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<h3>Job Description</h3>
We are seeking a highly skilled, passionate, and motivated scientist to join our diabetes research team. This position will play a key lab-based role in advancing iPSC stem cell engineering and contribute to the development of the next generation of islet cell therapies.
Responsibilities:
<ul>
<li>Enable and advance iPSC gene editing, cell line development, and evaluation of differentiated cells.</li>
<li>Perform routine iPSC cell culture, passaging, and media preparation.</li>
<li>Optimize workflows for iPSC CRISPR-based gene editing, gRNA screening, and delivery.</li>
<li>Develop and perform assays for on-/off-target analysis using PCR and NGS workflows.</li>
<li>Generate clonal gene-edited iPSC lines and characterize them via flow cytometry, ddPCR, dPCR, and qPCR.</li>
<li>Culture and execute routine directed differentiation of human iPSCs to pancreatic islets, performing assessments such as cell counts, viability, and metabolite analysis.</li>
<li>Assist scientists in evaluating and designing mitigation strategies to ensure genomic stability of iPSC lines and drug substances.</li>
<li>Collaborate cross-functionally to support the transfer of R&amp;D assays to GMP environments.</li>
<li>Maintain accurate and detailed experimental records, synthesize results, prepare reports, and present findings in meetings.</li>
<li>Contribute to the development and refinement of SOPs.</li>
<li>Execute work plans efficiently and meet established deadlines.</li>
</ul>
Qualifications:
<ul>
<li>BS or MS in Stem Cell Biology, Cell Biology, Bioengineering, or a related field.</li>
<li>3+ years of relevant industry experience for MS candidates, or 5+ years for BS candidates.</li>
<li>Extensive hands-on experience with human iPSC culture, gene editing, and molecular biology techniques.</li>
<li>Proficiency in gene editing and cell line development, including protocol optimization and flow-based sorting.</li>
<li>Hands-on experience with delivery methods for gene editing tools.</li>
<li>Strong communication and interpersonal skills, with the ability to work effectively in a collaborative team environment.</li>
<li>Excellent organizational skills and attention to detail in record keeping.</li>
<li>Experience in pancreatic islet directed differentiation is highly desirable.</li>
<li>Experience in transitioning research-grade processes to GMP-grade is highly desirable.</li>
</ul>

Biologist

<h3>Job Description</h3>
Job Description
Fully onsite 8-5. Cambridge site. Must be able to commute to site. Open to relocation candidates but must be willing to start ASAP. Must have: HPLC expertise and hands on lab experience. M.S. and 1 YOE would be ideal. B.S. and 3 YOE would be acceptable but a M.S is preferred. Managers ideal candidate: Someone who has a couple of years experience in biopharma working on bioanalytical assays such as SEC HPLC, Ion Exchange HPLC, and some basic assays like pH, osmolality, protein concentration etc. Good communication skills are also a must as they will work with a big group of people. Job Details: 1+ Years w/ Relevant MS OR equivalent 3+ Years w/ Relevant BS To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Responsibilities include: 1 Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision, 2 Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data, 3 Effectively transfers experimental methods from literature to the lab and makes modifications as necessary, 4 Develops and implements new protocols with moderate review, 5 Works efficiently in a matrix team environment and collaborates with coworkers, 6 Communicates data and interpretation to work group, 7 Skilled at developing systems to ensure quality data, 8 Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques (HPLC, CE, physical property testing...), 9 Effectively trouble-shoots equipment and experimental difficulties, 10 Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents, 11 Participates in department-wide support efforts such as safety, recruiting and committees, 12 May train staff and/or supervise others, 13 Coordinates and organizes resources needed to complete the task, 14 Understands when to seek input and when to make independent judgments. Requirements: Minimum BS degree (MS is preferred) in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology or related discipline and at least 2 year experience in a Biopharmaceutical working environment.
Top 3 Must Have Skill Sets:
BioPharma lab experience is a plus HPLC expertise - able to operate, process data, and report findings into electronic lab notebook. Good organizational skills - must be able to handle multiple tasks and communicate to different teams effectively and efficiently. Experience working in a biopharmaceutical lab showing analytical skills (compendial assays such as pH, osmolality, protein concentration, particle sizing etc).

Associate Scientist-HPLC (SEC/ Ion Exchange)

<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 is seeking a highly motivated Associate Scientist to join our Genomics &amp; Bioinformatics Group. In this role, you will use various CRISPR delivery systems to execute high-throughput screens to identify lead guides across our internal programs. You will be responsible for experimental design, analysis, and summarizing screens. In addition to screening efforts, you will be responsible for inventory and distribution of reagents within Sample Management. 
An ideal candidate has extensive experience handling and troubleshooting primary cells (HSC, T cells, Hepatocytes) and has experience screening in these cell types using various CRISPR delivery systems, including RNP and LNPs. The candidate should have a strong track record of creative thinking, strong drive, and the ability to be nimble while supporting multiple programs at a given time. Familiarity with liquid handling robots, such as the Biomek I7, and acoustic liquid transfers, like the Echo, is a plus. 
The position requires working effectively in a multi-disciplinary team, excellent written and verbal communication skills, and a capacity for creativity and innovation to efficiently execute screens that support the company achieve corporate objectives.
Requirements
Characterizing Your Impact:
As the Associate Scientist, Genomics and Bioinformatics you will:
<ul>
<li>Contribute to experimental design, execute screens, with editing and/or functional assays as readouts for internal programs. </li>
</ul>
<ul>
<li>Analyze and summarize screening results into proper documentation (ELN, Study Reports) and presentation slides.</li>
<li>Assist with Sample Management Support. </li>
</ul>
The Ideal Transcript:
To thrive in this role, you’ll need:
Minimum Qualifications 
<ul>
<li>B.S. in cell biology, or related field with 5+ years of relevant experience in industry; or M.S. in cell or molecular biology with 3+ years of relevant experience in industry</li>
<li>Independently design and run screening experiments, extract gDNA, submit for sequencing, analyze, and present data</li>
<li>Extensive experience handling primary cell lines. Proficient in performing cell-based assay development. Demonstrated ability to handle multiple cell lines simultaneously. </li>
<li>Proficient in multi-color flow cytometry, including design and data analysis using FlowJo.</li>
<li>Experience working with different screening modalities such as guide RNAs and LNPs.</li>
<li>Demonstrated ability to formulate both RNP and LNPs</li>
<li>Capable of independently using data analysis software such as PRISM, Tableau</li>
<li>Desire to learn new techniques and share expertise with colleagues</li>
<li>Self-motivated, detail-oriented problem solver with strong troubleshooting skills</li>
<li>Outstanding organizational skills and ability to multi-task in a fast-paced environment</li>
<li>Excellent communication and interpersonal skills fostering effective teamwork</li>
</ul>
Fundamentals That Set You Apart
Preferred Qualifications
<ul>
<li>Proficient in executing and analyzing functional assays including ELISAs and western blots</li>
<li>Familiar in molecular biology analyses such as qPCR and ddPCR</li>
<li>Prior experience operating lab automation including both liquid handling robots (Biomek I7s, Mantis, Echo) and plate readers (Envision). Bonus if prior experience writing methods on liquid handling robots. </li>
</ul>
Benefits
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.
Salary Range: 
$105,000 - $118,000
Pay Transparency
Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices.
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.

Associate Scientist, Genomics and Bioinformatics

<h3>Job Description</h3>
Job Description
Position: QC Chemist II / III
Location: Fall River, MA
Type: Direct Placement | First Shift (Monday–Friday, 8:30 AM – 5:00 PM)
A growing pharmaceutical manufacturer in Fall River, MA is seeking experienced Quality Control Chemists to join their team. This is a direct placement opportunity offering competitive compensation and the chance to work in a GMP-regulated environment. The ideal candidate will have hands-on experience with analytical instrumentation and raw material testing, and a strong understanding of cGMP and data integrity practices.
Key Responsibilities
<ul>
<li>Perform routine and advanced analytical testing using instruments such as HPLC, GC, Karl Fischer, ICP, and particle size analyzers.</li>
<li>Conduct raw material testing and release activities in compliance with regulatory standards.</li>
<li>Operate specialized lab equipment and perform wet chemistry techniques.</li>
<li>Lead and support investigation activities related to lab deviations or quality events.</li>
<li>Ensure strict adherence to cGMP, data integrity, and good documentation practices.</li>
<li>Collaborate with team members and department leadership to meet testing timelines and quality standards.</li>
<li>Perform other duties as assigned by department leadership.</li>
</ul>
Required Skills &amp; Qualifications
<ul>
<li>Bachelor’s degree in Physical Sciences (Chemistry, Biology, or related field); Master’s degree preferred.</li>
<li>2–5+ years of industry experience in a GMP pharmaceutical or biotech setting (co-op experience may be considered for entry-level).</li>
<li>Proficiency with analytical instruments including HPLC, GC-MS, Karl Fischer, ICP, and particle size analysis.</li>
<li>Strong understanding of GMP regulations and quality control procedures.</li>
<li>Excellent organizational, communication, and data analysis skills.</li>
<li>Ability to read, write, and communicate scientific information in English.</li>
<li>Comfortable working independently and collaboratively in a fast-paced lab environment.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience leading investigations or contributing to CAPA activities.</li>
<li>Familiarity with raw material release processes and documentation systems.</li>
<li>Strong attention to detail and ability to manage multiple priorities.</li>
</ul>
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com 
Job Type &amp; Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $65000.00 - $90000.00/yr.
Health Vision Dental 401K
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Nov 21, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist II, III

<h3>Job Description</h3>
Job Description
Title: Logistics Associate II
Pay Rate: $22/hour
Duration: 12-month contract
Location: Portsmouth, NH
Schedule: Monday – Friday, 7:00 AM – 3:30 PM
Job Summary
The Logistics Associate II is responsible for facilitating product shipping and distribution operations. This role involves working closely with management and team members to support logistics systems, implement new strategies, and ensure smooth warehouse operations.
Key Responsibilities
Perform general warehouse duties to support daily operations.
Facilitate product shipping, receiving, and distribution activities.
Collaborate with management on logistics systems and process improvements.
Assist in purchasing, warehousing, distribution, forecasting, and customer service.
Ensure freight is processed efficiently to maximize product service levels.
Process orders, prepare packing lists, and package outgoing materials.
Manage shipping logistics and ensure accuracy and timeliness of all orders.
Track shipment details, locations, and estimated times of arrival (ETAs).
Qualifications
3–5 years of relevant experience in logistics, warehouse operations, or supply chain management.
Strong attention to detail and organizational skills.
Ability to work effectively in a fast-paced environment.

Chemical Dispensing Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, 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.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!
Job Description 
We are seeking a highly motivated Analytical Development Scientist to join a collaborative team focused on supporting synthetic molecule development. This role involves designing, optimizing, and qualifying analytical methods to enable process and formulation development. The ideal candidate will bring strong technical expertise, problem-solving skills, and a proactive mindset to contribute meaningfully to project execution and innovation. The position is scheduled to start in January 2026.&nbsp;
Key Responsibilities:
<ul>
<li>Develop, optimize, and qualify analytical methods for synthetic molecules.</li>
<li>Provide analytical support for process and formulation development activities.</li>
<li>Independently plan and execute experiments; interpret and communicate complex data.</li>
<li>Troubleshoot technical issues and implement effective solutions.</li>
<li>Ensure compliance with cGMP/GLP, safety, and regulatory standards.</li>
<li>Write clear, concise technical reports and maintain accurate records.</li>
<li>Collaborate with cross-functional teams to meet project goals.</li>
<li>Coordinate lab work and contribute to team-based problem solving.</li>
<li>Learn and apply new techniques while managing multiple tasks efficiently.</li>
</ul>
Qualifications 
<ul>
<li>Working knowledge of analytical techniques with experience using multiple techniques (LC, GC, Dissolution, Karl Fisher, spectroscopic instruments, etc.) for synthetic molecules.</li>
<li>Basic understanding of industry practices and standards.</li>
<li>Experiences on method development and validation for synthetic molecule products</li>
<li>Strong computer, scientific, and organizational skills.</li>
<li>Analytical and Problem-Solving Skills - Able to troubleshoot critical issues or problems and determine causes and possible solutions using appropriate information</li>
<li>Ability to work well in a team environment&nbsp;</li>
<li>Communication&nbsp;and Organizational skills&nbsp;</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Education and Experience
<ul>
<li>Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 4+ years relevant industry experience&nbsp;&nbsp;</li>
<li>Master’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 2+ years relevant industry experience</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>
<li>45-60 Minute In-Person Meeting to Meet the Team and Discuss the Role&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to&nbsp;Cambridge, Massachusetts,&nbsp;are strongly encouraged to apply.&nbsp;
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>
<li>Hourly rate is between $39-$44,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

HPLC Development Specialist

<h3>Job Description</h3>
Job DescriptionCompany Description 
At Eurofins Professional Scientific Services (PSS), we believe the work we do matters—and so do our employees. We offer a unique opportunity to grow within the biopharmaceutical industry, supported by a collaborative team, professional development resources, and a competitive benefits package.
Eurofins Scientific is a global leader in analytical testing across food, environment, pharmaceutical, and cosmetic industries. Our mission is to make life and our environment safer, healthier, and more sustainable.
Job Description 
We are seeking a skilled HPLC Method Development Chemist to join our Cambridge-based team. This role focuses on developing, optimizing, and qualifying analytical methods for synthetic molecules, with a strong emphasis on HPLC and related chromatographic techniques.
Key Responsibilities
<ul>
<li>Develop and optimize HPLC methods for synthetic molecule analysis</li>
<li>Support process and formulation development through analytical testing</li>
<li>Interpret and communicate analytical data to cross-functional teams</li>
<li>Troubleshoot instrumentation and method-related issues</li>
<li>Author technical reports and documentation in compliance with cGMP/GLP standards</li>
<li>Independently design and execute experiments</li>
<li>Collaborate with team members to meet project goals</li>
<li>Maintain accurate records and adhere to safety and regulatory guidelines</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related field with 4+ years of relevant experience</li>
<li>OR Master’s degree with 2+ years of relevant experience</li>
<li>Hands-on experience with HPLC and other analytical techniques (e.g., GC, Dissolution, Karl Fischer, spectroscopy)</li>
<li>Strong problem-solving and organizational skills</li>
<li>Effective communication and teamwork abilities</li>
<li>Authorization to work in the U.S. without restriction or sponsorship</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>
<li>45-60 Minute In-Person Meeting to Meet the Team and Discuss the Role&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to&nbsp;Cambridge, Massachusetts,&nbsp;are strongly encouraged to apply.&nbsp;
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>
<li>Hourly rate is between $39-$44,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

HPLC Method Development Chemist

<h3>Job Description</h3>
Job Description
Job Description
We are seeking a Chemical / Process Engineer to join our team. The ideal candidate will develop, maintain, and optimize our chemical finishing processes while ensuring safety, quality, and compliance with industry standards. This role is hands-on and requires close collaboration with production, quality, and environmental health &amp; safety teams.
Responsibilities
<ul>
<li>Develop, implement, and improve electroplating, anodizing, conversion coating, and passivation processes.</li>
<li>Monitor and control chemical bath conditions, ensuring consistent performance and compliance with specifications.</li>
<li>Troubleshoot and resolve process issues related to adhesion, corrosion resistance, and finish quality.</li>
<li>Support audits and maintain compliance with NADCAP, ISO, AS9100D, and customer specifications.</li>
<li>Drive process improvements using Lean, Six Sigma, and data-driven problem solving.</li>
<li>Ensure compliance with environmental, health, and safety regulations for chemical handling and waste treatment.</li>
<li>Document standard operating procedures, work instructions, and process records.</li>
<li>Collaborate with cross-functional teams to meet production, quality, and cost goals.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Chemical Engineering, Materials Science, Chemistry, or a related field.</li>
<li>3+ years of experience in chemical or surface finishing processes (electroplating, anodizing, coatings, etc.).</li>
<li>Strong understanding of process control, bath chemistry, and troubleshooting.</li>
<li>Familiarity with NADCAP, ISO, and AS9100 requirements preferred.</li>
<li>Knowledge of safety practices for handling hazardous chemicals.</li>
<li>Excellent problem-solving, analytical, and communication skills.</li>
<li>Ability to work hands-on in a production environment.</li>
</ul>
Preferred Certifications (Not Required)
<ul>
<li>Lean Six Sigma (Green Belt or higher).</li>
<li>Certified Quality Engineer (CQE).</li>
<li>OSHA / HAZWOPER or other EHS-related training.</li>
<li>Professional Engineer (PE) license is a plus.</li>
</ul>
Benefits
<ul>
<li>Competitive salary with performance-based incentives.</li>
<li>Health, dental, and vision insurance.</li>
<li>Retirement plan with company match.</li>
<li>Paid time off and holidays.</li>
<li>Opportunities for career growth and professional development.</li>
</ul>
Company DescriptionCentral Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver. 
<h3>Company Description</h3>
Central Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver.

Chemical Process Engineer

<h3>Job Description</h3>
Job Title : QC Microbiology, Analyst ( Microbiology Analyst )
Location : Westborough, MA 01581
Duration : 06 Months 
Job Description : 
<ul>
<li>The primary purpose of the Analyst I position is to Support Quality Control Microbiological testing of drug substances, raw materials and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines, address excursions and conduct investigations.</li>
<li>Perform QC testing of samples for bioburden, microbial identification, growth promotion, and Endotoxin analysis.</li>
<li>Support cleanroom qualification, gowning qualification, aseptic process qualification, and personnel monitoring for manufacturing activities.</li>
<li>Experience in Environmental Monitoring and Pharma experience required</li>
</ul>

Microbiology Analyst

<h3>Job Description</h3>
Job Description
Mitsubishi Electric Research Laboratories (MERL) is seeking a self-motivated senior Ph.D. candidate in Computer Science or Electrical Engineering for a 3–month internship focused on developing and applying multi-modal large language models (LLMs) with application in anomaly detection, time sequence analysis, and predictive maintenance, etc. The ideal candidate will have a strong background in machine learning and signal processing, with a proven publication record in top conferences and journals. Experience in fine-tuning LLM foundation models is preferred. The intern will collaborate with MERL researchers to design and develop LLM-based frameworks for analyzing multi-modal sensor data, prepare technical reports, and contribute to manuscripts for scientific publications. The start date is flexible. 
Required Specific Experience 
<ul>
<li>Experience with LLMs. </li>
<li>Multi-modal time sequence data analysis</li>
<li>Ph.D Candidate </li>
</ul>
The pay range for this internship position will be 6-8K per month.
Mitsubishi Electric Research Labs, Inc. "MERL" provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, MERL complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
MERL expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of MERL’s employees to perform their job duties may result in discipline up to and including discharge.
Working at MERL requires full authorization to work in the U.S and access to technology, software and other information that is subject to governmental access control restrictions, due to export controls. Employment is conditioned on continued full authorization to work in the U.S and the availability of government authorization for the release of these items, which might include without limitation, obtaining an export license or other documentation. MERL may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to MERL facilities and information systems, as MERL deems appropriate, to ensure practical compliance with applicable employment law and government access control restrictions. 
In addition to base pay, interns receive a relocation stipend, covered travel to and from MERL, and a monthly Charlie Card for local commuting. Interns are invited to participate in weekly social gatherings and professional development opportunities, including research talks by both internal and external speakers. Interns who meet the 90-day waiting period are also eligible for health insurance coverage. MERL provides immigration support for qualified candidates as needed. Employment is considered “at-will,” and the Company reserves the right to modify base salary or any other compensation program at any time, including for reasons related to individual performance, departmental or Company performance, and market conditions.

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