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<h3>Job Description</h3>
Job Description
Job Title:&nbsp; Proteomics Bench Scientist
Location: &nbsp;Andover&nbsp;MA 01810
Duration: 12 months&nbsp;
POSITION SUMMARY
<ul>
<li>Candidate will be responsible for developing proteomics workflows using advanced high-resolution mass spectrometry techniques.</li>
<li>Key duties include development and optimization of sample preparation methods from cell lines and other matrices for mass spectrometry analysis and data processing with various bioinformatics tools; collaborative work with colleagues; accurately documenting all activities in an electronic lab notebook (ELN).</li>
<li>This role requires expertise in LC-MS based proteomics.</li>
<li>Experience with cell culture and cell manipulation is a plus.</li>
</ul>
POSITION RESPONSIBILITIES
• Applying knowledge of proteomics workflows to develop and implement optimal strategies for the preparation and analysis of cellular samples
• Working collaboratively with experts in the team to advance innovative proteomics strategies
• Employing different bioinformatics tools for data analysis and fitting
• Consistent record keeping using an electronic lab notebook (ELN)
ORGANIZATIONAL RELATIONSHIPS
• This hire will interact daily with the managers and 3-4 colleagues in the cross-functional team for method development, laboratory work prioritization, experiment planning and execution.
The hire might also work on common assignments with colleagues in a larger bioanalytical group at the same location, as needed.
The hire will participate in bi-weekly group meetings and other team meetings and discussions, as relevant to their work.
EDUCATION AND EXPERIENCE
• M.Sc 5+ years, PhD 0+ years in a relevant scientific field with a documented experience in proteomics and mass-spectrometry
TECHNICAL SKILLS REQUIREMENTS
Required:
• Advanced knowledge and documented expertise with mass-spectrometry based proteomics approaches: label- or label-free quantification (TMT or DIA)
• Experience with high-resolution mass-spectrometry instruments, such as Orbitraps and timsTOF
• Experience with sample preparation based on enrichment (incl. affinity purification), and universal protein extraction
• Bioinformatics skills relevant for mass-spec data search, statistical analysis and visualization
Preferable:
• Experience with membrane protein analysis and/or cell surface proteomics
• Knowledge of cell culture techniques and experience conducitng cell-based assays
PHYSICAL POSITION REQUIREMENTS
• Walking, taking the stairs, standing, sitting as appropriate for a laboratory-based position

Proteomics Bench Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Quality Control ChemistJob Description
The Quality Control Chemist will support method development using GC, HPLC, and UPLC, while performing essential analytical chemistry work. The role involves identifying and executing proper characterization methods and preparing technical data, reports, and standard operating procedures for internal use.
Responsibilities
<ul>
<li>Support and develop methods for GC, HPLC, and UPLC.</li>
<li>Identify and perform proper characterization methods.</li>
<li>Prepare and present technical data, reports, and standard operating procedures.</li>
<li>Run and support the development of the chemistry team.</li>
<li>Write and execute all methods used within the team.</li>
<li>Act as a supporting lead to drive research forward.</li>
</ul>
 Essential Skills
<ul>
<li>Proficiency in Chemistry, HPLC, UPLC, and method development.</li>
<li>Experience with analytical chemistry and gas chromatography.</li>
<li>Knowledge of capillary electrophoresis, conductivity, FTIR, GCMS, and UVVIS.</li>
<li>Experience in wet chemistry and quality control.</li>
</ul>
 Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's or Master's degree with 3-5 years of experience, preferably in chemistry or biochemistry.</li>
<li>Experience with independent method development using various chemistry instrumentation.</li>
<li>Proficiency in utilizing empower systems.</li>
<li>Hands-on experience with CE methods such as CE-SDS and cIEF for analyzing biological materials.</li>
</ul>
 Work Environment
The role requires 100% onsite work within the Quality Control chemistry group. The environment is business casual, operating on a first shift from Monday to Friday. The team values detail-oriented, collaborative, and hardworking individuals.
Job Type &amp; Location
This is a Contract position based out of Bedford, Massachusetts.
Pay and Benefits
The pay range for this position is $35.00 - $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 Bedford,MA.
Application Deadline
This position is anticipated to close on Sep 30, 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

<h3>Job Description</h3>
Job Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment.
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that foster a strong employee engagement, teamwork, safety and wellness.
We offer a competitive/generous benefits package that fits the needs of our employees. It includes health, dental, vision, wellness programs, employee discounts, 401k matches, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. (see E Ink │ Our Company)
About the position:
E Ink is the world leader in ePaper display technology. At the Billerica Innovation Center, we invent new materials for the development of next generation E Ink products. But we can’t improve product performance without evaluating the materials that go into them – that is where individuals like you come in. Reporting to the Senior Program Manager of the Analytical Chemistry Group, the Analytical Scientist will be a member of the Chemistry team responsible for carrying out and developing qualitative and quantitative analytical methods to measure critical component properties required to ensure the quality, performance, and reliability of our existing and future display products throughout their lifecycles.
Job Responsibilities
<ul>
<li>Support characterization of ePaper materials using a combination of techniques to include but not limited to GC-MS. LC-MS and NMR.</li>
<li>Be the analytical leader in root cause investigations to determine defects/failure mechanisms in ePaper coatings and laminates.</li>
<li>Develop and validate new quantitative analytical methods as needed to support product launch deadlines. Write SOP’s to support documentation of new procedures.</li>
<li>Be the owner responsible for maintenance and upkeep of assigned laboratory instrumentation.</li>
<li>Manage sample workflow of assigned test requests through the lab’s submission software.</li>
</ul>
Skill Requirements
<ul>
<li>B.S. in Science, Engineering or equivalent with minimum of 10 years chemical laboratory experience or M.S. in Science, Engineering with minimum of 4 years lab experience</li>
<li>In depth knowledge of and experience with quantitative gas chromatography-mass spectroscopy using a variety of sample introduction techniques (liquid injection, headspace, pyrolysis)</li>
<li>In depth knowledge of quantitative 1H and 13C NMR. Experience using Mnova NMR data processing software</li>
<li>Experience using Excel, Powerpoint and JMP to process and present data</li>
<li>Excellent organizational and communication skills, a strong sense of urgency and a performance metrics-driven style</li>
<li>Good analytical skills and attention to detail in a fast-paced environment</li>
</ul>
 Benefits
<ul>
<li>Competitive total compensation package</li>
<li>Medical, dental and vision on 1st day</li>
<li>Company 401K match</li>
<li>20 PTO days</li>
<li>Generous sick leave policy</li>
<li>Casual day to day work environment</li>
<li>Hybrid/flexible work environment (for some positions)</li>
</ul>
E ink is committed to a diverse and inclusive workforce. E Ink is an equal opportunity employer and does not discriminate on the basis of race, ethnicity, gender, identity, sexual orientation, veteran’s status, disability, age, or on any basis prohibited by federal and state law.

Senior Analytical Scientist 1050S-BFEW

<h3>Job Description</h3>
Job Description
In this vital role you will be developing, qualifying and transferring innovative and fit-for-purpose quantitative assays for the measurement of DNA, proteins and other biological analyzes for manufacturing process development. The Senior Associate in Process Development is instrumental in designing, developing, and optimizing manufacturing processes. They are involved in conducting experiments, analyzing results, and implementing process improvements to enhance efficiency and product quality.
 Responsibilities:
<ul>
<li>Routine testing support for PD DS process related impurity analysis</li>
<li>Preparation of lab buffers and reagents</li>
<li>Lab reagent and materials inventory</li>
<li>Maintenance of critical reagents stocks</li>
<li>General lab upkeep and equipment maintenance support</li>
<li>Provides critical evaluation of analytical data and results to support product development analytical testing activities.</li>
<li>Documentation of assays and laboratory activities in electronic notebook documentation system</li>
<li>Generating, analyzing, and interpreting analytical data</li>
<li>Supporting analytical projects involving method development, qualification, and transfer</li>
<li>Analyzing routine samples by qPCR and ELISA, data interpretation and reporting,</li>
<li>Documentation of results and peer review of electronic notebooks.</li>
<li>Preparation of lab buffers and reagents, maintenance of critical reagents stocks</li>
<li>Sample, reagent and materials inventory tracking and re-stocking</li>
<li>General lab upkeep and equipment maintenance support</li>
<li>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.</li>
</ul>
Requirements / Qualifications:
<ul>
<li>Associate’s degree in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field and 2 years of Scientific experience OR</li>
<li>Bachelor’s degree in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field</li>
<li>Experience and expertise with protein assays, especially immunoassays, ELISAs or qPCR.</li>
<li>Experience in GMP lab setting.</li>
<li>Experience and expertise with Microsoft Office software: Word, PowerPoint and Excel.</li>
<li>Enjoys participating in a cohesive, high performing team, establishes effective and adaptable relationships with colleagues, while contributing as an effective independent contributor.</li>
<li>Communication – establishes and maintains effective communication mechanisms to keep colleagues appropriately advised; bridges communication between individuals, team and other organizational units as necessary.</li>
<li>Social skills – communicates optimally, using appropriate tact and sensitivity; makes others feel respected, valued and understood.</li>
<li>ELISA, immunoassays and qPCR technologies</li>
<li>Familiarity with electronic laboratory notebook/record keeping system(s)</li>
<li>Familiarity with working in a GMP/GxP environment</li>
<li>Strong Communication skills</li>
<li>Team player</li>
</ul>
Company DescriptionThe Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search. 
<h3>Company Description</h3>
The Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search.

Associate Scientist

<h3>Job Description</h3>
Job Description
We’re seeking a Senior Dam Safety Engineer with deep expertise in geotechnical engineering and dam safety evaluations. This leadership role is ideal for someone with FERC Part 12 Independent Consultant approval—or the experience to qualify—and a passion for risk-based analysis and infrastructure resilience.
You’ll play a pivotal role in guiding project teams, mentoring junior staff, and shaping the future of our dam safety services. This is your opportunity to work on meaningful, high-impact projects in clean energy and environmental restoration. Ready to make a difference? Let’s build something lasting—together!
**Remote work options available
 
 
Key Responsibilities
<ul>
<li>Lead and coordinate design teams for FERC and state-regulated dam safety projects</li>
<li>Conduct dam safety evaluations, including FERC Part 12 inspections</li>
<li>Design earthen embankments and perform geotechnical assessments for dams and civil works</li>
<li>Develop and analyze geotechnical monitoring and testing programs</li>
<li>Review construction sequencing, design plans/specs, and permitting documents</li>
<li>Represent the firm in technical discussions with regulators, clients, and public forums</li>
<li>Author and review technical reports and project documentation</li>
<li>Mentor engineers in technical execution and career development</li>
<li>Support proposal writing, cost estimating, and project scheduling</li>
</ul>
Qualifications
<ul>
<li>B.S. in Civil or Geotechnical Engineering (M.S. preferred)</li>
<li>Licensed Professional Engineer (PE) with willingness to maintain multi-state registrations</li>
<li>FERC Part 12 Independent Consultant approval or eligibility</li>
<li>Comprehensive Assessments expert</li>
<li>Strong communication skills and attention to detail</li>
<li>Experience with risk-based analysis preferred</li>
<li>15+ years of experience in:
<ul>
<li>Dam safety evaluations and geotechnical design</li>
<li>Project management and client engagement</li>
<li>Earthquake response analysis for embankments</li>
<li>Proposal development and team mentoring</li>
<li>Familiarity with federal/state dam safety standards</li>
</ul>
</li>
<li>Some travel required to project sites</li>
</ul>
Benefits
We offer a competitive and comprehensive benefits package, including:
<ul>
<li>Medical, dental, and vision insurance</li>
<li>Generous vacation, comp time, and flexible holidays</li>
<li>Paid sick leave and extended medical leave account</li>
<li>Educational assistance and professional development support</li>
<li>Parental leave and Dependent Care FSA</li>
<li>Short and long-term disability coverage, Life Insurance</li>
<li>401K and profit-sharing program</li>
</ul>

Senior Geotechnical Dam Safety Engineer - PE

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting:
Director, Cancer Biology
 
Description: 
We are seeking an experienced Senior Research Associate or Scientist, Biology to join Marianas Biology organization, advancing personalized medicine and radiopharmaceuticals. In this role, you will contribute to target validation and execute preclinical studies that advance the next generation of radiotherapeutics. This is an exciting opportunity for someone eager to make an impact in science and in the lives of cancer patients, while growing their career within a dynamic biotech environment.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Design, plan, and execute preclinical experiments to demonstrate in vitro activity, in vivo efficacy, and elucidate mechanisms of action for novel radiopharmaceutical candidates.</li>
<li>Analyze, interpret, and present experimental data; prepare detailed study reports; communicate findings to internal project teams, leadership, and external collaborators.</li>
<li>Support target validation and model development to guide program advancement into translational and clinical stages.</li>
<li>Manage and engage with CROs and academic collaborators to accelerate key studies.</li>
<li>Maintain accurate and compliant laboratory records, ensuring data integrity.</li>
<li>Partner with cross-functional teams (chemistry, translational sciences, pharmacology) to align experimental design with overall strategy.</li>
<li>Contribute to scientific publications, presentations, and intellectual property generation.</li>
<li>Actively participate in lab meetings, project discussions, and strategic planning, offering scientific insight and innovative solutions.</li>
</ul>
Requirements/Skills:
<ul>
<li>Education/experience:
<ul>
<li>Sr. Research Associate I - BS or MS in Biology, Cell/Molecular Biology, Genetics, or related field with2 5+ years industry experience (BS)/ 1+ (MS) years industry experience in biotech or pharma R&amp;D.</li>
<li>Scientist II - BS or MS in Biology, Cell/Molecular Biology, Genetics, or related field with5 - 7+ years industry experience (BS/MS)/ 1+ years industry experience (PhD) in biotech or pharma R&amp;D.</li>
</ul>
</li>
<li>Strong background in cancer biology; experience in oncology drug discovery preferred.</li>
<li>Proven ability to independently design, execute, and troubleshoot experiments with high-quality, reproducible results.</li>
<li>Proficiency with standard laboratory techniques such as proliferation assays, Western blotting, ELISA, qPCR, and stable cell line generation.</li>
<li>Familiarity with in vivo oncology models or prior experience coordinating in vivo studies is a plus.</li>
<li>Strong data analysis and interpretation skills, with the ability to translate findings into actionable insights.</li>
<li>Excellent organizational skills with meticulous attention to detail and record-keeping.</li>
<li>Effective interpersonal and communication skills; thrives in a collaborative, fast-paced environment.</li>
<li>A proactive, self-motivated team player with urgency, accountability, and passion for advancing life-changing cancer therapeutics.</li>
</ul>
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

SRA/Scientist, Biology

<h3>Job Description</h3>
Job Description
Job Description 
<ul>
<li>
Developing proteomics workflows using advanced high-resolution mass spectrometry techniques. 
</li>
<li>
Key duties include development and optimization of sample preparation methods from cell lines and other matrices for mass spectrometry analysis and data processing with various bioinformatics tools; collaborative work with colleagues; accurately documenting all activities in an electronic lab notebook (ELN). 
</li>
<li>
Applying knowledge of proteomics workflows to develop and implement optimal strategies for the preparation and analysis of cellular samples
</li>
<li>
Working collaboratively with experts in the team to advance innovative proteomics strategies
</li>
<li>
Employing different bioinformatics tools for data analysis and fitting
</li>
<li>
Consistent record keeping using an electronic lab notebook (ELN)
</li>
<li>
Interact daily with the managers and 3-4 colleagues in the cross-functional team for method development, laboratory work prioritization, experiment planning and execution. 
</li>
<li>
Also work on common assignments with colleagues in a larger bioanalytical group at the same location, as needed. 
</li>
<li>
Participate in bi-weekly group meetings and other team meetings and discussions, as relevant to their work.
</li>
</ul>
QUALIFICATIONS:
<ul>
<li>
M.Sc with 5+ years experience; OR
</li>
<li>
PhD 0+ years in a relevant scientific field with a documented experience in proteomics and mass-spectrometry desired 
</li>
<li>
Advanced knowledge and documented expertise with mass-spectrometry based proteomics approaches: label- or label-free quantification (TMT or DIA)
</li>
<li>
Experience with high-resolution mass-spectrometry instruments, such as Orbitraps and timsTOF
</li>
<li>
Experience with sample preparation based on enrichment (incl. affinity purification), and universal protein extraction
</li>
<li>
Bioinformatics skills relevant for mass-spec data search, statistical analysis and visualization
</li>
<li>
Experience with membrane protein analysis and/or cell surface proteomics
</li>
<li>
Knowledge of cell culture techniques and experience conducitng cell-based assays
</li>
<li>
Walking, taking the stairs, standing, sitting as appropriate for a laboratory-based position
</li>
<li>
Experience with cell culture and cell manipulation is a plus.
</li>
<li>
Requires expertise in LC-MS based proteomics. 
</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 DescriptionNow Hiring: Analytical Bench Chemist – Food Industry
Hadley, MA 
Summary:
Are you passionate about science, precision, and food innovation? Join our dynamic team as an Analytical Bench Chemist, where you'll play a key role in ensuring the safety, quality, and consistency of our food ingredients and products.
This is a hands-on laboratory role ideal for someone who thrives in a fast-paced environment and enjoys solving complex analytical challenges. You’ll work closely with cross-functional teams in R&amp;D, Quality, and Production to support product development and ensure regulatory compliance.
 Job Details:
<ul>
<li>Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, titration, and more.</li>
<li>Develop, validate, and optimize analytical methods to support product innovation and quality assurance.</li>
<li>Maintain and calibrate laboratory instruments and ensure compliance with GLP/GMP standards.</li>
<li>Document results accurately and prepare detailed reports for internal and regulatory use.</li>
<li>Collaborate with QA and R&amp;D teams to troubleshoot formulation or process-related issues.</li>
<li>Support regulatory submissions and ensure compliance with FDA, USDA, and other relevant standards.</li>
<li>Participate in internal audits and contribute to continuous improvement initiatives.</li>
</ul>
Requirements:
<ul>
<li>Bachelor’s or Master’s degree in Chemistry, Food Science, Biochemistry, or related field.</li>
<li>2–5 years of experience in an analytical chemistry role, preferably in the food, beverage, or nutraceutical industry.</li>
<li>Strong proficiency in instrumental analysis (HPLC, GC, etc.) and wet chemistry techniques.</li>
<li>Familiarity with FDA regulations, food safety standards, and laboratory best practices.</li>
<li>Excellent attention to detail, organizational skills, and ability to work independently.</li>
<li>Strong communication skills and a collaborative mindset.</li>
</ul>
Why Join Us?
We’re a science-driven food company committed to innovation, sustainability, and quality. As part of our team, you’ll have the opportunity to work on exciting projects, grow your career, and make a meaningful impact on the food industry.
Pay and Benefits
The pay range for this position is $30.00 - $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 Sep 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.

Qc Lab Analyst - Food

<h3>Job Description</h3>
Job Description
We are looking for a skilled Research and Reporting Analyst to join a non-profit organization located in Andover, Massachusetts. In this long-term contract role, you will support the Institutional Research department, leveraging your expertise in data analysis and visualization to help drive informed decision-making across the campus.
 
Responsibilities:
• Extract, analyze, and interpret data to create reports, queries, and dashboards that support institutional objectives.
• Conduct detailed analyses on assigned projects and programs, ensuring accuracy and relevance in findings.
• Design, validate, and maintain Tableau dashboards and visualizations for use by campus stakeholders.
• Collaborate on the development and implementation of data management and quality control procedures to ensure consistency and reliability.
• Prepare responses to external surveys and data requests from organizations such as U.S. News &amp; World Report and The College Board.
• Maintain organized documentation of data sources, methodologies, and tracking systems for research requests.
• Update and publish annual summary reports on key metrics such as admissions, enrollment, retention, graduation, and degrees awarded.
• Partner with the web office to ensure reports and documents are accurately published online.
• Identify and resolve data discrepancies while contributing to the maintenance of secure and confidential data systems.
• Proven experience in business analysis, including data extraction, review, and reporting. • Proficiency in Tableau for creating dashboards and data visualizations. • Strong analytical skills with the ability to identify gaps and discrepancies in data. • Familiarity with university policies and procedures, particularly in a research setting. • Excellent organizational skills for managing documentation and tracking research requests. • Ability to handle sensitive data with a high degree of confidentiality. • Effective communication skills for presenting findings and collaborating with stakeholders. • Experience in preparing responses to external and internal data requests.

Research and Reporting Analyst

<h3>Job Description</h3>
Job Description
🚗 Why us? Your car and your home are the two most expensive things you’ll ever own — and the hardest to manage. At Jerry.ai, we’re building the first super app to help everyday Americans take control of both. From insurance and financing to repairs and real estate, we’re reimagining what it means to own and maintain your car and home. This is a $5 trillion+ problem — and we’re the only company tackling it end to end.
2024 was a milestone year for Jerry.ai. We delivered nearly 50% year-over-year revenue growth while reaching profitability for the first time in our history.
And we're just getting started! Our growth is driven by forward-thinking technology; Harvard Business Review covered the success of our chatbot less than a year after its launch and Jerry.ai is getting mentioned in many conversations about our use of GenAI, such as this Forbes article.
&amp;#x1F4BB; About the opportunity
We are looking for a Staff Applied Data Scientist (PhD) who is energized by working with a high caliber team and making a material difference in the lives of millions to join us! Reporting directly to our cofounder/CTO, you will architect and deploy advanced ML models with massive real-world applications (e.g. model &amp; predict user behavior, leverage LLMs and custom-built components to optimize our chatbot &amp; voicebot, etc). Come play a key role in helping us grow from 5M to 50M customers and become a $10B company in the next 4 years!
We have a fast-paced startup culture that empowers you to move quickly, test, iterate, and own projects end-to-end in an environment where your ideas matter and your impact is felt from day one. You’ll work with extremely talented and passionate engineers, data scientists, and analysts from companies like NVIDIA, Meta, Amazon, ByteDance, Square, Robinhood and more.
🫵 How you will make an impact
<ul>
<li>
Develop and architect complex machine learning models to address critical business challenges and drive company-wide strategic initiatives
</li>
<li>
Take ownership of the end-to-end modeling process, from initial ideation to model deployment and maintenance
</li>
<li>
Conduct thorough data preparation and analysis to ensure the quality and relevance of input data for modeling tasks
</li>
<li>
Collaborate closely with cross-functional teams, including Product and Data Engineering to productize and deploy models into production systems
</li>
<li>
Contribute to large-scale company initiatives aimed at solving problems that haven’t yet been touched by anyone at Jerry.ai
</li>
</ul>
🚀 Requirements
<ul>
<li>
PhD in Physics or related field
</li>
<li>
5+ years of experience building and deploying models from scratch.
</li>
<li>
Deep understanding of machine learning algorithms and techniques, with experience in building and deploying models from scratch.
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Strong analytical and problem-solving skills, with the ability to translate complex business requirements into practical modeling solutions.
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Passion for real-world application of machine learning, with a desire to make a significant impact on large-scale business initiatives.
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While we appreciate your interest and application, only applicants under consideration will be contacted.
Jerry.ai is proud to be an Equal Employment Opportunity employer. We prohibit discrimination based on race, religion, color, national origin, sex, pregnancy, reproductive health decisions or related medical conditions, sexual orientation, gender identity, gender expression, age, veteran status, disability, genetic information, or other characteristics protected by applicable local, state or federal laws. 
Jerry.ai is committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation due to a disability, please contact us at <a href="mailto:recruiting@jerry.ai" target="_blank">recruiting@jerry.ai</a>
The successful candidate’s starting pay will fall within the pay range listed on this job posting, determined based on job-related factors including, but not limited to, skills, experience, qualifications, work location, and market conditions. Ranges are market-dependent and may be modified in the future. In addition to base salary, the compensation may include opportunities for equity grants. 
We offer a comprehensive benefits package to regular employees, including health, dental, and vision coverage, paid time off, paid parental leave, 401(K) plan with employer matching, and wellness benefits, among others. Equity opportunities may also be part of your total rewards package. Part-time, contract, or freelance roles may not be eligible for certain benefits.
About Jerry.ai:
Jerry.ai is America’s first and only super app to radically simplify car ownership. We are redefining how people manage owning a car, one of their most expensive and time-consuming assets.&nbsp;
Backed by artificial intelligence and machine learning, Jerry.ai simplifies and automates owning and maintaining a car while providing personalized services for all car owners' needs. We spend every day innovating and improving our AI-powered app to provide the best possible experience for our customers. From car insurance and financing to maintenance and safety, Jerry.ai does it all.
We are the #1 rated and most downloaded app in our category with a 4.7 star rating in the App Store. We have more than 5 million customers — and we’re just getting started.&nbsp;
Jerry.ai was founded in 2017 by serial entrepreneurs and has raised more than $240 million in financing.
Join our team and work with passionate, curious and egoless people who love solving real-world problems. Help us build a revolutionary product that’s disrupting a massive market.

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