISA, HTRF, and proliferation assays).
</li>
<li>
Utilize technical knowledge and experience to effectively troubleshoot and optimize assays.
</li>
<li>
Maintaining laboratory notebooks to the required company standard.
</li>
<li>
Communicating results to internal meetings.
</li>
<li>
Interpret findings and effectively present scientific data, concepts, and recommendations to various internal audiences.
</li>
<li>
Compile and review technical reports, protocols, manuscripts, and other key documents.
</li>
</ul>
Requirements:
<ul>
<li>
Current or perspective BS/MS/PHD students in Biotechnology, Immunology, Molecular Biology, Cell Biology or Microbiology
</li>
<li>
PHD students in Biotechnology, Immunology, Molecular Biology, Cell Biology or Microbiology
</li>
<li>
5 + years' experience
</li>
<li>
Ability to work in a fast-paced environment and delivery results in a timely and agile manner.
</li>
<li>
Ability to work independently and collaboratively with cross-functional teams.
</li>
<li>
Willing to learn new techniques and develop new assays as needed
</li>
<li>
Extensive cell biology and immunology experience, proficiency in working with human primary cells and immortalized cell lines.
</li>
<li>
Experience with co-culture systems or complex in invitro systems with primary human cells esp. T Cells. 
</li>
<li>
Demonstrated knowledge and experience of key cell biology assays and techniques.
</li>
<li>
Genetic manipulation of human cells using shRNA/siRNA/CRISPR tools.
</li>
<li>
Proficiency in molecular biology skills such as qPCR analysis, flow cytometry, and Western Blotting analysis.
</li>
<li>
Trouble-shooter able to adapt ideas and experiments to achieve key project objectives and adhere to timelines.
</li>
<li>
Excellent communication of complex scientific ideas (written and verbal) and interpersonal skills.
</li>
<li>
Strong organizational skills required, in particular good time management skills.
</li>
<li>
Inclusive, open-minded, collaborative, and forward-thinking.
</li>
<li>
Background in cell biology of inflammation or Immunology
</li>
<li>
Excellent oral and written communication, analytical, and computer skills.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist

<h3>Job Description</h3>
Job DescriptionOverview: HIFIBIO Therapeutics is a cutting-edge biotechnology company focused on developing curative immunotherapies for patients. We leverage single-cell technologies with AI/ML analysis to enhance success from target to patient. We are seeking a highly motivated and innovative intern to assist in the development of novel applications for our single-cell RNA sequencing platform. The ideal candidate will work closely with a multidisciplinary team of scientists to design, test, and optimize experimental protocols. The intern will gain hands-on experience with state-of-the-art laboratory techniques and contribute to ongoing research aimed at improving single-cell analysis methodologies using our in-house microfluidic-based platform. The successful candidate is a proactive and flexible scientist with a curiosity for novel technologies, prioritizes tasks effectively in a fast-paced environment, communicates clearly and efficiently, and thinks nimbly about conveying biological results. This is a unique opportunity to contribute to drug development in a biotherapeutics company positioned at the cutting edge for treating cancer and autoimmune diseases.&nbsp; Responsibilities: 
<ul>
<li>Develop, optimize, and validate protocols for single-cell RNA sequencing from various tissue types </li>
<li>Conduct laboratory experiments including tissue dissociation, sample labelling and sequencing library preparation </li>
<li>Operates our in-house microfluidic platform </li>
<li>Troubleshoot technical challenges and propose solutions to improve workflow efficiency and reproducibility </li>
<li>Maintain detailed records of experimental procedures, results, and analysis </li>
<li>Stay up to date with the latest scientific literature on single-cell RNA sequencing technologies and related methodologies </li>
</ul>
Qualifications:&nbsp; 
<ul>
<li>Enrolled in a 4-year college or university and having completed at least their sophomore year the semester before the internship OR have graduated within the past year&nbsp; </li>
<li>Major in biomedical engineering, biology, chemistry, or other related experimental sciences&nbsp; </li>
<li>Familiarity with standard cell biology and molecular biology techniques (Cell culture, PCR, ligations, microscopy) strongly preferred </li>
</ul>
&nbsp;&nbsp;MLSC Intern Eligibility: 1. Must meet at least one of the following:
<ul>
<li>Massachusetts resident (proof of residency required)</li>
<li>Attend an accredited college or university located in Massachusetts (enrollment verification required)</li>
<li>Attend a Minority Serving Institution (MSI), such as a Historically Black College or University (HBCU)</li>
</ul>
2. Must meet one of the following:
<ul>
<li>Currently enrolled in a 2-year community college or a certificate program (or have completed one within the past year)</li>
<li>Enrolled in a 4-year college or university or have graduated within the past year. Four-year college/university students must be completing at least their freshman year prior to the start of the internship.</li>
<li>Graduate students must be enrolled in a Master’s program or have received their Master’s degree within the past year. Doctoral students/candidates and post-docs are not eligible for the Internship Challenge.</li>
</ul>
To Apply:&nbsp; 
<ul>
<li>Please apply through <a href="http://www.hifibio.com" target="_blank">www.hifibio.com</a> </li>
<li>And through the internship challenge program at MLSC <a href="http://www.masslifesciences.com" target="_blank">www.masslifesciences.com</a></li>
</ul>
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RYdy4Cz233

Wet Lab Summer Intern

<h3>Job Description</h3>
Job Description
Job Description
<ul>
<li>
Biologics Developability Screening and Automation
</li>
<li>
The Biologics CMC Developability team is an integral part of the Biologics CMC Drug Product Development organization.
</li>
<li>
The Biologics CMC Developability team is responsible for- (1) the identification of biophysical- and chemical liabilities in discovery-stage biologic drug candidates to guide lead selection, and (2) for characterization of the key CMC attributes important for biologic drug development. 
</li>
<li>
We have an exciting opportunity for a motivated scientist to join the Biologics CMC Developability team based in Worcester, MA.
</li>
<li>
Perform in-depth LC-MS based characterization of therapeutic biologic molecules and their post-translational modifications.
</li>
<li>
Conduct biophysical and biochemical characterization of biologic drug candidates, as needed.
</li>
<li>
Execute experimental protocols, collect results, and perform data analysis carefully and independently.
</li>
<li>
Maintain excellent documentation of work including electronic lab notebook and protocols.
</li>
<li>
Prepare and deliver concise scientific presentations of experimental results.
</li>
<li>
Oversee maintenance of key laboratory equipment and routine laboratory operations.
</li>
<li>
Build strong relationships with other team members and across groups.
</li>
<li>
Understand and adhere to corporate standards regarding code of conduct, safety, and documentation compliance.
</li>
</ul>
Qualifications:
<ul>
<li>
BS or MS in Biochemistry, Biology, Chemistry (or equivalent, e.g., Chemical Engineering, Pharmaceutical Sciences) with 5+ (BS) or 2+ years (MS), or Ph.D. with 0+ years of biopharmaceutical industry experience. 
</li>
<li>
Candidates with less than 5 years/ BS will be considered for Scientist II-3-5 years
</li>
<li>
Hands-on experience with protein mass-spectrometry (subunit analysis, peptide mapping, disulfide mapping).
</li>
<li>
Experience with biochemical and biophysical characterization of biologic proteins would be preferred.
</li>
<li>
Experience with liquid handling robots and their programming would be highly beneficial.
</li>
<li>
Demonstrated track record of independent thinking, creativity, and scientific accomplishment.
</li>
<li>
Highly responsible and self-motivated. 
</li>
<li>
Skills to plan and conduct experiments with high quality and timely deliverables. 
</li>
<li>
Able to perform data analysis using MS Excel and GraphPad.
</li>
<li>
Team player with excellent collaboration and communication skills.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

<h3>Job Description</h3>
Job Description
At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases. 
Why Choose Editas?
At Editas Medicine, we’re a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor!
Decoding The Role:
Editas Medicine is seeking an accomplished Scientist to join our Molecular Biology &amp; Gene Editing group. This individual will support the design and execution of novel engineered gene editing technologies by leveraging their expertise in molecular biology techniques, such as plasmid design and various molecular cloning techniques. The Scientist will play a key role in evolving the current and next generation of gene editing platforms at Editas. 
Characterizing Your Impact:
As the Scientist II, Molecular Biology &amp; Gene Editing, you will:
<ul>
<li>Be part of a dedicated team to develop innovative gene editing platform technologies.</li>
<li>Design and execute directed evolution and/or rational design processes to engineer gene editing technologies with desired properties, including precision genomic editing technologies.</li>
<li>Design and construct libraries using rational and combinational molecular biology methods.</li>
<li>Develop in vitro or cell-based high throughput screening methods for functional readout.</li>
<li>Build assays to quantify and measure efficacy and specificity of novel gene editing technologies in vivo and in vitro.</li>
<li>Provide training, scientific and personnel management for junior team members.</li>
</ul>
Requirements
The Ideal Transcript:
To thrive in this role, you’ll need:
Qualifications
· Ph.D. in cell biology, molecular biology, bioengineering, or a related field
<ul>
<li>2+ years of industry experience in molecular biology or a related field</li>
<li>Molecular and cell biology expertise including plasmid design and library preparation, molecular cloning techniques such as Gibson assembly and golden gate cloning, primer design, PCR, gel electrophoresis, DNA and RNA purification, in vitro transcription, LNP formulation, qPCR/RT-qPCR, ddPCR/RT-ddPCR, and flow cytometry.</li>
<li>Extensive experience in mammalian cell culture, transfections, and cell-based assays </li>
<li>Experience working with CRISPR and non-viral (LNP) and/or viral (AAV, lentivirus) delivery vectors </li>
<li>Familiarity with DNA analysis software such as VectorNTI, Geneious, Benchling </li>
</ul>
Fundamentals That Set You Apart
· Preferably knowledge in genetic diseases, precision gene editing, and gene therapy.
<ul>
<li>Experience in protein structure-function study, protein engineering, and directed evolution.</li>
<li>An ability to work in a fast-paced, team-oriented, multidisciplinary environment. </li>
</ul>
Benefits
Benefits Summary:
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases..

Scientist II, Molecular Biology & Gene Editing

<h3>Job Description</h3>
Job Description
Overview
The Advanced Regenerative Manufacturing Institute (ARMI) is a member-based, non-profit organization whose mission is to advance the bioeconomy of the United States. As part of its technical efforts, ARMI is applying advanced automation and analytical techniques to develop scalable, consistent, and cost-effective manufacturing processes for cells, tissues, and organs.
The Impact That You Will Make
ARMI is seeking an Associate Scientist to assist in the manufacturing of cell-based products. This is an on-site role that will spend most of the workday in the lab. To be successful in this role, candidates need previous experience with bioreactors, automated manufacturing systems, and/or iPSC differentiation protocols. The position requires excellent communication skills, creative troubleshooting, and a drive to learn.
Your Role
<ul>
<li>Hands-on participation in automated cell-based product manufacturing</li>
<li>Participate in troubleshooting and transfer of processes from R&amp;D</li>
<li>Function within a high-paced environment with a focus on teamwork and flexibility</li>
<li>Maintenance of ARMI's documentation standards through proper record keeping</li>
<li>Wear proper PPE and observe all safety/environmental and ARMI guidelines to ensure that a safe and professional work environment is maintained</li>
</ul>
Your Skills and Experiences
<ul>
<li>B.S with 2+ years of experience in cell-based product manufacturing</li>
<li>Experience with closed, scalable manufacturing systems</li>
<li>Experience with aseptic technique and cleanroom gowning </li>
<li>Experience with processes involving a variety of cell types, including Pluripotent Stem Cell expansion and differentiation Pancreatic islet differentiation experience preferred</li>
<li>Experience with technical SOPs and master batch records</li>
<li>Experience with GMP and/or GLP</li>
<li>Preferred knowledge of one or more of a variety of untargeted and targeted characterization methods, including analytical assays such as real-time PCR, ELISA, or flow cytometry</li>
</ul>

Associate Scientist

<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>

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