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<h3>Job Description</h3>
Job Description
We are looking for a Senior Food Scientist to lead product development for nutritional beverages and powders. This role drives innovation from concept to commercialization, ensuring product quality, stability, and clinical effectiveness.
Key Responsibilities:
<ul>
<li>Develop and optimize nutritional beverage and powder formulations</li>
<li>Conduct R&amp;D on new ingredients and nutrition solutions</li>
<li>Collaborate with Medical Nutrition, Marketing, and Sales</li>
<li>Provide scientific guidance for product and clinical development</li>
<li>Ensure compliance with GMP, food safety, and aseptic processing</li>
<li>Build vendor relationships and source high-quality ingredients</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's in Food Science, Nutrition, or related field (Master's preferred; PhD/PharmD a plus)</li>
<li>5+ years in product development in food, beverage, supplement, nutraceutical, or biotech</li>
<li>Experience with R&amp;D, ingredient interactions, and nutrient stability</li>
<li>Knowledge of GMP, food safety standards, and aseptic processing</li>
</ul>
Benefits:
<ul>
<li>Competitive salary + performance-based bonus</li>
<li>Health, dental, and vision insurance</li>
<li>Paid time off and holidays</li>
<li>401(k) with company match</li>
<li>Professional development and career growth opportunities</li>
<li>Employee discounts</li>
</ul>

Senior Food Scientist - Product Development

<h3>Job Description</h3>
Job Description
Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics.
 
We are seeking a Senior Associate Scientist, Viral Vector to join our Cell Line Development team in Boston, MA. The ideal candidate will have a proven track record performing lentiviral vector stable packaging or producer cell line development in an industry setting. They will be a key contributor to our team, participating in the creation of stable producer cell lines for lentiviral vector therapeutics and research projects to improve our cell line development workflows. They will also work closely with Asimov’s synthetic biology and process development teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering.
About the Role:
<ul>
<li>
Perform lentiviral vector stable producer cell line development processes including transfection, pool generation, single cell cloning, characterization, and cell banking using state-of-the-art equipment.&nbsp;
</li>
<li>
Perform assays to assess quantity, potency and infectivity of lentiviral vector preparations.
</li>
<li>
Support innovation through development of novel workflows and applications
</li>
<li>
Support research projects to develop viral vector production methods to enhance product quality attributes such as empty/full ratio, potency and/or cell targeting.
</li>
<li>
Work effectively as part of a cross-functional team in support of a Lentiviral CLD platform and in collaboration with Synthetic Biology and Process Development teams.
</li>
<li>
Design experiments, analyze data, troubleshoot, and maintain detailed records.&nbsp;
</li>
<li>
Represent LV CLD on project teams, making decisions for cell line development activities and effectively communicating results, progress and plans.
</li>
</ul>
About You:
<ul>
<li>
B.S or M.S. in Biological Engineering, Virology, Cell Biology, Molecular Biology, or a related field.
</li>
<li>
5+ years of hands-on experience in biopharma with a minimum of 3 years focused on lentiviral vector producer cell line development in support of GLP or GMP production of cell or gene therapies.
</li>
<li>
Extensive experience performing viral transductions, flow cytometry, and quantitative gene expression analyses (ddPCR or qPCR).&nbsp;
</li>
<li>
Experience with downstream purification of lentiviral vectors, T-cell transduction assay, viral genome engineering, and/or host cell genome engineering related to virus production or producer cell line technologies is highly desired.
</li>
<li>
Comfortable working with large, multidimensional datasets and applying statistical or computational methods to extract actionable biological or process insights.
</li>
<li>
Strong written and verbal communication skills required.
</li>
</ul>
We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.
Compensation Range: $115K - $120K

Senior Associate Scientist, Viral Vector Cell Line Development

<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 24, 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
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.

<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 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
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 Description
Description
What are the top 3-5 skills, experience or education required for this position: 1. Immunohistochemistry experience acquired at pharmaceutical, CRO or biotechnology company 2.Working knowledge of performing IHS and in situ hybridization (ISH) on the Leica Bond Rx. 3.BS in Science/Chemistry/related 4.Team-oriented We are seeking an individual who will perform routine single plex and multiplex immunohistochemistry in drug discovery programs. The successful candidate will work in a group providing research support in target validation, target distribution, animal model development, pharmacology, and exploratory safety studies. Being detailed oriented is critical to this role. Specific activities will include immunohistochemistry performed on the Leica Bond Rx platform therefore, familiarity with this technology is important. Exposure to multiplex using the Lumiphores COMET platform will be available. Additional tasks include using computer-based laboratory tracking system (Sample Manager), Dream Path, interaction with study pathologists and project teams as well as inclusion in a highly dynamic, motivated team of immunohistochemistry scientists and histotechnologists. The candidate must be comfortable working independently after a thorough period of training and onboarding as well as the ability to prioritize workload to manage several tasks. If you are willing to work as part of a multidisciplinary research team in an exciting, friendly, fast-paced environment, please consider joining our team! Other Desirable Attributes: Well organized Attention to detail Adherence to established protocols and laboratory documentation requirements Ability to work and effectively communicate within a team environment Ability to handle multiple projects simultaneously Delivery of high-quality, timely results Excellent oral and written communication skills Enthusiastic Independent, analytical, innovative thinker Proficiency with MS office-Excel, OneNote Significant Work Activities and Conditions Continuous standing for prolonged periods (more than 2 consecutive hours in an 8-hour day) Routine work with chemicals
 
Skills
immunohistochemistry, leica bond RX, chemistry, In Situ Hybridization, histology, pathology
 
Top Skills Details
immunohistochemistry,leica bond RX,chemistry,In Situ Hybridization,histology,pathology
 
Additional Skills &amp; Qualifications
Basic Qualifications: B.S./B.A. in Biology/Chemistry or related field Microsoft office skills Preferred Qualifications: Qualification in IHC (QIHC) preferred but not required Working knowledge of the Leica Bond Rx IHC platform Ability to troubleshoot IHC Ideally 3-5 years of experience within a histology/ pathology laboratory
 
Experience Level
Intermediate Level
Job Type &amp; Location
This is a Contract position based out of Worcester, MA.
Pay and Benefits
The pay range for this position is $45.00 - $50.00/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 Worcester,MA.
Application Deadline
This position is anticipated to close on Nov 26, 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.

Scientist II

<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 Job Title: Bench Chemist
Location: Hadley, MA
Job Type: Contract-to-Hire
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
About the Role
Are you passionate about chemistry and eager to make an impact in a dynamic laboratory setting? We’re looking for a Bench Chemist who thrives on precision, problem-solving, and innovation. In this role, you’ll work with cutting-edge instrumentation and collaborate with a team dedicated to delivering high-quality results that drive product excellence.
This is an exciting opportunity to join a growing organization where your expertise will directly contribute to advancing science and improving product quality.
What You’ll Do
<ul>
<li>Perform LC and GC testing on raw materials, in-process samples, and finished goods.</li>
<li>Prepare samples, run calibration curves, and ensure system suitability through integration reviews.</li>
<li>Execute wet chemistry techniques such as pH measurement, titrations, and loss on drying (LOD).</li>
<li>Conduct first-line instrument maintenance and troubleshooting to keep operations running smoothly.</li>
<li>Support method validation efforts focusing on accuracy, precision, and detection limits.</li>
<li>Maintain a clean, organized lab environment and assist with inventory management.</li>
<li>Draft and review SOPs to uphold compliance and quality standards.</li>
</ul>
What We’re Looking For
<ul>
<li>Education: Master’s degree in Chemistry or Analytical Chemistry with 3–5 years of QC lab experience (food or supplement industry preferred).</li>
<li>Technical Skills: Proficient in HPLC and GC systems, chromatography software (OpenLab, ChemStation), and wet chemistry techniques.</li>
<li>Knowledge: Familiarity with USP/AOAC methods and cGMP documentation.</li>
<li>Strong commitment to lab safety, accuracy, and continuous improvement.</li>
</ul>
Preferred:
<ul>
<li>Bachelor’s degree in Chemistry with equivalent experience.</li>
<li>Background in organic chemistry, formulation, or R&amp;D.</li>
</ul>
Why Join Us?
<ul>
<li>Work with state-of-the-art equipment in a collaborative, science-driven environment.</li>
<li>Opportunity for career growth through a contract-to-hire pathway.</li>
<li>Be part of a team that values innovation, quality, and professional development.</li>
</ul>
Job Type &amp; Location
This is a Permanent position based out of Hadley, MA.
Pay and Benefits
The pay range for this position is $40.00 - $40.00/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 Hadley,MA.
Application Deadline
This position is anticipated to close on Nov 27, 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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