Research and development technician jobs in Lewiston, ME - 32 jobs

**About ETS:** ETS is a global education and talent solutions organization enabling lifelong learners worldwide to be future-ready. For more than 75 years, we've been advancing the science of measurement to build benchmarks for fair and valid skill assessment across cultures and borders. Our worldwide impact extends through our renowned assessments including TOEFL , TOEIC , GRE and Praxis tests, serving millions of learners in more than 200 countries and territories. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere. With offices and partners across Asia, Europe, the Middle East, Africa, and the Americas, we deliver nearly 50 million tests annually. Join us in our journey of measuring progress to power human progress worldwide. The Associate R&D Data Scientist contributes to the planning, development, and execution of data science analyses for research and development projects within the ETS Research Institute. This role focuses on applying advanced data science, statistics, machine learning, and AI to make inferences and/or predictions from data. The position requires expertise in modern frameworks and cloud computing environments to support innovative research in educational measurement and assessment. **Primary Responsibilities** _Technical Responsibilties:_ Data Management and Analysis + Collect, preprocess, and manage structured and unstructured data from diverse sources, ensuring data quality and integrity. + Perform exploratory data analysis to identify trends, patterns, and actionable insights. Model Development and Evaluation + Design, implement, and validate predictive models and machine-learning algorithms using frameworks such as PyTorch/TensorFlow, and scikit-learn. + Experiment with large language models and generative AI techniques (e.g., working with large language model APIs, prompt engineering) to support innovative research. Deployment and Scalability + Develop and maintain pipelines for model deployment in cloud computing environments (e.g., AWS, Azure) to ensure scalability and reproducibility. _Research and Collaboration_ + Collaborate with scientists and cross-functional research teams to align data science efforts with program objectives + Contribute to technical reports, presentations, and publications that disseminate research findings. + Communicate complex technical concepts clearly to both technical and non-technical stakeholders. \#LI-MM1 \#Remote + Demonstrable proficiency and experience in Python and/or R for data analysis and modeling. + Hands-on experience with PyTorch/TensorFlow, Scikit-learn, and other machine learning frameworks. + Familiarity with generative AI methods and their practical applications. + Strong understanding of statistical methods, experimental design, and data visualization. + Ability to work in cloud computing environments (e.g., AWS) for model deployment and data processing. + Excellent problem-solving skills and adaptability to evolving research priorities. + Effective written and verbal communication skills for collaborative research environments. + Exceptional attention to detail, ensuring accuracy and reliability in data analysis, modeling, and reporting. **Education:** Master's degree in Data Science, Computer Science, Statistics, or a related quantitative field; or equivalent combination of education and experience. **ETS is mission driven and action oriented** + We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning. + We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders. In support of this ETS offers multiple Business Resource Groups (BRG) for you to learn and advance your career growth! + As a not-for-profit organization we will encourage you to lean in to your passion for volunteering. At ETS you may qualify for up to an additional 8 hours of PTO for volunteer work on causes that are important to you! **ETS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. We believe in creating a work environment where all individuals are treated with respect and dignity.**

As a Global Supply Chain Manufacturing Scientist, you'll support the Bio-Rad manufacturing plant that produces recombinant proteins and other specialized life science products that researchers and scientists need to make health-care breakthroughs and save lives. Collaborating with internal and external stakeholders, you'll help to implement continuous process improvement projects, perform investigations related to product issues, and identify solutions to address manufacturing issues. In this role, you'll work with a team of scientist to apply innovative cell and molecular biology approaches to develop and manufacture recombinant proteins. How You'll Make An Impact: * Develop experiments and tests, including writing and executing protocols, to qualify and validate manufacturing processes; analyze results, make recommendations, and develops reports. * Analyze and resolve basic Manufacturing and Compliance risks via CAPA, non-conformances, audit observations, risk analysis. Mitigate the risks and implements longterm solutions. * Support production teams with hands on training and manufacturing documentation reviews and updates. While also guiding the seamless knowledge transfer of projects and manufacturing processes. * Develop methods for process improvements by applying technical design skills to ensure equipment, tools, fixtures, and processes are lean and efficient. * Design and develop new products, that support our recombinant protein production pipeline, using molecular biology and biochemistry methodologies. What You Bring: * Education/Work Experience: Bachelor's Degree in a Scientific field, in biologic and/or chemistry disciplines, prefer biochemistry, immunology, cell biology. Up to 4 years' experience required in related industry. Prefer 5+ years related experience working in a cGMP manufacturing environment. Not required but would prefer experience working in an ISO13485 environment. * Strong biochemistry background and some molecular biology knowledge (e.g. chromatography, bio-processing, ELISA, electrophoresis, and western blotting) also preferred. * Organizational, analytical, and written and oral communication skills. * Must be able to convey complex technical topics to diverse audiences (business, QA/QC, etc.) * Design control and experience driving projects through the various phase-gates (e.g. feasibility, validation, verification, and development) desired. Total Rewards Package: At Bio-Rad, we're empowered by our purpose and recognize that our employees are as well. That's why we offer a competitive and comprehensive Total Rewards Program that provides value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Bio-Rad's robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee's work and life cycle. Benefits: We're proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability, paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG's), and more! Compensation: The estimated base salary range for this position is $76,200 - $104,900 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is also eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance. Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply. Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes. Fraud Alert: Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake "recruiters" and job scams. Click here for more information on this scam and how to avoid it. #LI-LL1 Legal Entity: (USA_1000) Bio-Rad Laboratories, Inc.

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. **Job Overview** We are currently seeking a dynamic, highly motivated, and experienced individual for the position of **Manager, Clinical Systems R&D IT Business Applications** who will serve as the primary liaison between R&D Clinical Operations team and IT, responsible for the delivery and support of technology solutions that align with business needs and operational demands. **_This role requires proficiency in implementing, integration, and managing Medidata & Veeva clinical systems (e.g. CTMS, EDC etc.) in a regulated environment_** **Job Duties and Responsibilities** + Partner with Clinical business stakeholders to co-create technology plans which support their business objectives and operational demands + Continuously assess current systems environment and identify changes (process and/or system) that enhance effectiveness + Assist in the evaluation of new technology systems and/or service providers + Oversee end-to-end management of IT projects-including planning, design, and implementation-ensuring projects are delivered on time, within scope, and with measurable business impact + Work with a team of managed service providers supporting the lines of business technology needs including project delivery, solution design, enhancement requests and support services + Accountable for managing clinical application systems through their full lifecycle, from implementation to ongoing optimization + Lead and initiate troubleshooting quality and/or functionality issues associated with technology systems in scope + Develop and maintain comprehensive project documentation, ensuring centralized storage and accessibility for knowledge management + Manage and prioritize system enhancements and fixes in collaboration with business stakeholders + Provide regular project status reports, manage issues proactively, and adjust schedules as needed while maintaining alignment with the overall program plan + Responsible for timely execution of all GxP system commitments and compliance activities (Backup recovery, Disaster Recovery testing etc.) + Collaborate with cross-functional IT teams to ensure seamless delivery of services, efficient communication, and shared accountability for outcomes + Establish clear performance metrics and service level agreements (SLAs) to monitor IT service delivery, project outcomes, and stakeholder satisfaction + Stay informed of emerging industry trends, best practices, and regulatory changes to proactively recommend technologies and process adaptations that empower the company during phases of rapid expansion + Serve as the IT subject matter expert for application upgrades, integrations, and system enhancements across supported business areas **Key Core Competencies** + Strong understanding of Clinical business processes, requirements and technology systems supporting Clinical Trials (e.g. EDC, CTMS, ETMF, Payments etc.) + 7+ years of progressively increasing experience managing clinical applications in a Pharma/Biotech company + Strong understanding of building and operating a technology support function + Proficient in implementing, integration and managing Medidata & Veeva clinical systems (e.g. CTMS, EDC etc.) in a regulated environment **Education and Experience** + BS/BA degree in a related discipline is required. Training or equivalent experience in IT or business management is beneficial but not required + 7+ years of experience in life sciences with a focus on IT system delivery + 5+ years of experience in implementing, integration and managing Medidata & Veeva clinical systems (e.g. CTMS, EDC etc.) in a regulated environment + Experience in Program & Project Management, including the Software Development Lifecycle and Computer Systems Validation process + Excellent communication skills The base salary range for this role is $127,440 to $159,300. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. **Confidential Data** : All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential. **Compliance** : Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards. 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. **Mental/Physical Requirements** : Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time. **Sumitomo Pharma America (SMPA)** **is an Equal Employment Opportunity (EEO) employer** Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. Sumitomo Pharma America (SMPA) endeavors to make its application process accessible to all. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact SMPA at ********************************************** This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company's cultural pillars. **Our** **Mission** _To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_ **Our** **Vision** _For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_

Responsibilities Conduct research on individual, corporate, and foundation prospects using established tools and resources. Prepare profiles, briefings, and reports for fundraisers and university leadership as directed. Assist with maintaining and updating prospect records in the fundraising CRM . Support the Vice President of Institutional Advancement at Board of Trustees Trusteeship Committee meetings by preparing meeting collateral and taking minutes. Assist the Vice President of Institutional Advancement and the University President in their work with principal gift prospects by entering actions into the fundraising CRM , identifying new prospects, and supporting related research and administrative tasks. Serve as the point person for collecting and tracking data on corporate partners, collaborating with Career Readiness and academic deans to support institutional relationship management and reporting. Support Major Gift Officers (MGOs) by conducting prospect research, assisting with moves management tracking, and helping maintain and update donor portfolios in the fundraising CRM . Follow established procedures for prospect management and data privacy. Ensure accuracy and integrity of prospect data in the fundraising CRM through regular review and updates. Respond to ad hoc research requests from advancement staff in a timely and professional manner. Stay current with best practices in prospect research and data management through ongoing professional development. Collaborate with team members to support donor-related initiatives and events. Perform other duties as assigned by supervisor. Qualifications Bachelor's degree with at least three years of prospect research or library science experience or a combination of education and experience from which comparable knowledge and skills are acquired. Strong information literary skills, including knowledge of industry-standard search techniques and software, and ability to navigate resources on the web (such social media and business websites). Understanding of prospect development and management concepts. Experience with fundraising CRMs (preferably The Raiser's EdgeNXT, ResearchPoint, Target Analytics). Experience with MS Office (Word, Excel, PowerPoint, OneNote). Ability to work independently and proactively on concurrent projects and collaboratively with others. Strong planning, communication, time management and organizational skills. Previous experience in advancement/development preferred. General understanding of fundraising terminology and practices. General understanding of higher education organizational structure and administrative operations. Ability to deal effectively with a wide variety of University personnel, students, and/or outside individuals/organizations. Adherence to the American Prospect Research Association (APRA's) Code of Ethics and the Family Educational Rights and Privacy Act ( FERPA ), which includes sensitivity to confidential information. Previous UNE experience desirable.

The Muskie School of Public Service at the University of Southern Maine (USM) is pleased to announce an opening for a full-time, Research Associate II position. The Research Associate II (RAII) carries out a full range of complex epidemiologic and surveillance activities, with a focus on Environmental and Occupational Health. This position is part of a team of USM epidemiologists and health communication specialists dedicated to building epidemiology and communication capacity at USM and the Maine CDC (the state's public health agency). The RAII provides epidemiology and subject matter expertise to state, federal, and local partners. The RAII, in partnership with Maine CDC staff and other USM staff, is responsible for developing, implementing and sustaining public health surveillance systems within the Maine CDC's Environmental Health Program (EHP); this includes assessing the burden and trends of environmental health-related outcomes, exposures, and risk factors in the general population and among sub-populations; and coordinating grant deliverables and reports and overseeing technical staff in the execution of grant activities. In addition, the RAII will lead and collaborate on epidemiologic studies with various Maine CDC programs and with partners in other state and federal agencies. The Muskie School of Public Service is Maine's distinguished public policy school, combining an extensive applied research and technical assistance portfolio with rigorous undergraduate and graduate degree and certificate programs in geography-anthropology; tourism and hospitality; policy, planning, and management (MPPM); and public health (MPH). The school is nationally recognized for applying innovative knowledge to critical issues in the fields of sustainable development and health and human service policy and management and is home to the Cutler Institute for Health and Social Policy. The Muskie School and Cutler Institute engage in cross-disciplinary opportunities through the University of Maine Graduate & Professional Center, which brings together programs in business, law, policy, and public health. This is a full-time position located on either our Portland Campus or Augusta location with a starting annual salary of $70,000. The University of Southern Maine offers highly competitive benefits for full-time and eligible part-time employees that includes (but is not limited to): 13 paid holidays plus earned vacation time and sick time. Health, dental and vision insurance. Low-cost short-term disability insurance and employer-paid long-term disability insurance. Employer-paid basic life insurance and supplemental life insurance. A tuition waiver program for employees and their spouse or dependent child(ren). A 403(b)-retirement plan with employer contribution. Free access to the METRO system, including the Husky Line with service between our Portland and Gorham campuses. To learn more, please review the Benefits Information Summary. The University of Southern Maine is a vibrant academic community located in the greater Portland, Maine area, including campuses in Portland, Gorham, Lewiston, and online. USM is part of the University of Maine System and offers a comprehensive array of undergraduate and graduate programs, emphasizing hands-on learning, community engagement, and interdisciplinary collaboration. With a highly engaged student-centered learning environment, USM is a steward of higher education, helping drive the economic, cultural, and civic life in the communities where our campuses are located and beyond. USM is committed to providing expanded access to high-quality education that elevates economic opportunity and contributes significantly to the vitality of a diverse society. To learn more about USM, visit About Our University. The University of Southern Maine fosters a welcoming and supportive campus environment that respects and appreciates varied perspectives, enhancing teaching, learning, personal growth, and overall institutional achievement. We welcome applications from candidates of all backgrounds who share our dedication to academic excellence and the enrichment of our community. We are dedicated to our Service Promise, Student Focused Every Day and seek a team member who embraces this commitment and upholds our core values of Respect & Care, Integrity, Equity, and Responsiveness. Required Qualifications: Master's degree in Epidemiology, Public Health or related field, preferably from an accredited school of public health, and a minimum of 6 years of epidemiologic-related work experience. Demonstrated mastery of principles of epidemiology and public health. Experience developing and implementing public health surveillance systems. Experience building partnerships and successfully collaborating with internal and external partners. Ability to identify the need for applied epidemiologic studies. Strong quantitative and qualitative research skills, including experience with major computer-based statistical packages, preferably SAS and/or R. How To Apply: Click on the ‘Apply Now' button below or visit our USM Careers Page and submit the following: Cover Letter Resume/Curriculum Vitae Finalist candidates will be asked to provide a list of the names and contact information for references. For full consideration please submit all required materials by November 30, 2025. We are not able to consider applicants who require Visa sponsorship support. Appropriate background screening will be conducted for the successful candidate. Clery Act: The Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act, or Clery Act, mandates that all Title IV institutions, such as the University, prepare, publish, and distribute an Annual Security Report (ASR), and provide notice of the availability of the ASR to all prospective employees. This report consists of two basic parts: disclosure of the University's crime statistics for the past three calendar years; and disclosures regarding the University's current campus security policies. View the University's Annual Security Report (PDF). If you wish to have a paper copy of the ASR or need to have a copy of the ASR in an accessible format, the University will provide such a copy upon request. Please contact our Public Safety Office at ************. EEO Statement: The University of Maine System (the System) is an equal opportunity institution committed to fostering a nondiscriminatory environment and complying with all applicable nondiscrimination laws. Consistent with State and Federal law, the System does not discriminate on the basis of race, color, religion, sex, sexual orientation, transgender status, gender, gender identity or expression, ethnicity, national origin, citizenship status, familial status, ancestry, age, disability (physical or mental), genetic information, pregnancy, or veteran or military status in any aspect of its education, programs and activities, and employment. The System provides reasonable accommodations to qualified individuals with disabilities upon request. If you believe you have experienced discrimination or harassment, you are encouraged to contact the System Office of Equal Opportunity and Title IX Services at 5713 Chadbourne Hall, Room 412, Orono, ME 04469-5713, by calling ************, or via TTY at 711 (Maine Relay System). For more information about Title IX or to file a complaint, please contact the UMS Title IX Coordinator at ************************

Job DescriptionJoin Our Discovery Team as a Discovery Associate Scientist Are you the kind of scientist who can't stop asking “why” and “what if”? Do you get excited about trying new techniques, optimizing protocols, and uncovering data that can push a project in a fresh direction? Do you learn from failures in the lab? If so, this Discovery Associate Scientist role may be the perfect next step in your career. We seek a team member driven to impact patient lives through precision quality controls who thrive in a culture of respect, open communication, and innovation where every voice matters. About the Role As a Discovery Associate Scientist, you will be at the bench every day, supporting early-stage molecular biology and molecular diagnostics projects. You will work side-by-side with Discovery Scientists, running experiments, testing new ideas, and helping turn early concepts into real technologies. This is a hands-on role for someone who loves the lab and wants to grow by learning new methods, taking initiative, and contributing ideas. What We're Looking For B.S. in biology, molecular biology, biochemistry, chemistry, or a related field with experience in Molecular Biology research. Hands-on experience with core molecular biology techniques (pipetting, reagent prep, amplification, electrophoresis, and nucleic acid extraction) from coursework and research lab experience, internships, or prior work. Innate curiosity, coupled with the drive and initiative needed to satisfy it. A team-oriented attitude, strong communication skills, and enthusiasm for learning from and collaborating with experienced scientists. Strong attention to detail, careful documentation habits, and the ability to follow SOPs while also helping refine them. Comfortable using basic software tools (e.g., Excel or equivalent) for data handling and simple calculations. What You'll Do Perform a wide range of molecular biology techniques (e.g., buffer and reagent prep, nucleic acid extraction, plasmid prep, in vitro transcription, PCR/qPCR/dPCR, and related techniques) to support feasibility and exploratory projects. Run carefully designed experiments under the direction of Discovery Scientists, record your work in detail, and help organize, interpret, present data so the team can quickly decide on next steps. Learn and adopt new technologies and protocols as the Discovery group evaluates innovative tools and methods. Contribute to daily lab operations, including reagent prep, routine laboratory cleaning, dishes, and chores, inventory management, and basic equipment checks, keeping the Discovery lab running smoothly. Why You'll Love Working Here You will learn rapidly by working closely with senior Discovery Scientists on cutting-edge molecular projects. You will be encouraged to ask questions, propose new ideas, and develop new capabilities. You will see how early-stage discovery work evolves into the development of useful products and technologies that impact molecular diagnostics and patient care. You will join a collaborative, energetic team that values curiosity, initiative, and scientific rigor. If you are a hands-on scientist who wants to grow, experiment, and help shape new molecular solutions from the ground up, we want to hear from you. Apply now and bring your curiosity to the Discovery lab. Benefits We Offer: • Medical insurance • Dental insurance • 401(k) • Profit Sharing Plan • Vacation • Holidays • Sick leave Get to know the MMQCI team! ********************************************************************* Maine Molecular Quality Controls, Inc. (MMQCI) designs, develops, manufactures, and markets unique quality control products used by hospital laboratories to monitor the accuracy of tests for inherited disease, pharmacogenetics, oncology, and infectious diseases. MMQCI has developed technologies to stabilize DNA and RNA for use as quality controls and continues to pursue the discovery of novel techniques useful for the development of new quality control products. MMQCI is conveniently located in beautiful southern coastal Maine, minutes from the Maine Turnpike, Portland International Jetport, and less than 2 hours from Boston. Close by are fabulous Portland restaurants, sandy beaches, and a plentiful supply of Maine lobsters! Many terrific outdoor activities are easily accessible including hiking, biking, kayaking, fishing, skiing and snowshoeing. We're in a state-of-the-art facility, located in Saco, right next to the Eastern Trail. Come join us! Powered by JazzHR fDNtgelzL9

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Job Description **Technical Manufacturing Chemist I** **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to: + Career development with an international company where you can grow the career you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. + An excellent retirement savings plan with a high employer contribution + Tuition reimbursement, the Freedom 2 Save (******************************************************************************************************* student debt program, and FreeU (*************************************************************************************************************** education benefit - an affordable and convenient path to getting a bachelor's degree. + A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. + A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. **The Opportunity** Abbott Rapid Diagnostics is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. The position of **Technical Manufacturing Chemist I** is within our Infectious Disease Developed Markets business unit located at **Scarborough, Maine.** In this role you will produce material for use in immunology-based chromatography and enzyme tests. **What You'll Work On** + Maintains and supports the production schedule. + Investigates problem areas and areas of desirable improvement. + Undertakes new procedures and observes proper safety precautions. + Responsible for in-process QC testing of manufacturing material as it relates. to qualifications, quality inspections and titration. + Maintains quality systems and proper GMP/GLP. + Creates and follows protocols designed around product improvement. + Responsible for making critical and non-critical bioreagents for use in product. and manufacturing processes using Standard Operating Procedures (SOPs). + Works in a team setting and coordinates manufacturing efforts based upon a set production schedule and maintaining the raw bioreagent supply as needed to support this schedule. **Required Qualifications** + Bachelor's Degree in a Chemistry, Life Sciences, or related field or equivalent combination of education and experience. + Prior Experience in the following areas: Pipette, Spectrophotometry, HPLC, pH meters, Gel Electrophoresis, SDS Page, ELISA assays **COMPETENCIES:** + Ability to work successfully as a member of a team and independently with moderate supervision. + Skill in using computer applications including spreadsheet, database, manufacturing, and word processing software. Apply Now (****************************** **Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ********************** (http://**********************/pages/candidate.aspx) Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ************** , on Facebook at *********************** , and on Twitter @AbbottNews. The base pay for this position is $20.50 - $41.00 per hour. In specific locations, the pay range may vary from the range posted. An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call ************ or email ******************

The Muskie School of Public Service at the University of Southern Maine (USM) is pleased to announce an opening for a full-time, Research Associate II position. The Research Associate II (RAII) carries out a full range of complex epidemiologic and surveillance activities, with a focus on Environmental and Occupational Health. This position is part of a team of USM epidemiologists and health communication specialists dedicated to building epidemiology and communication capacity at USM and the Maine CDC (the state's public health agency). The RAII provides epidemiology and subject matter expertise to state, federal, and local partners. The RAII, in partnership with Maine CDC staff and other USM staff, is responsible for developing, implementing and sustaining public health surveillance systems within the Maine CDC's Environmental Health Program (EHP); this includes assessing the burden and trends of environmental health-related outcomes, exposures, and risk factors in the general population and among sub-populations; and coordinating grant deliverables and reports and overseeing technical staff in the execution of grant activities. In addition, the RAII will lead and collaborate on epidemiologic studies with various Maine CDC programs and with partners in other state and federal agencies. The Muskie School of Public Service is Maine's distinguished public policy school, combining an extensive applied research and technical assistance portfolio with rigorous undergraduate and graduate degree and certificate programs in geography-anthropology; tourism and hospitality; policy, planning, and management (MPPM); and public health (MPH). The school is nationally recognized for applying innovative knowledge to critical issues in the fields of sustainable development and health and human service policy and management and is home to the Cutler Institute for Health and Social Policy. The Muskie School and Cutler Institute engage in cross-disciplinary opportunities through the University of Maine Graduate & Professional Center, which brings together programs in business, law, policy, and public health. This is a full-time position located on either our Portland Campus or Augusta location with a starting annual salary of $70,000. The University of Southern Maine offers highly competitive benefits for full-time and eligible part-time employees that includes (but is not limited to): 13 paid holidays plus earned vacation time and sick time. Health, dental and vision insurance. Low-cost short-term disability insurance and employer-paid long-term disability insurance. Employer-paid basic life insurance and supplemental life insurance. A tuition waiver program for employees and their spouse or dependent child(ren). A 403(b)-retirement plan with employer contribution. Free access to the METRO system, including the Husky Line with service between our Portland and Gorham campuses. To learn more, please review the Benefits Information Summary. The University of Southern Maine is a vibrant academic community located in the greater Portland, Maine area, including campuses in Portland, Gorham, Lewiston, and online. USM is part of the University of Maine System and offers a comprehensive array of undergraduate and graduate programs, emphasizing hands-on learning, community engagement, and interdisciplinary collaboration. With a highly engaged student-centered learning environment, USM is a steward of higher education, helping drive the economic, cultural, and civic life in the communities where our campuses are located and beyond. USM is committed to providing expanded access to high-quality education that elevates economic opportunity and contributes significantly to the vitality of a diverse society. To learn more about USM, visit About Our University. The University of Southern Maine fosters a welcoming and supportive campus environment that respects and appreciates varied perspectives, enhancing teaching, learning, personal growth, and overall institutional achievement. We welcome applications from candidates of all backgrounds who share our dedication to academic excellence and the enrichment of our community. We are dedicated to our Service Promise, Student Focused Every Day and seek a team member who embraces this commitment and upholds our core values of Respect & Care, Integrity, Equity, and Responsiveness. Required Qualifications: Master's degree in Epidemiology, Public Health or related field, preferably from an accredited school of public health, and a minimum of 6 years of epidemiologic-related work experience. Demonstrated mastery of principles of epidemiology and public health. Experience developing and implementing public health surveillance systems. Experience building partnerships and successfully collaborating with internal and external partners. Ability to identify the need for applied epidemiologic studies. Strong quantitative and qualitative research skills, including experience with major computer-based statistical packages, preferably SAS and/or R. How To Apply: Click on the ‘Apply Now' button below or visit our USM Careers Page and submit the following: Cover Letter Resume/Curriculum Vitae Finalist candidates will be asked to provide a list of the names and contact information for references. For full consideration please submit all required materials by November 30, 2025. We are not able to consider applicants who require Visa sponsorship support. Appropriate background screening will be conducted for the successful candidate. Clery Act: The Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act, or Clery Act, mandates that all Title IV institutions, such as the University, prepare, publish, and distribute an Annual Security Report (ASR), and provide notice of the availability of the ASR to all prospective employees. This report consists of two basic parts: disclosure of the University's crime statistics for the past three calendar years; and disclosures regarding the University's current campus security policies. View the University's Annual Security Report (PDF). If you wish to have a paper copy of the ASR or need to have a copy of the ASR in an accessible format, the University will provide such a copy upon request. Please contact our Public Safety Office at ************. EEO Statement: The University of Maine System (the System) is an equal opportunity institution committed to fostering a nondiscriminatory environment and complying with all applicable nondiscrimination laws. Consistent with State and Federal law, the System does not discriminate on the basis of race, color, religion, sex, sexual orientation, transgender status, gender, gender identity or expression, ethnicity, national origin, citizenship status, familial status, ancestry, age, disability (physical or mental), genetic information, pregnancy, or veteran or military status in any aspect of its education, programs and activities, and employment. The System provides reasonable accommodations to qualified individuals with disabilities upon request. If you believe you have experienced discrimination or harassment, you are encouraged to contact the System Office of Equal Opportunity and Title IX Services at 5713 Chadbourne Hall, Room 412, Orono, ME 04469-5713, by calling ************, or via TTY at 711 (Maine Relay System). For more information about Title IX or to file a complaint, please contact the UMS Title IX Coordinator at ************************

The R&D Discovery and Technology Futures Team at IDEXX Laboratories is seeking a motivated early career Associate Scientist to join our LCMS group in advancing the next generation of multiomic biomarker assays. In this highly collaborative role, you will work alongside a team of talented scientists at the BS, MS, and PhD levels to support biomarker discovery projects that drive innovation in veterinary diagnostics. The successful candidate will be innately curious about mass spectrometry and proteomics, eager to develop technical expertise with cutting-edge instrumentation, and thrive in a fast-paced, scientifically diverse environment. In this role, you will contribute to large-scale biomarker discovery studies using state-of-the-art UPLC-MS/MS platforms. You will work closely with a scientifically diverse team with expertise in proteomics, glycoproteomics, metabolomics, and lipidomics to process and analyze complex biological samples from blood, urine, tissue, and fecal matrices. This position offers significant opportunities for hands-on learning and professional growth as you develop mastery of advanced analytical techniques and contribute to projects that directly impact animal health. What You'll Do: Perform large biomarker studies, including sample preparation, fractionation, UPLC-MS/MS analysis, and data processing across diverse sample types Prepare materials, execute experiments, gather and analyze data, and reach conclusions with guidance from senior team members Use cutting-edge instrumentation and analysis software to explore the world of proteomics, glycoproteomics, metabolomics, and lipidomics Perform basic maintenance and troubleshooting of UPLC and mass spectrometry systems Document experiments and lab activities with meticulous attention to detail; prepare reports and summaries; present results and conclusions to team members Order and maintain necessary reagents, consumables, and laboratory supplies Collaborate with multiple cross-functional teams to support new product development and on-market products Contribute to method development and optimization efforts for novel biomarker assays What You Need to Succeed: Bachelor's degree in Chemistry, Biochemistry, or related fields with 0-3 years of relevant experience in mass spectrometry, proteomics, or analytical chemistry (industry or academic research) Hands-on laboratory bench and instrumentation skills, including experience with chromatography and/or mass spectrometry systems Strong analytical and problem-solving skills with exceptional attention to detail Ability to quickly learn new techniques and adapt to changing priorities Excellent organizational and time management abilities Strong communication skills, both verbal and written, with ability to present data clearly Ability to work independently and cooperatively as part of a team Demonstrated initiative, accountability, and ownership of assigned tasks Highly Desirable: Experience with UPLC-MS/MS systems, particularly Thermo instruments (Vanquish UPLC, Orbitrap, or Q Exactive platforms) Familiarity with proteomic sample preparation techniques (protein extraction, digestion, fractionation) Exposure to proteomic or metabolomic software packages (e.g., Proteome Discoverer, Skyline, MaxQuant, Compound Discoverer) Experience working with biological matrices such as plasma, serum, urine, or tissue Physical Demands and Work Environment: Laboratory setting with varying levels of noise and exposure to various potential chemical and biological hazards Compliance with approved laboratory practices is required Extensive sitting, standing, and computer use Ability to extend and reach with hands and arms May be required to lift, move, and carry up to 50 pounds Occasional travel may be required What You Can Expect From Us: Base salary range starting at $62,000 based on experience Opportunity for annual cash bonus Health / Dental / Vision Benefits Day-One 5% matching 401k Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more If you're looking for a role that'll challenge you, offer a variety of work and learning opportunities in a cutting-edge analytical field, while helping an amazing industry, we'd love to hear from you! Why IDEXX: We're proud of the work we do because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. While we appreciate our staffing partners, we are unable to accept unsolicited agency resumes. #LI-CAG

The Orthopaedic Surgery Research Associate will administer and execute all research projects within the Department of Orthopaedic Surgery. The individual filling this position will work closely with the pediatric orthopaedic surgery faculty members and lead the division in all ongoing research including the administration of multi-center clinical trials and internal clinical studies and will be responsible for the education and training of clinical staff, identification of eligible patients and their surrogates, consent and recruitment as well as IRB application, compliance and ongoing reporting. Additionally, this individual will play an integral part in the conception, design, IRB application process, data collection, analysis, writing, editing and submission process of all future research projects within the division. The individual filling this position will also be responsible for training and supervising research assistants within the department as well as assisting, guiding and mentoring orthopaedic surgery residents and medical students who are working on research projects within the division and department. The Research Associate may do some occasional travel for site visits and training in multi-center studies and for research presentations at national and international meetings. This is a grant funded position. Requirements PhD required Three years experience required Experience in a clinical research capacity including conducting clinical research trials and interfacing with sponsoring agencies is preferred. Computer literacy and competency with e-mail Outlook,internet search, MS Excel and MS Word Experience with electronic Data Entry and Retrieval systems Clinical Research experience preferred Human subject protection training Demonstrates critical thinking skills to problem-solving and clinical decision making for expected and unexpected problems Is responsible and accountable for own schedule Provides a safe environment for patients/involved others Comfortable giving input and leading others in research meetings and conferences Department: Orthopedic Surgery Bargaining Unit: Non Union Campus: EINSTEIN Employment Status: Regular Full-Time Address: 1250 Waters Place, Bronx Shift: Day Scheduled Hours: 8:30 AM-5 PM Req ID: 224684 Salary Range/Pay Rate: $62,400.00 - $73,000.00 For positions that have only a rate listed, the displayed rate is the hiring rate but could be subject to change based on shift differential, experience, education or other relevant factors. To learn more about the “Montefiore Difference” - who we are at Montefiore and all that we have to offer our associates, please click here. Montefiore is an equal employment opportunity employer. Montefiore will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law. N/A

The Muskie School of Public Service at the University of Southern Maine (USM) is pleased to announce an opening for a full-time, Research Associate II position. The Research Associate II (RAII) carries out a full range of complex epidemiologic and surveillance activities, with a focus on Environmental and Occupational Health. This position is part of a team of USM epidemiologists and health communication specialists dedicated to building epidemiology and communication capacity at USM and the Maine CDC (the state's public health agency). The RAII provides epidemiology and subject matter expertise to state, federal, and local partners. The RAII, in partnership with Maine CDC staff and other USM staff, is responsible for developing, implementing and sustaining public health surveillance systems within the Maine CDC's Environmental Health Program (EHP); this includes assessing the burden and trends of environmental health-related outcomes, exposures, and risk factors in the general population and among sub-populations; and coordinating grant deliverables and reports and overseeing technical staff in the execution of grant activities. In addition, the RAII will lead and collaborate on epidemiologic studies with various Maine CDC programs and with partners in other state and federal agencies. The Muskie School of Public Service is Maine's distinguished public policy school, combining an extensive applied research and technical assistance portfolio with rigorous undergraduate and graduate degree and certificate programs in geography-anthropology; tourism and hospitality; policy, planning, and management (MPPM); and public health (MPH). The school is nationally recognized for applying innovative knowledge to critical issues in the fields of sustainable development and health and human service policy and management and is home to the Cutler Institute for Health and Social Policy. The Muskie School and Cutler Institute engage in cross-disciplinary opportunities through the University of Maine Graduate & Professional Center, which brings together programs in business, law, policy, and public health. This is a full-time position located on either our Portland Campus or Augusta location with a starting annual salary of $70,000. The University of Southern Maine offers highly competitive benefits for full-time and eligible part-time employees that includes (but is not limited to): * 13 paid holidays plus earned vacation time and sick time. * Health, dental and vision insurance. * Low-cost short-term disability insurance and employer-paid long-term disability insurance. * Employer-paid basic life insurance and supplemental life insurance. * A tuition waiver program for employees and their spouse or dependent child(ren). * A 403(b)-retirement plan with employer contribution. * Free access to the METRO system, including the Husky Line with service between our Portland and Gorham campuses. To learn more, please review the Benefits Information Summary. The University of Southern Maine is a vibrant academic community located in the greater Portland, Maine area, including campuses in Portland, Gorham, Lewiston, and online. USM is part of the University of Maine System and offers a comprehensive array of undergraduate and graduate programs, emphasizing hands-on learning, community engagement, and interdisciplinary collaboration. With a highly engaged student-centered learning environment, USM is a steward of higher education, helping drive the economic, cultural, and civic life in the communities where our campuses are located and beyond. USM is committed to providing expanded access to high-quality education that elevates economic opportunity and contributes significantly to the vitality of a diverse society. To learn more about USM, visit About Our University. The University of Southern Maine fosters a welcoming and supportive campus environment that respects and appreciates varied perspectives, enhancing teaching, learning, personal growth, and overall institutional achievement. We welcome applications from candidates of all backgrounds who share our dedication to academic excellence and the enrichment of our community. We are dedicated to our Service Promise, Student Focused Every Day and seek a team member who embraces this commitment and upholds our core values of Respect & Care, Integrity, Equity, and Responsiveness. Required Qualifications: * Master's degree in Epidemiology, Public Health or related field, preferably from an accredited school of public health, and a minimum of 6 years of epidemiologic-related work experience. * Demonstrated mastery of principles of epidemiology and public health. * Experience developing and implementing public health surveillance systems. * Experience building partnerships and successfully collaborating with internal and external partners. * Ability to identify the need for applied epidemiologic studies. * Strong quantitative and qualitative research skills, including experience with major computer-based statistical packages, preferably SAS and/or R. How To Apply: Click on the 'Apply Now' button below or visit our USM Careers Page and submit the following: * Cover Letter * Resume/Curriculum Vitae * Finalist candidates will be asked to provide a list of the names and contact information for references. For full consideration please submit all required materials by November 30, 2025. We are not able to consider applicants who require Visa sponsorship support. Appropriate background screening will be conducted for the successful candidate. Clery Act: The Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act, or Clery Act, mandates that all Title IV institutions, such as the University, prepare, publish, and distribute an Annual Security Report (ASR), and provide notice of the availability of the ASR to all prospective employees. This report consists of two basic parts: disclosure of the University's crime statistics for the past three calendar years; and disclosures regarding the University's current campus security policies. View the University's Annual Security Report (PDF). If you wish to have a paper copy of the ASR or need to have a copy of the ASR in an accessible format, the University will provide such a copy upon request. Please contact our Public Safety Office at ************. EEO Statement: The University of Maine System (the System) is an equal opportunity institution committed to fostering a nondiscriminatory environment and complying with all applicable nondiscrimination laws. Consistent with State and Federal law, the System does not discriminate on the basis of race, color, religion, sex, sexual orientation, transgender status, gender, gender identity or expression, ethnicity, national origin, citizenship status, familial status, ancestry, age, disability (physical or mental), genetic information, pregnancy, or veteran or military status in any aspect of its education, programs and activities, and employment. The System provides reasonable accommodations to qualified individuals with disabilities upon request. If you believe you have experienced discrimination or harassment, you are encouraged to contact the System Office of Equal Opportunity and Title IX Services at 5713 Chadbourne Hall, Room 412, Orono, ME 04469-5713, by calling ************, or via TTY at 711 (Maine Relay System). For more information about Title IX or to file a complaint, please contact the UMS Title IX Coordinator at ************************

Are you looking to build your career in environmental fieldwork and permitting with a company that values collaboration, professional growth, and work-life balance? Join Haley Ward, a 100% employee-owned, multidisciplinary firm named one of the Best Places to Work in Maine and one of the Best Firms to Work For in the country! AND, as an added benefit, we will offer you a $2,500 signing bonus. About Haley Ward At Haley Ward, our 300+ employee-owners provide environmental, engineering, and architectural services across the Northeast. We believe in teamwork, mentoring, and professional development, and we take pride in delivering high-quality, practical solutions for our clients. What We Offer $2,500 Signing Bonus Employee Stock Ownership Plan (ESOP) you ll be an owner! Competitive salary and benefits package, including health, dental, and vision insurance 401(k) with company match and Roth option Paid time off and 11 holidays Company-paid life and disability insurance Flexible Spending Accounts (FSA), Health Savings Accounts (HSA), and Health Reimbursement Arrangement (HRA) options Culture that values mentorship, flexibility, and volunteerism What You ll Do We are seeking a motivated Natural Resources Scientist to join our Environmental Team. This position will support senior permitting specialists and project managers with field investigations, data collection, and environmental documentation for permitting and compliance projects. Typical Responsibilities Conduct wetland delineations, vernal pool surveys, and wildlife and habitat assessments. Assist with soil evaluations, vegetation inventories, and hydrology observations. Collect and organize field data using GPS and mobile data collection tools. Prepare field forms, maps, and technical figures to support environmental reports and permit applications. Support preparation of Maine Department of Environmental Protection (MDEP), Maine Land Use Planning Commission (LUPC), Natural Resources Protection Act (NRPA), and U.S. Army Corps of Engineers (USACE) permit applications. Collaborate with multidisciplinary teams on environmental and infrastructure projects. Maintain accurate field records and contribute to project documentation. Note: Approximately 50% of work is conducted in the field, varying with project requirements, with the balance of time in an office setting. What You ll Bring Bachelor s degree in Environmental Science, Ecology, Natural Resources, Biology, or related field. 5+ years of field experience in wetlands, wildlife, or environmental science. Familiarity with state and federal environmental permitting preferred. Strong field identification skills for vegetation, soils, and hydrology indicators. Proficiency with GPS data collection and Microsoft Office; GIS or AutoCAD skills a plus. Excellent written and verbal communication. Ability to work independently outdoors and as part of a team. Valid driver s license and satisfactory driving record. Location: Saco, ME reliable commute or relocation required Haley Ward is proud to be an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, age, national origin, disability, or veteran status.

Are you looking to build your career in environmental fieldwork and permitting with a company that values collaboration, professional growth, and work-life balance? Join Haley Ward, a 100% employee-owned, multidisciplinary firm named one of the Best Places to Work in Maine and one of the Best Firms to Work For in the country! AND, as an added benefit, we will offer you a $2,500 signing bonus. About Haley Ward At Haley Ward, our 300+ employee-owners provide environmental, engineering, and architectural services across the Northeast. We believe in teamwork, mentoring, and professional development, and we take pride in delivering high-quality, practical solutions for our clients. What We Offer * $2,500 Signing Bonus * Employee Stock Ownership Plan (ESOP) youll be an owner! * Competitive salary and benefits package, including health, dental, and vision insurance * 401(k) with company match and Roth option * Paid time off and 11 holidays * Company-paid life and disability insurance * Flexible Spending Accounts (FSA), Health Savings Accounts (HSA), and Health Reimbursement Arrangement (HRA) options * Culture that values mentorship, flexibility, and volunteerism What Youll Do We are seeking a motivated Natural Resources Scientist to join our Environmental Team. This position will support senior permitting specialists and project managers with field investigations, data collection, and environmental documentation for permitting and compliance projects. Typical Responsibilities * Conduct wetland delineations, vernal pool surveys, and wildlife and habitat assessments. * Assist with soil evaluations, vegetation inventories, and hydrology observations. * Collect and organize field data using GPS and mobile data collection tools. * Prepare field forms, maps, and technical figures to support environmental reports and permit applications. * Support preparation of Maine Department of Environmental Protection (MDEP), Maine Land Use Planning Commission (LUPC), Natural Resources Protection Act (NRPA), and U.S. Army Corps of Engineers (USACE) permit applications. * Collaborate with multidisciplinary teams on environmental and infrastructure projects. * Maintain accurate field records and contribute to project documentation. Note: Approximately 50% of work is conducted in the field, varying with project requirements, with the balance of time in an office setting. What Youll Bring * Bachelors degree in Environmental Science, Ecology, Natural Resources, Biology, or related field. * 5+ years of field experience in wetlands, wildlife, or environmental science. * Familiarity with state and federal environmental permitting preferred. * Strong field identification skills for vegetation, soils, and hydrology indicators. * Proficiency with GPS data collection and Microsoft Office; GIS or AutoCAD skills a plus. * Excellent written and verbal communication. * Ability to work independently outdoors and as part of a team. * Valid drivers license and satisfactory driving record. Location: Saco, ME reliable commute or relocation required Haley Ward is proud to be an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, age, national origin, disability, or veteran status.

Trueline's client is seeking a Vision System R&D Engineer to join their team in Biddeford. This role will focus on developing next generation automated inspection systems from concept through integration leveraging software, machine learning, and hardware in a fast moving manufacturing R&D environment. It's an excellent opportunity to bridge advanced vision/ML work with real industrial impact. What You'll Do as the Vision System R&D Engineer: Lead the design and development of custom automated vision systems: hardware selection, image acquisition, processing, and user interface. Select, train, validate and deploy machine/deep learning models for inspection tasks: defect detection, measurement, classification. Collaborate with engineering, technicians, and customers to integrate these vision systems into production and legacy automation. Contribute to the broader automation agenda by designing and programming machine control logic (PLCs, HMIs, robots) tied to vision or non vision systems. Produce and maintain clear technical documentation for prototypes, software architecture and vision system manuals. Manage R&D project timelines and deliverables, ensuring performance targets are met or exceeded. Configure and troubleshoot machine networking systems (Ethernet based industrial networks) in support of integration. Vision System R&D Engineer Requirements: Bachelor of Science in Computer Science, Engineering or related field (or equivalent experience). Strong software development skills: Python, C++ and/or C#. Demonstrated experience diagnosing/troubleshooting complex electro mechanical systems. Experience with machine learning frameworks (e.g., TensorFlow, PyTorch) and open source computer vision libraries. A minimum of 1+ year of professional experience deploying or supporting deep learning models (preferred). Strong analytical and problem solving skills, with the ability to thrive when dealing with undefined challenges. Excellent communication and teamwork abilities; comfortable working in a fast paced, collaborative environment. Willingness to travel for system deployment and customer support. Nice to Haves as the Vision System R&D Engineer: Experience deploying applications to edge devices (embedded vision/ML). Direct experience with industrial automation systems, robotics, PLCs or HMI design. Hands on familiarity with industrial networking protocols (e.g., EtherNet/IP, OPC UA). Prior involvement in manufacturing R&D or production automation environments. Truline Offers: A role at the frontier of industrial vision + machine learning application-real impact in manufacturing. Collaborative, engineering driven culture with opportunity for innovation and autonomy. A competitive salary and benefits package (please insert specifics if available: bonus, equity, travel, training). Exposure across software, hardware, controls, and production systems-broadening your skill set and career growth. Opportunity for travel and customer facing work, enabling a blend of development and deployment. Trueline and its clients are unabashed equal opportunity employers committed to a diverse workforce. We welcome smart and ambitious applicants and recruit, refer, hire, place, and promote without regard to race, color, gender, religion, national origin, ancestry, citizenship, disability, age, sexual orientation, or any other characteristic protected by federal or state law.

April - August 16 weeks Reporting to the Compliance Specialist Responsibilities: Assist with monitoring of upstream and downstream fish passages at Brookfield owned hydroelectric dams on rivers in Maine consistent with established Operation and Maintenance plans. Daily operation of fish lifts to capture, sort, and count various species of migratory and resident fish. Migratory fish species will be transported a short distance upstream in tanks hauled by truck and trailer. Monitor eelways for proper water flow, remove debris, change batteries for water systems, etc. Perform quality control checks to ensure that all data collected are accurate and complete. Assist with fish passage studies. This position will often require working longer than 8 hours per day. This position will require working weekends and holidays. Required Skills: Must be highly motivated and have the ability to work both independently and cooperatively with others. Must be able to learn identify a variety of migratory and resident fish species. Ability to keep data organized and error free. Must have good time management skills. Must be able to identify safety and environmental hazards, and then prepare and follow job safety plans appropriate for all work. Must make safety the highest priority in performing all work activities. Pre-employment drug testing required. Valid driver's license required. Pay: $18/hr

The Prospect Research Associate supports the Institutional Advancement team by conducting research on individual, corporate, and foundation prospects; assisting with data management and integrity; and preparing reports and profiles to inform fundraising activities. This role works under the direction of the Vice President of Institutional Advancement, collaborating with fundraisers, university leadership, Career Readiness, and academic deans to ensure accurate and timely information is available for donor engagement, portfolio management, principal and major gift support, and institutional partnership tracking. About the University of New England UNE is Maine's largest private university, with two beautiful coastal campuses in Maine, a one-of-a-kind study-abroad campus in Tangier, Morocco, and an array of flexible online offerings. In an uncommonly welcoming and supportive community, we offer hands-on learning, empowering students to positively impact a world full of challenges. We are the state's top provider of health professionals and home to Maine's only medical and dental colleges, a variety of other interprofessionally aligned health care programs, and nationally recognized programs in the marine sciences, the natural and social sciences, business, the humanities, and the arts. Benefits Overview * Multiple health and dental plan options, plus vision coverage. * Up to 8% retirement plan match. * Generous leave time, including vacation, sick, and personal time, and 12+ holidays per year. * Educational benefits: * UNE tuition waiver for employees, spouses, and domestic partners. * UNE tuition waiver for dependents of employees with 1 year of full-time service. * 50% tuition reduction if less than 1 year of full-time service. For more information about our outstanding benefits, please visit: UNE Benefits Overview. Responsibilities * Conduct research on individual, corporate, and foundation prospects using established tools and resources. * Prepare profiles, briefings, and reports for fundraisers and university leadership as directed. * Assist with maintaining and updating prospect records in the fundraising CRM. * Support the Vice President of Institutional Advancement at Board of Trustees Trusteeship Committee meetings by preparing meeting collateral and taking minutes. * Assist the Vice President of Institutional Advancement and the University President in their work with principal gift prospects by entering actions into the fundraising CRM, identifying new prospects, and supporting related research and administrative tasks. * Serve as the point person for collecting and tracking data on corporate partners, collaborating with Career Readiness and academic deans to support institutional relationship management and reporting. * Support Major Gift Officers (MGOs) by conducting prospect research, assisting with moves management tracking, and helping maintain and update donor portfolios in the fundraising CRM. * Follow established procedures for prospect management and data privacy. * Ensure accuracy and integrity of prospect data in the fundraising CRM through regular review and updates. * Respond to ad hoc research requests from advancement staff in a timely and professional manner. * Stay current with best practices in prospect research and data management through ongoing professional development. * Collaborate with team members to support donor-related initiatives and events. * Perform other duties as assigned by supervisor. Qualifications * Bachelor's degree with at least three years of prospect research or library science experience or a combination of education and experience from which comparable knowledge and skills are acquired. * Strong information literary skills, including knowledge of industry-standard search techniques and software, and ability to navigate resources on the web (such social media and business websites). * Understanding of prospect development and management concepts. * Experience with fundraising CRMs (preferably The Raiser's EdgeNXT, ResearchPoint, Target Analytics). * Experience with MS Office (Word, Excel, PowerPoint, OneNote). * Ability to work independently and proactively on concurrent projects and collaboratively with others. * Strong planning, communication, time management and organizational skills. * Previous experience in advancement/development preferred. * General understanding of fundraising terminology and practices. * General understanding of higher education organizational structure and administrative operations. * Ability to deal effectively with a wide variety of University personnel, students, and/or outside individuals/organizations. * Adherence to the American Prospect Research Association (APRA's) Code of Ethics and the Family Educational Rights and Privacy Act (FERPA), which includes sensitivity to confidential information. * Previous UNE experience desirable. EEO Statement Summary Consistent with federal and state law and University policy, the University of New England is committed to the fundamental concept of equal opportunity for all of the members of the University community. The University prohibits, and will not tolerate, discrimination in employment, the provision of academic services or in any other area of University life based on race, color, sex, physical or mental disability, religion, age, ancestry, national origin, sexual orientation, gender identity and/or expression, ethnicity, genetic information, HIV status, or status as a veteran. Prohibited bias factors should not motivate decisions regarding students, employees, applicants for admission, applicants for employment, contractors, volunteers or participants in and/or users of institutional programs, services, and activities. COVID Vaccination Statement (PLEASE NOTE) Employees in clinical settings must meet the State of Maine's immunization requirements for clinical activity. Additional Note This position is not eligible for H-1B visa sponsorship.

**About ETS:** ETS is a global education and talent solutions organization enabling lifelong learners worldwide to be future-ready. For more than 75 years, we've been advancing the science of measurement to build benchmarks for fair and valid skill assessment across cultures and borders. Our worldwide impact extends through our renowned assessments including TOEFL , TOEIC , GRE and Praxis tests, serving millions of learners in more than 200 countries and territories. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere. With offices and partners across Asia, Europe, the Middle East, Africa, and the Americas, we deliver nearly 50 million tests annually. Join us in our journey of measuring progress to power human progress worldwide. **About the role** ETS is seeking a dynamic and strategic Manager of Research Proposal Development to lead the end-to-end proposal process for federal and non-federal funding opportunities. This role is central to advancing ETS's mission by securing resources that fuel innovation across the ETS Research Institute and enterprise-wide initiatives. You'll manage a high-volume pipeline of proposals, guide researchers through complex funding landscapes, and ensure every submission meets the highest standards of quality, compliance, and impact. **What you'll do** Strategic leadership + Serve as a trusted advisor to researchers, guiding engagement with program officers and navigating regulatory requirements-especially with NSF, IES, and other key agencies and foundations. + Interpret funding structures and review cultures to align proposals with agency priorities and long-term trends. + Foster collaboration across ETS and with external partners to support proposal and budget development. + Contribute to the evolution of Strategic Research Alliances' strategy and stay informed on emerging trends and best practices. Proposal development & pipeline management + Identify and share relevant funding opportunities, encouraging timely and strategic proposal submissions. + Provide insights into funding cycles and program structures to align ETS initiatives with external opportunities. + Maintain proposal calendars and assign writers based on expertise and capacity. + Manage a pipeline of 40-60 proposals annually using Salesforce and grants management tools. + Support proposal drafting, including boilerplate content, staffing charts, budget justifications, and organizational materials. + Repurpose technical documentation for future opportunities when appropriate. Quality control & compliance + Review and edit proposals for clarity, consistency, and alignment with funder requirements. + Ensure compliance with federal, state, and institutional guidelines, including FAR and agency-specific standards. + Proactively identify and resolve compliance issues, keeping leadership informed of risks and solutions. Monitoring & reporting + Track proposal outcomes and lead post-submission reviews to drive continuous improvement. + Provide regular status updates and maintain RFP distribution lists. Budget & grant management Draft proposal budgets and narratives aligned with ETS best practices. + Implement process improvements, including external proposal platforms. + Advise leadership on budgetary risks and collaborate with finance teams to monitor project expenses. **What success looks like** + Seamless management of a multimillion-dollar portfolio of research grants. + Formation of high-performing proposal teams. + Proposals meet ETS's editorial and technical standards and are recognized as "best in class." + Grants are implemented effectively and aligned with funder priorities. + ETS intellectual property is protected and aligned with mission-driven goals. + Funders are informed and satisfied with grant progress and outcomes. **Why this role matters** This is a high-impact, high-visibility position. You'll work with confidential materials, lead strategic initiatives, and represent ETS to government agencies and private foundations. Your leadership ensures ETS secures the funding needed to advance research that powers human progress. **Reporting structure** This role reports to the Associate Vice President of Strategic Research Alliances and works closely with the Strategic Research Alliances team, ETS General Counsel, and Finance. \#LI-NK1 + Position requires a Bachelor's degree and 5+ years of directly relevant experience. + Much of the work of the Manager, Research Proposal Development is self-directed. The position reports to the Associate Vice President for Strategic Research Alliances, and by extension to the Senior Vice President, Global Research. + Requires strong writing, interpersonal, and organizational skills, as well as the ability to work effectively as part of a team. + Requires the ability to exercise a significant amount of judgement, technical expertise, professionalism, and experience. + Must be knowledgeable of the policies and procedures of federal funding agencies, private foundations and corporations and other funding bodies. + Must have some knowledge of the electronic proposal submission and project management systems. + Must be able to communicate effectively with ETS researchers and the representatives of federal funding agencies, private foundations and corporations and other funding bodies. + Requires not only operational knowledge but also a scholarly understanding of the evolving funding landscape-including agency missions, program call structures, and peer-review practices-to anticipate shifts in priorities and guide ETS researchers accordingly. + Stakeholders include senior management, departmental professional and support staff and other ETS researchers, external clients, external boards, councils and committees, government organizations and other external agencies. **ETS is mission driven and action oriented** + We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning. + We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders. In support of this ETS offers multiple Business Resource Groups (BRG) for you to learn and advance your career growth! + As a not-for-profit organization we will encourage you to lean in to your passion for volunteering. At ETS you may qualify for up to an additional 8 hours of PTO for volunteer work on causes that are important to you! **ETS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. We believe in creating a work environment where all individuals are treated with respect and dignity.**

Join Our Discovery Team as a Discovery Associate Scientist Are you the kind of scientist who can't stop asking “why” and “what if”? Do you get excited about trying new techniques, optimizing protocols, and uncovering data that can push a project in a fresh direction? Do you learn from failures in the lab? If so, this Discovery Associate Scientist role may be the perfect next step in your career. We seek a team member driven to impact patient lives through precision quality controls who thrive in a culture of respect, open communication, and innovation where every voice matters. About the Role As a Discovery Associate Scientist, you will be at the bench every day, supporting early-stage molecular biology and molecular diagnostics projects. You will work side-by-side with Discovery Scientists, running experiments, testing new ideas, and helping turn early concepts into real technologies. This is a hands-on role for someone who loves the lab and wants to grow by learning new methods, taking initiative, and contributing ideas. What We're Looking For B.S. in biology, molecular biology, biochemistry, chemistry, or a related field with experience in Molecular Biology research. Hands-on experience with core molecular biology techniques (pipetting, reagent prep, amplification, electrophoresis, and nucleic acid extraction) from coursework and research lab experience, internships, or prior work. Innate curiosity, coupled with the drive and initiative needed to satisfy it. A team-oriented attitude, strong communication skills, and enthusiasm for learning from and collaborating with experienced scientists. Strong attention to detail, careful documentation habits, and the ability to follow SOPs while also helping refine them. Comfortable using basic software tools (e.g., Excel or equivalent) for data handling and simple calculations. What You'll Do Perform a wide range of molecular biology techniques (e.g., buffer and reagent prep, nucleic acid extraction, plasmid prep, in vitro transcription, PCR/qPCR/dPCR, and related techniques) to support feasibility and exploratory projects. Run carefully designed experiments under the direction of Discovery Scientists, record your work in detail, and help organize, interpret, present data so the team can quickly decide on next steps. Learn and adopt new technologies and protocols as the Discovery group evaluates innovative tools and methods. Contribute to daily lab operations, including reagent prep, routine laboratory cleaning, dishes, and chores, inventory management, and basic equipment checks, keeping the Discovery lab running smoothly. Why You'll Love Working Here You will learn rapidly by working closely with senior Discovery Scientists on cutting-edge molecular projects. You will be encouraged to ask questions, propose new ideas, and develop new capabilities. You will see how early-stage discovery work evolves into the development of useful products and technologies that impact molecular diagnostics and patient care. You will join a collaborative, energetic team that values curiosity, initiative, and scientific rigor. If you are a hands-on scientist who wants to grow, experiment, and help shape new molecular solutions from the ground up, we want to hear from you. Apply now and bring your curiosity to the Discovery lab. Benefits We Offer: • Medical insurance • Dental insurance • 401(k) • Profit Sharing Plan • Vacation • Holidays • Sick leave Get to know the MMQCI team! ********************************************************************* Maine Molecular Quality Controls, Inc. (MMQCI) designs, develops, manufactures, and markets unique quality control products used by hospital laboratories to monitor the accuracy of tests for inherited disease, pharmacogenetics, oncology, and infectious diseases. MMQCI has developed technologies to stabilize DNA and RNA for use as quality controls and continues to pursue the discovery of novel techniques useful for the development of new quality control products. MMQCI is conveniently located in beautiful southern coastal Maine, minutes from the Maine Turnpike, Portland International Jetport, and less than 2 hours from Boston. Close by are fabulous Portland restaurants, sandy beaches, and a plentiful supply of Maine lobsters! Many terrific outdoor activities are easily accessible including hiking, biking, kayaking, fishing, skiing and snowshoeing. We're in a state-of-the-art facility, located in Saco, right next to the Eastern Trail. Come join us!

IDEXX is looking for an experienced Principal R&D Engineer, Diagnostic Consumables to lead the development of high-volume, single-use consumables for our veterinary diagnostics platforms. In this role, you'll work at the intersection of engineering, life sciences, and manufacturing-collaborating with assay scientists, instrument teams, and external partners to bring innovative, cost-effective products to market. From early material selection to physics-based modeling and USDA-compliant commercialization, your impact will be felt across the entire product lifecycle. What you'll do: Own the technical vision for diagnostic consumables, guiding concept development from material selection through commercialization. Drive advanced modeling and simulation (ANSYS, COMSOL) to establish design principles across fluidic, thermal, and mechanical domains. Shape cross-functional strategy by partnering with assay scientists, instrument engineers, and external vendors to deliver integrated, scalable solutions. Lead design reviews and risk assessments ensuring robust validation strategies and regulatory compliance under USDA standards. Mentor and develop junior engineers, fostering technical excellence and building organizational capability in diagnostic system engineering. Influence long-term roadmaps, contributing to portfolio planning and innovation pipelines that expand IDEXX's diagnostic capabilities. Champion manufacturability and cost-effectiveness, ensuring designs translate seamlessly into high-volume, regulated production environments. Contribute to technical roadmaps and mentor junior team members What you need to succeed: Ph.D. or Master's in Mechanical Engineering, Biomedical Engineering, Materials Science, or related field 8+ years of experience in diagnostic consumables or medical device development Strong proficiency in analytical modeling; SolidWorks experience is a plus Proven success in high-volume, regulated manufacturing environments Excellent communication, leadership, and cross-functional collaboration skills Experience designing and integrating microfluidic systems Familiarity with high-volume web-based manufacturing technologies Track record of developing high-volume assay consumables or diagnostic products What you can expect from us: Salary range starting at $160,000 based on experience Opportunity for annual cash bonus Health / Dental / Vision Benefits Day-One 5% matching 401k Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more If you're looking for a role that'll challenge you, offer a variety of work and learning, while helping an amazing industry, we'd love to hear from you! Why IDEXX: We're proud of the work we do because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. About the job location: If you're thinking about relocating for this role, here are a few things to know about living in Maine (often called “Vacationland”). The Westbrook, ME area provides great access to active downtown areas and the outdoors, with the coast and numerous mountains and hiking trails nearby. You'll also find a number of large companies like ours in the area, creating a vibrant work culture. You can learn more on the Portland tourism website: ************************************************************** IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. While we appreciate our staffing partners, we are unable to accept unsolicited agency resumes. #LI-CAG