Chemist jobs in Bend, OR - 104 jobs

Element has an opening for a Chemist III position at our extractables and leachables (E&L) testing Center of Excellence in Bend, OR. The Chemist III position will work in a cGMP-regulated environment under the direction of the GC Lead or other senior staff member in laboratory and office settings. The position will work with a team completing E&L project work using internal methods, protocols and SOPs according to customer specific requirements. The position requires working in a collaborative manner with other team members to accomplish organizational goals, providing ideas to improve efficiency and actively contributing to positive co-worker/customer relationships through efficient interaction on current projects. The Chemist III will also contribute to team continuous improvement initiatives. In this position, there are many opportunities for developing strong analytical skills in GC-MS and for industry advancement. Element Bend is known for focus, expertise, and scientific contributions in the field of E&L testing for the biopharmaceutical, pharmaceutical and medical device industries. We are a fast-paced and quick-thinking scientific organization that excels in customer service. At the same time, we foster a casual, flexible, and fun supportive team environment. Pay Range: $78k-$92k Responsibilities Member of GC-MS team utilizing advanced analytical instrumentation to perform E&L sample and data analysis. Effectively perform project tasks under direction of GC Lead and Chromatography Manager. Create, revise or review controlled procedures and participate in the maintenance and continuous improvement of our Quality System. Promote growth and development within the GC Team and greater Element Bend organization. Depending on experience, may assist with protocol and report writing and reviewing Skills / Qualifications Bachelor's Degree in Chemistry or related field is required. Minimum 4 years experience in a laboratory setting, cGMP experience preferred. Prior experience in GC-MS required. #LI-TK1 Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world's most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) “If you need an accommodation filling out an application, or applying to a job, please email ***********************”

Element has an opening for a Chemist III position at our extractables and leachables (E&L) testing Center of Excellence in Bend, OR. The Chemist III position will work in a cGMP-regulated environment under the direction of the GC Lead or other senior staff member in laboratory and office settings. The position will work with a team completing E&L project work using internal methods, protocols and SOPs according to customer specific requirements. The position requires working in a collaborative manner with other team members to accomplish organizational goals, providing ideas to improve efficiency and actively contributing to positive co-worker/customer relationships through efficient interaction on current projects. The Chemist III will also contribute to team continuous improvement initiatives. In this position, there are many opportunities for developing strong analytical skills in GC-MS and for industry advancement. Element Bend is known for focus, expertise, and scientific contributions in the field of E&L testing for the biopharmaceutical, pharmaceutical and medical device industries. We are a fast-paced and quick-thinking scientific organization that excels in customer service. At the same time, we foster a casual, flexible, and fun supportive team environment. Pay Range: $78k-$92k Responsibilities * Member of GC-MS team utilizing advanced analytical instrumentation to perform E&L sample and data analysis. * Effectively perform project tasks under direction of GC Lead and Chromatography Manager. * Create, revise or review controlled procedures and participate in the maintenance and continuous improvement of our Quality System. * Promote growth and development within the GC Team and greater Element Bend organization. * Depending on experience, may assist with protocol and report writing and reviewing Skills / Qualifications * Bachelor's Degree in Chemistry or related field is required. * Minimum 4 years experience in a laboratory setting, cGMP experience preferred. * Prior experience in GC-MS required. #LI-TK1 Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) "If you need an accommodation filling out an application, or applying to a job, please email ***********************"

Element has an opening for a Chemist III position at our extractables and leachables (E&L) testing Center of Excellence in Bend, OR. The Chemist III position will work in a cGMP-regulated environment under the direction of the GC Lead or other senior staff member in laboratory and office settings. The position will work with a team completing E&L project work using internal methods, protocols and SOPs according to customer specific requirements. The position requires working in a collaborative manner with other team members to accomplish organizational goals, providing ideas to improve efficiency and actively contributing to positive co-worker/customer relationships through efficient interaction on current projects. The Chemist III will also contribute to team continuous improvement initiatives. In this position, there are many opportunities for developing strong analytical skills in GC-MS and for industry advancement. Element Bend is known for focus, expertise, and scientific contributions in the field of E&L testing for the biopharmaceutical, pharmaceutical and medical device industries. We are a fast-paced and quick-thinking scientific organization that excels in customer service. At the same time, we foster a casual, flexible, and fun supportive team environment. Pay Range: $78k-$92k Responsibilities Member of GC-MS team utilizing advanced analytical instrumentation to perform E&L sample and data analysis. Effectively perform project tasks under direction of GC Lead and Chromatography Manager. Create, revise or review controlled procedures and participate in the maintenance and continuous improvement of our Quality System. Promote growth and development within the GC Team and greater Element Bend organization. Depending on experience, may assist with protocol and report writing and reviewing Skills / Qualifications Bachelor's Degree in Chemistry or related field is required. Minimum 4 years experience in a laboratory setting, cGMP experience preferred. Prior experience in GC-MS required. #LI-TK1 Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to ‘Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world's most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) “If you need an accommodation filling out an application, or applying to a job, please email ***********************”

OMIC USA Inc. is seeking motivated and skilled Chemist 2s (Analytical Chemists) to join our expanding laboratory teams. This posting covers several open positions across three of our main analytical departments: Inorganic, Gas Chromatography, and Liquid Chromatography. Applicants will be reviewed for all Chemist 2 roles, and final placement will be based on each candidate's technical background, experience, and best departmental fit. Whether your strengths are in trace element analysis, pesticide residue testing, or general instrumental quantitation, we invite you to apply and become part of a rewarding, collaborative analytical laboratory environment. OMIC USA, Inc. is an International Analytical Testing Laboratory and is committed to global food health and safety through the analytical testing services we offer to our clients. MISSION OF THE ROLE: Chemist 2 performs an essential role in the Residue Chemistry and Inorganic Laboratories by providing analytical services and results accurately, efficiently, and in a timely manner to clients through (1) analyzing samples by GC, LC, or ICP instrumentation using conventional, MS, MSMS, and other analytical detection techniques, (2) proposing improvements, (3) stabilizing analytical processes, and (4) contributing to innovation to achieve the Company's mission and objectives. RESPONSIBILITIES: Other duties may be assigned. Performs sample analysis as per documented methods and Standard Operating Procedures (SOPs). This includes but is not limited to: Operating analytical instrumentation, chromatographic and other, such as a GC, LC, or ICP that is equipped with conventional, MS, and MSMS detection. Utilizing multiple vendor acquisition and quantitative analysis software packages to evaluate, interpret, and report test results, including QA/QC data. Vendors could include, Agilent, SCIEX, Waters, CETAC, LECO, and others. Entering data into the LIMS for the tests performed and is responsible for the results. Independently performing analysis for simple and complex test methods for routine and non-routine samples and matrix types. Issues with complex analyses are discussed with and potential solutions proposed to the Group Leader. Depending on skill level and training, test responsibility may include more complex or challenging analyses, advanced data interpretation, and independent decision making with little supervision or consultation needed. Scheduling activities to provide accurate and timely service to support business requirements. Ensuring that samples are extracted and analyzed in accordance with registered and in-house validated methods. Ensuring that reference materials and working standards are maintained and documented according to relevant regulated documents and SOPs. Compiling and maintaining Internal Quality Control (IQC) data for analytes and tests assigned and performing periodic assessments of positive fortification extraction efficiency/recovery trends. Consults with Group Leader to determine cases where QC or analytical data do not meet acceptable criteria based on established procedures and suggests course(s) of action. Remaining informed of hazards associated with chemicals, equipment, and their use in a laboratory setting. Works in a safe manner, using appropriate safeguards and personal protective equipment, to prevent injury to self and co-workers. Reports all accidents or unsafe working conditions to the safety committee or management. Performs responsibilities and duties of Chemist 1 (Extraction Chemist); this may include extractions, as needed, assigned, and directed by the Group Leader. Troubleshoots issues with analytical procedures and coordinates with Chemist 3 (Senior Chemist) or Group Leader on resolutions. Troubleshoots and performs routine and preventative maintenance, verification, and calibration of chromatographic and other analytical instrumentation possessing conventional, MS, and MSMS detectors in accordance with documented procedures. Escalates to Chemist 3 or Group Leader if issues cannot be resolved. Develops and updates controlled documents and SOPs, ensuring that current versions are up to date and are available to other Chemists. As directed by Group Leader, may perform secondary review on data packages submitted by other Chemists for quality, accuracy, consistency, and completeness ensuring proper procedures are followed for ISO17025 compliance. Participates in special analytical projects, as directed by Group Leader. Develops improved and/or new methodology using published sources and finalizes supporting data which is verified by Chemist 3 or Group Leader. Assists Chemist 3 and Group Leader with new equipment recommendations, implementation, instrument verification, and method optimization. Assists Chemist 3 in R&D projects. Contributes to the continuous improvement of laboratory operations by proposing and implementing changes for improving extraction and analysis method quality and performance, reducing cost, and increasing efficiency. Obtains and retains an up-to-date knowledge of analytical techniques, equipment, and technologies. Participates in internal and external training as assigned. Participates in external professional and technical meetings for obtaining latest market insights, new technologies, and building networks as assigned and directed by Group Leader or Management. Trains and mentors Chemists within department and is a resource to other Chemists as needed or directed. Supports and provides assignments for Chemist 1 as directed by Group Leader. SUPERVISORY RESPONSIBILITIES: This role has no direct supervisory responsibilities. SKILLS AND EXPERIENCE: EDUCATION Bachelor's degree (B.S. or B.A.) in Chemistry or related science from a four-year college or university or equivalent combination of education and experience. CERTIFICATES, LICENSES, REGISTRATIONS None SKILLS & EXPERIENCE At least 1 year of successful experience working independently with and proven competency in daily operation, maintenance, and troubleshooting of Gas or Liquid Chromatographic or Inductively Coupled Plasma Spectrometric instrumentation utilizing conventional, MS, and MSMS detectors (GC, GCMS, GCMSMS, HPLC, LCMSMS, ICPMS, etc.). Experience routinely analyzing and producing data packages for small and larger data sets. Thorough understanding and demonstrable working knowledge of analytical instrumentation and data analysis software packages such as: Agilent MassHunter, Agilent OpenLAB CDS, SCIEX Analyst, SCIEX MultiQuant, SCIEX OS, Waters Acquity or equivalent. Successful experience collaborating with different or dissimilar business departments. Familiar with the commercial fast-paced laboratory business environment. Experience with and participation in improvement and learning initiatives. Ability to handle multiple priorities and deadlines. Able to gather and communicate technical information clearly, both orally and through writing, with respect to analytical and problem-solving skills. High Emotional Intelligence. Good cultural awareness and ability to communicate with people of diverse backgrounds. Experienced user of MS Office and Adobe Acrobat. PERFORMANCE FACTORS Quality of Work Communication Adaptability Teamwork Time Management Knowledge and Skills Initiative Dependability LANGUAGE SKILLS Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write Standard Operating Procedures, analytical methods, reports, business correspondences, and additional laboratory documentation. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, and quadratic equations. Ability to apply mathematical operations to tasks such as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. SKILLS & EXPERIENCE 3 or more years of experience with GCMS, GCMSMS, LCMS, LCMSMS, and/or ICPMS instrumentation; routinely creating and running analytical sequences, performing primary data analysis and review, as well as compiling and submitting finalized data package deliverables in a commercial high-throughput laboratory environment. 3 or more years of experience in analytical method development with an emphasis on optimization of MS and MSMS instrumentation and data acquisition parameters. 3 or more years of experience working with one or more of the following software platforms: Agilent MassHunter, Agilent OpenLAB CDS, SCIEX Analyst, SCIEX MultiQuant, SCIEX OS, and Waters Acquity. 3 or more years of experience routinely analyzing, which includes screening, quantitation, and reporting, of large-scale pesticide panels (> 100 compounds per sample) or moderate metal and minerals panels. Proficient hands-on experience and expertise in employing the QuEChERS extraction technique, along with processing and analyzing the resulting data. Proficient hands-on experience employing microwave acid digestions for metals and minerals testing. At least 1 year of experience with sample processing and extraction method development, particularly for pesticides, process contaminants, and/or metals and minerals in food matrices. Experience with high resolution accurate mass spectrometry (HRMS), Time of Flight (TOF), and/or other cutting-edge analytical technologies. Knowledge of other relevant laboratory technologies. Successful experience in mentoring and training others, specifically in extraction, analytical, and instrument methodology. Experience interacting with representatives of relevant external agencies and organizations. Experience working in international businesses. OTHERS: TRAINING REQUIREMENTS OJT in understanding company operating systems, including the maintenance and operation of laboratory extraction and analytical equipment, and passing the Initial Demonstration of Capability (IDOC) for existing SOPs or other laboratory procedures. PHYSICAL DEMANDS While performing the duties of this job, the employee is regularly required to be able to hear and understand instructions and handle items involving repetitive hand and wrist movement. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. WORK ENVIRONMENT Works in a laboratory using laboratory extraction and analytical equipment. Employee may have exposure to hazardous chemicals and solvents. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Chemist 2 Department: Nutrition JD-036 Reports To: Inorganic/Nutrition Group Leader FLSA Status: Non-Exempt OMIC USA, Inc. is an international Analytical Laboratory and is committed to global food health and safety through the analytical testing services we offer to our clients. MISSION OF THE ROLE: The Chemist II performs an essential role by providing accurate, efficient, and timely nutritional analytical services to clients. This position focuses on the analysis of nutrients in food, dietary supplements, and related matrices using validated analytical methods and advanced instrumentation. The role supports continuous improvement, method optimization, and innovation aligned with the Company's mission and quality objectives. RESPONSIBILITIES: Other duties may be assigned. Perform nutritional analyses for minerals, trace elements, vitamins, proximates, amino acids, and fatty acids in accordance with SOPs and validated methods (AOAC, USP, ISO, FDA, and in-house). Prepare, extract, digest, and analyze samples, including complex matrices, ensuring data integrity and accuracy. Operate, maintain, and troubleshoot analytical instruments, including GC-FID and associated sample preparation equipment; escalate unresolved technical issues to senior staff and propose solutions. Enter analytical data into the Laboratory Information Management System (LIMS) and assume responsibility for reported results. Prepare, maintain, and document reference materials, calibration standards, and quality control materials. Compile and trend Internal Quality Control (IQC) data; assess method performance and recommend corrective actions for out-of-specification (OOS) or out-of-trend (OOT) results. Review analytical data packages for completeness, accuracy, and procedural compliance. Develop, revise, and maintain controlled documents and SOPs, ensuring ISO 17025 compliance. Support method development, validation, transfer, and optimization projects. Assist with evaluation, implementation, and qualification of new equipment and analytical methods. Contribute to continuous improvement initiatives to enhance data quality, method performance, efficiency, and turnaround time. Manage laboratory inventory for consumables, reagents, and supplies, ensuring adequate stock levels and timely replenishment. Schedule and prioritize analytical work to meet client and business timelines. Train and mentor Chemist I staff and provide technical support to the laboratory team. Maintain knowledge of current analytical techniques, technologies, and regulatory expectations through ongoing training. Independently perform simple and complex analyses across routine, non-routine, and complex sample matrices; escalate technical challenges and propose solutions to improve workflow and method performance SUPERVISORY RESPONSIBILITIES: This role has no direct supervisory responsibilities. SKILLS AND EXPERIENCE: EDUCATION Bachelor's degree (B.S.) in Chemistry or related science from a four-year college or university in addition to at least 3 years of directly applicable experience (Chemist I or II role); or equivalent combination of education and experience. CERTIFICATES, LICENSES, REGISTRATIONS None SKILLS & EXPERIENCE Experience in quantitative nutritional analysis and laboratory operations. Proficiency with GC-FID and other analytical instrumentation. Strong understanding of QA/QC practices and regulatory standards (AOAC, USP, ISO, FDA). Successful experience working independently and demonstrating competency using and maintaining department-specific instruments, including conventional, MS, and MS/MS detectors, with operation, maintenance, and troubleshooting. Experience routinely analyzing small and large data sets. Experience in analytical and extraction method troubleshooting, development, and optimization. Successful experience mentoring and training others, specifically in extraction, analytical, and instrument methodology. Successful experience collaborating with different business departments. Familiarity with the laboratory business environment. Involvement in improvement and learning initiatives. Ability to handle multiple priorities and deadlines effectively. Ability to gather and communicate technical information clearly, both orally and in writing, with respect to analytical and problem-solving skills. High emotional intelligence and cultural awareness, with strong communication skills for working with people from diverse backgrounds. Experienced user of MS Office and Adobe Acrobat. PERFORMANCE FACTORS Page Break Quality of Work Communication Adaptability Teamwork Time Management Knowledge and Skills Initiative Dependability Page Break LANGUAGE SKILLS Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write Standard Operating Procedures, analytical methods, reports, business correspondences, and additional laboratory documentation. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, and quadratic equations. Ability to apply mathematical operations to tasks such as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. SKILLS & EXPERIENCE Experience with high resolution accurate mass spectrometry (HRMS) and/or cutting-edge new technologies Experience with analytical method development Experience with sample processing and extraction method development, particularly for pesticides and process contaminants in food matrices Knowledge of other relevant technologies and markets Well connected or having experience interacting with representatives of relevant external agencies and organizations Experience working in international businesses OTHERS: TRAINING REQUIREMENTS OJT in understanding company operating systems, including the maintenance and operation of laboratory extraction and analytical equipment, and passing the Initial Demonstration of Capability (IDOC) for existing SOPs or other laboratory procedures. PHYSICAL DEMANDS While performing the duties of this job, the employee is regularly required to be able to hear and understand instructions and handle items involving repetitive hand and wrist movement. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. WORK ENVIRONMENT Works in a laboratory using laboratory extraction and analytical equipment. Employee may have exposure to hazardous chemicals and solvents. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

We are looking to fill a **Scientist 3 -** **Third Shift** **Analytical Chemist Pilot Plant** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ** . This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **Description** The Scientist III **Third Shift** - Analytical Chemist Pilot Plant operates and maintains a myriad of analytical instrumentation and other duties as assigned by the client. **Responsibilities** + Experience in routine and real-time testing for high-performance liquid chromatography (HPLC), gas chromatography (GC), ultraviolet (UV) spectroscopy, infrared (IR) spectroscopy, titrations, Karl Fischer (KF) testing, and other wet chemistry methods + Experience in HPLC and GC is required with an interest in expanding the knowledge and background in method development and optimization, validation, data analysis, and sample preparation techniques + Routine use of modern analytical techniques such as HPLC, GC, KF, ultraviolet-visible spectroscopy (UV-VIS), and IR spectroscopy + Comfortable working in a cGMP environment; knowledgeable in various GMP analytical activities, such as documentation procedures, abiding by relevant department SOPs and generation and second scientist review of GMP data + Experience with automated liquid handling systems (Tecan) for high throughput testing + Experience with a myriad of software platforms used in the compilation, processing, and reporting of data, such as Waters Empower, Relational Laboratory Information Management System (RLIMS), Lab X, etc. **Qualifications** + BA/BS (3-5 yrs.) of relevant experience in n chemistry or a related discipline testing lab + MS (1-2 yrs.) of relevant experience in chemistry or a related discipline testing lab **Desired Skills and Experience** + Effective organizational, multi-tasking, and oral/written communications skills + Ability to work under pressure and provide reliable results with quick turnarounds + Consistently deliver high quality and fully compliant results and interact with a diverse customer base daily + Proficient in written and spoken English, is required **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Hexion is entering a bold new chapter, and we're looking for talented scientists, engineers, and innovators to be part of it. With our newly announced expansion of the research and development headquarters in Dublin, Ohio, we're creating high-impact roles that will shape the future of sustainable materials, advanced chemistry, and AI-driven manufacturing. (Learn more about our expansion here: Hexion Selects Columbus Region for Global R&D Center) At Hexion, you won't just work on products-you'll build real-world solutions that power industries and make a global impact. Hexion is a place where curiosity is rewarded, innovation is constant, and the possibilities are endless. If you're looking for a career that challenges you, inspires you, and puts you at the forefront of what's next, we encourage you to apply today and join us in building the future. Anything is possible when you imagine everything. Position Overview Based in our Dublin, OH R&D Laboratory, we are seeking a highly motivated and innovative Research Chemist with a Ph.D. in Chemistry, Polymer Science, or a related field to join our R&D team. The ideal candidate will be responsible for recommending and leading research programs targeted at new molecules, formulations, novel polymers, and advanced materials. This role will contribute directly to our strategic innovation initiatives and product development pipeline. Why Join US * Opportunity to work on cutting-edge research with real-world impact. * Collaborative and intellectually stimulating work environment. * Competitive salary and benefits package. * Career development opportunities through training and innovation programs. Job Responsibilities * Ensure compliance with all safety, regulatory, and environmental guidelines. * Stay current with advancements in polymer science and related disciplines through patent searching, literature review, conferences, and academic collaboration. * Utilize open innovation to identify new research programs, as well as accelerate the progress of existing programs. * Design and execute experiments to develop and characterize new molecules, polymers, formulations, or chemical processes. * Conduct fundamental and applied research in areas such as polymerization methods, structure-property relationships, and materials performance. * Analyze data using advanced techniques (e.g., NMR, FTIR, GPC, DSC, TGA, rheology) and interpret results to guide research direction. * Collaborate with cross-functional teams including product development, engineering, and manufacturing to translate lab-scale research into commercial applications. * Maintain comprehensive documentation of research activities, including lab notebooks, technical reports, and scientific publications. Minimum Qualifications * Ph.D. in Chemistry, Polymer Science, Materials Science, or a related field. * 4+ years of experience working in a laboratory environment. * Background in at least one of the following: small molecule or polymer synthesis, formulation of adhesives, additives or formulations targeted at oil and gas applications, mining applications, or agricultural applications. * Hands-on experience with analytical instrumentation and techniques relevant to polymer/material characterization. * Demonstrated ability to identify, design and lead independent research projects. * Excellent problem-solving skills, with a creative and inquisitive mindset. * Strong written and verbal communication skills, including the ability to prepare technical documents and present findings clearly. * Experience in industrial or applied research (preferred but not required). * Strong computer skills with experience in Excel, Word, PowerPoint and statistical programs such as JMP and/or MiniTab. * Must be highly organized and self-directed with good time management skills. Preferred Qualifications * Familiarity with thermosets, thermoplastics, bio-based polymers, adhesives, chemical products for oil and gas applications, additives for mining applications, or formulations for agricultural applications. * Experience with scale-up and process development. * Knowledge of regulatory requirements (e.g., REACH, TSCA) for chemical products. Other We are an Equal Opportunity, Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to gender, pregnancy, race, national origin, religion, age, sexual orientation, gender identity, veteran or military status, status as a qualified individual with a disability or any other characteristic protected by law. To be considered for this position candidates are required to submit an application for employment through our career site and, be at least 18 years of age. Any offer of employment will be conditioned upon successful completion of a drug test and background investigation, as well as authorization for the Company to conduct additional periodic background checks as required by the Chemical Facility Anti-Terrorism Standards (CFATS) or regulations adopted by the department of Homeland Security or other regulatory agencies. A prior criminal record is not an automatic bar to employment, and the Company will conduct an individualized assessment and reassessment, consistent with applicable law, prior to making any final employment decision.

Analytical Chemist, Springfield, OR Arclin USA is currently looking to fill a Analytical Chemist Job at our Springfield, OR location. Reporting into the Analytical Services Manager, this position is responsible for providing pertinent, timely and reliable analytical chemistry support that allows us to quickly deliver on emergent technologies and be the undisputed technology leader in the markets we serve. This position is also responsible for supporting Technical Sales, Manufacturing and Quality in instances requiring a deeper chemical understanding of a product or by-product. Analytical Chemist Job Requirements: Assist in the development of novel analytical methods to better support R&T's objectives Write analytical reports and maintain proper written records of results and activities Operate and maintain chromatography, spectroscopy, thermal and mechanical analysis instrumentation. This includes, but is not limited to, routing instrument operation, tracking and validating instrument performance metrics, performing preventative and emergency instrument maintenance, and ensuring necessary stocking of solvents, reagents and consumables. Communicate with product groups requesting analysis to fully understand the problem they wish to solve. Choose analytical methods and experimental designs to best meet those needs. Maintain a clean and safe lab environment in compliance with Arclin HSE policies and procedures. Ensure that all lab equipment is maintained and operating optimally Analytical Chemist Job Qualifications: Bachelors of Science (BS) in Chemistry, Materials Science, Polymer Science or related fields 3-5 years' experience within an analytical chemistry laboratory environment; MS degree will substitute for two years of experience Experience in thermal analysis, spectroscopy and chromatography Knowledge of experimental design, laboratory equipment and project planning skills. Attention to detail and accuracy. Ability to document and write technical reports. Strong logical reasoning and problem solving skills. Proficiency in the use of computer and analytical instrument software

The R&D chemist position is in HP's imaging and printing business in our Corvallis, Oregon facility. The work will be focused on development of new ink formulations through a combination of empirical design and modeling methods. Our group is responsible for the design and formulation of inkjet printing inks including the characterization of the print attributes and robustness. The project will focus on developing components that expand various ink attributes such as optical density and durability on different media. The project will also involve optimizing the new inks for drop formation and the printing process. Part of the role is to collaborate with the printer component designers to implement system level changes to balance tradeoffs in the various components. Aspects of the role include: Component development Formulation design (includes design for performance, manufacturing and chemical regulatory guidelines) Print system characterization Cross-functional/pan global team participation and leadership External supplier material co-development and manufacturing Our group is part of a chemistry center of excellence that develops inks for the different print businesses. While we work across several sites, this project will partner primarily with colleagues in our Corvallis, Oregon location. The Corvallis site includes a combination of F&D and manufacturing facilities with work ranging from MEMS fabs to large industrial printing presses. Qualifications Ph. D. in chemistry, chemical engineering, or related field Understanding of fundamental chemical mechanisms. Key areas include: Pigment and dye chemistry Polymers in solution Organic and inorganic nanoparticle suspensions Interfacial and surface chemistry Proficiency in appropriate analytical instruments and the data interpretation Wet chemistry or ink formulation experience Strong written and spoken communication skills Ability to creatively solve problems in a fast-paced product development environment Ability to work and effectively interact (remotely, as needed) with team members from other disciplines, projects, organizations, cultures, and companies Demonstrated leadership, teamwork/interpersonal, communication and technical skills Resourceful, creative, and flexible Fluency in English Desired qualifications Programming skills Familiarity with printing technology and color science Formulation experience is a plus The pay range for this role is $93,400 to $143,800 USD annually with additional opportunities for pay in the form of bonus and/or equity (applies to United States of America candidates only). Pay varies by work location, job-related knowledge, skills, and experience. Benefits: HP offers a comprehensive benefits package for this position, including: Health insurance Dental insurance Vision insurance Long term/short term disability insurance Employee assistance program Flexible spending account Life insurance Generous time off policies, including; 4-12 weeks fully paid parental leave based on tenure 11 paid holidays Additional flexible paid vacation and sick leave (US benefits overview) The compensation and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law. Job - Engineering Schedule - Full time Shift - No shift premium (United States of America) Travel - Relocation - Equal Opportunity Employer (EEO) - HP, Inc. provides equal employment opportunity to all employees and prospective employees, without regard to race, color, religion, sex, national origin, ancestry, citizenship, sexual orientation, age, disability, or status as a protected veteran, marital status, familial status, physical or mental disability, medical condition, pregnancy, genetic predisposition or carrier status, uniformed service status, political affiliation or any other characteristic protected by applicable national, federal, state, and local law(s). Please be assured that you will not be subject to any adverse treatment if you choose to disclose the information requested. This information is provided voluntarily. The information obtained will be kept in strict confidence. For more information, review HP's EEO Policy or read about your rights as an applicant under the law here: “Know Your Rights: Workplace Discrimination is Illegal"

Job Title: (PART- TIME) R&D Lab Technician Department: Research & Development Reports To: R&D Manager / Food Scientist The R&D Lab Technician supports the Research & Development team by preparing samples, executing lab trials, maintaining lab organization, and accurately documenting results. This is a hands-on role focused on supporting new product development while following food safety and quality standards. Key Responsibilities Prepare R&D samples according to formulas and test plans Accurately weigh and measure ingredients using laboratory scales Assist with lab trials, product testing, and sensory evaluations Maintain a clean, organized, and food-safe R&D lab Wash, sanitize, and store lab equipment and tools Manage ingredient inventory, labeling, and storage Record formulations, weights, observations, and results clearly Follow GMPs, food safety, and sanitation procedures Support sample preparation for internal reviews or customer presentations Qualifications Required High school diploma or equivalent 1-3 years of experience in a food, lab, or manufacturing environment preferred Strong attention to detail and ability to follow written instructions Ability to stand for extended periods and lift up to 50 pounds Preferred Degree or coursework in Food Science or a related field Experience with frozen desserts or dairy products Familiarity with GMPs or food safety programs Work Environment R&D lab and production-adjacent areas Exposure to cold environments (freezers) Requires use of appropriate PPE

Serán BioScience is looking for a scientist with laboratory experience to support manufacturing of pharmaceutical drug products within our In-Process Control group. As a scientist within the Quality Control department you will work alongside a team of scientists and operators to ensure the highest quality product by testing raw materials and production equipment within GMP manufacturing and laboratory environments. Qualified candidates will demonstrate expertise in utilizing specialized laboratory equipment, techniques, and methodologies for technical assessments and data analysis purposes. Preference will be given to those with experience in GMP environments and technical data review specific to the pharmaceutical industry. Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.Duties and Responsibilities Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies Performs routine testing using analytical equipment including but not limited to HPLC, GC, KFC, Disso, etc. Conducts appearance testing, solution preparation, raw material sampling, and pH measurement Drafts stability tables, sets-up stability studies, logs-in samples and standards Cleans lab and glassware and disposes of analytical waste appropriately Participates in process improvement and other non-routine projects Enters clean spaces with appropriate PPE to collect various samples Is familiar with introductory analytical equipment (e.g., HPLC, GC-HS, TOC, FT-IR) Is familiar with raw materials testing requirements (compendial and client testing) Conducts peer review of routine testing at the discretion of the relevant supervisor Performs technical writing and reporting including but not limited to: incident reporting, laboratory investigations, CAPAs, SOPs, trend reports, risk assessments, etc. Performs hypothesis testing or investigative work for OOS results under management and SME guidance Demonstrates cross-functional support capabilities with other QC teams Responsibilities may increase in scope to align with company initiatives All other related duties as assigned Required Skills and Abilities Hands-on lab experience in HPLC, CG-HS, TOC, FT-IR Hands-on lab experience with raw materials testing Strong verbal and written communication skills Demonstrated ability to collaborate and work in cross-functional teams Strong organizational skills and attention to detail Follows detailed written and oral instructions Strong time management skills with a proven ability to meet variable and competing deadlines Strong analytical and problem-solving skills Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs Accepts feedback from a variety of sources and constructively manages conflict Ability to prioritize tasks and to keep leadership apprised of performance to timelines Ability to function well in a high-paced and at times stressful environment Proficient with Microsoft Office Suite or related software Education and Experience Bachelor's degree in related scientific discipline 3 years of hands-on laboratory experience required, cGMP preferred Minimum of 2 years of GMP experience required to be considered for Scientist II Physical Requirements Prolonged periods of sitting or standing at a desk and working on a computer Prolonged periods of sitting or standing in laboratory environment Must be able to lift up to 25 pounds at times Adheres to predicable in-person attendance Motor skills required for basic laboratory operations Compensation correlates to skills and experience presented by selected candidate. Visit ******************************** to learn more about company culture and the community of Bend, Oregon. Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Benefits Summary:Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees' wellbeing, along with access to pet insurance. The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701

Job Title: (PART- TIME) R&D Lab Technician Department: Research & Development Reports To: R&D Manager / Food Scientist Location: Eugene, Oregon The R&D Lab Technician supports the Research & Development team by preparing samples, executing lab trials, maintaining lab organization, and accurately documenting results. This is a hands-on role focused on supporting new product development while following food safety and quality standards. Key Responsibilities Prepare R&D samples according to formulas and test plans Accurately weigh and measure ingredients using laboratory scales Assist with lab trials, product testing, and sensory evaluations Maintain a clean, organized, and food-safe R&D lab Wash, sanitize, and store lab equipment and tools Manage ingredient inventory, labeling, and storage Record formulations, weights, observations, and results clearly Follow GMPs, food safety, and sanitation procedures Support sample preparation for internal reviews or customer presentations Qualifications Required High school diploma or equivalent 1-3 years of experience in a food, lab, or manufacturing environment preferred Strong attention to detail and ability to follow written instructions Ability to stand for extended periods and lift up to 50 pounds Preferred Degree or coursework in Food Science or a related field Experience with frozen desserts or dairy products Familiarity with GMPs or food safety programs Work Environment R&D lab and production-adjacent areas Exposure to cold environments (freezers) Requires use of appropriate PPE

At Mission Driven Data, we empower transformational leaders of social services agencies by providing access to meaningful data tools and passionate support. We're looking for a detail-oriented, product-focused team member, with experience working in behavioral health or social services, to join our Product Development team in support of the Director of Product Development. This role focuses on the careful, sometimes time-consuming work that helps our products scale and stay reliable. We're seeking someone comfortable writing SQL to build and maintain the structured datasets behind our products - creating clear, consistently named tables and views that behave predictably and are easy to build on. This work matters because those datasets directly support the Power BI dashboards you'll also help build, which are designed to work well for dozens of agencies, not just one. In this role, attention to detail matters more than cleverness. We value people who enjoy following patterns, learning established standards, and producing work that holds up over time. We care deeply about quality and durability, and we expect this role to grow as it encounters new constraints and challenges. In addition, this position will frequently interface directly with clients, helping to onboard our customers into specific products built by Product Development. While Solutions Consultants handle much of our client work, some products require our team's centralization, technical skills, and administrative access to Mission Driven Data's infrastructure. In those cases, this role coordinates setup steps, tracks progress, and follows up to ensure nothing falls through the cracks. Some parts of this job are deeply satisfying; others are less glamorous but essential. This role is a good fit for someone who takes direction well, handles nuance thoughtfully, and manages their own work with a steady hand. About Your Technical Skills You don't need to be an expert in everything listed below, but you should feel comfortable with the core ideas and willing to deepen your skills as you go. * SQL You're comfortable writing and reading SQL to build and maintain structured datasets. You care about correctness, consistency, readability, and clear naming. * Working with structured data You understand relational concepts like unique IDs, relationships, and how tables fit together. You can reason about how data changes ripple through a system. * Data structure & taxonomy awareness You understand how metadata and taxonomies are used to describe and organize entities, and why consistency matters for reporting and usability. * Power BI (or similar tools) You've built dashboards or reports and care about clarity, usability, and visual quality. You're comfortable learning new standards to support many users, not just one. * Very basic comfort with Systems Administration You're comfortable following documentation and performing well-defined tasks carefully in a shared environment. * Documentation & reproducibility You can document what you build so others can understand, maintain, and reuse it. Non-Technical Skills for This Role * Behavioral Health Experience: You've worked in or alongside behavioral health or social services organizations, or you're motivated by building tools that support the people doing that work. * Attention to detail: You notice inconsistencies and care about accuracy and completeness. * Project management and follow-through: You track work, manage multiple threads, and close loops. * Comfort taking direction: You listen carefully, ask clarifying questions, and execute thoughtfully. * Nuance awareness: You handle edge cases and ambiguity without freezing or overcomplicating things. * Clear, kind communication: Especially when following up or nudging busy humans. * Self-management: You organize your work without needing close supervision. * Patience and persistence: You stay steady when progress is slow or work is repetitive. * Collaborative mindset: You work well with people across roles and technical backgrounds. This Role Might Be a Fit If… * You enjoy careful, well-structured work that holds up over time. * You like following standards and making things consistent. * You're comfortable taking direction and executing thoughtfully. * You notice details others miss and care about fixing them. * You can keep track of multiple threads without dropping balls. * You're okay being gently persistent with clients and teammates. * You value reliability, usefulness, and quality over novelty. What "Good" Looks Like After 6 Months By around six months, someone doing well in this role would typically: * Write SQL that fits our standards with minimal guidance. * Build clean, reliable datasets others can trust. * Independently produce solid Power BI dashboards. * Manage client onboarding tasks end to end without things slipping. * Complete basic system administration tasks accurately and confidently. * Stay organized and communicate clearly about progress and risks. * Catch small issues early and handle nuance thoughtfully. * Make small improvements to documentation or processes along the way. About Mission Driven Data Our vision is to be the catalyst for change in the community mental health treatment system, by kindling the curiosity and creativity of emerging leaders and creating a new vocabulary of metrics that truly measure the quality and value of community services Logistics If this sounds like an awesome opportunity that fits what you're looking for, please let us know that you're interested by sending your resume and a brief note explaining your interest in this position to *********************************, using the subject line "Product Development Analyst". If selected for the next round, we'll be in touch with next steps. Listing Type Jobs | Hybrid Categories Business Development | Consultant | Healthcare | Information Technology | Professional Services | Social Services | Technology Position Type Contract Experience Level Mid Level Employer Type Direct Employer Salary Min 40 Salary Max 65 Salary Type /hr.

Nova Analytic Labs is seeking a highly motivated and qualified scientist to join our cannabis testing laboratory startup, located in Portland, ME. The testing Nova Analytic Labs will perform is critical to the health and safety of recreational and medicinal cannabis and hemp products. Nova Analytic Labs will provide the highest quality and safety in testing to the community by combining advanced technology and innovative scientific methods. As a startup, we are particularly interested in individuals with well\-rounded capabilities and an eager appetite to grow and build a successful enterprise. The ideal candidate will possess sound scientific knowledge, management skills, and an eye for continuous improvement. Flexibility and dedication are a must. The Lab Analyst I works directly under Lab Manager and ensures all samples are received, extracted, analyzed and reported in compliance with company policies and procedures. Other duties may be assigned as necessary. Duties and Responsibilities Responsible for day to day receipt and analysis of samples Responsible for solution prep and tracking Responsible for maintaining equipment logs and maintenance Perform extractions and prepare samples for analysis on LC\/MS, GC\/MS and ICP\/MS Responsible for data entry of samples in the lab Responsible for understanding and following all necessary SOPs Produce quality, mistake\-free work in the lab Ensures resolution of errors before results are released to clients Continuously seeks out new and better ideas, driving best practices Ensure samples are received, requisitioned and extracted in a manner that is compliant with SOPs Other duties as assigned by management Requirements Bachelor degree in a science related field or one year experience in a high complexity laboratory, food testing, or environmental testing laboratory High school diploma with at least 2 years experience in a high complexity laboratory, food testing, or environmental testing laboratory Some experience in a high complexity laboratory preferred Some experience with LC\/MS, GC\/MS and ICP\/MS Benefits Health care, Employee bonus\/profit sharing "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"658476418","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Cannabis Testing"},{"field Label":"Work Experience","uitype":2,"value":"1\-3 years"},{"field Label":"Salary","uitype":1,"value":"50k\-60k annually"},{"field Label":"City","uitype":1,"value":"Portland"},{"field Label":"State\/Province","uitype":1,"value":"Maine"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"04103"}],"header Name":"Lab Analyst I","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********00217001","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":false,"job Id":"**********00944085","FontSize":"12","google IndexUrl":"https:\/\/nova\-analyticlabs.zohorecruit.com\/recruit\/ViewJob.na?digest=hy RQVBoMJAbuDRSyhPCH4wc6IBmI3C5h5aYJJV25G8I\-&embedsource=Google","location":"Portland","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"keztafeaadcb89cb34a278aa494453c4c0a8d"}

Pay range: $31.72 - $47.57 hourly, varies on experience. Sleep Center - Bend, Oregon Work Shift - Variable (Day & Night) Differentials: Relief - 15% Evening - $2.50 Night - $6.50 ST. CHARLES HEALTH SYSTEM JOB DESCRIPTION TITLE: Sleep Technologist - Night Shift REPORTS TO POSITION: Clinical Supervisor, RPSGT DEPARTMENT: St. Charles Sleep Center DATE LAST REVIEWED: July 2024 OUR VISION: Creating America's healthiest community, together OUR MISSION: In the spirit of love and compassion, better health, better care, better value OUR VALUES: Accountability, Caring and Teamwork DEPARTMENT SUMMARY: St. Charles Medical Group encompasses practices in three Central Oregon counties and numerous specialties including family care, internal medicine, obstetrics and gynecology, pediatrics, immediate/urgent care, cardiology, pulmonology, rheumatology, general surgery, cancer care, and sleep medicine. We encourage collaboration between clinical and non-clinical staff to assure we are providing our community with comprehensive and compassionate health care. Sleep Medicine provides diagnostic and therapeutic services to patients. POSITION OVERVIEW: A Sleep Technologist at St. Charles Health System works under the general supervision of the medical director or designee to provide comprehensive evaluation and treatment of sleep disorders including in center and out of center sleep testing, diagnostic and therapeutic interventions, comprehensive patient care and direct patient education. A sleep technologist is able to perform the duties defined for a sleep technician and is able to provide oversight of other sleep center staff. The sleep technologist is credentialed in sleep technology. This position does not directly manage other caregivers. ESSENTIAL FUNCTIONS AND DUTIES: Collects, analyzes, scores, and integrates patient information in order to identify and meet the patient-specific needs. Performs sleep study data acquisition for pediatric and adult PSGs according to ordering provider. Determines final testing parameters/procedures in conjunction with the ordering physician or clinical director and laboratory protocols. Reviews the patient's history and verify the medical order. Follows sleep center protocols related to the sleep study. Prepares bedroom to accommodate patient's need and comfort. When patient arrives, verifies identification, collects documents, and obtains consent for the study. Selects appropriate equipment, calibrates for testing to determine proper functioning, and adjusts if necessary. Applies electrodes and sensors according to accepted published standards. Performs routine positive airway pressure (PAP) interface fitting and desentization/acclimation. Responsible for patient care during overnight testing procedures. Educates and informs patients about sleep procedures. Performs appropriate physiological calibrations to ensure proper signals and make required adjustments. Performs basic troubleshooting to maintain data integrity. Administers supplemental low flow oxygen therapy per ordering provider or as direct by oxygen therapy protocol. Implements appropriate interventions (including actions necessary for patient safety and therapeutic intervention such as positive airway pressure, oxygen administration, etc.) Documents routine observations, including sleep stages and clinical events, changes in procedure, and other significant events in order to facilitate scoring and interpretation of polysomnographic results Monitors capnography during polysomnogram. Scores sleep/wake stages by applying professionally accepted guidelines. Scores clinical events (such as respiratory events, cardiac events, limb movements, arousals, etc.) utilizing AASM standards. Generates accurate reports by tabulating sleep/wake and clinical event data. Demonstrates the knowledge and skills necessary to recognize and provide age specific care in the treatment, assessment, and education of neonatal, pediatric, adolescent, adult, and geriatric patients. Demonstrates the knowledge and skills necessary to perform portable monitoring equipment preparation and data download. Performs patient education and instruction appropriate for out of center sleep testing. Demonstrates adherence to cleaning and disinfection procedures for portable monitoring devices. Fields patient questions on Home Sleep Apnea Testing. Participates and completes Monthly interscore reliability Exams to meet QA on Sleep Record Scoring. Recognizes and activates emergency precautions. Participates in and assists with training Sleep tech I staff and/or students from accredited sleep programs. Supports the vision, mission and values of the organization in all respects. Supports Lean principles of continuous improvement with energy and enthusiasm, functioning as a champion of change. Provides and maintains a safe environment for caregivers, patients and guests. Conducts all activities with the highest standards of professionalism and confidentiality. Complies with all applicable laws, regulations, policies and procedures, supporting the organization's corporate integrity efforts by acting in an ethical and appropriate manner, reporting known or suspected violation of applicable rules, and cooperating fully with all organizational investigations and proceedings. Delivers customer service and/or patient care in a manner that promotes goodwill, is timely, efficient and accurate. May perform additional duties of similar complexity within the organization, as required or assigned. _________________________________________________________________________________________________ EDUCATION: Required: High school diploma or GED. Preferred: Associate's degree or higher. LICENSURE/CERTIFICATION/REGISTRATION: Required: RPSGT, RST or Respiratory Therapist with SDS certification. Licensed the by the state of Oregon through the Polysomnographic Technologist Licensing Board. -Or- Respiratory Therapist, RRT credentialed. SDS credentialed required within 6 months of hire. Licensed the by the state of Oregon through the Polysomnographic Technologist Licensing Board. Current BLS certification. Preferred: Certification in Clinical Sleep Health (CCSH). EXPERIENCE: Required: N/A Preferred: Two (2) years of patient care experience as a sleep technician/technologist. PERSONAL PROTECTIVE EQUIPMENT: Must be able to wear appropriate Personal Protective Equipment (PPE) required to perform the job safely. ADDITIONAL POSITION INFORMATION: Demonstrates St. Charles Health System values of Accountability, Caring and Teamwork in every interaction. Must have excellent communication skills and ability to interact with a diverse population and professionally represent St. Charles Health System. Strong team working and collaborative skills. Ability to effectively reach consensus with a diverse population with differing needs. Ability to manage facilitation and consensus building among health care professionals and agencies and achieve expected results. Ability to work under pressure in a fast-paced environment. Ability to multi-task and work independently. Attention to detail. Excellent organizational skills, written and oral communication and customer service skills, particularly in dealing with stressful personal interactions. Strong analytical, problem solving and decision-making skills. Excellent organizational and multi-tasking skills. Performs basic math (add, subtract, multiply and divide) calculations. Read, write, speak and understand English PHYSICAL REQUIREMENTS: Category: Patient Care Level #3 Continually (75% or more): Standing and walking, keyboard operation, use of clear and audible speaking voice and the ability to hear normal speech level. Frequently (50%): Sitting, lifting, carrying, pushing, or pulling 1-25 pounds. The use and operation of a motor vehicle for Home Health and Wound Caregivers. Occasionally (25%): Bending, stooping/kneeling/crouching, climbing ladder/stepstool (varies by area), reaching overhead, lifting, carrying, pushing, or pulling 25-50 pounds, grasping/squeezing, ability to hear whispered speech level. Rarely (10%): Climbing stairs. Never (0%): Climbing ladder/stepstool (varies by area), operation of a motor vehicle. Exposure to Elemental Factors Rarely (10%): Wet/slippery area, chemical solution. Never (0%): Heat, cold, noise, dust, vibration, uneven surface. Blood-Borne Pathogen (BBP) Exposure Category Risk for Exposure to BBP . Schedule Weekly Hours: 0 Caregiver Type: Relief Shift: Variable (United States of America) Is Exempt Position? No Job Family: SLEEP TECHNICIAN Scheduled Days of the Week: Variable Shift Start & End Time:

Site: North Shore Medical Center, Inc. Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. $20,000 Sign On Bonus! 4 (10) hour days! Free Parking and excellent benefits that start on day one - no waiting period. On call is required for this position. Benefits start on day one and include: Medical, Dental, and Vision insurance * Tuition Reimbursement * Generous Paid Time Off * 50% Off MBTA passes or free parking pass * Access to childcare resources and emergency backup care * 403(b), Cash Balance Retirement Plan, and Tax-Sheltered Annuity options * Exclusive "Perks" - enjoy discounts on tickets and passes for everything from ski resorts to museums to sporting events) Minimum pay for this role is 40.95 per hour Job Summary Summary Responsible for performing specialized diagnostic and therapeutic procedures using imaging techniques such as X-rays, fluoroscopy, and ultrasound. This role works closely with physicians and other medical staff to ensure accurate and safe procedures for patients. Essential Functions Conducts various diagnostic imaging procedures, including angiography, cardiac catheterization, interventional radiology, and vascular procedures. * Prepares the patient for procedures, explains the process, and positions the patient appropriately for optimal imaging results. * Operates specialized imaging equipment to capture images of the patient's internal structures. * Ensures that equipment is functioning correctly, makes adjustments as necessary, and maintains a sterile and safe environment. * Works closely with radiologists, cardiologists, and other physicians during procedures. * Ensures patient safety during procedures by monitoring vital signs, responding to patient discomfort or emergencies, and maintaining a sterile environment. Qualifications Education High School Diploma or Equivalent required and Associate's Degree Radiologic Technology preferred Can this role accept experience in lieu of a degree? No Licenses and Credentials Radiologic Technologist [State License] - Generic - HR Only required Registered Technologist [ARRT-R] - American Registry of Radiologic Technologists (ARRT) preferred Experience Experience with imaging techniques, including X-rays, fluoroscopy, and ultrasound 0-1 year preferred Knowledge, Skills and Abilities - Strong understanding of human anatomy and physiology, particularly in relation to the cardiovascular and interventional radiology systems. - Proficiency in various imaging techniques used in special procedures, such as X-rays, fluoroscopy, and ultrasound. - Skilled in operating and maintaining specialized imaging equipment. - Understanding of radiation safety principles including radiation protection measures, safety protocols, and guidelines to minimize radiation exposure to patients and staff. - Strong patient care skills, including ability to communicate effectively, provide emotional support, and ensure patient comfort during procedures. - Skilled in critical thinking and problem-solving. Additional Job Details (if applicable) Physical RequirementsStanding Frequently (34-66%) Walking Frequently (34-66%) Sitting Occasionally (3-33%) Lifting Frequently (34-66%) 35lbs+ (w/assisted device) Carrying Frequently (34-66%) 20lbs - 35lbs Pushing Occasionally (3-33%) Pulling Occasionally (3-33%) Climbing Rarely (Less than 2%) Balancing Frequently (34-66%) Stooping Occasionally (3-33%) Kneeling Occasionally (3-33%) Crouching Occasionally (3-33%) Crawling Rarely (Less than 2%) Reaching Frequently (34-66%) Gross Manipulation (Handling) Frequently (34-66%) Fine Manipulation (Fingering) Frequently (34-66%) Feeling Constantly (67-100%) Foot Use Rarely (Less than 2%) Vision - Far Constantly (67-100%) Vision - Near Constantly (67-100%) Talking Constantly (67-100%) Hearing Constantly (67-100%) Remote Type Onsite Work Location 81 Highland Avenue Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range $29.23 - $44.48/Hourly Grade 5 At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package. EEO Statement: 3200 North Shore Medical Center, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at **************. Mass General Brigham Competency Framework At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Temp Food Production Quality Control Pay: Day Shift $23.60/hour (+ $2.50 night shift differential for hours worked between 5pm - 5am) Schedule: 3 - 4 day work weeks with set shifts 8pm - 8am Shift 4 - Thursday - Saturday every other Wednesday Night Shift Location: Mcminnville, OR GLISS General Labor & Industrial Staffing Solutions is hiring for Food Production Quality Control Technicians. In this role you are responsible for testing materials and finished products to ensure they conform to all applicable laws and company standards. Quality control technicians test products across the three stages of production (before, in-process, and final) to ensure quality levels are met. If you have QC/QA experience and looking for a temp-to hire position APPLY TODAY Responsibilities: Coach and train employees on GMP's. Enforce GMP's to maintain a quality product manufactured in a safe environment and meeting all targeted requirements. Maintain, and enforce company quality standards. Ensure plant operations staff delivers quality products within specification. Provide regular and timely feedback to production operations and Supervision as to critical process analytical measurements. Conduct routine testing and quality checks per schedule. Conduct allergen verification testing and gluten testing in accordance with certifying bodies and internal procedures. Assess product quality and accept or reject from processing. Ensure date codes are changed on containers to reflect proper identification of product being processed. The ability to work with individuals at all levels of the organization, including appropriate confrontation as needed when any individual or department is not compliant with quality expectations. Audit and analyze food contact equipment for cleanliness. Perform sanitation inspection of production workstations prior to startup, changeover or shift relief and communicate deficiencies to supervisor. Reject unsanitary production equipment. Calibrate or replace malfunctioning equipment. Properly and timely complete all shift documentation. Routine housekeeping of assigned workstation and adjacent areas. Manage any and all HOLDS from assigned shift and ensure product, material disposition is following Food Safety requirements. Perform required line checks. Examples are metal detection, weight checks, lot checks, etc. Inspect raw materials upon arrival, ensure proper paperwork accompanies the raw materials and pull raw material retains as required. Inspect packaging materials upon arrival, ensure proper paperwork accompanies the packaging material and pull packaging material retains as required. Communicate any non-conformance issues to the Quality Supervisor or Director of Quality. Ensure team members follow all appropriate SOPs, GMPs and safety requirements. Verify equipment is calibrated as required and documented accordingly. Provide proper paperwork to the operations and warehouse teams. Qualifications: Quality Control/Assurance experience in a manufacturing or food production facility 6 months+ Knowledge of HACCP with HACCP training Must work well in a team environment and have strong communication skills. Work independently, set priorities to meet deadlines, handle multiple tasks, and make decisions under pressure. Excellent analytical and problem-solving skills with heightened attention to detail Required: - Ability to commit to a 12-hour workday & standing/walking the entirety of the shift - Working overtime weekly & working weekend days - Speak, read & write fluent English as orientation is required and material available at this time is only in English - Ability to lift up to 50lbs - Resume & longevity of past jobs is important to this position BENEFITS OFFERED TO ELIGIBLE EMPLOYEES: Medical Insurance Dental Insurance Vision Insurance 401(k) retirement plan Referral bonuses HOW TO APPLY: 1. Online Application: Start the first part of your application online at WWW.GENERAL-LBR.COM 2. Call to Schedule: Once your application is complete, call us at ************ to schedule an interview. Applications are accepted by appointment only, Office Hours: Monday-Thursday, 8:00 AM-5:00 PM 3070 Lancaster Dr NE Salem, OR 97305

Join our dynamic team as a General Laborer with a focus on production for a local parts cleaning company. You will play a crucial role in processing, cleaning, and inspecting parts and assemblies from high-tech semiconductor manufacturing in a controlled cleanroom environment. **Responsibilities** + Process, clean, and inspect parts and assemblies from semiconductor manufacturing. + Disassemble, clean/refurbish, reassemble, perform final clean, and prepare parts. + Maintain highest safety and quality standards while focusing on customer needs and company values. + Practice inventory management to ensure proper stocking levels. + Receive, inspect, process, package, and transport parts and components. + Use and support maintenance of processing equipment such as media blasters, solvent benches, ultrasonic tanks, and ovens. + Utilize a combination of mechanical and chemical cleaning techniques. + Use safety equipment including hearing protection, safety glasses, face shields, chemical-resistant aprons, and gloves. + Handle potentially hazardous materials following manufacturing and safety procedures. + Work in a cleanroom environment, wearing appropriate garments and following micro-contamination protocols. + Adhere strictly to corporate, industry, and site protocols and procedures. + Ensure work area, equipment, and tools are clean and properly maintained. **Essential Skills** + Experience with production, hand tools, power tools, and measuring tools. + Ability to lift up to 25 - 50 lbs. + Familiarity with chemical handling and inspection processes. + Understanding of cleanroom protocols. **Additional Skills & Qualifications** + General labor experience. + Assembly experience. + Experience in semiconductor industry preferred. + Chemical Handling experience **Why Work Here?** Join a stable company with opportunities for growth and training in other areas. This role serves as a great entry point into semiconductor roles, offering a solid foundation for career advancement. **Work Environment** Work in a cleanroom, shop, and warehouse environment, adhering to strict safety and contamination protocols. **Job Type & Location** This is a Contract to Hire position based out of Hillsboro, OR. **Pay and Benefits** The pay range for this position is $21.00 - $23.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) **Workplace Type** This is a fully onsite position in Hillsboro,OR. **Application Deadline** This position is anticipated to close on Feb 3, 2026. **About Aerotek:** We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Title: Lab Technician II Duration: 0-12+ Months Shift: 8am -4: 30pm Monday through Friday Pay Rate: $23.00/- Hourly Responsibilities: The lab technician will be supervised by engineers and lab manager and is expected to be able to independently function in the scope provided below. •Perform lab experiments daily, document and communicate results to support customer-oriented R&D projects •Adhere to all safety procedures in conducting daily work, handling chemical and operating lab equipment •Support customer sample manufacturing in pilot scale •Assist shipping and receiving of chemicals •Responsible for lab maintenance and inventory •Exhibit flexibility and the ability to adapt to shifting priorities •Contribute ideas that improve the safety, efficiency and/or the overall effectiveness of the laboratory and team Education: Bachelor's degree Experience: At least 2 years of lab experience;preferably in an industrial or pilot plant environment Skills: •Wet chemistry skills (required) •Basic computer skills (Microsoft Office) •Good oral and written communication skills •Experience with semiconductor processing is a plus