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<h3>Job Description</h3>
Job DescriptionJob Summary Medicilon is seeking an entry-level Research Associate to support in vivo, non-tumor disease model studies using rodent models. This role focuses on hands-on animal study execution while ensuring animal health, welfare, and regulatory compliance. You will work closely with scientists and veterinary staff to support preclinical research programs. Key Responsibilities 
<ul>
<li>Perform routine animal handling and restraint using approved procedures</li>
<li>Understand and adherence to safety, animal welfare, and regulatory standards</li>
<li>Prepare formulations and perform dose calculations</li>
<li>Administer test articles via common routes (e.g., oral gavage, IV, SC, IP)</li>
<li>Conduct basic tissue and blood collection (e.g., spleen, liver, cardiac puncture, IV sampling)</li>
<li>Monitor animals during in-life phases, including body weight, clinical observations, and measurements</li>
<li>Observe and report animal health and welfare concerns during procedures</li>
<li>Support study setup activities, including: &nbsp;
<ul>
<li>IACUC and protocol review&nbsp;</li>
<li>Labeling of collection materials&nbsp;</li>
<li>Animal room and study room preparation</li>
</ul>
</li>
<li>Execute laboratory work in accordance with approved study plans, IACUC protocols, and SOPs</li>
</ul>
QualificationsRequired:
<ul>
<li>A.A./A.S. or B.A./B.S. in animal science, life sciences, or a related field</li>
<li>6–12 months of hands-on laboratory animal experience</li>
</ul>
Preferred:
<ul>
<li>Basic in vivo technical skills</li>
<li>ALAT certification&nbsp;</li>
<li>Familiarity with regulated research environments (GLP experience a plus)</li>
</ul>

Research Associate I Non-Tumor Disease Models

<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:
E Ink is seeking a highly motivated, creative and hands-on scientist to conduct leading-edge materials and process research for novel electrophoretic display technology. The Senior Scientist will be a subject-matter expert in coating method and formulation development to support new designs and materials introduction into the next generation of ePaper devices. This individual will be based in Billerica, MA, and engage globally with E Ink’s R&amp;D and manufacturing departments to champion technical innovations from conception to commercialization.
Key Responsibilities:
<ul>
<li>Drive the design and development of microcapsule slurry and coating</li>
<li>Develop a deep understanding of the interplay between material properties, ink formulation, fluid dynamics, substrate interactions and drying mechanisms to improve coating quality and large area uniformity</li>
<li>Identify correlation between critical properties of individual layers and electro-optical performance of multilayer device stack, and develop in-line and off-line characterization methods to ensure quality</li>
<li>Provide technical leadership and hands-on support across all stages of the coating process, including compounding, slurry delivery, coating application, post-coating treatments, and film characterization</li>
<li>Work with and contribute to an agile, inspiring and supportive team to rapidly advance project goals and actively pursue contingency plans</li>
<li>Document the results in comprehensive technical reports and in patents for intellectual property</li>
</ul>
<ul></ul>
Qualifications
<ul>
<li>Ph.D. in materials science, chemical engineering or a related field and 2+ years of experience in thin film coating process development or M.S. in materials science, chemical engineering or a related fields and 5+ years of experience in thin film coating process development</li>
<li>Expertise in heterogeneous fluid rheology, surface interactions, drying behavior and characterizations</li>
<li>Expertise in a wide range of coating technologies such as slot-die, gravure, blade and multilayer lamination techniques</li>
<li>Knowledge of Design of Experiments and Statistical Analysis</li>
<li>Excellent troubleshooting, teamwork, communication, and interpersonal skills</li>
<li>Self-directed, motivated, and hands-on personality. Ability to work in a fast-paced, open-minded, highly interdisciplinary work environment</li>
</ul>
Preferences
<ul>
<li>Experience with microcapsule-based functional coating is highly preferred</li>
<li>Knowledge of electrical and optical characterization in thin film devices</li>
<li>Technical project management experience</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>Sick time</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. 
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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.

Senior Formulation and Coating Scientist 1060H-2

<h3>Job Description</h3>
Job DescriptionJob Title: Process Engineer - Chemical Manufacturing Location: Manchester, NH Job Type: Full-time, on-site Pay Range: $95,000 to $105,000 Benefits: Medical, dental, vision insurance, and 401(k) Job Summary Adecco Permanent Recruitment is partnered with a well-established specialty chemical manufacturing company in the Manchester, New Hampshire area to help them hire a Process Engineer. This role supports a manufacturing operation producing customer specific polymer products in an industrial environment. The Process Engineer will play a critical role in maintaining process stability, supporting production, and driving improvements tied to quality, efficiency, and future growth. Key Responsibilities
<ul>
<li>Support day-to-day manufacturing operations in a continuous production environment</li>
<li>Lead root cause analysis for quality, process, and production issues and implement corrective actions</li>
<li>Evaluate process performance and identify optimization and standardization opportunities</li>
<li>Serve as a technical escalation point for supervisors and operations teams</li>
<li>Assess feasibility of new customer formulations prior to production to prevent scrap and delays</li>
<li>Analyze process data to drive continuous improvement initiatives</li>
<li>Support training and communication related to updated procedures and management of change activities</li>
<li>Collaborate with operations leadership, process improvement, and R&amp;D teams on scale up and expansion projects</li>
</ul>
 Qualifications and Must-Haves
<ul>
<li>Bachelor’s degree in Engineering required, Chemical Engineering strongly preferred</li>
<li>3 to 10 years of hands-on experience in manufacturing or industrial operations</li>
<li>Experience with chemical processing, plastics, compounding, extrusion, pelletizing, or similar processes</li>
<li>Strong root cause analysis and data driven problem solving skills</li>
<li>Ability to communicate technical findings clearly to operators, supervisors, and leadership</li>
<li>Comfortable working in a true industrial manufacturing environment</li>
<li>Experience solely in clean-room, biomedical, or medical device manufacturing is not a fit for this role</li>
</ul>
 Pay Details: $95,000.00 to $105,000.00 per year Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.adecco.com/en-us/candidate-privacy" target="_blank">https://www.adecco.com/en-us/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Process Engineer - Chemical Manufacturing

<h3>Job Description</h3>
Job Description
Principal Biostatistician
Statistics &amp; Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials. 

Job Summary
Apply a high level of technical expertise to help guide and develop the more junior biostatistics staff members. Serve as a lead statistician on clinical studies and provide senior level peer review of work being accomplished by other biostatisticians in the department. Maintain the statistical and analytical integrity of clinical trials analyzed by SDC. Actively participate in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies as required. Support business development and project management with strategic planning, proposals, pricing, and timeline planning.

Primary Responsibilities
· Serve as an internal consultant for biostatistics analysis tools and methods. 
· Serve as a subject matter expert during client and vendor meetings for biostatistics analysis support.
· Actively support business development in capabilities presentations to prospective and current clients
· Effectively manage assigned clinical study budgets for biostatistics analysis support.
· Develop, coach and mentor junior biostatistics department personnel.
· Act as the lead statistician on clinical research projects and help with SAS programming.
· Provide statistical expertise for study design of clinical trial protocols. 
· Write statistical methods section of the study protocol, as needed.
· Write statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed.
· Review CRFs to ensure consistency with protocol and statistical analysis plan (SAP)
· Program summary tables, data listings and graphical representations of clinical trials data
· Perform all analyses defined in the statistical analysis plan as well as any post-hoc analyses and relevant exploratory analyses of clinical trial data. 
· Prepare/review key sections of clinical study reports and various regulatory documents.
· Perform statistical QC of all department outputs including analyses and clinical study reports.
· Provide statistical support to answer questions from external clients (such as FDA, Investigators)
· Contribute to the development, maintenance, and training of standard operating procedures (SOPs)
· Represent the biostatistics department at regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed.
· Manage biostatistics timelines, budgets, and client expectations.
· Adhere to all aspects of the Statistics &amp; Data Corporation’s quality system.
· Comply with Statistics &amp; Data Corporation’s data integrity &amp; business ethics requirements.
· Perform other related duties incidental to the work described herein.
· Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements. 

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified. 
Requirements

Required Skills
· Effective leadership, budget forecast and implementation skills.
· Excellent analytical skills, with the ability to process scientific and medical data.
· Able to work independently and in teams.
· Project management abilities including analytical evaluation, organization, delegation, flexible team management, negotiating and resource management skills.
· Excellent knowledge of statistical programming.
· Expertise in manipulating and analyzing SAS data. 
· Able to identify data issues, present problems, and implement solutions. 
· Capable of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues and clients.
· Excellent organizational and time management skills, with the ability to multi-task.
· Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).
· Strong interpersonal communication and presentation skills.
· Able to effectively collaborate across cross-functional teams. 
· Focus on quality at all times and in all situations.

Education or Equivalent Experience
· Typically a Master’s degree in biostatistics, statistics or other related, scientific field and four years of relevant professional experience; or a PhD in biostatistics, statistics or other related, scientific field and three years of relevant experience; or equivalent combination of experience, education, and/or demonstrated ability.
Benefits
Why SDC
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances, positive work/life balance and 401k matching (US), we are able to attract some of the most talented people in the industry. 

•We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits. 
•We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment. 
•We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.
•We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry. 
•With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

#LI-Hybrid

Principal Biostatistician

<h3>Job Description</h3>
Job DescriptionAbout Phoenix Tailings:Phoenix Tailings is a rapidly growing clean mining and metals production startup dedicated to sustainable and economic critical metals production. Our mission is to be the world's first fully clean mining and metals production company, producing the resources needed for the next generation of our economy. We are seeking a Junior Chemical Engineer to join our dynamic team and contribute to the design, development, and optimization of innovative critical metals production systems. Why Phoenix Tailings:At Phoenix, we believe that nothing great is ever accomplished alone or without the passion of people who push and motivate one another. If you are someone who shares our relentless pursuit of a better future, passion for innovation, and are excited about working with some of the top innovators in the world, then this is the place for you. Our Values:● You are only crazy if you are wrong, it’s ok to be wrong● Lead with Compassion● Be Resourceful● Listen● Hustle Who We Are Looking For:Phoenix Tailings is looking for a Chemical Process Technician to join our Separations Team in Burlington, MA. This individual will work a 12-hour overnight shift (6 PM–6 AM) and must be comfortable with rotating shift work. In this hands-on role,&nbsp;you’ll&nbsp;play a vital part in operating and improving our rare earth metals separation processes by working with strong acids, bases, and wet chemistry systems. Your work will directly enable the clean, scalable production of the critical materials powering the technologies of tomorrow.&nbsp; This pay range reflects the expected compensation for this role and may vary based on experience and qualifications. Salary Range: $60,000/year- $80,000/yearKey Responsibilities:
<ul>
<li>Operate chemical separation processes during overnight shifts, ensuring accuracy and safety in all activities&nbsp;</li>
<li>Safely handle strong acids, bases, and other hazardous materials using&nbsp;appropriate PPE&nbsp;and safety protocols&nbsp;</li>
<li>Execute wet chemistry procedures and follow SOPs precisely to support critical metals separation&nbsp;</li>
<li>Monitor and adjust process conditions based on lab results and performance data&nbsp;</li>
<li>Conduct in-process sampling and testing to ensure process targets are met&nbsp;</li>
<li>Document experimental data, deviations, and observations with high attention to detail&nbsp;</li>
<li>Support troubleshooting efforts and recommend improvements to&nbsp;optimize&nbsp;separation performance&nbsp;</li>
<li>Perform routine cleaning, inspections, and maintenance of process and lab equipment&nbsp;</li>
<li>Maintain a clean, organized, and compliant work environment aligned with EHS standards&nbsp;</li>
</ul>
Qualifications:
<ul>
<li>2+ years of hands-on experience in chemical processing, laboratory work, or industrial operations&nbsp;</li>
<li>Strong experience working with wet chemistry, including handling of strong acids and bases&nbsp;</li>
<li>Proven ability to follow SOPs and&nbsp;maintain&nbsp;strict adherence to safety and quality standards&nbsp;</li>
<li>Comfortable working a rotating overnight shift (12-hour shifts, including weekends and holidays as needed)&nbsp;</li>
<li>Familiarity with basic lab instrumentation, data collection, and documentation practices&nbsp;</li>
<li>High school diploma or equivalent&nbsp;required; associate degree or vocational training in chemistry, chemical engineering, or a related field preferred&nbsp;</li>
<li>Must be self-motivated, dependable, and capable of working independently during overnight hours&nbsp;</li>
</ul>
We offer a competitive compensation package that is based on expertise. We also offer the following benefits:
<ul>
<li>Healthcare, we care about you and your family:&nbsp;100% Medical, dental, and vision coverage&nbsp;</li>
<li>Stock:&nbsp;Ownership in a fast-growing venture-backed company.&nbsp;</li>
<li>Family Focus:&nbsp;Parental leave and flexibility for families.&nbsp;</li>
<li>Time Off:&nbsp;Flexible vacation policy to encourage people to get out and see the world.&nbsp;</li>
<li>Team Fun:&nbsp;Regularly scheduled events, and celebrations.&nbsp;</li>
<li>Learning:&nbsp;Learning and development Opportunities to grow your skills and career.&nbsp;</li>
<li>Great team:&nbsp;Working with fun, hard-working, kind people committed to making a difference!&nbsp;</li>
<li>Flexible culture:&nbsp;We are results-focused. We don’t work at the office every day.&nbsp;</li>
</ul>
We offer a competitive compensation package based on expertise, including healthcare coverage (100% medical, dental, and vision), stock ownership, parental leave, flexible vacation policy, learning and development opportunities, and a great team culture that values making a difference and encourages results-focused work. At Phoenix Tailings, we have an open culture that values learning and growth, and we are looking for enthusiastic individuals who share our vision of sustainable mining. Phoenix Tailings, Inc. is an Equal Opportunity Employer, and we value diversity at all levels. All qualified candidates will receive consideration for employment without regard to race, color, religion, sex (including gender identity, sexual orientation, and pregnancy), national origin, age, disability, genetic information, or any other applicable protected characteristics. These characteristics will not be a factor for consideration of any work-related decisions, including but not limited to hiring, firing, compensation, and discipline.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

3.5. Chemical Process Technician

<h3>Job Description</h3>
Job Description
We are seeking a highly motivated Project Coordinator to manage the DMPK operational logistics of our early-stage drug discovery assays, pharmacokinetics studies, and compound management processes. This role is crucial for maintaining efficient workflows between internal research teams and external Contract Research Organizations (CROs), ensuring smooth execution of experiments, data tracking, and financial administration during the contract term.
 
Key Accountabilities and Responsibilities:
 
The primary responsibilities for this contract role are:
• Assay Request System (ARS) Management: manage the end-to-end process for incoming assay requests using the internal ARS platform. Create and track study orders, troubleshoot system issues, and register new assay codes as needed. Facilitate the onboarding process for new CROs within the ARS ecosystem.
• Compound Management and Logistics: Oversee compound sourcing and logistics, including availability checks, internal ordering, and external shipping coordination. Manage compound plating, tracking, and inventory updates. Coordinate seamlessly with internal compound management teams, external CROs, and third-party vendors to ensure timely delivery and accurate handling of research materials. Onsite presence may be required for some shipments.
• Data Management and Integrity: Ensure the timely and accurate upload of assay data into our primary data repository (e.g., D360, similar internal system). Maintain rigorous documentation and ensure all relevant information within the ARS is current and accurate.
• Contracts, Financials, and Vendor Management: Establish, review, and maintain annual Statements of Work (SOWs) and rate cards with key vendors. Monitor Purchase Orders (POs), manage change orders efficiently, and review CRO cost summaries for accuracy and compliance.
• Study Support Coordination: Manage the quotation process for new studies and draft study-specific SOWs. Obtain necessary internal tracking numbers (e.g., G-TRAKS) and set up new studies on external collaboration platforms (e.g., Science Exchange).
• CRO Communications and Relationship Management: Serve as the primary liaison for day-to-day ARS communications with external partners. Coordinate subject matter expert (SME) and CRO meetings and support the logistical implementation of new assay protocols at vendor sites.
• Data Analytics and Metrics Reporting: Track and analyze assay submissions, execution metrics (turnaround times, success rates) across both internal teams (TAS) and external CROs. Perform spend analytics and provide comprehensive monthly reports and key performance indicator (KPI) dashboards to management.
 
Qualifications and Desired Experience
• Education: Bachelor’s degree (BS) in Biology, Chemistry, or another related scientific field is highly recommended.
• Experience: 4-7 years of experience in biotech, pharmaceuticals, or a research operations role (Intermediate Level), specifically within assay operations, compound management, or vendor management. Note: 0-3 years is suitable for an Associate level; 8+ years is suitable for a Senior level hire.
• Attributes: Excellent organizational skills, meticulous attention to detail, strong problem-solving abilities, and superior communication skills. Proven ability to operate independently and manage multiple projects and priorities effectively in a dynamic environment.
Company Description<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a> 
<h3>Company Description</h3>
<a href="http://www.techdataservice.com" target="_blank">www.techdataservice.com</a>

DMPK Logistics Project Coordinator (LC9862)

<h3>Job Description</h3>
Job DescriptionJob Title: Associate Scientist Location: Devens MA 01434 Duration: 12 months Pay Range - $40 - $45/hr. on w2 Job Description: 100% onsite Work Schedule: Mon- Fri (normal business hours) Description: The Associate Scientist in Manufacturing Sciences &amp; Technology will support the Materials and Cryogenics Science group in the run the business work for cryogenics, consumables and single-use systems for biopharmaceuticals commercial manufacturing operations. The successful candidate will collaborate closely with Manufacturing, Manufacturing Technology, Quality Assurance, Quality Control, Supply Chain, and Global Procurement groups on cross-functional teams.
<ul>
<li>The subject matter expert for this position will be primarily required to:</li>
<li>Support material and cryogenics technical evaluations, risk assessment and change management activities</li>
<li>Executes material control strategies, validations and qualifications, as appropriate, including life-cycle management.</li>
<li>Evaluate and manage material associated supplier changes notifications to maintain GMP compliance.</li>
<li>Support cryogenics and cold-chain transportation related lab studies or activities.</li>
<li>Assist material and cryogenics manufacturing investigations.</li>
<li>Author and revise CMC documents as appropriate.</li>
<li>Author protocols, reports, and technical presentations. </li>
</ul>
Requirements:
<ul>
<li>Minimum BS with 2+ years of industry experience or MSc in Chemical Engineering, Biochemical Engineering, Material Science Engineering, Chemistry or equivalent scientific background.</li>
<li>Awareness of cGMP compliance and regulatory agency requirements.</li>
<li>Knowledge of common protein analytical tools and demonstrated experimental skills for lab work are required.</li>
<li>Knowledge of manufacturing process validation is desired.</li>
<li>Strong organizational, oral communication and technical writing skills. Strong attention to details, excellent experimental/troubleshooting aptitude, and self-motivated.</li>
<li>Effective team player and strong individual contributor.</li>
</ul>
 #sczr2

Associate Scientist

<h3>Job Description</h3>
Job DescriptionWe are seeking a detail-oriented Electronics Assembly Technician to join our team. This role involves performing a wide variety of electronic and electro-mechanical assembly operations in a clean room environment.Key Responsibilities:
<ul>
<li>Perform bench-level electronic and electro-mechanical assembly using skilled hand techniques and/or automated production equipment</li>
<li>Interpret technical specifications, drawings, and documentation</li>
<li>Follow established methods and sequences for wiring, component installation, hand soldering, and cable harnessing</li>
<li>Set up and adjust assemblies while holding tight tolerances to blueprint specifications</li>
<li>Maintain clean room standards and procedures</li>
</ul>
Qualifications:
<ul>
<li>Experience working in a clean room environment</li>
<li>High School Diploma or equivalent with a minimum of 4 years of relevant experience OR</li>
<li>Associate’s Degree (or post-secondary education) with 0–2 years of related experience</li>
<li>Strong attention to detail and ability to work from technical documentation</li>
</ul>
This is a great opportunity for someone who enjoys hands-on assembly work in a precision-driven environment. #INDNashua #ZipNashuaCompany DescriptionWe are HW Staffing, and our mission is to “Connect Great People with Great Companies.” Collectively, we are revolutionizing how staffing services support the employee and client. HW Staffing jobs encompass meaningful work, a sense of purpose with career development, and a welcoming community. Our jobs inspire and reward independence. Our organizational culture of teamwork and inclusivity supports our spirit and commitment to helping people. Together we can help people find meaningful work - we’re just getting started #wearehwstaffing 
<h3>Company Description</h3>
We are HW Staffing, and our mission is to “Connect Great People with Great Companies.” Collectively, we are revolutionizing how staffing services support the employee and client. HW Staffing jobs encompass meaningful work, a sense of purpose with career development, and a welcoming community. Our jobs inspire and reward independence. Our organizational culture of teamwork and inclusivity supports our spirit and commitment to helping people. Together we can help people find meaningful work - we’re just getting started #wearehwstaffing

Clean Room Assembly NH

<h3>Job Description</h3>
Job DescriptionDescription:
About Lux
Lux Research is a leading research and advisory firm, helping clients navigate emerging technologies and drive growth through innovation. We support C-level executives in the world’s largest companies. Our culture is high-energy, detail-obsessed and relentlessly focused on performance. If you thrive in a fast-paced, demanding environment where results, accountability and engagement matter, join our team for what may be the most rewarding job you have ever had.
 
Role Description
Lux Research is seeking a Research Associate specializing in Industrial Process and Manufacturing Innovation with a strong emphasis on industrial wastewater treatment. The ideal candidate will bring a solid foundation in a STEM discipline — such as chemical engineering, environmental engineering, industrial engineering, materials science, or a related technical field — and a passion for applying scientific and technical expertise to strategic innovation questions.
As a Research Associate at Lux, you will investigate emerging technologies that are reshaping industrial operations, resource efficiency, and environmental performance. Your work will guide clients in understanding technological transformation across manufacturing systems, chemical and material processes, and wastewater treatment infrastructures. You will develop thought leadership through analytical research on breakthrough technologies, innovative companies, and evolving industry practices, delivering actionable insights that support investment, partnership, and strategic planning for global industrial leaders.
 
Salary Range: $65,000 - $75,000
Requirements:
Responsibilities:
<ul>
<li>Lead research on emerging technologies transforming industrial operations, including advanced manufacturing systems, process intensification, automation, industrial decarbonization, and next-generation materials processing.</li>
<li>Investigate innovation in industrial wastewater treatment, including physical, chemical, biological, and hybrid treatment approaches; water reuse and recycling; resource recovery; and zero-liquid-discharge systems.</li>
<li>Master a toolkit of research skills, synthesize data from diverse sources, and produce findings that help clients navigate innovation opportunities.</li>
<li>Advise and support clients through written deliverables, direct consultations, and public presentations, providing insightful, evidence-based perspectives on technology and market trends.</li>
<li>Produce high-quality research reports and analyses that connect innovation in the industrial sector to broader regulatory and consumer dynamics.</li>
<li>Represent Lux Research at industry conferences, webinars, and client events as a recognized thought leader in industrial innovation, environmental technologies, and manufacturing transformation.</li>
<li>Collaborate with analysts across disciplines and geographic regions to deliver integrated insights on cross-sector innovation challenges, including circular economy strategies, resource efficiency, digitalization of industrial systems, and infrastructure modernization.</li>
</ul>
 
Minimum Qualifications:
<ul>
<li>Bachelor’s degree in a STEM field related to chemical engineering, process engineering, or related disciplines focusing on industrial processes (e.g., chemicals production, manufacturing, etc.)</li>
<li>1-2 years of experience in the manufacturing or industrials sectors, ideally involving technology analysis, R&amp;D, project management, or strategic consulting.</li>
<li>Demonstrated ability to analyze technical and market data, develop original insights, and communicate them effectively to business and technical audiences.</li>
<li>Exceptional writing and presentation skills, with experience crafting incisive, data-driven reports and delivering client presentations.</li>
<li>Strong quantitative and qualitative analytical skills, with the ability to translate complex scientific concepts into business implications.</li>
</ul>
 
Desired Qualifications
<ul>
<li>A Master’s degree is highly preferred, especially with a STEM background in chemical engineering, process engineering, or related disciplines focusing on industrial processes (e.g., chemicals production, manufacturing, etc.)</li>
<li>Intellectual curiosity and a deep interest in innovation, energy transition, and the future of manufacturing and industrials.</li>
<li>Entrepreneurial and collaborative mindset, with a willingness to go the extra mile in a fast-paced environment.</li>
<li>High degree of organization, attention to detail, and commitment to delivering high-quality research that drives impact.</li>
</ul>
Lux Research is an Equal Opportunity Employer
Lux Research is an equal opportunity employer. In accordance with anti-discrimination law, Lux prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Lux Research conforms to the spirit as well as to the letter of all applicable laws and regulations. law. Lux Research conforms to the spirit as well as to the letter of all applicable laws and regulations.

Research Associate- Industrials

<h3>Job Description</h3>
Title:- Research Associate I
Location: Framingham, MA
Duration: Contract until Feb 2027 (Possible extension) 
 
Job Summary:
Position Overview/Department Description
We are seeking a contract upstream Research Associate to join our Cell Culture Platform group in Cell Culture Development department (CCD-CCP). CCD-CCP is a global business unit responsible for the development of cell culture platforms including media and bioprocess technologies for both fed-batch and perfusion from early and late-stage biologics projects, as well as all upstream CMC development activities for early phase projects (up to Phase II).
The candidate will be self-motivated and strongly driven to succeed while demonstrating the ability to function well within a fast-paced and collaborative team-oriented environment. The candidate will also be inquisitive and innovative, exhibiting scientific curiosity and the ability to acquire new skills for fed-batch and perfusion based upstream cell culture processes.
This is an exciting opportunity to learn cutting-edge cell culture techniques and develop cell culture subject matter expertise. This role will have significant impacts on early pipeline projects, next generation cell culture process development and manufacturing strategies within the global *** network.
 
Main Duties &amp; Responsibilities
• Require to be on site daily; Weekend work required occasionally.
• Plan and execute experiments to optimize upstream cell culture platform process at different scales (shake flasks, AMBR, 3L/10L bioreactors, etc.)
• Perform upstream experiments and collaborate with other functional groups to speed Phase I pipeline projects
• Contribute to technical reports, experimental protocols, and technical summaries for presentation internally and externally
• Participate in the technology transfer of processes into manufacturing facilities
• Ensure safety and environmental compliance are maintained in the workplace
• Some weekend working may be required for this role
Basic Qualifications
• Bachelor or Master's degree in Chemical Engineering, Biochemical Engineering, Cell Biology, Biochemistry or a related discipline
• Post-education experience ?=3 years
• Understanding of aseptic technique and principles of mammalian cell culture
• Detailed in lab operations and quick learner for new technologies
 
Preferred Qualifications
• Experience in the operation of fed-batch and/or perfusion-based cell culture bioreactors
• Knowledge of CMC
 
 
MINAKSHI SANGWAN
Recruiting Lead - US Recruitment
O 732-339-3518
E <a href="mailto:Minakshi.sangwan@aequor.com" target="_blank">Minakshi.sangwan@aequor.com</a>
W <a href="http://www.aequor.com/" target="_blank">http://www.aequor.com/</a>

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