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<h3>Job Description</h3>
Job DescriptionDescription:
Nobis Group is an integrated consulting firm providing engineering and engineering solutions for public and private projects of all sizes. We are committed to solving the challenges of making the Earth a better place to live - community by community, and project by project.
 
Overview
Do you want to expand your career as a Chemist in Environmental Engineering? If so, Nobis wants you! 
 
Nobis is looking for a Senior Chemist in our Environmental Engineering group based in Lowell, Massachusetts. The ideal candidate will have demonstrated experience and a desire to join our remarkable team of forward thinking committed partners. 
 
What You’ll Do
<ul>
<li>Effectively collaborate with team members (internal and external) and others to execute assignments efficiently and effectively. Provide technical support and direction to junior staff members.</li>
<li>Assist in development and/or review of planning documents such as Quality Assurance Project Plans (QAPPs), technical specifications for analytical service procurement;</li>
<li>Perform validation of analytical data in accordance with current EPA data validation guidance as modified by each EPA region, or reviewing the work output from others on Nobis’ chemistry team;</li>
<li>Serve as primary liaison between Nobis technical staff and subcontracted laboratory staff;</li>
<li>Serve as primary liaison between Nobis technical staff and client chemistry staff (such as EPA and their Contract Laboratory Program, and USACE);</li>
<li>Serve as the primary Nobis Environmental Data Management System administrator. The administrator is responsible for overall operations and maintenance of the EDMS. In this capacity, the administrator would work with other chemistry staff to evaluate and commit valid data to the EDMS, and would be responsible for preparing specific SQL queries and database reports per technical staff requests;</li>
<li>Communicate technical information with other Nobis staff, clients, regulators, and in a professional, clear, and concise manner. Accurately document such communications, and apply the information obtained to the relevant project work; </li>
<li>Fluent in and promote compliance with applicable federal and state analytical services requirements and guidance;</li>
<li>Travel to and perform quality assurance audits of analytical laboratory subcontractor operations and performance in accordance with program or project-level QAPPs and/or contract requirements;</li>
<li>Provide mentoring to junior staff in the application of analytical chemistry services; and</li>
<li>May perform senior technical review of certain calculations and technical documents.</li>
</ul>
What It’s Like Working at Nobis
We are 100% Employee-Owned and that makes you an owner. As a Nobis Employee-Owner, you will become part of a team that thrives on diversity of thought, encourages out-of-the-box ideas, and strives to fulfill our mission to deliver unparalleled engineering and environmental solutions that drive employee-owner, client, and community success.
 
We offer highly competitive salaries, generous paid time off, and a flexible hybrid schedule that allows our employee-owners to maintain a comfortable balance between life and work. In addition to our extensive benefits package, you will have access to all the advantages that come with working for an ESOP.
 
Nobis is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, veteran status, sexual orientation, or gender identity.
Requirements:
What You’ll Need to Bring With You
<ul>
<li>Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) degree from an accredited four-year college or university in chemistry or chemical engineering is required. Ten years minimum of related experience and/or training; or equivalent combination of education and experience, is required. A Master of Science (M.S.) degree is desirable.</li>
<li>Must possess a valid driver’s license, have own transportation, and be able to travel for project site visits, meetings, training, and quality control audits. Travel is expected to be minimal for this position.</li>
<li>A working knowledge of SQL coding and SQL Server databases is preferred, and be able to prepare queries and reports based on parameters established by other project staff.</li>
</ul>

Senior Chemist

<h3>Job Description</h3>
Job DescriptionDescription:
Nobis Group is an integrated consulting firm providing engineering and engineering solutions for public and private projects of all sizes. We are committed to solving the challenges of making the Earth a better place to live - community by community, and project by project.
 
Overview
Do you want to expand your career as a Project Manager in Geotechnical Engineering? If so, Nobis wants you! 
 
Nobis is looking for a Project Manager with a concentration on commercial projects for our Geotechnical Engineering group based in Concord, New Hampshire. The ideal candidate will have demonstrated experience and a desire to join our remarkable team of forward thinking committed partners. 
 
What You’ll Do
<ul>
<li>Generate and manage proposals, contracts, and subcontracts.</li>
<li>Communicate with clients, state and local regulators, contractors, and subcontractors.</li>
<li>Track project schedules, budgets, and prepare monthly invoices.</li>
<li>Oversee the technical performance of projects to provide high-quality solutions (design plans, specifications, reports, and other design documents).</li>
<li>Perform on-the-job training and mentoring of junior staff.</li>
<li>Provide technical review for environmental investigations, remedial actions, and environmental due diligence projects for a variety of environmental project types throughout New England.</li>
<li>Communicate with Nobis’ internal Resource Center Manager and Account Manager regularly on the status and performance of projects.</li>
<li>Identify, prioritize, and build relationships that will support Nobis’ long-term commercial strategies for growth.</li>
<li>Build strategic alliances and teaming relationships that enable Nobis to pursue commercial contracts as both a prime and subcontractor.</li>
<li>Participate in commercial development team to develop strategy, identify leads, and position the team to grow commercial market sector revenues.</li>
<li>Assist in development of commercial market sector strategic plans, prepare revenue and labor utilization projections, and meeting revenue targets for commercial services.</li>
</ul>
What It’s Like Working at Nobis
We are 100% Employee-Owned and that makes you an owner. As a Nobis Employee-Owner, you will become part of a team that thrives on diversity of thought, encourages out-of-the-box ideas, and strives to fulfill our mission to deliver unparalleled engineering and environmental solutions that drive employee-owner, client, and community success.
 
We offer highly competitive salaries, generous paid time off, and a flexible hybrid schedule that allows our employee-owners to maintain a comfortable balance between life and work. In addition to our extensive benefits package, you will have access to all the advantages that come with working for an ESOP.
 
Nobis is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, veteran status, sexual orientation, or gender identity.
Requirements:
What You’ll Need to Bring With You
<ul>
<li>A Bachelor of Science (B.S.) or Bachelor of Arts (B.A.) degree in geotechnical engineering or a civil engineering curriculum with a strong concentration in geotechnical engineering from an accredited four-year college or university. It’s a plus to have a Master’s degree with a concentration of geotechnical engineering.</li>
<li>A minimum of five years related experience and/or training.</li>
<li>Professional Engineer (P.E.) licensure with specialized experience in geotechnical engineering (required).</li>
<li>Knowledge of local regulations, environmental standards, and construction practices in target markets.</li>
<li>Demonstrated experience with sales and marketing processes in commercial engineering or construction sectors at a management level.</li>
<li>Valid driver’s license, reliable transportation, and proof of auto insurance (required).</li>
</ul>

Geotechnical Project Manager

<h3>Job Description</h3>
Job DescriptionCompany Description 
At Eurofins Professional Scientific Services (PSS), we believe the work we do matters—and so do our people. We offer a unique opportunity to launch or grow your career in the biopharmaceutical industry, with a strong focus on professional development, work-life balance, and a competitive benefits package.
As part of Eurofins Scientific, a global leader in life sciences testing, we support the world’s top companies in ensuring the safety and quality of food, water, pharmaceuticals, and more. Join us in shaping a safer, healthier, and more sustainable world
ics, 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 HPLC/LCMS Specialist to support analytical method development and data generation for product development. This role emphasizes hands-on expertise in chromatography and mass spectrometry, scientific rigor, and cross-functional collaboration.
Key Responsibilities
<ul>
<li>Develop, optimize, and implement robust HPLC, UPLC, and LC-MS methods to support product development and manufacturing.</li>
<li>Independently generate and interpret analytical data to inform decision-making.</li>
<li>Collaborate with cross-functional teams to transfer and validate analytical methods.</li>
<li>Troubleshoot and maintain analytical instrumentation (e.g., Waters I-Class, Thermo Vanquish Flex).</li>
<li>Ensure compliance with safety protocols and laboratory best practices.</li>
<li>Contribute to continuous improvement initiatives and scientific innovation.</li>
</ul>
Qualifications 
Minimum Requirements:
<ul>
<li>B.S. (3–4 years experience) or M.S. (1+ year experience) in Analytical Chemistry, Biochemistry, or related field.</li>
<li>Strong hands-on experience with HPLC, UPLC, and LC-MS.</li>
<li>Familiarity with analytical software (Empower, Xcalibur, BioPharma Finder).</li>
<li>Working knowledge of chromatography techniques (IPRP, AEX/IEX, HILIC).</li>
<li>Solid understanding of method validation parameters (e.g., linearity, precision, LOD/LOQ).</li>
<li>Excellent troubleshooting, communication, and problem-solving skills.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with RNA or oligonucleotide analysis.</li>
<li>Familiarity with additional techniques: FTIR, NMR, UV-Vis, KF, ICP, DSC, TGA, XRPD.</li>
<li>Exposure to lean lab practices or 5S methodologies</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>60 Minute Onsite Meeting with Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Boston, MA are strongly encouraged to apply.
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 $36-$41,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Copy of Analytical Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Discovery Biotherapeutics and Genetic Medicine (BGM) at AbbVie is seeking a highly motivated and experienced scientist to join its Protein Sciences Analytical Team. This position offers a unique opportunity to contribute to various Discovery Research Therapeutic Areas (TAs) and Projects by providing in-depth analytical and functional characterization of biologics and biopharmaceutical products, such as complex protein antigens, monoclonal antibodies, multi-specifics, and other antibody-like biologics. The ideal candidate will have a strong background in protein analytical characterization, particularly mass spectrometry, to discern protein critical quality attributes (identity, post-translational modifications, physiochemical properties), prior demonstration of innovative problem solving and troubleshooting, and will foster productive collaborations with other functional groups and TAs. This is an excellent opportunity for a motivated scientist to make a significant impact in a collaborative and innovative environment. Join us in bringing innovative medicines to patients!
Key responsibilities:
<ul>
<li>Independently develop and execute mass spectrometry workflows for comprehensive characterization of biologics and biotherapeutics (including intact, reduced, subunit, and peptide mapping).</li>
<li>Develop, optimize, validate, and execute innovative analytical methods to characterize complex proteins/glycoproteins, antigens, and novel protein-based therapeutics.</li>
<li>Ensure optimal functioning, calibration, and maintenance of laboratory equipment; proactively troubleshoot and resolve technical or experimental issues to minimize operational downtime.</li>
<li>Resolve key project challenges and obstacles by leveraging available analytical tools, literature, and technical expertise, and proactively proposing solutions.</li>
<li>Demonstrate scientific initiative and creativity in developing novel workflows and strategies for biologics characterization and screening—including non-traditional modalities (e.g., multi-specifics, alternative scaffolds, and fusion proteins)—to support BGM and TA projects.</li>
<li>Collaborate with external partners, CROs, or vendors as appropriate to advance project goals.</li>
<li>Analyze, document, and report data concisely, formulate conclusions, and design follow-on experiments based on multidisciplinary data.</li>
<li>Provide direct mentorship and guidance to junior scientists and team members, fostering their scientific development and growth.</li>
<li>Communicate project progress, data analyses, and technical recommendations to cross-functional teams and senior management in a clear and timely manner.</li>
<li>Present original research and findings both internally and at external scientific conferences; contribute to scientific papers, patents, and technical reports as author or co-author.</li>
</ul>
Qualifications 
Qualifications:
<ul>
<li>Scientist II: BS or equivalent education with typically 7 or more years of experience or MS or equivalent education with typically 5 or more years of experience.</li>
<li>Sr. Scientist I:&nbsp;Bachelor’s Degree or equivalent education and typically, 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no experience necessary.</li>
<li>Extensive hands-on experience with commercial mass spectrometry platforms (e.g., Orbitrap, Q-ToF), advanced MS workflows for protein characterization, and use of MS data analysis software for both routine and complex sample sets.</li>
<li>Direct, hands-on experience with biologics, monoclonal antibodies, and/or protein therapeutics, including characterization and analytical techniques.</li>
<li>Demonstrated experience operating laboratory automation systems (e.g., Andrew+, Assaymap Bravo) for automated, high-throughput sample processing and preparation.</li>
<li>Proficient in a range of analytical techniques, including chromatography (e.g., HPLC, UPLC) and capillary electrophoresis, with ability to troubleshoot and optimize these methods as needed.</li>
<li>Working knowledge of biophysical and structural biology methods, such as DLS, DSF, HDX-MS, X-ray crystallography, or NMR spectroscopy (preferred).</li>
<li>Familiarity or experience with coding/programming (e.g., Python, R, or relevant scripting languages) and in developing automated data workflows or solutions (preferred but not required).</li>
<li>Demonstrated strong theoretical and practical foundation in the relevant scientific discipline, with proven ability to rapidly learn, master, and apply innovative technologies.</li>
<li>Exceptional organizational skills and the ability to manage multiple concurrent projects and tasks efficiently within established timelines.</li>
<li>Team-oriented and collaborative mindset, with excellent verbal and written communication skills; able to thrive in a fast-paced, dynamic, and multidisciplinary environment.</li>
<li>The levelling of the role will be decided based on candidate qualifications.</li>
</ul>
Key AbbVie Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable high performance.</li>
<li>Learns fast, grasps the “essence” and can change course quickly when indicated.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;ofthis posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location,and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.&nbsp;​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of anybonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's soleand&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Scientist II/Senior Scientist I, Protein Analytical Characterization

<h3>Job Description</h3>
Job Description
Are you a highly motivated microbiologist ready to be the frontline defender of quality for groundbreaking clinical and commercial manufacturing?
We are seeking a meticulous and experienced Quality Control Microbiology Associate I to join our team. In this critical role, your expertise in environmental and utility monitoring will directly ensure the safety, compliance, and integrity of our entire manufacturing operation. If you thrive on precise execution, love troubleshooting, and are ready to contribute to a Bold, Relentless, and Collaborative culture, this is your next career challenge!
Required QualificationsEducation: Bachelor's Degree (Master's Degrees will not be considered).Technical Skills: Proficiency with Microsoft Office Programs and electronic databases (LIMS, SAP, eQMS).Experience:3+ years of experience in a GMP QC laboratory setting, specifically focusing on microbiology.Instrumentation:Hands-on experience with particle counters, viable air samplers, and gas equipment.Core Knowledge:Knowledge of GMP, microbiology, aseptic techniques, and general laboratory instrumentation.Regulatory: Familiarity with relevant FDA, EU, ICH guidelines, and regulations.Communication:solid written and oral communication skills and organizational abilities.Environment:Ability to work effectively in a fast-paced, cross-functional matrix environment.Compensation &amp; Culture
<ul>
<li>
Pay: Competitive rate of $43.00/hour (with shift differential, potentially $49.45/hour).
</li>
<li>
Culture: Join a high-growth, transformational company that values curiosity, boldness, and collaboration.
</li>
</ul>
If you are ready to apply your microbiology expertise where it matters most, ensuring product safety from the ground up, apply today!FOR MORE IMMEDIATE CONSIDERATION, email a current resume to <a href="mailto:iris.levy@randstadusa.com" target="_blank">iris.levy@randstadusa.com</a>
salary: $42 - $43 per hour shift: Second work hours: 10 AM - 8 PM education: Bachelors 
Responsibilities
The Mission: What You'll Be Doing
You will be responsible for the routine monitoring and control of our critical manufacturing environment and utilities:
<ul>
<li>
Routine &amp; Critical Sampling: Conduct routine Environmental Monitoring (EM), including In-Process and EMPQ's, WFI Sampling, and Compressed Gas Sampling across clinical and commercial operations.
</li>
<li>
Compliance &amp; Documentation: Write, revise, and strictly follow SOPs, protocols, and reports. You will support quality systems records such as deviations, change controls, and CAPAs.
</li>
<li>
Data Integrity: Ensure meticulous data entry, review, and trending using LIMS (Laboratory Information Management System).
</li>
<li>
Lab Operations &amp; Collaboration: Maintain lab equipment, perform housekeeping tasks, and collaborate with internal and external labs for sample coordination and testing.
</li>
<li>
Troubleshooting: Actively troubleshoot equipment and test methods and participate in audits and continuous improvement initiatives.
</li>
</ul>
The essential functions of this role include: 
<ul>
<li>working weekends</li>
 Skills
<li>Quality Control</li>
<li>microbiology</li>
<li>GMP (1 year of experience is required)</li>
<li>QC laboratory</li>
 Qualifications
<li>Years of experience: 3 years</li>
<li>Experience level: Experienced</li>
 Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. 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. 
</ul>

Quality Control Microbiology Associate I

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose
The Associate QC Scientist performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab Investigation reports.
Responsibilities
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>2+ years of related work experience</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, Quality Control (Wednesday-Saturday 4pm-2:30am)

<h3>Job Description</h3>
Job DescriptionClean Room Assembler – Chicopee, MA
We are seeking a detail-oriented Clean Room Assembler to support precision manufacturing in a controlled environment. This role involves assembling components, performing quality inspections, and following strict operational procedures.
Key Responsibilities:
<ul>
<li>Assemble parts and sub-assemblies per SOPs</li>
<li>Conduct in-process quality inspections</li>
<li>Maintain compliance with cleanroom standards and safety protocols</li>
</ul>
Qualifications:
<ul>
<li>Prior experience in cleanroom or assembly environments</li>
<li>Proficiency with microscopes and fine motor tasks</li>
<li>Ability to follow detailed instructions and work under supervision</li>
</ul>
Why Join Us:
<ul>
<li>Structured, supportive work environment</li>
<li>Opportunities to build technical skills</li>
<li>Contribute to high-quality production in a specialized setting</li>
</ul>
Pay and Benefits
The pay range for this position is $17.65 - $19.40/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 Chicopee,MA.
Application Deadline
This position is anticipated to close on Nov 6, 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.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
Ink Materials Process Engineer South Hadley
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer and commercial leader in ePaper technology (see E Ink │ About Us). E Ink’s South Hadley, MA production facility is increasing its chemical manufacturing capability because of increased global demand for E Ink ePaper display products. We are seeking qualified candidates who are self-driven, looking to advance their career and be a high-impact player on a team.
Our diversity of people, backgrounds, experiences, thoughts and perspectives are 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 │ Life at E Ink).
About the Role:
Are you passionate about transforming innovative ideas into scalable manufacturing processes? As a key member of our Operations Engineering team, you will play a pivotal role in developing and optimizing systems that produce our unique pigments and dispersions. Your work will directly impact the efficiency, quality, and sustainability of our manufacturing operations.
In this hands-on role, you will collaborate with cross-functional teams to troubleshoot challenges, implement improvements, and drive innovation from the lab to full-scale production. We're seeking a proactive engineer who thrives in dynamic environments and is eager to contribute to our mission of delivering high-quality pigment solutions.
Key Responsibilities: 
<ul>
<li>Monitor and enhance ink and pigment manufacturing processes to ensure consistency, efficiency, and quality</li>
<li>Utilize statistical tools (e.g., SPC, SQC) to analyze process data and identify areas for improvement</li>
<li>Develop and maintain comprehensive process documentation, including SOPs and batch records</li>
<li>Lead investigations into process deviations, implementing corrective actions to prevent recurrence</li>
<li>Identify and execute projects aimed at improving safety, reducing costs, and enhancing product quality</li>
<li>Work closely with Development, Quality, and Supply Chain teams to support new product introductions and raw material qualifications</li>
<li>Oversee small to medium-scale capital projects, from conception through implementation</li>
<li>Promote a culture of safety by adhering to and advocating for best practices and regulatory compliance</li>
</ul>
Qualifications:
<ul>
<li>BS degree in Chemical Engineering, Materials Science, Chemistry, or a related field</li>
<li>5–10 years of experience in manufacturing or process engineering, ideally within pigment, chemical, or related industries. Candidates with strong technical foundations and demonstrated learning agility are also encouraged to apply.</li>
<li>Demonstrated ability to identify issues, analyze root causes, and implement effective solutions</li>
<li>Proficiency or the ability to master statistical analysis software (e.g. JMP, Minitab) and familiarity with process control methodologies</li>
<li>Ability to prioritize assignments, multi-task and work both independently and with cross-functional teams</li>
<li>Able to communicate technical information clearly and adapt messaging to different audiences</li>
<li>Ability to work in areas requiring the use of a full-face respirator, with training and equipment provided to ensure comfort and safety</li>
</ul>
Preferences:
<ul>
<li>Experience with formal root cause analysis tools (e.g., 8D, DMAIC)</li>
<li>Familiarity with ISO standards and quality management systems</li>
<li>Working knowledge of lean and Six Sigma methodologies</li>
<li>Lean Six Sigma Green Belt or equivalent certification</li>
<li>Familiarity with solvent handling and an understanding of OSHA Process Safety Management (PSM) principles</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 $90,000 to $125,000 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.

Ink Materials Process Engineer South Hadley

<h3>Job Description</h3>
Job Description
Job Title: Clean Room Assembler
Shift : 7am - 3pm Monday through Friday
Pay : $21/hour 
Job Description : The Clean Room Assembler is responsible for assembling product parts on the assembly line in accordance with production guidelines. The role involves performing spot checks to ensure product quality and adherence to approved standards. The assembler must notify management of any product discrepancies or equipment malfunctions, adhere to company policies and safety regulations, wear personal protective equipment as required, and perform other related duties as assigned.
Responsibilities
<ul>
<li>Assemble product parts on the assembly line according to production guidelines.</li>
<li>Perform spot checks on products to ensure quality standards are met.</li>
<li>Notify management of any product discrepancies or equipment malfunctions.</li>
<li>Adhere to established company policies and safety regulations.</li>
<li>Wear personal protective equipment in accordance with training guidelines.</li>
<li>Perform other related duties as assigned.</li>
</ul>
Pay and Benefits
The pay range for this position is $22.00 - $24.00/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 NASHUA,NH.
Application Deadline
This position is anticipated to close on Oct 28, 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.

<h3>Job Description</h3>
Job DescriptionSalary: $50K - $55K 
The Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute that is addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. Our research strategy uses molecular and genomic technologies to address questions related to Oceans and Human Health in two divisions (1) Marine Biomedical Discovery and (2) Healthy Oceans and Fisheries. GMGI is looking for a highly motivated Research Associate who will play an important role in contributing to our eDNA Service Lab within the Healthy Oceans and Fisheries Division.
 
The ideal candidate will have strong experience in molecular biology/ecology applied to fisheries and knowledge of common molecular laboratory techniques and data analysis. The candidate must be capable of working independently to design experiments, generate high quality data, and analyze results for a variety of projects directed by GMGI research staff. Experience with eDNA is highly desirable. This position is an extraordinary opportunity for an ambitious and entrepreneurial person who is interested in helping to contribute to a world-class research institute.
 
Responsibilities
 Design and execute experiments using molecular biology/genomics techniques
 Perform DNA/RNA isolations and quantification, PCR, qPCR, RT-qPCR, ddPCR
 Prepare libraries and run Illumina next-generation sequencing
 Conduct eDNA metabarcoding and species presence/absence assays
 Apply knowledge of experimental design, bioinformatics, and statistics to analyze results
 Participate in field collections for eDNA samples, including tissue dissection and processing
 Organize, process, and archive field and lab samples following established protocols
 Prepare client-facing reports and scientific communications (presentations, manuscripts, etc)
 Communication with clients via email and meetings to provide updates, answer questions, and ensure project success.
 
Qualifications
 Bachelors or Masters degree in biology, molecular biology, marine biology, or related discipline
 Hands-on experience with molecular biology techniques including qPCR, RT-qPCR, and Next-Generation Sequencing
 Experience working with genomics instruments and laboratory automation tools
 Demonstrated ability to plan and carry out experiments independently
 Familiarity with the command line interface, Linux, and R; hands-on experience in analyzing metabarcoding data
 Strong scientific writing and documentation skills
 Excellent verbal communication skills and comfort working in a team setting and with clients
 Commitment to scientific integrity and rigorous data quality standards; willingness to troubleshoot
 Adaptability and initiative in a fast-paced, start-up and research-driven environment
 Enthusiasm and commitment to GMGIs mission for science and education
 Self-starting, independent, creative thinker with strong problem-solving skills
 
This position will report to the eDNA Service Platform Manager.
Salary commensurate with experience.
 
It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes:
 Health and Dental Insurance
 Medical and Dependent Flex Spending Accounts
 Long Term Disability
 Life Insurance
 Paid Time Off
 403(b) Retirement Plan
 12 Paid Holidays
 
Applicants must be authorized to work in the US.
 
About GMGI
Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics.
GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need.
 
In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization, and in building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: <a href="http://www.gmgi.org" target="_blank">www.gmgi.org</a>

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