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<h3>Job Description</h3>
Job Description
MERL is looking for a highly motivated intern to work on an original research project in reconstruction/rendering dynamic 3D scenes. A strong background in 3D computer vision and/or computer graphics is required. Experience in the latest advances of deep learning in this area, such as neural radiance fields (NeRFs)/Gaussian Splatting (GS)/Point Map reconstruction methods, is an added plus and will be valued. The successful candidate is expected to have published at least one paper in a top-tier computer vision/graphics or machine learning venue, such as CVPR, ECCV, ICCV, SIGGRAPH, 3DV, ICML, ICLR, NeurIPS or AAAI, and possess solid programming skills in Python and popular deep learning frameworks like Pytorch. The goal would be for such a candidate to collaborate with MERL researchers to develop algorithms and prepare manuscripts for scientific publications. The position is available for graduate students on a Ph.D. track or those that have recently graduated with a Ph.D. Duration and start dates are flexible but are expected to last for at least 3 months. This internship is preferred to be onsite at MERL’s office in Cambridge, MA.
Required Specific Experience 
<ul>
<li>Prior publications in top computer vision/graphics and/or machine learning venues, such as CVPR, ECCV, ICCV, SIGGRAPH, 3DV, ICML, ICLR, NeurIPS or AAAI.</li>
<li>Experience in the latest novel-view synthesis approaches such as Neural Radiance Fields (NeRFs) or Gaussian Splatting (GS) and/or in the latest 3D point map reconstruction methods.</li>
<li>Proficiency in coding (particularly scripting languages like Python) and familiarity with deep learning frameworks, such as PyTorch or Tensorflow.</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.

Internship - Reconstruction/Novel View Synthesis of Dynamic Scenes

<h3>Job Description</h3>
Job Description
Senior Chemical Process Engineer Tewksbury, MA Direct Hire |
Summary
We are seeking a Senior Chemical Process Engineer with experience in process development, design, and construction of industrial facilities. This role will lead engineering efforts for complex process-facility projects, including new plant design, facility upgrades, and rehabilitation of high-hazard environments. The Senior Engineer will work closely with clients, vendors, contractors, and internal teams to deliver projects successfully.
Qualifications
<ul>
<li>B.S. in Chemical Engineering (minimum)</li>
<li>10+ years’ experience in chemical process engineering</li>
<li>Experience in process development, design, and construction</li>
<li>Ability to manage multiple projects and shifting priorities</li>
<li>Strong time management and leadership skills</li>
<li>Comfortable supervising junior engineers and collaborating with multidisciplinary teams</li>
<li>Background in chemical processing or related industries</li>
<li>Capital project management experience is a plus</li>
</ul>
Responsibilities
<ul>
<li>Lead and support engineering design for process-facility projects</li>
<li>Supervise and mentor engineering team members</li>
<li>Develop material &amp; energy balances and process flow diagrams (PFDs)</li>
<li>Prepare piping &amp; instrumentation diagrams (P&amp;IDs)</li>
<li>Size, specify, and procure equipment</li>
<li>Provide equipment and piping layout design support</li>
<li>Perform process and utility calculations</li>
<li>Support construction activities and process startups</li>
<li>Coordinate closely with vendors and clients to ensure requirements are met</li>
</ul>
Preferred Experience
<ul>
<li>Project management of capital projects</li>
<li>Construction support and startup/commissioning</li>
</ul>
Company DescriptionWhy Join · Collaborative, experienced engineering team. · Competitive salary &amp; full benefits. · Opportunity to deliver impactful next-generation products. 
<h3>Company Description</h3>
Why Join\r\n· Collaborative, experienced engineering team.\r\n· Competitive salary &amp; full benefits.\r\n· Opportunity to deliver impactful next-generation products.

Senior Chemical Process Engineer

<h3>Job Description</h3>
Job DescriptionCompany Description 
Are you ready to take the next step in your career and join a company that truly values your contributions? At Eurofins PSS, we offer more than just a job—we provide a rewarding, enriching, and fulfilling career path with opportunities for growth and advancement.
As part of our team, you’ll work in state-of-the-art laboratories alongside passionate professionals dedicated to the testing, development, and advancement of life-saving drug products. Together, we’re making the world a healthier and happier place to live.
Eurofins PSS is a global leader in life sciences, delivering a unique range of analytical testing services that help ensure the safety, authenticity, and accuracy of products and their ingredients. We partner with some of the world’s largest companies to make life and our environment safer, healthier, and more sustainable.
Our people are our chemistry—and we’re looking for talented individuals like you to join us in making a difference.
Job Description 
Advance your scientific career in&nbsp;Indianapolis, a thriving center for pharmaceutical and biotech innovation. We’re seeking a&nbsp;Metrologist Group Leader&nbsp;to oversee equipment maintenance, qualification, and team development in a GMP-regulated lab environment. This is a full-time leadership role with&nbsp;relocation assistance provided&nbsp;to support your move.
&nbsp;Why Relocate to Indianapolis?
<ul>
<li>Affordable cost of living with vibrant urban and suburban options</li>
<li>Expanding life sciences and pharmaceutical ecosystem</li>
<li>Relocation support and onboarding assistance to help you settle in smoothly</li>
</ul>
&nbsp;What You’ll Do
<ul>
<li>Lead equipment maintenance and qualification activities across lab operations</li>
<li>Troubleshoot technical issues and serve as a subject matter expert on lab instrumentation</li>
<li>Collaborate cross-functionally with internal teams, vendors, and global quality groups</li>
<li>Recommend and implement process improvements to enhance lab efficiency</li>
<li>Supervise and mentor team members, manage workflow, and conduct performance reviews</li>
<li>Ensure compliance with GMP standards and maintain accurate documentation</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in physical sciences (e.g., chemistry, physics)</li>
<li>4+ years of&nbsp;industry lab experience, including leadership responsibilities</li>
<li>Strong troubleshooting skills and familiarity with CMMS systems</li>
<li>Excellent communication, organizational, and team leadership abilities</li>
<li>Authorization to work in the U.S. indefinitely without sponsorship</li>
<li>Willingness to relocate to Indianapolis –&nbsp;relocation support is available</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, 8:00 am- 5:00 pm Overtime as needed.&nbsp;</li>
<li>Position is located in downtown Indianapolis, IN.&nbsp;</li>
<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 holidays</li>
<li>#LI-EB1</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Metrologist Group Leader - Relocation Opportunity to Indianapolis

<h3>Job Description</h3>
Job DescriptionDescription:
Technical/Field Service Customer Support
· Assists customers with instrumentation selection, installation practices based on project requirements/RFQ’s. Liaise with Sales and Engineering departments to realize compelling and competitive solutions to monitoring challenges.
· Provides technical troubleshooting and support for existing installations via phone/email.
· Provides data analysis to assess proper functionality and installation of instrumentation.
Field Service Coordination
· Manages Field Service activities, coordinating requests from customers with GEOKON personnel, and provide field services as needed.
· Prepares quotes and sales orders for field services, and occasional instrumentation products as needed.
Sales/Training Support
· Assists with providing training on the overview and application of GEOKON products and instrumentation in general. This includes in-house training, on-site training, and webinars.
Requirements:
Technical Skills/Knowledge
· Pile design and pile testing
· Slope stability
· Groundwater hydrology
· Understanding and use of various field instrumentation
· Awareness of soil and concrete testing procedures
· Familiarity with multiple aspects of geotechnical engineering
 
Other Requirements
· Managing and interpreting customer requirements and project applications
· General knowledge of a wide range of Civil Engineering projects and terminology
· Exceptional analytical and problem solving skills
· Strong writing capabilities and the skill to write clear, concise technically correct technical documents with high attention to detail
· Ability to exercise a high degree of independent judgment and professionalism
· Comfortable presenting in front of others and fielding technical questions
· Ability to travel 10-20% per year
· Fluent English language required
· Fluent Spanish languish/speaking preferred

ENGINEER - GEOTECHNICAL SVCS

<h3>Job Description</h3>
WuXi AppTec is looking for a highly motivated Research Associate II to join our biophysics team in Natick, MA.&nbsp; This role will provide lab support for both small and large molecule client projects using a range of biophysical techniques. 
 
<ul>
<li>Support biophysical binding assays </li>
<li>Follow SOP’s and perform SPR, TSA, MST, and other biophysical assays as required </li>
<li>Support instrument maintenance</li>
<li>Understanding of protein sciences, including binding affinity and kinetics</li>
<li>Effectively communicate with internal team colleagues and external clients to promote world class services</li>
</ul>
 
Experience / Education&nbsp;&nbsp;&nbsp; 
<ul>
<li>Bachelor's degree in biochemistry, biophysics, chemistry, or a lab-based discipline required. 2+ year of work experience is preferred</li>
<li>Demonstrated strong understanding of complex scientific procedures and technical proficiency with in vitro based assays</li>
<li>Outstanding written and oral communication and interpersonal skills to seamlessly fit into a team-oriented environment</li>
</ul>
Knowledge / Skills / Abilities:
<ul>
<li>Basic troubleshooting and planning skills</li>
<li>Excellent written, oral and interpersonal communication abilities</li>
<li>In vitro lab skills (pipetting, measuring, following lab protocols)</li>
<li>Proficient in Microsoft (Excel, Word, Outlook)</li>
<li>Ability to work in a team environment</li>
<li>Must be able to read, write and understand English. </li>
</ul>
Physical Requirements:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 
<ul>
<li>Must be able to work in an office environment with minimal noise conditions. </li>
<li>Must be able to work in Lab setting with exposure to biohazards, chemicals </li>
<li>Must be able to wear appropriate PPE</li>
<li>Must be able to work in environment with variable noise levels</li>
<li>Ability to stand/sit/walk for long periods of time </li>
<li>Ability to Lift 10 lbs. routinely</li>
<li>Ability to crouch, bend, twist, and reach</li>
<li>Ability to push/pull 10 lbs. routinely</li>
<li>Clarity of Vision</li>
</ul>
The anticipated base pay rate for this role is $21.00 - $28.00/hour
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, or protected veteran status and will not be discriminated against on the basis of disability
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.&nbsp; Employees holding this position will be required to perform any other job-related duties as requested by Management.

Research Associate II, Biophysics

<h3>Job Description</h3>
Job DescriptionSalary: $160,000 - $180,000 
About Acrivon Therapeutics
 Acrivon is a clinical stage biopharmaceutical company discovering and developing precision medicines utilizing its proprietary Generative Phosphoproteomics AP3 platform. The platform allows the company to interpret and quantify compound specific, drug-regulated pathway activity levels inside the intact cell in an unbiased manner, yielding terabytes of proprietary data and delivering rapid, actionable insights. The Generative Phosphoproteomics AP3 platform is comprised of a growing suite of powerful, internally-developed tools, including the AP3 Data Portal, converting multimodal data into structured data for generative AI analyses, the AP3 KaiSR Kinase Substrate Relationship Predictor, and the AP3 Interactome. These distinctive capabilities enable the company to go beyond the limitations of traditional drug discovery, as well as current AI-based target-centric drug discovery, and rapidly design highly differentiated compounds with desirable pathway effects through intracellular protein network analyses and advance these agents into the clinic for streamlined development.
 
Acrivon is currently advancing its lead program, ACR-368 (also known as prexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2b trial for endometrial cancer. The company has received Fast Track designation from the Food and Drug Administration, or FDA, for the investigation of ACR-368 as a monotherapy based on OncoSignature-predicted sensitivity in patients with endometrial cancer. The FDA has granted a Breakthrough Device designation for the ACR-368 OncoSignature assay for the identification of patients with endometrial cancer who may benefit from ACR-368 treatment. In addition, the company has initiated a third arm to the Phase 2b study without the need for a pre-treatment biopsy to evaluate ACR-368 with ultra-low-dose gemcitabine (ULDG) sensitization in all-comer, biomarker-unselected 2nd line patients with endometrial cancer who have all received prior treatment with chemotherapy and anti-PD-1.
 
Acrivon is also leveraging its proprietary Generative Phosphoproteomics AP3 platform for developing its co-crystallography-driven, internally discovered pipeline programs. These include ACR-2316, the companys second clinical stage asset, a novel, potent, selective WEE1/PKMYT1 inhibitor designed for superior single-agent activity through strong activation of not only CDK1 and CDK2, but also of PLK1 to drive pro-apoptotic cell death, as observed in preclinical studies against benchmark inhibitors. The Phase 1 trial of ACR-2316 is advancing with enrollment in the first three dose-escalation cohorts completed. Drug target engagement was observed at DL1 and 2 using the companys clinical mass spectrometry-based AP3 profiling, with evidence of approximate dose proportionality based on plasma pharmacokinetic analyses, and initial clinical activity and confirmed partial response. In addition, the company is advancing a preclinical program directed against an undisclosed cell cycle regulatory target.
Position Overview:
This position will apply technical expertise to support biomarker assaysprimarily digital imaging, analysis and associated workflows, data analysis, scripting and LIMSwithin our CLIA/CAP framework, and work closely with our biomarker platform team to advance our precision medicines in oncology.
Location:
This position will report to the CLIA Laboratory Director and be based at least 60% in our Watertown, MA facility, with no more than 40% in a home office.
Duties and Responsibilities:
<ul>
<li>Execute validated slide scanning and quantitative image analysis protocols for highcomplexity tests, including IHC and multiplex immunofluorescence assays.</li>
<li>Develop and execute validation plans for equipment and assay procedures including software and electronic workflow.</li>
<li>Collaborate with cross-functional teams to develop image analysis algorithms, scripts and workflows to support clinical and research assay development.</li>
<li>Lead all LIMS efforts including configurations, validations, document support and training.</li>
<li>Provide technical guidance on laboratory automation, data tracking and workflow optimization.</li>
<li>Assist with biostatistics for validation protocols and result analysis.</li>
<li>Collaborate with Quality, Regulatory, and IT teams to maintain a compliant, efficient laboratory.</li>
<li>Participate in proficiency testing and regulatory compliance.</li>
<li>Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed.</li>
<li>Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.</li>
<li>Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor, or Laboratory Director.</li>
<li>Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.</li>
<li>Work on special projects as assigned by management.</li>
</ul>
Required Skills/Abilities:
<ul>
<li>Minimum of masters degree in computer science, medical technology, histology, biology, or related field.</li>
<li>Minimum of 5 years of experience in clinical or research pathology laboratory.</li>
<li>Expertise in digital pathology platforms including multispectral imaging systems.</li>
<li>Familiarity with histology and IHC (including both bright field and fluorescence techniques).</li>
<li>Proficiency in Python, RStudio, HTML and laboratory information systems.</li>
<li>Familiarity with machine learning/AI applications</li>
<li>Detailoriented, precise, and adept at working in regulated environments.</li>
<li>Excellent communication, problem-solving, and leadership skills.</li>
<li>Ability to participate constructively on cross-functional and diverse teams.</li>
<li>Visual acuity for microscopic examination and computer use.</li>
</ul>
Acrivon Therapeutics is proud to be an equal opportunity employer and to provide equal opportunities to all employees and applicants for employment without regard to race, color, religion, sex or gender identity, national origin, age, disability, sexual orientation, or genetics. In addition to federal law requirements, Acrivon Therapeutics complies with applicable state and local laws governing nondiscrimination in employment.

Laboratory Information and Workflow Manager, CLIA Immunohistochemistry (IHC) Laboratory

<h3>Job Description</h3>
Job Description
WHDH-TV in Boston, MA is looking for an accurate weather forecaster for our newscasts. Must be able to generate creative, animated weather graphics. Must have an AMS Seal and a minimum of 3-5 years experience. WHDH-TV is an Equal Opportunity Employer. This position requires candidate to work 100% in Boston office.

Meteorologist - Weekend Mornings-FT

<h3>Job Description</h3>
Job DescriptionThis is an Associate Scientist/Scientist role in the Bioanalytical Group to help developing, qualifying/validating bioanalytical methods, and analyzing small and large molecule in different biological matrix. Experienced in analytical techniques such as ELISA, MSD, PCR is preferred. Job title and compensation will be based on candidates credentials

Associate Scientist/Scientist

<h3>Job Description</h3>
Job Description
Description
 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.
Job Type &amp; Location
This is a Contract position based out of Cambridge, MA.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Cambridge,MA.
Application Deadline
This position is anticipated to close on Nov 20, 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.

Associate Scientist

<h3>Job Description</h3>
Job Description
Description
• Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP • Conduct routine testing or other analysis in a specific group or department setting. • Conduct advanced testing and/or critical testing, as required. • Operate specialized equipment or conduct specialized skill testing • Working knowledge of raw materials testing and release • Lead investigation activities. • Ensure compliance to all data integrity and cGMP practices, procedures, and expect • Ensure compliance with all good documentation practices. • Other duties and responsibilities as assigned by the Head of the Department or Section Head
 
Skills
Hplc, Gmp, Karl Fisher, Particle size, icp, gc-ms, quality control, raw material, data entry, Wet chemistry, Analytical chemistry
 
Top Skills Details
Hplc,Gmp,Karl Fisher,Particle size,icp,gc-ms,quality control
 
Additional Skills &amp; Qualifications
Frist Shift- General Shift: 8:30AM – 5:00PM Monday -Friday Level II Pay Rate- $5,000K-$82,500K Level III-$83,000-$90,000 They’re hiring across levels (QC Chemist II &amp; III). QC Chemist II should be between 2-3 years’ experience in industry. Co-op experience in a cGMP pharmaceutical manufacturing setting is also acceptable especially for a level I. QC Chemist III should be at least 3-5 industry experience not academic experience. I’d prefer to focus on the Level II based on our previous experience with the hiring team and the level of expertise they desire. • Bachelor's degree (BS or BA), physical sciences required • Master's degree preferred • Minimum of 3-5+ years' experience. • Proficiently speak English as a first or second language • Proficiently communicate and understand (read and write) scientific work in English • Have excellent organization, learning and teaching skills required to work in teams • Ability to understand and analyze complex data sets.
 
Experience Level
Intermediate Level
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 13, 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.

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