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<h3>Job Description</h3>
Summary:
Under the general direction of the Laboratory Managers and Medical Director, is responsible for staff orientation, training, and competency assessment, and daily supervision of work activities of personnel.
 
Does this position require Patient Care? No
 
Essential Functions:
-Provides daily supervision of technical, clerical, and service employees.
-Plans, organizes, delineates, and schedules duties and responsibilities of Laboratory staff in conjunction with the Laboratory Managers. 
-Assists other technologists as needed with technical problems and interpretation of results. 
-Determines the priority of work at the laboratory, assuring the timely completion of work. 
-Is responsible for ordering and maintaining an appropriate level of inventory and laboratory supplies. 
-Maintains manuals on all Standard Operating Procedures and required records and reports. 
-Responsible for ensuring staff adhere to all safety policies and procedures. 
-Responsible for orientation, training, and competency assessments, assuring staff:
1. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results.
2. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient samples.
3. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed.
4. Follow the laboratory's established corrective action policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.
5. Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical consultant, technical supervisor, clinical consultant or director; and
6. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.
 
Education:
Bachelor's Degree Medical Technology required or Bachelor's Degree Laboratory Sciences required and Other Certificate/Diploma Clinical Laboratory Sciences required.
 
Can this role accept experience in lieu of a degree?
No
 
Licenses and Credentials:
Medical Technologist (ASCP) [MLT, MT, MLA, Histologists] - American Society for Clinical Pathology Board of Certification (ASCP-BOC) required.
 
Experience:
Lab experience 3-5 years required and Supervisory experience 1-2 years preferred.
 
Knowledge, Skills and Abilities:
- The knowledge, both practical and theoretical, of tests and procedures necessary to review findings and advise and direct subordinates in action.
- Demonstrates advanced level of analytical skills and judgment.
- Must have a relatively high level of analytical ability to work with complex instrumentation, resolve technical equipment problems, relate test results to normal and pathological states, and interpret quality control data.
- Must have understanding of computer technology and its application to analytical procedures and quality control.
- Must have a comprehensive understanding of laboratory equipment and its operation, maintenance and repair, and analytic techniques.
- Must have the ability to work independently, evaluate situations and act appropriately.
- Detailed knowledge of applicable federal, state and accreditation requirements.
- Ability to multitask in a fast-paced environment.
- Advanced computer skills.
- Comprehensive understanding of test principles, equipment operation and computer system operations.
- Make appropriate decisions, develop and complete follow-up actions in conjunction with lab leadership.
- Must be able to perform as a senior team member, providing direction and guidance to less experienced technologists.
- Must have the ability to pay careful attention to detail and to adhere to written protocols, including communication to lab leadership when issues are identified.
- Must be able to perform as a team member.
- Excellent interpersonal skills.
- Ability to interact professionally and effectively with numerous staff, including physicians, hospital personnel, employees, and patients.

Supervisor, Clinical Laboratory

<h3>Job Description</h3>
Job Description
Job Description
We are seeking a Chemical / Process Engineer to join our team. The ideal candidate will develop, maintain, and optimize our chemical finishing processes while ensuring safety, quality, and compliance with industry standards. This role is hands-on and requires close collaboration with production, quality, and environmental health &amp; safety teams.
Responsibilities
<ul>
<li>
Develop, implement, and improve electroplating, anodizing, conversion coating, and passivation processes.
</li>
<li>
Monitor and control chemical bath conditions, ensuring consistent performance and compliance with specifications.
</li>
<li>
Troubleshoot and resolve process issues related to adhesion, corrosion resistance, and finish quality.
</li>
<li>
Support audits and maintain compliance with NADCAP, ISO, AS9100D, and customer specifications.
</li>
<li>
Drive process improvements using Lean, Six Sigma, and data-driven problem solving.
</li>
<li>
Ensure compliance with environmental, health, and safety regulations for chemical handling and waste treatment.
</li>
<li>
Document standard operating procedures, work instructions, and process records.
</li>
<li>
Collaborate with cross-functional teams to meet production, quality, and cost goals.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s degree in Chemical Engineering, Materials Science, Chemistry, or a related field.
</li>
<li>
3+ years of experience in chemical or surface finishing processes (electroplating, anodizing, coatings, etc.).
</li>
<li>
Strong understanding of process control, bath chemistry, and troubleshooting.
</li>
<li>
Familiarity with NADCAP, ISO, and AS9100 requirements preferred.
</li>
<li>
Knowledge of safety practices for handling hazardous chemicals.
</li>
<li>
Excellent problem-solving, analytical, and communication skills.
</li>
<li>
Ability to work hands-on in a production environment.
</li>
</ul>
Preferred Certifications (Not Required)
<ul>
<li>
Lean Six Sigma (Green Belt or higher).
</li>
<li>
Certified Quality Engineer (CQE).
</li>
<li>
OSHA / HAZWOPER or other EHS-related training.
</li>
<li>
Professional Engineer (PE) license is a plus.
</li>
</ul>
Benefits
<ul>
<li>
Competitive salary with performance-based incentives.
</li>
<li>
Health, dental, and vision insurance.
</li>
<li>
Retirement plan with company match.
</li>
<li>
Paid time off and holidays.
</li>
<li>
Opportunities for career growth and professional development.
</li>
</ul>
Company DescriptionCentral Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver. 
<h3>Company Description</h3>
Central Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver.

Chemical Process Engineer

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
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. 
</li>
<li>
Analyzes test data and evaluates results. 
</li>
<li>
Writes procedures with guidance. 
</li>
<li>
Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties.
</li>
<li>
Assists in trending data to support assay performance. 
</li>
<li>
Assists in writing lab Investigation reports.
</li>
<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>
3 + years of related work experience
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Chemist

<h3>Job Description</h3>
Job Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment. Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that 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:
The Chemical Engineer will perform hands-on laboratory and pilot-scale operations to support the synthesis, processing, and finishing of organic pigments. This role involves preparing and operating chemical equipment, performing wet chemistry reactions, monitoring process parameters, and conducting quality control tests to ensure materials meet specifications.
Key Responsibilities
<ul>
<li>Carry out chemical reactions of organic synthesis of organic pigments and dyes, etc.</li>
<li>Operate wet chemistry equipment such as reactors, filtration units, washing stations, and dryers</li>
<li>Carry out pigment finishing process steps (flushing, drying, grinding, surface treatment)</li>
<li>Take in-process samples and perform analytical tests (pH, solids content, particle size, color strength, shade, etc.)</li>
<li>Record all process parameters and observations accurately in batch records</li>
<li>Work closely with R&amp;D scientists and engineers to scale up reactions from lab to pilot plant</li>
<li>Support process optimization and troubleshooting efforts</li>
<li>Work with senior technical staff to conduct laboratory experiments in the area of pigment surface modification and ink formulations</li>
<li>Perform electrical and electro-optical measurements for new color displays</li>
</ul>
Qualifications
<ul>
<li>Bachelor or associate’s degree in Chemistry, Chemical Engineering, Material Engineering, Polymer Engineering or a related field; or equivalent hands-on industrial experience</li>
<li>1–3 years in chemical manufacturing, preferably with pigments, dyes, or fine chemicals</li>
<li>Experience with wet chemistry techniques (organic and polymer synthesis, media milling, precipitation, filtration, washing, drying)</li>
</ul>
Skills &amp; Competencies:
<ul>
<li>Strong understanding of basic chemistry principles and chemical safety</li>
<li>Ability to follow detailed batch instructions and standard operating procedures (SOPs)</li>
<li>Hands-on experience with laboratory and pilot-scale chemical equipment</li>
<li>Good record-keeping, observation, and problem-solving skills</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.

Chemical Engineer - Color Pigment 1060S-4

<h3>Job Description</h3>
Job DescriptionThe Lehigh Valley Justice Institute at United Way GLV is a nonpartisan research, policy, and advocacy program working to develop and promote a reimagined justice system that is equitable and fair for all communities. LVJI employs a data-driven approach focused on the criminal justice processes within the Lehigh Valley area of Pennsylvania. We believe that solutions borne in the Lehigh Valley, due to the region’s unique and diverse political, economic, and demographic climates, are portable in nature and can thus be applied to communities throughout the United States. At LVJI, we understand you are a student and are still learning. We believe internships are opportunities to learn how to apply what you’ve learned in the classroom to real-world scenarios. We are committed to providing an internship experience that grows your skills, introduces you to the professional workforce, and bolsters your career in a nurturing environment. If you want to work on a real project, start your professional journey, and make some real change, we’d love to hear from you! Benefits Professional Development Responsibilities The Lehigh Valley Justice Institute (LVJI) at United Way of the Greater Lehigh Valley (UWGLV) is looking for Research Interns to study the effect of technology in K-12 classrooms. This hands-on project includes an intense literature review, synthesizing research and best practices, and writing a final research report. Interns will review published and unpublished academic literature on the impact of technology on child learning and produce a set of best practices. At the end, there may be internal presentations or presentations to local committees or organizations. We hope to answer the following research questions. What effects does integrating cell phone, tablet, laptop, etc., technology have on student learning in K-12 classrooms? Is there a “sweet spot” of technology integration that best facilitates learning? What are the best practices of integrating technology into K-12 classrooms? Responsiblities: Attend meetings with supervisors and team members Conduct literature searches to answer the research questions Execute basic data analysis as needed Add/modify research questions as needed Write a report describing research procedures, results, and interpretation Communicate and collaborate with other interns or team members Requisition #cmfe4kb2sx6o20jo5xdtj1jni

Research Intern - Technology in Classrooms - Virtual/Remote

<h3>Job Description</h3>
Job DescriptionThe Lehigh Valley Justice Institute at United Way GLV is a nonpartisan research, policy, and advocacy program working to develop and promote a reimagined justice system that is equitable and fair for all communities. LVJI employs a data-driven approach focused on the criminal justice processes within the Lehigh Valley area of Pennsylvania. We believe that solutions borne in the Lehigh Valley, due to the region’s unique and diverse political, economic, and demographic climates, are portable in nature and can thus be applied to communities throughout the United States. At LVJI, we understand you are a student and are still learning. We believe internships are opportunities to learn how to apply what you’ve learned in the classroom to real-world scenarios. We are committed to providing an internship experience that grows your skills, introduces you to the professional workforce, and bolsters your career in a nurturing environment. If you want to work on a real project, start your professional journey, and make some real change, we’d love to hear from you! Benefits Professional Development Responsibilities The Lehigh Valley Justice Institute (LVJI) at the United Way of the Greater Lehigh Valley (UWGLV) is seeking Research Interns to investigate the impact of Federally Qualified Health Centers (FQHCs). FQHCs are community-based health organizations that provide comprehensive primary care, dental, and behavioral health services to underserved populations in the United States. Interns will review published and unpublished academic literature on the impact of these health centers on the populations they serve and produce a set of best practices. There may be internal presentations or presentations to local committees or organizations. We are hiring 1-2 interns for this role. We hope to answer the following research questions. What effects do FQHCs have on underserved populations in removing barriers to care, improving mental health, or even downstream impacts on financial stability, housing security, or food security? Do these effects differ by population? Do some groups benefit more from FQHCs than others, and if so, why? What is the current state of FQHCs? Can we identify any areas in the Lehigh Valley region that could benefit from an FQHC? What are the best practices for implementing and running FQHCs? Responsibilities: Attend meetings with supervisors and team members Conduct literature searches to answer the research questions Execute basic data analysis as needed Add/modify research questions as needed Write a report describing research procedures, results, and interpretation Communicate and collaborate with other interns or team members Requisition #cmfe51z91x6s90jo5vt8njzn5

Research Intern - Federally Qualified Health Centers - Virtual/Remote

<h3>Job Description</h3>
Job Description
We are currently hiring a full-time Research Associate to support the investment team in our Needham, MA office. There is flexibility for hybrid work with at least two days in the office. The Research Associate will be focused on thematic research across areas targeted by proprietary Portfolio Managers and will conduct fundamental research of companies within proprietary equity strategies. A successful Research Associate is intellectually curious, detail oriented, flexible in thought, and willing to put in the effort to build the knowledge base required to add value in the research process.
Job Responsibilities Work with the investment team and through self-study to build the skills required to effectively: • Conduct fundamental company research including industry analysis, financial statement review, modeling, valuation, materiality assessment, management interaction and written research findings. • Conduct original research across targeted market, industry, and sustainability themes in collaboration with the investment team. This work forms the foundation of sustainable growth opportunities across strategies. • Publish written reports across thematic and company-level research to support proprietary strategy management and reporting/marketing efforts.
Qualifications: • Bachelor's degree with a record of high academic achievement • Relevant work or internship experience preferred • Demonstrated interest in investing, capital markets and sustainability • Clear desire to work toward attainment of the CFA charter • Proficiency with MS Excel and familiarity with Bloomberg helpful • Excellent writing and oral communication skills • Demonstrated team-player with the ability to work efficiently independently
F.L.Putnam is an equal opportunity employer. We are committed to promoting an inclusive environment in service to one another and our clients. We do all of this with kindness, empathy, and respect for one another.

Research Associate

<h3>Job Description</h3>
Job Description Position Title: Senior Geotechnical Engineer Location: Boston, Massachusetts, United States Department: Civil Description: We are offering an exciting opportunity for a Senior Geotechnical Engineer to join our team in our Boston MA office. The successful candidate will provide geotechnical design and construction related services for bridge and highway projects. With over 138 years of experience, H&amp;H is a trusted full-service infrastructure engineering firm. Our clients, including infrastructure owners, contractors, and colleagues, rely on us for intricate and innovative engineering solutions. They trust our time-tested ability to manage the entire life cycle of a project, from the study and planning phase through to design and construction. With over 600 talented employees located across 30 offices nationwide, H&amp;H can efficiently and effectively handle assignments of all sizes, types, and delivery methods around the country and across the globe. Requirements: 
<ul>
<li>Master's Degree in Geotechnical Engineering (required)</li>
<li>Five+ years of experience in Geotechnical Engineering</li>
<li>PE Licensed required</li>
<li>Experience with Deep Foundation design and construction, AASHTO LRFD</li>
<li>Familiar with Numerical modeling of soil-structure interaction using Fb-MultiPier, Stress and Ground Improvement Analysis</li>
<li>Experience with Finite Element software, Geosynthetics, Soil Liquefaction, Slope Stability and all aspects of Pile Analysis for bridge foundations are required</li>
</ul>
 Benefits: We offer a professional work environment, a competitive salary, a benefits package, and 401(k). EOE M/F/DISABILITY/VETS 
PI8a29bce31247-25405-37252376

Senior Geotechnical Engineer

<h3>Job Description</h3>
Job Description
🧪 Quality Control Lab Analyst – Contract to Hire
📍&nbsp;Location: Hadley, MA
🕒&nbsp;Schedule: Monday–Friday, 8:30 AM–4:30 PM or 9:00 AM–5:00 PM
🔬&nbsp;Join a growing team in a cutting-edge lab environment
&amp;#x1F31F;&nbsp;Help Us Ensure Quality from Molecule to Market
Are you a hands-on chemist with a passion for precision and product safety? Join our expanding team as a&nbsp;Quality Control Lab Analyst&nbsp;and play a critical role in testing and validating the ingredients that power health and wellness products. You’ll work in a dynamic lab setting, using advanced instrumentation and wet chemistry techniques to ensure every batch meets the highest standards.
This is a fantastic opportunity for someone who thrives in a collaborative, science-driven environment and wants to grow with a company that values innovation and integrity.
💼&nbsp;What You’ll Do
<ul>
<li>Prepare and test samples using GC and wet chemistry methods (pH, titrations, LOD).</li>
<li>Run calibration curves and system suitability tests to ensure accuracy.</li>
<li>Perform first-line instrument care and basic troubleshooting (GC, HPLC).</li>
<li>Support method validation efforts (accuracy, precision, LOD, LOQ).</li>
<li>Maintain lab inventory, cleanliness, and documentation standards.</li>
<li>Draft and review SOPs and participate in notebook peer reviews.</li>
</ul>
✅&nbsp;What You Bring
<ul>
<li>Bachelor’s degree in Chemistry (Master’s preferred).</li>
<li>3–5 years of QC lab experience in food, supplements, or natural products.</li>
<li>Independent operation of&nbsp;GC and HPLC&nbsp;instruments.</li>
<li>Experience with lipid-rich or natural product matrices (e.g., vitamins, fats, emulsifiers).</li>
<li>Familiarity with&nbsp;USP/AOAC methods&nbsp;and&nbsp;cGMP documentation.</li>
<li>Proficiency in chromatography software (OpenLab, ChemStation).</li>
<li>Strong lab safety mindset and attention to detail.</li>
</ul>
&nbsp;Why You’ll Love This Role
<ul>
<li>Work in a growing organization with room to influence lab operations.</li>
<li>Be part of a team that values scientific rigor and continuous improvement.</li>
<li>Enjoy a stable weekday schedule with flexibility in start time.</li>
<li>Opportunity to transition into a permanent role with long-term growth potential.</li>
</ul>
Ready to make your mark in quality control?
Apply today and help us deliver safe, effective products backed by science.
Pay and Benefits
The pay range for this position is $30.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hadley,MA.
Application Deadline
This position is anticipated to close on Sep 19, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

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