field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<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 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier, and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!
Job Description 
We are seeking a highly motivated Analytical Development Scientist to join a collaborative team focused on supporting synthetic molecule development. This role involves designing, optimizing, and qualifying analytical methods to enable process and formulation development. The ideal candidate will bring strong technical expertise, problem-solving skills, and a proactive mindset to contribute meaningfully to project execution and innovation. The position is scheduled to start in January 2026.&nbsp;
Key Responsibilities:
<ul>
<li>Develop, optimize, and qualify analytical methods for synthetic molecules.</li>
<li>Provide analytical support for process and formulation development activities.</li>
<li>Independently plan and execute experiments; interpret and communicate complex data.</li>
<li>Troubleshoot technical issues and implement effective solutions.</li>
<li>Ensure compliance with cGMP/GLP, safety, and regulatory standards.</li>
<li>Write clear, concise technical reports and maintain accurate records.</li>
<li>Collaborate with cross-functional teams to meet project goals.</li>
<li>Coordinate lab work and contribute to team-based problem solving.</li>
<li>Learn and apply new techniques while managing multiple tasks efficiently.</li>
</ul>
Qualifications 
<ul>
<li>Working knowledge of analytical techniques with experience using multiple techniques (LC, GC, Dissolution, Karl Fisher, spectroscopic instruments, etc.) for synthetic molecules.</li>
<li>Basic understanding of industry practices and standards.</li>
<li>Experiences on method development and validation for synthetic molecule products</li>
<li>Strong computer, scientific, and organizational skills.</li>
<li>Analytical and Problem-Solving Skills - Able to troubleshoot critical issues or problems and determine causes and possible solutions using appropriate information</li>
<li>Ability to work well in a team environment&nbsp;</li>
<li>Communication&nbsp;and Organizational skills&nbsp;</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Education and Experience
<ul>
<li>Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 4+ years relevant industry experience&nbsp;&nbsp;</li>
<li>Master’s degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 2+ years relevant industry experience</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>45-60 Minute In-Person Meeting to Meet the Team and Discuss the Role&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to&nbsp;Cambridge, Massachusetts,&nbsp;are strongly encouraged to apply.&nbsp;
Excellent full-time benefits include:
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Hourly rate is between $39-$44,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

HPLC Development Specialist

<h3>Job Description</h3>
Job DescriptionSalary: 
The Opportunity
The Sr. Scientist, Preclinical Development is responsible for activities related to transitioning drug development candidates into early development with a focus on the execution of preclinical studies to support health authority submissions (i.e. IND, CTA). The Sr. Scientist will collaborate with Research teams positioning their pipeline programs to make the Research to Development transition through candidate screening, hit to lead, and final candidate nomination. The Sr. Scientist will work side by side with their research team colleagues to ensure a smooth transition of lead candidates into early clinical development. This includes obtaining a deep understanding of the target biology and the drugs mechanism of action to facilitate the design and management of non-regulated pharmacokinetic and pharmacodynamic studies in relevant species. The Sr. Scientist will collaborate with the Research team to document all preclinical PK/PD study findings and contribute to the pharmacology sections of regulatory submissions.
Visterra is seeking a flexible candidate with a broad-based knowledge of immunology and biologics drug development. The primary focuses will be in vivo pharmacology, defining pharmacodynamic endpoints, establishment of pharmacokinetic/pharmacodynamic relationships and identification of key efficacy thresholds, as well as immunogenicity assessments and mechanistic studies addressing mechanism of action and safety. This individual is responsible for design, technical oversight, and documentation for preclinical programs. The individual will actively participate in program teams, as well as collaborate effectively across functions. The successful candidate shall demonstrate a proven track record in development and have experience with biologics and understanding of INDs and FDA/EMA guidelines. This individual will be highly analytical, goal-oriented, and timeline sensitive while maintaining high quality standards.
This is an onsite position in Waltham, MA.
Responsibilities 
<ul>
<li>Oversee external contractors and internal staff to leverage appropriate preclinical in-vitro and in-vivo models and procedures to support development programs.</li>
<li>Oversee and conduct preclinical efficacy and mechanism of action studies.</li>
<li>Prepare and review reports and packages for regulatory submissions.</li>
<li>Identify translation biomarkers for pharmacology endpoints and oversee technology transfer if applicable for assay method development and validation to support regulated studies.</li>
<li>Review and analyze preclinical study data to support late-stage research and development activities.</li>
<li>Present data at cross functional team meetings, summarize data in reports to support IND filings.</li>
<li>Organize reports (pharmacology, pharmacokinetics, toxicology) from research and preclinical groups and track statuses to support timely regulatory filings</li>
<li>Assist in collecting and summarizing data from reports into regulatory documents (from briefing books for early regulatory interactions through to IND modules and Investigators Brochures)</li>
<li>Oversee method development at CROs to support pharmacodynamic assessments</li>
<li>Establish and maintain high-quality systems for outsourcing, managing and reporting data from preclinical studies that meet both regulatory guidelines and industrys best practices.</li>
<li>Effectively present data to mixed audiences both internally and to external partners.</li>
<li>Demonstrates a strong ability to effectively communicate in a cross-functional team setting.</li>
<li>Proven ability to meet deliverables and timelines.</li>
</ul>
<ul>
<li>Maintains a contemporary knowledge of current industry and regulatory trends, standards and methodologies.</li>
<li>Performs other duties as required.</li>
</ul>
Requirements 
<ul>
<li>A minimum of five years of working experience in academia or the biotech industry, including strong track record of hands-on experience in R&amp;D.</li>
<li>S. or Ph.D. in Immunology, Biology or related field of study is preferable. Candidates with a Bachelor of Science degree with significant research experience are also encouraged to apply.</li>
<li>Working experiences with biologics drug discovery and development is highly desirable.</li>
<li>Familiarity with antibody pharmacokinetics and WinNonlin software a plus</li>
<li>Knowledge of regulatory requirements, including GLP, GCP, ICH and other applicable guidelines for Nonclinical development in support of regulatory submissions.</li>
<li>Experience in outsourcing and managing CROs for assay development and preclinical studies.</li>
<li>Ability to think critically, synthesize and extract simple principles from complex datasets, communicate effectively across broad spectrum of audience both internal and external, excellent written skills.</li>
</ul>
Benefits
We provide comprehensive benefits and resources to support your work, life, and balance.
<ul>
<li>A 401(k) retirement plan with a 10% dollar-for-dollar match.</li>
<li>Medical, dental and vision benefits, with Visterra contributing 85% to the monthly premium.</li>
<li>A rich mental &amp; behavioral wellness program.</li>
<li>Short- and long-term disability programs.</li>
<li>Group and voluntary life insurance.</li>
<li>Pre-tax flexible spending and commuter accounts.</li>
<li>17 days of personal time, discretionary sick time, and 11 holidays per calendar year. Personal time accrual grows to 22 days after 3 years, with an additional one-time grants of 5 days every 5 years.</li>
<li>Twelve weeks of paid parental leave for birth or adoption.</li>
<li>A broad fitness reimbursement program.</li>
<li>Tuition and student loan reimbursement.</li>
<li>A variety of employee discounts.</li>
</ul>
 
About Us
Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney diseases and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs.
Visterra is a wholly-owned subsidiary of Otsuka America, Inc., which is a U.S. holding company and a wholly owned subsidiary of Otsuka Pharmaceutical Co., Ltd. of Japan. Visterra has approximately 125 employees and is located in Waltham, Massachusetts.
Visterra provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Sr. Scientist, Preclinical Development

<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
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 fosters 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:
We are seeking a highly skilled and innovative Organic Synthesis Chemist with proven industry experience in a research and development (R&amp;D) environment, specifically focused on the synthesis and development of organic color pigments, dyes, and related chromophores. The successful candidate will be responsible for designing synthetic routes, developing new pigment molecules, and supporting scale-up for commercial applications of electrophoretic displays.
Key Responsibilities:
<ul>
<li>Design and execute multi-step organic synthesis of dyes, pigments, and intermediates to meet the color spectra requirements of E Ink products</li>
<li>Develop and optimize synthetic pathways with a focus on scalability, yield, purity, cost-effectiveness, and sustainability</li>
<li>Characterize synthesized compounds using NMR, HPLC, UV-Vis, IR, MS, and other analytical techniques</li>
<li>Lead pigment finishing efforts, including crystal form control, particle size management, and surface treatments to enhance application properties such as surface charge, dispersibility, color strength, thermal stability, and lightfastness</li>
<li>Collaborate with application scientists, formulation chemists, and process engineers to evaluate pigment performance in electrophoretic display systems and support pilot-to-commercial scale-up</li>
<li>Maintain detailed laboratory records, contribute to technical documentation, patent filings, and internal knowledge sharing</li>
<li>Monitor emerging pigment technologies, competitor activity, and market trends to identify new innovation opportunities</li>
<li>Ensure all R&amp;D activities are conducted in compliance with environmental, health, and safety regulations</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. or M.S. in Organic Chemistry, Synthetic Chemistry, or a closely related field</li>
<li>3+ years of hands-on industry experience in organic synthesis within an R&amp;D environment, with a focus on color pigments, dyes, or organic colorants</li>
<li>Solid knowledge of pigment chemistry, including azo, quinacridone, phthalocyanine, perylene, or anthraquinone classes</li>
<li>Strong command of modern analytical tools and structure elucidation</li>
<li>Track record of working in cross-functional industrial teams and delivering on project timelines\</li>
<li>Excellent problem-solving, project management, and scientific communication skills</li>
</ul>
Preferred Skills &amp; Attributes:
<ul>
<li>Familiarity with regulatory and safety requirements for pigments and dyes (e.g., REACH, TSCA)</li>
<li>Experience with crystallization techniques, polymorphism, and pigment surface modification</li>
<li>Experience collaborating with external research partners, toll manufacturers, or academic institutions</li>
<li>Exposure to high-performance pigment development for applications such as inkjet inks, automotive coatings, or high-end plastics</li>
<li>Commitment to green chemistry and sustainable pigment solutions</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.
Salary Range Disclosure: The annual base salary range for this position is $120,000 to $150,000, not including any variable pay. The total compensation package may include performance-based incentives, discretionary bonuses, and other variable pay components. The salary range for this position reflects a reasonable estimate at the time of posting and may vary based on factors such as experience, skills, education, certifications, and location.

Organic Synthesis Chemist - Color Pigments & Dyes 1060S-3

<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
About the Company:
Biotechnology company pioneering a genetics-informed precision medicine approach to develop functional antibodies for the treatment of I&amp;I disorders. The company’s approach establishes proof-of-concept at the earliest stages of drug development. Through a strong understanding of genetics and mechanistic biology, our pipeline is powered for indication expansion where we know we can have the most impact.
Description:
Seeking a motivated 9-months full time contract Biostatistician. This is a hybrid position (requires minimum of 1 day/week in the office). In this role, you will be supporting all statistical activities across multiple studies including study monitoring, reporting, simulation studies and generating real word evidence. The position reports to the Head of Biometrics.
Responsibilities
• Perform simulations, modeling, and validation of datasets, tables, listings, and figures to ensure accuracy and compliance.
• Independently perform statistical analyses as per the analysis plan. Collaborate with study teams to ensure the delivery of high-quality outputs according to the timelines. Identify and anticipate issues arising in the study design, conduct and propose scientifically sound approaches.
• Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.
• Work collaboratively with multifunctional study teams.
Top Skills Details
• Biostatistics, Programming, Python, R
Additional Skills &amp; Qualifications
• Minimum Ph.D. in Statistics or related field
• Strong proficiency in R and Python
• Extensive experience in simulation, various data visualization, and analytics
• Previous internship or work experience at a biotech or CRO is a plus
• Excellent communication skills, strong organizational skills, and ability to work independently in a fast-paced setting.
Job Type &amp; Location
This is a Contract position based out of Watertown, MA.
Pay and Benefits
The pay range for this position is $45.00 - $55.00/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 hybrid position in Watertown,MA.
Application Deadline
This position is anticipated to close on Nov 14, 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.

Biostatistician (Hybrid)

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom Assembler Job Description
Join our dynamic team as a Cleanroom Assembler, where you will play a crucial role in assembling and packaging high-quality medical products. We seek individuals who are eager to learn and grow, with a keen eye for detail and a passion for precision work in a regulated environment.
Responsibilities
<ul>
<li>Assemble and package products with meticulous attention to detail.</li>
<li>Complete paperwork related to assemblies and production activities.</li>
<li>Communicate discrepancies or potential issues effectively.</li>
<li>Understand and utilize measuring devices, prints, and quality control documents.</li>
<li>Operate mechanical, electrical, and optical tools for quality inspection.</li>
<li>Ensure high quality standards in assembly production.</li>
<li>Use programs to collect and evaluate operating data for on-line adjustments.</li>
<li>Perform operational tests and fault isolation on systems.</li>
</ul>
Essential Skills
<ul>
<li>0-2 years of manufacturing experience, or willingness to learn.</li>
<li>Good attendance and reliability.</li>
<li>Comfortable working with a microscope for 4-6 hours daily.</li>
<li>Experience in a cleanroom or regulated environment.</li>
<li>Good hand-eye dexterity and proficiency with small hand tools.</li>
<li>Attention to detail and ability to read drawings.</li>
<li>Basic computer skills, including Microsoft Office.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School diploma or equivalent.</li>
<li>Ability to perform basic mathematical calculations.</li>
<li>Familiarity with Good Manufacturing Practices (GMP) and Standard Operating Procedures.</li>
<li>Manual dexterity, eye-hand coordination, and visual acuity.</li>
<li>Ability to maintain product traceability and identify non-conforming products.</li>
<li>Basic understanding of electricity.</li>
</ul>
Why Work Here?
We offer a financially stable environment with large contracts and plenty of work. Enjoy uncapped overtime and the opportunity to grow within the company. Many of our leaders began as operators, showcasing our commitment to investing in our employees' growth. If you're passionate and eager to learn, you'll find ample opportunities to advance.
Work Environment
Work in a clean, regulated environment that fosters a friendly, hard-working culture. This role involves repetitive tasks and requires a full gowning process. Initially, train on the first shift from 5 AM to 3:30 PM, then transition to the second shift from 3 PM to 1:30 AM, Monday through Thursday.
Job Type &amp; Location
This is a Contract to Hire position based out of Billerica, MA.
Pay and Benefits
The pay range for this position is $21.00 - $23.00/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 Billerica,MA.
Application Deadline
This position is anticipated to close on Nov 15, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Assembler

<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.

Chemist - Bench Work

<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.

725 Science Jobs