Senior scientist jobs in Portland, ME - 22 jobs

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza is currently seeking an experienced MSAT Senior Scientist to join their team in Portsmouth, NH. POSITION: MSAT Senior Scientist JOB LOCATION: 101 International Dr. Portsmouth, NH 03801 [and various unanticipated locations throughout the U.S.; may work from home] MSAT Senior Scientist needed by Lonza Biologics Inc. in Portsmouth, NH [and various unanticipated locations throughout the U.S.; may work from home] to perform all functions associated with process transfer and process support including developing process understanding, performing gap analysis/FMEA, generating process models, authoring/reviewing Process Descriptions and Batch Records, authoring/reviewing planned deviations and change controls, performing process monitoring (manufacturing data summary and analysis and data presentation), authoring campaign summary reports, and performing activities for lot release (assess deviations and process changes). Recommend improvements for MSAT practices and procedures. Provide guidance on process transfer and support activities to junior members of the team. Assess all major deviations including those that impact product quality as well as post lot release deviations that may impact multiple products. Identify potential Root causes using a systematic approach. Apply knowledge in use/application of variety of problem-solving tools including Fishbone, Kepner-Tregoe, etc. Identify potential solutions and lead multidisciplinary teams in developing and implementing solutions. Perform, understand, and interpret all types of complex data analysis including multiple linear regression analysis, ANOVA, and multivariate analysis and identify applications where appropriate. Authors and reviews process descriptions, definitive formulations, batch records, raw material listings, change controls independently and authors/reviews/modifies the corresponding templates. Identify and create new documents that would aid in process transfer or support activities. Identify process changes and assess change controls for impact of process/equipment or procedural changes that can affect both process performance and product quality. Support documentation preparation for regulatory purposes. Represent MSAT on project teams and interfaces with customer technical and quality representatives. Represent MSAT on internal teams including Deviation and Run Daily Management System meetings. Participate in Customer and Regulatory Audits. Interact with site leadership on matters concerning several functional areas, divisions, and/or customers. Follow all training and policy guidelines established for the facility as well as all cGMP requirements. Ensure employee training profile is up to date at all times by regular monitoring of training lists including Compliance Wire and SAP Learning Portal and complete all training in a timely fashion. Perform other duties as assigned. Work on computer skills allowing interface with critical software. Work on Teams, Word, Excel, Outlook, PowerPoint, Planview, DMS document management system, Statistica, Trackwise, Simca, Global Data Mart, Pi DataLink software, Pi Vision software, Syncade, SAP, Delta V, Power BI, Orchestrate scheduling systems, and various cloud based data storage systems including SharePoint. Work on aseptic technique and mammalian cell culture. Demonstrate knowledge of cell culture bioreactors with sufficient acumen to perform troubleshooting on active cultures during processing. Understand and interpret statistical models including multivariate analysis presented through Excel, Statistica, Power BI, and similar software. Demonstrate proficiency with Statistica, Power BI, Simca, and Pi Vision to remotely monitor processing and prepare technical presentations for customers. Perform product impact assessments of deviations within a process by requiring investigation to identify potential impacts and data to be reviewed to determine impact to process. MINIMUM REQUIREMENTS: Requires a Bachelor degree, or foreign equivalent degree, in Biological Sciences, Biomedical Engineering, Chemical Engineering, or Biotechnology and Bioinformatics and 9 years of progressive, post-baccalaureate experience in the job offered, or 9 years of progressive, post-baccalaureate experience in a related occupation working on computer skills allowing interface with critical software; working on Teams, Word, Excel, Outlook, PowerPoint, Planview, DMS document management system, Statistica, Trackwise, Simca, Global Data Mart, Pi DataLink software, Pi Vision software, Syncade, SAP, Delta V, Power BI, Orchestrate scheduling systems, or any other equivalent data analysis and monitoring tools and software (Spotfire or JMP), as well as quality management programs (CDOCS or Veeva Vault); utilizing various cloud based data storage systems including SharePoint; working on aseptic technique and mammalian cell culture; demonstrating knowledge of cell culture bioreactors with sufficient acumen to perform troubleshooting on active cultures during processing; understanding and interpretating statistical models including multivariate analysis presented through Excel, Statistica, Power BI, and similar software; demonstrating proficiency with Statistica, Power BI, Simca, and Pi Vision to remotely monitor processing and prepare technical presentations for customers; and performing product impact assessments of deviations within a process by requiring investigation to identify potential impacts and data to be to determine impact to process. Alternatively, the employer will accept a Master degree, or foreign equivalent degree, in Biological Sciences, Biomedical Engineering, Chemical Engineering, or Biotechnology and Bioinformatics, and 5 years of experience in the job offered or 5 years of experience in a related occupation working on computer skills allowing interface with critical software; working on Teams, Word, Excel, Outlook, PowerPoint, Planview, DMS document management system, Statistica, Trackwise, Simca, Global Data Mart, Pi DataLink software, Pi Vision software, Syncade, SAP, Delta V, Power BI, Orchestrate scheduling systems, or any other equivalent data analysis and monitoring tools and software (Spotfire or JMP), as well as quality management programs (CDOCS or Veeva Vault); utilizing various cloud based data storage systems including SharePoint; working on aseptic technique and mammalian cell culture; demonstrating knowledge of cell culture bioreactors with sufficient acumen to perform troubleshooting on active cultures during processing; understanding and interpretating statistical models including multivariate analysis presented through Excel, Statistica, Power BI, and similar software; demonstrating proficiency with Statistica, Power BI, Simca, and Pi Vision to remotely monitor processing and prepare technical presentations for customers; and performing product impact assessments of deviations within a process by requiring investigation to identify potential impacts and data to be reviewed to determine impact to process. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

MaineHealth Institute for Research Management/Leadership The Center for Interdisciplinary Population & Health Research (CIPHR) is recruiting a Principal Investigator to bring their research program to the MaineHealth Institute for Research (MHIR) as a Faculty Scientist II (Associate Professor) or Faculty Scientist III (Full Professor). We are interested in a population health researcher whose focus is on social determinants/drivers of health, with preference for an investigator whose work aligns with cancer control or implementation science.

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.

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.

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!

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.

The LCMS group within the R&D Discovery and Technology Futures group is looking for a creative and energetic Senior Scientist specializing in proteomics to join the discovery team. The successful candidate will join a team of experienced scientists at the BS/MS and PhD levels to support biomarker discovery projects. We are looking for a highly motivated individual who has strong wet-bench and data analysis skills, curiosity, and is a team player. What you can expect: Integral part of a dynamic LCMS Discovery team that develops novel and robust multi-omic biomarker assays. Use cutting edge instrumentation and analysis software to dig deep into the world of proteomics, metabolomics, lipidomics and post-translational modifications across blood, urine, tissue and fecal samples. Drive experimental design for large biomarker experiments and optimize sample preparation protocols for expanding reach of discovery programs. Develop top-down workflows with immunoaffinity capture for characterization of proteins of interest. Prepares materials, performs experiments, analyzes data, and reaches conclusions. Perform troubleshooting of UPLCs and mass spectrometers. Document experiments and other lab activities. Prepare reports and summaries. Present results and conclusions. Interface with multiple cross-functional teams to support new product development and on-market products. Communicate and clearly present results to a broad audience within R&D, including IDEXX senior leadership What you need to succeed: PhD in scientific or related discipline or equivalent combination of education and experience. Background in Biochemistry or Chemistry. Demonstrated experience working with and developing protocols for a wide variety of sample types; plasma/serum proteomic experience preferred. Hands-on experience with and demonstrated understanding of Thermo Orbitrap and Bruker tims TOF mass spectrometers and UPLCs. Hands-on experience with and demonstrated understanding of proteomic software. Detail-oriented and ability to adapt quickly to changing priorities. Demonstrated ability to critically evaluate and interpret results. Excellent communication and organizational skills. Ability to work independently and collaboratively in a team environment. Ability to take initiative and be accountable. Demonstrated ability to critically evaluate techniques and results and implement improved practices. What you can expect from us: Salary range starting at $110,000 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 diseases. 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, LGBT 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. #LI-CAG

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza is currently seeking an experienced MSAT Senior Scientist to join their team in Portsmouth, NH. POSITION: MSAT Senior Scientist JOB LOCATION: 101 International Dr. Portsmouth, NH 03801 [and various unanticipated locations throughout the U.S.; may work from home] MSAT Senior Scientist needed by Lonza Biologics Inc. in Portsmouth, NH [and various unanticipated locations throughout the U.S.; may work from home] to perform all functions associated with process transfer and process support including developing process understanding, performing gap analysis/FMEA, generating process models, authoring/reviewing Process Descriptions and Batch Records, authoring/reviewing planned deviations and change controls, performing process monitoring (manufacturing data summary and analysis and data presentation), authoring campaign summary reports, and performing activities for lot release (assess deviations and process changes). Recommend improvements for MSAT practices and procedures. Provide guidance on process transfer and support activities to junior members of the team. Assess all major deviations including those that impact product quality as well as post lot release deviations that may impact multiple products. Identify potential Root causes using a systematic approach. Apply knowledge in use/application of variety of problem-solving tools including Fishbone, Kepner-Tregoe, etc. Identify potential solutions and lead multidisciplinary teams in developing and implementing solutions. Perform, understand, and interpret all types of complex data analysis including multiple linear regression analysis, ANOVA, and multivariate analysis and identify applications where appropriate. Authors and reviews process descriptions, definitive formulations, batch records, raw material listings, change controls independently and authors/reviews/modifies the corresponding templates. Identify and create new documents that would aid in process transfer or support activities. Identify process changes and assess change controls for impact of process/equipment or procedural changes that can affect both process performance and product quality. Support documentation preparation for regulatory purposes. Represent MSAT on project teams and interfaces with customer technical and quality representatives. Represent MSAT on internal teams including Deviation and Run Daily Management System meetings. Participate in Customer and Regulatory Audits. Interact with site leadership on matters concerning several functional areas, divisions, and/or customers. Follow all training and policy guidelines established for the facility as well as all cGMP requirements. Ensure employee training profile is up to date at all times by regular monitoring of training lists including Compliance Wire and SAP Learning Portal and complete all training in a timely fashion. Perform other duties as assigned. Work on computer skills allowing interface with critical software. Work on Teams, Word, Excel, Outlook, PowerPoint, Planview, DMS document management system, Statistica, Trackwise, Simca, Global Data Mart, Pi DataLink software, Pi Vision software, Syncade, SAP, Delta V, Power BI, Orchestrate scheduling systems, and various cloud based data storage systems including SharePoint. Work on aseptic technique and mammalian cell culture. Demonstrate knowledge of cell culture bioreactors with sufficient acumen to perform troubleshooting on active cultures during processing. Understand and interpret statistical models including multivariate analysis presented through Excel, Statistica, Power BI, and similar software. Demonstrate proficiency with Statistica, Power BI, Simca, and Pi Vision to remotely monitor processing and prepare technical presentations for customers. Perform product impact assessments of deviations within a process by requiring investigation to identify potential impacts and data to be reviewed to determine impact to process. MINIMUM REQUIREMENTS: Requires a Bachelor degree, or foreign equivalent degree, in Biological Sciences, Biomedical Engineering, Chemical Engineering, or Biotechnology and Bioinformatics and 9 years of progressive, post-baccalaureate experience in the job offered, or 9 years of progressive, post-baccalaureate experience in a related occupation working on computer skills allowing interface with critical software; working on Teams, Word, Excel, Outlook, PowerPoint, Planview, DMS document management system, Statistica, Trackwise, Simca, Global Data Mart, Pi DataLink software, Pi Vision software, Syncade, SAP, Delta V, Power BI, Orchestrate scheduling systems, or any other equivalent data analysis and monitoring tools and software (Spotfire or JMP), as well as quality management programs (CDOCS or Veeva Vault); utilizing various cloud based data storage systems including SharePoint; working on aseptic technique and mammalian cell culture; demonstrating knowledge of cell culture bioreactors with sufficient acumen to perform troubleshooting on active cultures during processing; understanding and interpretating statistical models including multivariate analysis presented through Excel, Statistica, Power BI, and similar software; demonstrating proficiency with Statistica, Power BI, Simca, and Pi Vision to remotely monitor processing and prepare technical presentations for customers; and performing product impact assessments of deviations within a process by requiring investigation to identify potential impacts and data to be to determine impact to process. Alternatively, the employer will accept a Master degree, or foreign equivalent degree, in Biological Sciences, Biomedical Engineering, Chemical Engineering, or Biotechnology and Bioinformatics, and 5 years of experience in the job offered or 5 years of experience in a related occupation working on computer skills allowing interface with critical software; working on Teams, Word, Excel, Outlook, PowerPoint, Planview, DMS document management system, Statistica, Trackwise, Simca, Global Data Mart, Pi DataLink software, Pi Vision software, Syncade, SAP, Delta V, Power BI, Orchestrate scheduling systems, or any other equivalent data analysis and monitoring tools and software (Spotfire or JMP), as well as quality management programs (CDOCS or Veeva Vault); utilizing various cloud based data storage systems including SharePoint; working on aseptic technique and mammalian cell culture; demonstrating knowledge of cell culture bioreactors with sufficient acumen to perform troubleshooting on active cultures during processing; understanding and interpretating statistical models including multivariate analysis presented through Excel, Statistica, Power BI, and similar software; demonstrating proficiency with Statistica, Power BI, Simca, and Pi Vision to remotely monitor processing and prepare technical presentations for customers; and performing product impact assessments of deviations within a process by requiring investigation to identify potential impacts and data to be reviewed to determine impact to process. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. This position is responsible for being the primary technical Upstream MSAT support person for manufacturing processes. This person has in-depth experience with manufacturing processes and/or technical transfer. The individual is an Upstream MSAT subject matter expert for key aspects of the role, and it is expected that questions on tasks or issues will be raised by this individual when clarification or greater technical expertise is required. What you will get * An agile career and dynamic working culture * An inclusive and ethical workplace * 401(k) matching plan * Competitive compensation programs that reward high performance * Comprehensive medical, dental, and vision insurance Access to our full list of global benefits: ************************************** What you will do * Perform all functions associated with upstream process transfer and/or process support. Recommend improvements for MSAT practices and procedures. * May provide guidance on process transfer and support activities to junior members of the team. * Deviations / Problem Solving / Data Analysis: Assess deviations that may impact multiple products. Identifies potential Root causes using a systematic approach. * Able to identify potential solutions and lead multidisciplinary teams in developing and implementing solutions. Performs and is able to understand and interpret all types of complex data analysis. * Documentation and Change assessments: Authors and reviews process documents. Able to identify and create new documents that would aid in process transfer or support activities. Identifies process changes and assess change controls for impact of process / equipment or procedural changes that can affect both process performance and product quality. * Represent Upstream MSAT: Represents Upstream MSAT on project teams and interfaces with customer technical and quality representatives. Represents MSAT on internal teams. * Participates in Customer and Regulatory Audits. Regularly interacts with site leadership on matters concerning several functional areas, divisions and/or customers. What we are looking for * Bachelor's degree in Biotechnology, Biological Sciences, or Chemical Engineering * 6+ years of biotech experience (or equivalent with advanced degrees) * Experience in commercial manufacturing and GMP regulations * Strong communication and technical writing skills * Proficiency in data analysis and problem-solving * Knowledge of cell culture and process development * Willingness to provide 24/7 on-call support during manufacturing About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values-Collaboration, Accountability, Excellence, Passion, and Integrity-reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Job Description 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.

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

The LCMS group within the R&D Discovery and Technology Futures group is looking for a creative and energetic Senior Scientist specializing in proteomics to join the discovery team. The successful candidate will join a team of experienced scientists at the BS/MS and PhD levels to support biomarker discovery projects. We are looking for a highly motivated individual who has strong wet-bench and data analysis skills, curiosity, and is a team player. What you can expect: * Integral part of a dynamic LCMS Discovery team that develops novel and robust multi-omic biomarker assays. * Use cutting edge instrumentation and analysis software to dig deep into the world of proteomics, metabolomics, lipidomics and post-translational modifications across blood, urine, tissue and fecal samples. * Drive experimental design for large biomarker experiments and optimize sample preparation protocols for expanding reach of discovery programs. * Develop top-down workflows with immunoaffinity capture for characterization of proteins of interest. * Prepares materials, performs experiments, analyzes data, and reaches conclusions. * Perform troubleshooting of UPLCs and mass spectrometers. * Document experiments and other lab activities. Prepare reports and summaries. Present results and conclusions. * Interface with multiple cross-functional teams to support new product development and on-market products. * Communicate and clearly present results to a broad audience within R&D, including IDEXX senior leadership What you need to succeed: * PhD in scientific or related discipline or equivalent combination of education and experience. * Background in Biochemistry or Chemistry. * Demonstrated experience working with and developing protocols for a wide variety of sample types; plasma/serum proteomic experience preferred. * Hands-on experience with and demonstrated understanding of Thermo Orbitrap and Bruker tims TOF mass spectrometers and UPLCs. * Hands-on experience with and demonstrated understanding of proteomic software. * Detail-oriented and ability to adapt quickly to changing priorities. * Demonstrated ability to critically evaluate and interpret results. * Excellent communication and organizational skills. * Ability to work independently and collaboratively in a team environment. * Ability to take initiative and be accountable. * Demonstrated ability to critically evaluate techniques and results and implement improved practices. What you can expect from us: * Salary range starting at $110,000 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 diseases. 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, LGBT 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. #LI-CAG

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.

The MSAT Scientist II is responsible for being the primary technical support lead during technology transfer activities and/or process support lead for manufacturing processes. The supervisor/manager provides direction and oversight, as this level of Process Scientist is expected to have a good grasp of the requirements of the role. The individual is a subject matter expert for several aspects of the role and it is expected that questions on tasks or issues will be raised by this individual when clarification or greater technical expertise is required. What you will get: An agile career and dynamic working culture An inclusive and ethical workplace Competitive salary and performance-based bonuses 401(k) matching plan Competitive compensation programs that reward high performance Comprehensive medical, dental, and vision insurance Access to our full list of global benefits: ************************************** What you will do: Represent Manufacturing Science and Technology (MSAT) on project teams as technical subject matter expert (SME) and interface with customer technical and quality representatives. Author, review and owns process related documentation example process description and batch records. Author/review change controls including managing the implementation of the change as the assigned change agent. Monitor and reports on process performance manufacturing data analysis and delivery of data in the form of live presentations. Perform or is able to understand all types of complex data analysis, such as interpreting process trends and data in the context of prior runs. Supports documentation preparation for regulatory purposes. Practice safety awareness at all times and considers impact of actions prior to executing activities. What we are looking for: Minimum of Bachelor of Science degree required, preferred in Biotechnology area, Biological Sciences, or Chemical Engineering. Typically requires 3+ years of experience (2+ years with Masters, 0+ years with PhD) in process support role, process development, and/or process scale up and manufacturing Arrange of experience with biotech, process development, process scale up, tech transfer or manufacturing. Experience with cell biology, cell culture, scale up and mass transfer, bioreactor operation, disc. stack centrifugation, and statistical data analysis Strong knowledge of aseptic technique and mammalian cell culture. Strong communication skills. Able to clearly express ideas and point of view both verbally and in writing. Has good interpersonal skills. Shows commitment and dedication and strives to be ahead of schedule. Ability to share 24/7 on-call support while process is being manufactured. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

IDEXX is growing rapidly, and our New Product Development Team is seeking to hire an Associate Scientist in the Assay Design & Development Team. In this role, you will perform a variety of scientific activities to support design, development, characterization of new products and reagent processes. You will join a scientifically diverse team including staff with expertise in biochemistry, analytical chemistry, molecular biology, protein expression and purification. You will design, execute, and analyze laboratory experiments to accelerate our rich pipeline of new products and technologies. We invite applicants with a range of relevant educational and work experience. What You'll Do: Independently perform multi-variable experiments. Assist with designing experiments and communicate findings. Analyze data generated and troubleshoot as needed. Perform Maintain electronic lab notebook and databases, prepare reports, and make regular presentations to summarize results. As an integral member of our functional group, this individual will collaborate closely with other team members within R&D. Strong technical aptitude for lab work, documentation, and a problem-solving mindset. What You Need to Succeed: Bachelors in Biochemistry, Chemistry, Biotechnology or related fields (3-5 years of relevant experience in industry or academic lab) Aptitude for detail-oriented work and following SOPs Aptitude for learning new techniques Ability to work independently or with limited direct supervision Fast learner with creative problem-solving ability Ability to present and communicate data at team meetings What you can expect from us: Salary range starting at $65,000 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, our team members help pet owners worldwide keep their companion animals healthy and happy, ensure safe drinking water for billions, and help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a collaborative global workforce. Our culture is one that embraces challenges and encourages learning and discovery. At IDEXX, you'll be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Knowing our work has a meaningful impact on the health and well-being of pets and people is what motivates us every day. If meaningful work and a sense of purpose are at the top of your list, you'll find it here. 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 MSAT Scientist II is responsible for being the primary technical support lead during technology transfer activities and/or process support lead for manufacturing processes. The supervisor/manager provides direction and oversight, as this level of Process Scientist is expected to have a good grasp of the requirements of the role. The individual is a subject matter expert for several aspects of the role and it is expected that questions on tasks or issues will be raised by this individual when clarification or greater technical expertise is required. What you will get: * An agile career and dynamic working culture * An inclusive and ethical workplace * Competitive salary and performance-based bonuses * 401(k) matching plan * Competitive compensation programs that reward high performance * Comprehensive medical, dental, and vision insurance Access to our full list of global benefits: ************************************** What you will do: * Represent Manufacturing Science and Technology (MSAT) on project teams as technical subject matter expert (SME) and interface with customer technical and quality representatives. * Author, review and owns process related documentation example process description and batch records. * Author/review change controls including managing the implementation of the change as the assigned change agent. * Monitor and reports on process performance manufacturing data analysis and delivery of data in the form of live presentations. * Perform or is able to understand all types of complex data analysis, such as interpreting process trends and data in the context of prior runs. * Supports documentation preparation for regulatory purposes. * Practice safety awareness at all times and considers impact of actions prior to executing activities. What we are looking for: * Minimum of Bachelor of Science degree required, preferred in Biotechnology area, Biological Sciences, or Chemical Engineering. Typically requires 3+ years of experience (2+ years with Masters, 0+ years with PhD) in process support role, process development, and/or process scale up and manufacturing * Arrange of experience with biotech, process development, process scale up, tech transfer or manufacturing. * Experience with cell biology, cell culture, scale up and mass transfer, bioreactor operation, disc. * stack centrifugation, and statistical data analysis * Strong knowledge of aseptic technique and mammalian cell culture. * Strong communication skills. Able to clearly express ideas and point of view both verbally and in writing. Has good interpersonal skills. Shows commitment and dedication and strives to be ahead of schedule. * Ability to share 24/7 on-call support while process is being manufactured. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Job Description 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.

As an Associate Scientist I in Technical Manufacturing, you will be involved in the production of nanoparticle bioconjugations that are components of high quality veterinary diagnostic products. Your work will be performed by utilizing different chemistries to manipulate and prepare material to be coated on nanoparticles. Your focus of responsibility will be on the preparation of solutions and reagents by following standard protocols at the laboratory bench, as well as a BL2 suite, to support the production build plan. You will have the opportunity to cross train across multiple processes and participate on a technically focused team as an approach to support lab work and solve problems. You will communicate and present to colleagues. You will operate under 5S and Lean Manufacturing principles and ISO standards. You can make a difference by producing innovative products that keep people and animals healthy. Exceeding customer expectations is one of our guiding principles at IDEXX. Our credibility as a company relies on our ability to deliver quality products to our customers on time and with no disruption to their business. IDEXX's Worldwide Operations Team works to meet this challenge each day with a global network of distribution hubs and a focus on efficiency, regulatory compliance, and continuous improvement. PRIMARY DUTIES AND RESPONSIBILITIES: Produce coated microparticles and other rare reagents. Order and maintain equipment and work area. Use strong documentation skills to ensure records are filled out according to standard operating procedures. Accurately report data and labor to the inventory control system. Adhere to appropriate procedures and regulatory requirements. Operate within an ISO 9001:2008 / 14001:2004 Quality Management System. Partner with manufacturing staff and production or product support groups to recommend, investigate, and/or implement modification of existing reagents and processes to improve quality and production efficiency. Have opportunities to participate in continuous improvement initiatives. REQUIRED SKILLS AND ABILITIES: Bachelors degree or equivalent combination of education and experience required. Specific technical skills related to the applicable scientific specialty. Laboratory bench and instrumentation skills. Analytical and problem solving skills. Strong communication skills, both verbal and written. Ability to work independently and cooperatively as part of a team. Organizational skills and ability to plan work. Takes initiative and is accountable (shows ownership); focuses on task at hand; detail oriented. Adaptable. Ability to work well under pressure and handle the stress of deadlines. What you can expect from us: An annual salary target of $59,000K - $62,000 based on experience Opportunity for annual cash bonus Opportunity for performance based annual merit increase Health / Dental / Vision Benefits Day - One 5% matching 401k Generous PTO benefits Additional benefits including but not limited to pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more! Why IDEXX? We're proud of the work we do, because our work matters. Every role at IDEXX contributes to enhancing the health and wellbeing of pets, people, and livestock. With over 10,000 global team members, customers in over 175 countries, and a fast-growing industry - we're always looking for motivated and inspiring people to join us. We offer competitive compensation, incentives, and benefits. You'll be part of a double-digit growth company in a quickly growing market and we are leading the way forward with innovative products, services, and a strong focus on our customers. 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. #LI-JH1

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