Quality control analyst jobs in Schenectady, NY - 74 jobs

Ready to be pushed beyond what you think you're capable of? At Coinbase, our mission is to increase economic freedom in the world. It's a massive, ambitious opportunity that demands the best of us, every day, as we build the emerging onchain platform - and with it, the future global financial system. To achieve our mission, we're seeking a very specific candidate. We want someone who is passionate about our mission and who believes in the power of crypto and blockchain technology to update the financial system. We want someone who is eager to leave their mark on the world, who relishes the pressure and privilege of working with high caliber colleagues, and who actively seeks feedback to keep leveling up. We want someone who will run towards, not away from, solving the company's hardest problems. Our ******************************** is intense and isn't for everyone. But if you want to build the future alongside others who excel in their disciplines and expect the same from you, there's no better place to be. While many roles at Coinbase are remote-first, we are not remote-only. In-person participation is required throughout the year. Team and company-wide offsites are held multiple times annually to foster collaboration, connection, and alignment. Attendance is expected and fully supported. The Complaints Quality Control (CQC) team plays a critical role in ensuring our global complaints operations are efficient, compliant, and consistently deliver high-quality outcomes. As an Analyst III on the team, you'll conduct quality control (QC) reviews across Consumer Complaints, Regulatory Complaints, and Litigation Support investigations, while helping refine complaint processes and providing actionable feedback to agents. This role requires strong independence, the ability to manage multiple priorities, and a commitment to continuous improvement through open, collaborative feedback. *What you'll be doing (ie. job duties):* * Perform QC reviews of complaint cases based on the quality rubric, ensuring compliance with established guidelines. * Provide constructive feedback to agents based on QC findings to support performance improvement. Feedback will be documented in written reports, and agents may need to set up meetings to discuss and clarify scores if needed. * Assist in refining and updating the complaints review process, contributing feedback and suggestions for ongoing improvements. * Conduct root cause analysis (RCA) to identify trends and areas for process enhancements. * Collaborate with cross-functional teams to improve the efficiency and effectiveness of complaints handling. * Independently balance and prioritize multiple tasks to ensure timely and accurate completion of QC reviews. * Be receptive to feedback from all levels and foster a collaborative environment that encourages open communication and continuous improvement. * Ensure compliance with global regulatory guidelines, including MiCA and CF8, across all complaint handling. * Contribute to reporting and visualizations that highlight complaint trends and areas for process optimization. * Support the troubleshooting and resolution of escalated and complex complaint cases, ensuring alignment with company standards. *What we look for in you (ie. job requirements):* * Minimum of 3 years of relevant experience in financial services, crypto, investigations, legal, or the tech industry, with a focus on complaints handling, compliance, or regulatory matters. * Ability to work independently, manage multiple priorities, and balance tasks with minimal guidance. * Strong analytical skills with the ability to perform root cause analysis and provide actionable insights. * Comfortable providing feedback to agents and open to receiving feedback from peers and leadership. * Exceptional communication skills to collaborate with cross-functional teams and present findings effectively. * Adaptability to thrive in a fast-paced, high-growth environment and adjust priorities as needed. * Proven attention to detail, with a focus on accuracy and quality in QC reviews and reporting. *Nice to haves:* * Experience in project management, analytics, or vendor management. * Advanced degree in business, finance, or customer experience (CX). * Proficiency with tools such as Google apps, JIRA, and Salesforce Service Cloud. * Experience collaborating with external outsource business partners. Position ID: P74727 \#LI-Remote *Pay Transparency Notice*: Depending on your work location, the target annual *base *salary for this position can range as detailed below. Full time offers from Coinbase also include bonus eligibility + equity eligibility + benefits (including medical, dental, vision and 401(k)). Base salary range shown. Total compensation also includes equity and bonus eligibility and benefits: $38.01-$40.01 USD Please be advised that each candidate may submit a maximum of four applications within any 30-day period. We encourage you to carefully evaluate how your skills and interests align with Coinbase's roles before applying. Commitment to Equal Opportunity Coinbase is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law. Coinbase will also consider for employment qualified applicants with criminal histories in a manner consistent with applicable federal, state and local law. For US applicants, you may view the *********************************************** in certain locations, as required by law. Coinbase is also committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact us at accommodations*********************************** *Global Data Privacy Notice for Job Candidates and Applicants* Depending on your location, the General Data Protection Regulation (GDPR) and California Consumer Privacy Act (CCPA) may regulate the way we manage the data of job applicants. Our full notice outlining how data will be processed as part of the application procedure for applicable locations is available ********************************************************** By submitting your application, you are agreeing to our use and processing of your data as required. *AI Disclosure* For select roles, Coinbase is piloting an AI tool based on machine learning technologies to conduct initial screening interviews to qualified applicants. The tool simulates realistic interview scenarios and engages in dynamic conversation. A human recruiter will review your interview responses, provided in the form of a voice recording and/or transcript, to assess them against the qualifications and characteristics outlined in the job description. For select roles, Coinbase is also piloting an AI interview intelligence platform to transcribe and summarize interview notes, allowing our interviewers to fully focus on you as the candidate. *The above pilots are for testing purposes and Coinbase will not use AI to make decisions impacting employment*. To request a reasonable accommodation due to disability, please contact accommodations[at]coinbase.com

We are always looking forward to receiving resumes from candidates with skills and technical experience in the aerospace sector. We are very happy to receive speculative resumes if you are looking for a career change within the aerospace industry. Our flexible recruitment services will provide you with the following employment options: * Contract * Contract to Direct * Direct Our experienced consultants are experts in their field and are well placed to advise you on all aspects of aerospace recruitment opportunities, and employment trends.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Responsibilities Include: Working in a cleanroom environment by aseptically gowning and sampling raw materials Performing inspection of containers, components, and other consumables. Receiving, handling, and disposing of samples Calibrates or verifies calibration of instruments/devices before use. Accurately records test results and reports any quality anomalies Maintains laboratory supplies and performs laboratory housekeeping as assigned Ensures excellent customer service to clients Participates in required training activities Complies with all pertinent regulatory agency requirements Potential cross-training opportunity with sampling and testing of compressed gas systems and sampling and testing of compressed gas tankers This position is an indoor lab-based position working in biopharmaceutical manufacturing cleanrooms and lab spaces. Position requires aseptic gowning techniques. Position requires significant time spent in ISO 8 cleanrooms with the following restrictions: No cosmetic products or applications (such as makeup, false lashes, spray tans etc) are permitted and must be removed prior to entry Nails must be kept short, trimmed, and unadorned (no nail polish, rhinestones, etc) No jewelry may be worn, (exceptions are medical alert related and one smooth ring band that can be easily covered by a glove) Hair must be able to be neatly tied back and contained in a hairnet and all facial hair must be neatly trimmed and able to be secured in a beard cover. Qualifications The Ideal Candidate Would Possess: Is self-motivated, adaptable, team-oriented, and has a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Knowledgeable of aseptic techniques Excellent communication (oral and written) and attention to detail Desire to work in a moderately physical role that requires standing much of the time Strong computer and organizational skills Fosters a healthy, trusting environment and champions transparency and communication GMP, biopharmaceutical, or other related industry experience Familiarity with LIMS Minimum Qualifications: Bachelor's degree in chemistry or other science-related degree concentration, or equivalent directly related experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information What to Expect in the Hiring Process: 10-15 Minute Phone Interview with Region Recruiter 45-60 Minute Virtual Interview with Manager and/or Group Leader 30 Minute Virtual Meeting with Site Director Additional Details: The position is full-time, Monday through Friday, 8am-4:30pm. Candidates living within a commutable distance of Rensselaer, New York, are encouraged to apply. Excellent full-time benefits include: comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Hourly rate is 19.00-22.00 Ready to make an impact? Join a team where your scientific skills matter, and your growth is supported. If you're passionate about quality, collaboration, and continuous improvement, we want to hear from you. Apply today and take the next step in your career with Eurofins PSS! Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Responsibilities Include: Working in a cleanroom environment by aseptically gowning and sampling raw materials Performing inspection of containers, components, and other consumables. Receiving, handling, and disposing of samples Calibrates or verifies calibration of instruments/devices before use. Accurately records test results and reports any quality anomalies Maintains laboratory supplies and performs laboratory housekeeping as assigned Ensures excellent customer service to clients Participates in required training activities Complies with all pertinent regulatory agency requirements Potential cross-training opportunity with sampling and testing of compressed gas systems and sampling and testing of compressed gas tankers This position is an indoor lab-based position working in biopharmaceutical manufacturing cleanrooms and lab spaces. Position requires aseptic gowning techniques. Position requires significant time spent in ISO 8 cleanrooms with the following restrictions: No cosmetic products or applications (such as makeup, false lashes, spray tans etc) are permitted and must be removed prior to entry Nails must be kept short, trimmed, and unadorned (no nail polish, rhinestones, etc) No jewelry may be worn, (exceptions are medical alert related and one smooth ring band that can be easily covered by a glove) Hair must be able to be neatly tied back and contained in a hairnet and all facial hair must be neatly trimmed and able to be secured in a beard cover. Qualifications The Ideal Candidate Would Possess: Is self-motivated, adaptable, team-oriented, and has a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Knowledgeable of aseptic techniques Excellent communication (oral and written) and attention to detail Desire to work in a moderately physical role that requires standing much of the time Strong computer and organizational skills Fosters a healthy, trusting environment and champions transparency and communication GMP, biopharmaceutical, or other related industry experience Familiarity with LIMS Minimum Qualifications: Bachelor's degree in chemistry or other science-related degree concentration, or equivalent directly related experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information What to Expect in the Hiring Process: 10-15 Minute Phone Interview with Region Recruiter 45-60 Minute Virtual Interview with Manager and/or Group Leader 30 Minute Virtual Meeting with Site Director Additional Details: The position is full-time, Monday through Friday, 8am-4:30pm. Candidates living within a commutable distance of Rensselaer, New York, are encouraged to apply. Excellent full-time benefits include: comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Hourly rate is 19.00-22.00 Ready to make an impact? Join a team where your scientific skills matter, and your growth is supported. If you're passionate about quality, collaboration, and continuous improvement, we want to hear from you. Apply today and take the next step in your career with Eurofins PSS! Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Rensselaer, NY, USA Full-time ** **Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.** **Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.** **In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.** **In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.** **Job Description** **Responsibilities Include:** + Working in a cleanroom environment by aseptically gowning and sampling raw materials + Performing inspection of containers, components, and other consumables. + Receiving, handling, and disposing of samples + Calibrates or verifies calibration of instruments/devices before use. + Accurately records test results and reports any quality anomalies + Maintains laboratory supplies and performs laboratory housekeeping as assigned + Ensures excellent customer service to clients + Participates in required training activities + Complies with all pertinent regulatory agency requirements + Potential cross-training opportunity with sampling and testing of compressed gas systems and sampling and testing of compressed gas tankers This position is an indoor lab-based position working in biopharmaceutical manufacturing cleanrooms and lab spaces. Position requires aseptic gowning techniques. Position requires significant time spent in ISO 8 cleanrooms with the following restrictions: + No cosmetic products or applications (such as makeup, false lashes, spray tans etc) are permitted and must be removed prior to entry + Nails must be kept short, trimmed, and unadorned (no nail polish, rhinestones, etc) + No jewelry may be worn, (exceptions are medical alert related and one smooth ring band that can be easily covered by a glove) + Hair must be able to be neatly tied back and contained in a hairnet and all facial hair must be neatly trimmed and able to be secured in a beard cover. **Qualifications** **The Ideal Candidate Would Possess:** + Is self-motivated, adaptable, team-oriented, and has a positive attitude + Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies + Knowledgeable of aseptic techniques + Excellent communication (oral and written) and attention to detail + Desire to work in a moderately physical role that requires standing much of the time + Strong computer and organizational skills + Fosters a healthy, trusting environment and champions transparency and communication + GMP, biopharmaceutical, or other related industry experience + Familiarity with LIMS **Minimum Qualifications:** + Bachelor's degree in chemistry or other science-related degree concentration, or equivalent directly related experience + Authorization to work in the United States indefinitely without restriction or sponsorship **Additional Information** **What to Expect in the Hiring Process:** + 10-15 Minute Phone Interview with Region Recruiter + 45-60 Minute Virtual Interview with Manager and/or Group Leader + 30 Minute Virtual Meeting with Site Director **Additional Details:** The position is full-time, Monday through Friday, 8am-4:30pm. Candidates living within a commutable distance of Rensselaer, New York, are encouraged to apply. Excellent full-time benefits include: + comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays + **Hourly rate is 19.00-22.00** **Ready to make an impact?** Join a team where your scientific skills matter, and your growth is supported. If you're passionate about quality, collaboration, and continuous improvement, we want to hear from you. Apply today and take the next step in your career with Eurofins PSS! **Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

Within Accenture's Utilities (Energy Retail and Customer Experience) Practice, We use our deep industry expertise in digital customer engagement and operations, connected energy services and customer platforms to help retail energy and utility providers with cost effectiveness, revenue assurance/extension and customer satisfaction and loyalty. In Strategy & Consulting we work with C-suite executives, leaders and boards of the world's leading organizations, helping them reinvent every part of their enterprise to drive greater growth, enhance competitiveness, implement operational improvements, reduce cost, deliver sustainable 360° stakeholder value, and set a new performance frontier for themselves and the industry in which they operate. Our deep industry and functional expertise is supported by proprietary assets and solutions that help organizations transform faster and become more resilient. Underpinned by technology, data, analytics, AI, change management, talent and sustainability capabilities, our Strategy & Consulting services help architect and accelerate all aspects of an organization's total enterprise reinvention. Benefits of Working at Accenture: + Impactful Projects with Leading Clients: Opportunity to partner with top-tier clients in the CNR Industry on transformative projects. + Collaborative Work Culture: Join a dynamic and collaborative environment that values professional growth and development. + Competitive Compensation and Benefits: Enjoy a rewarding compensation package, including extensive benefits. Key Responsibilities: + Lead strategic consulting engagements in energy retail and customer service, focusing on digital transformation, customer experience enhancement, and operational efficiencies. + Serve as a primary client contact for senior executives, building trusted advisory relationships and ensuring alignment with client business objectives. + Develop and execute strategies to improve client business performance, drive revenue growth, and support customer-centric transformation initiatives. + Manage project teams, guiding junior members and ensuring project delivery meets quality, timeline, and budgetary expectations. + Lead business development activities by identifying new opportunities, crafting proposals, and representing Accenture's Utilities practice in sales pursuits. + Actively contribute to thought leadership, staying current on industry trends, regulatory changes, and technological advancements in the energy retail sector. + Drive team development and growth by mentoring team members and fostering a collaborative, high-performance work Note: We are open to hiring in most major cities in the US that are near to an Accenture corporate office. Here's what you need: + Minimum of 3 years of experience in the Utility Industry, Customer Service project delivery / Customer Transformation project delivery + Minimum of 2 years of functional experience with either an SAP or Oracle platform. + Expertise in Meter to Cash operations, functions, and technologies. + Expertise in major Customer Transformation and technology implementations (e.g., CIS replacements) + Bachelor's degree or equivalent work experience. + Ability to travel as needed. Bonus Points If: + You have at least 2 years of experience in an advisory or consulting role Professional Skill Requirements: + You improvise and adapt to lead clients and teams through change and ambiguity + You've gained the trust of your clients and partnered with them to: design business process, lead design thinking workshops, develop business case, deliver agile projects, develop new operating model, manage talent and change, co-create intellectual property Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below.We anticipate this job posting will be posted on 01/22/2026 and open for at least 3 days. Accenture offers a market competitive suite of benefits including medical, dental, vision, life, and long-term disability coverage, a 401(k) plan, bonus opportunities, paid holidays, and paid time off. See more information on our benefits here: U.S. Employee Benefits | Accenture (******************************************************* Role Location Annual Salary Range California $70,350 to $205,800 Cleveland $59,100 to $164,600 Colorado $63,800 to $177,800 District of Columbia $68,000 to $189,300 Illinois $59,100 to $177,800 Maryland $63,800 to $177,800 Massachusetts $63,800 to $189,300 Minnesota $63,800 to $177,800 New York $66,300 to $205,800 New Jersey $68,000 to $205,800 Washington $80,200 to $189,300 #LI-NA #LI-MP Requesting an Accommodation Accenture is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Accenture and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired. If you would like to be considered for employment opportunities with Accenture and have accommodation needs such as for a disability or religious observance, please call us toll free at **************** or send us an email or speak with your recruiter. Equal Employment Opportunity Statement We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. For details, view a copy of the Accenture Equal Opportunity Statement (******************************************************************************************************************************************** Accenture is an EEO and Affirmative Action Employer of Veterans/Individuals with Disabilities. Accenture is committed to providing veteran employment opportunities to our service men and women. Other Employment Statements Applicants for employment in the US must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States. Candidates who are currently employed by a client of Accenture or an affiliated Accenture business may not be eligible for consideration. Job candidates will not be obligated to disclose sealed or expunged records of conviction or arrest as part of the hiring process. Further, at Accenture a criminal conviction history is not an absolute bar to employment. The Company 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. Additionally, 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 Company's legal duty to furnish information. California requires additional notifications for applicants and employees. If you are a California resident, live in or plan to work from Los Angeles County upon being hired for this position, please click here for additional important information. Please read Accenture's Recruiting and Hiring Statement for more information on how we process your data during the Recruiting and Hiring process.

SummaryJob Description Collaborate with GE Vernova's Controls & Electrical Systems teams and MIT partners to design and implement innovative control strategies for variable grid strength and dynamic load demands. Intern 1 (Grid/Controls - load flow, parameter estimation, scenarios) - Grid modeling (in GE PSLF)and studies: Build and validate a power system model; run ≥10 load-flow and dynamic scenarios (varying SCR, renewables 20-80%, AI DC step/ramp loads). Outcome: quantified voltage profiles, congestion, losses, and stability margins. - Parameter estimation: Identify key plant/control parameters (governor, AVR, PSS) from operational/PMU data or simulations with ≤5-10% error (NRMSE ≥0.9). Deliver a calibrated model with uncertainty bounds. - Control strategy prototype: Design and simulate an adaptive/predictive control update that improves frequency/voltage recovery time by ≥20% and limits overshoot to ≤5% across scenarios. Scenario playbook: Produce a controls adaptation playbook for weak-grid and high-ramp AI load events, with trigger conditions, setpoint/limit adjustments, and rollback criteria. Intern 2 (ML/System ID - data-driven modeling, predictive control) - Data pipeline: Curate a clean, labeled dataset (signals, events, load profiles); document data quality metrics (missingness, latency, drift). - System identification/modeling: Develop and validate a predictive model (e.g., state-space/N4SID, ARX, or ML) with ≤5-10% MAPE on key outputs (e.g., bus voltage, frequency, torque) and calibrated time constants. - Predictive control prototype: Implement an MPC or equivalent controller using the learned model; demonstrate closed-loop stability and constraint handling with control latency ≤100 ms in simulation/HIL. - Performance gains: Show ≥15-25% reduction in oscillations or curtailment during AI load ramps and improved stability margin (e.g., damping ratio +10%). Explainability and governance: Provide feature importance/ablation results, model risk/assumptions, and retraining criteria for production handoff. Project Outcomes: Deliver validated models and control prototypes that address electrical and mechanical challenges from renewables and AI data center integration on power plants and grids, with clear evidence of stability/resilience gains. Intern1 Deliverables: Model files and scripts, study report with KPIs, control design rationale, and a reproducible runbook. Intern2 Deliverables: Trained models, evaluation notebooks, controller prototype, and concise documentation. Shared outcomes (both interns): - Communication: Midterm and final presentations to internal stakeholders and MIT collaborators; 8-10 page tech note plus a 1-page executive summary. - Integration: Joint demo where ML model informs scenario/control tuning in the grid model; side-by-side baseline vs. improved results. - Documentation and handoff: Versioned artifacts, how-to guides, and issue/risk log to enable continuity after the internship. - Stakeholder impact: Clear mapping from findings to operational decisions (setpoints, limits, protection coordination) and next-step recommendations. Primary Skills Developed: • Lead the development of advanced controls and electrical system scenarios for variable grid strength adaptation. • Gain exposure to cutting-edge research in power system control, predictive modelling, and real-time system optimization. • Work directly with MIT and GE Vernova experts to address real-world challenges and deliver impactful solutions for the energy sector. • Build expertise in power generation operational challenges, control techniques, and next-generation energy system integration. Basic Qualifications: • Currently pursuing a master's in electrical engineering, Mechanical Engineering, Controls Engineering, Computer Science, or a related field. • Minimum of 4.0 GPA out of 5.0. Desired Qualifications: • Foundational knowledge and Demonstrated interest on advanced control concepts & Load flow calculations for power systems (academic, research, or project-based). • Exposure to machine learning techniques applied to system modelling and control (coursework, academic projects, or research experience). • Strong analytical and problem-solving skills, with experience in data-driven modelling, simulation, or algorithm development as part of studies or projects. • Ability to work collaboratively in multidisciplinary and research-driven environments. • Proficiency in programming languages such as C/C++, Python, R, or similar, for algorithm development, data analysis, and simulation. • Exposure to power plant control systems, grid modelling, and turbine control operational challenges. • Familiarity with AI data Center load profiles and their impact on electrical grid and power plant operations. • Working knowledge of model-based engineering and real-world power system simulation tools. • Strong communication and presentation skills for cross-functional and academic collaboration. Benefits Available to you: Addressing the climate crisis is an urgent global priority, and at GE Vernova, we take our responsibility seriously. That is the singular mission of GE Vernova: to continue electrifying the world while simultaneously working to help decarbonize it. In order to meet this mission, we provide varied, competitive benefits to help support our workforce: Our Culture | GE Vernova (gecareers.com) The pay for this position is $34/hr. This position is also eligible for: Relocation Assistance: Co-op/Interns will be reimbursed for reasonable, proper, and documented expenditures incurred while initially reporting to work and returning to school/home upon completion of the assignment. Employees with a permanent address greater than 50 miles away from the work location are eligible. Housing Allowance: Co-op/Interns employees receive a weekly housing allowance to help off-set living expenses when the co-op/Intern's permanent residence is at least 50 miles away from the work location. Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services GE Retirement Savings Plan (RSP) after their accumulated service reaches 90 days, and they meet any other eligibility requirements as defined in the plans. (Eligibility occurs on the 1st of the month following the 90th day.) General Electric Company, Ropcor, Inc., their successors, and in some cases their affiliates, each sponsor certain employee benefit plans or programs (i.e., is a Sponsor”). Each Sponsor reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual. Inclusion At GE Vernova, we believe in the value of your unique identity, background and experiences. We are committed to fostering an inclusive culture, where everyone feels empowered to do their best work because they feel accepted, respected and that they belong. Click here to learn more: ************************************************** Additional Information GE Vernova offers a great work environment, professional development, challenging careers, and competitive compensation. GE Vernova is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Vernova will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). Relocation Assistance Provided: No

Overview: Responsible for conducting qualitative and quantitative testing of raw materials and finished goods. Responsibilities: Safely perform laboratory tests on beverages to ensure product is produced within established parameters and make adjustments where necessary. Conduct qualitative and quantitative testing of beverages, syrups, and raw materials throughout the entire production process. Analyze syrup beverage and/or water attributes Audit container rinsers, air blowers, filters, and coders to ensure proper operations. Conduct package quality inspection and quality audits and isolate product that does not meet standards. Maintain highest possible housekeeping standards to prevent microbial contamination Monitoring package appearance, integrity and correct package codes. Requires working with other lab technicians, line foreman, line operators, fork truck drivers, and other production personnel. Responsible for Food Safety and Food Quality Requirements: Demonstrated attention to detail and accuracy Strong analytical skills Ability to read, write and keep records Good computer skills including literacy with Excel and Word Ability to “be on your feet” from beginning to end of shift. Able to lift materials up to 50 pounds Ability to pass pre-employment math test

Summer 2026 Internship Program - Quality Intern, Health Nutrition and Care Schenectady, NY, US If you're looking to grow your network and gain new skills within a global company, an internship with dsm-firmenich could be the program for you. Our summer internships provide students opportunities to work on real business projects and gain invaluable professional experience. As an intern, you'll have exposure to many different areas of global flavors, fragrances, and ingredients organization that works with some of the biggest brands in the world, along with opportunities to network with your peers and leadership. From engaging events to mentoring opportunities and valuable resume-building experiences, we're committed to preparing you for a fulfilling and enduring career, both at dsm-firmenich and beyond. We are currently looking for a Quality summer intern at our Schenectady, NY office. The 2026 dsm-firmenich Summer Internship Program will run from June 1, 2026 to August 14, 2026. Working Hours: Monday - Friday, 8:00am - 5:00pm Join our Health Nutrition and Care Quality team as an intern and gain invaluable professional experience. Enhance your skills and contribute to real projects that have visibility across the business through a Summer internship. Come discover all we have to offer! Your key responsibilities * Assist the local Quality unit's day-to-day operations in a 24 / 5 food, dietary supplement and infant formula manufacturing facility * Participate in customer-facing activities such as facility audits and complaint handling * Gather Quality data to aid in decision making and continuous improvement initiatives * Review and update documentation to enhance our current documented processes in line with our quality and regulatory requirements (FSSC 22000, US FDA) We bring * Build Your Future Skills: Gain hands-on experience and develop practical skills that prepare you for a successful career. * Expand Your Network: Connect with professionals and peers in a company where sustainability drives every decision and action. * Thrive in an Inclusive Culture: Join a community that values and respects every individual-regardless of background, beliefs, or identity. * Grow Through Curiosity: Work in an environment that encourages open-mindedness, learning, and collaboration to create a better future together. You Bring * Currently working on completion of a bachelor's degree in engineering, life sciences or a related field * Must be available to work full-time on-site beginning on June 1, 2026 to August 14, 2026. * Excellent communication and interpersonal skills * Strong analytical skills and ability to synthesize and parse data * Strong organizational, problem-solving, and analytical skills; able to manage priorities and workflow * Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm The hourly rate for this position is $23.00 - $26.00 per hour. Compensation will be dependent on factors that include location, education, training, specific skills, and years of experience. At the end of this internship, you will: * Develop a deeper understanding of the ways of working within a world-class quality system * Gain an appreciation of a complex manufacturing process and the inter-departmental work that supports it * Sharpen your presentation, communication, and interpersonal skills by engaging with multiple levels of a large organization About dsm-firmenich: At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we go beyond, together. Inclusion, belonging and equal opportunity statement: At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. Agency statement: We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.

ABOUT US R&D Lab Technician Schenectady Permanent Full-time Von Roll Group is the global market leader for insulation products and the only company to offer the complete range of insulation products, composites, consulting, tests and services for the electrical industry. Von Roll USA Ltd. Inc. in Schenectady is part of Von Roll Group, active in the development and production of resins and varnishes, potting compounds, mica tapes, coated glass, flexible laminates and prepregs. This site serves its customers by supplying electrical insulation components for the design of reliable electric motors, traction drive systems, coils, generators, transformers and several ballistic applications. Here, we go with the future, and we improve constantly - especially with experts like you! As a R&D Lab Technician you will be responsible for working closely with our R&D group contributing to the development of research projects, manufacturing support and other various related activities. YOUR RESPONSIBILITY AND TASKS Prepare lab-scale samples via chemical synthesis. Collaborate with R&D chemist and engineers to optimize/analyze resin formulations. Perform chemical and physical tests to help manufacture and develop new polymer or other materials. Run standard polymer characterization tests and interpret the measurements. Interpret lab standards and follow procedures for processing and testing samples. Prepare test reports based on testing results and customer provided or development team requirements. Support lab activities including keeping the lab organized and up to cleanliness standards, maintain laboratory equipment and perform routine maintenance YOUR PROFILE Minimum Qualifications: Two-year OR Four-year degree, in physical science such as chemistry, physics, biology or science related field. Minimum of 1-2 years experience in testing processes, within a lab environment, or working with chemical manufacturing equipment Experience in an industrial R&D laboratory in the resin, paints or coatings field preferred but not required Physical Demands: While performing the duties of this job, the employee is regularly required to talk and hear. This position is very active and requires standing, walking, bending, kneeling, stooping, crouching, crawling and climbing all day. The employee must frequently lift and move items over 50 pounds. Work Environment: This position will operate in a professional office and a chemical lab environment. This role will require the use of standard and technical office programs as well as chemical and other volatile laboratory equipment and products While performing the duties of this job, the employee is frequently exposed to fumes or airborne particles, moving mechanical parts and vibration. The noise level in the work environment and job sites can be loud. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. WE OFFER 401k Retirement Plan Dynamic environment Health Benefits International environment Medical, Dental and Vision Benefits Highly motivated team Salary range: $50,000-$60,000 CONTACT Your contact person is: Ms Christina Carnavale

We are looking for a Sr Quality Control Scientist in the Technical Resources Department. This position performs assay development, characterization, optimization, transfer, validation, and investigations for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development. As a Sr QC Scientist for Chemistry in the Technical Resources Department, a typical day might include the following: + Performs assay development/validation for QC. + Reviews new test procedures and assays. + Evaluates and bring in new methodologies/techniques when needed. + Facilitate assay transfer from R&D and to business partners + Organize analytical assay transfer internally and externally. + Set product specification. + Participates in technical troubleshooting and problem investigation. + Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance. + Participates in training programs for analysts. This job might be for you if: + You have in-depth knowledge with HPLC based assays. + You like dealing with technical issues, troubleshooting, and constant change + You are a team player who can work with a variety of different people on different tasks + You have strong written and verbal communication skills + You enjoy mentoring and training others on systems, processes and problem solving + You enjoy working in a fast-paced environment and are flexible to changing requirements + You can take on new and sometimes ambiguous challenges and learn quickly To be considered for a Sr QC Scientist (Chemistry) Technical Resources role you must be willing and able to work onsite Monday-Friday, 8am-4:30pm. A PhD in Chemistry, Biochemistry, Biology, or a related field is required. Experience with cell or gene therapy in a Biopharmaceutical environment is strongly preferred. Level is determined based on experience relevant to the role. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. **Salary Range (annually)** $77,600.00 - $126,800.00

Solid Sealing Technology (SST) designs and manufactures small-scale electrical components used around the world. Our parts are found in many types of industrial, medical, and research facilities, and you will work with technologies used on equipment like energy storage systems, MRI machines, and particle accelerators. We have even sent parts to Mars! NASA's Mars Insight Mission uses components made right here in Watervliet, NY. Position Summary: The Quality Control Technician is responsible for providing quality control and assurance throughout all phases of the production process by inspecting and testing incoming and outgoing products to determine if all requirements have been met. The Quality Control Technician also performs various administrative duties associated with the operation of the company's quality system. Essential Duties and Responsibilities: Reads drawings; work instructions and referenced procedures to determine requirements. Performs dimensional and visual inspection and basic electrical and mechanical testing on products received from suppliers and on internally processed products to be shipped to customers. Includes use of: Basic hand measurement tools such as calipers and micrometers. Coordinate Measuring Machine (CMM) and automated Vision Inspection System. High voltage electrical test system. Uses observation and testing to identify faults in materials and manufacturing process. Compares results of inspections and tests to company's quality standards; reports the results to supervisor for final analysis and action steps. Generates inspection reports and certifications for customers. Records logs, charts, and forms detailing quality levels, inspection data, and results of special quality studies for review by supervisor, and other production staff. Records completion of work steps, rework, and scrap transactions, in computer system. Participates in activities in response to quality issues to achieve root-cause solutions and recurrence prevention. Documents and properly handles nonconforming material. Consults with supervisor to determine appropriate recommendations and remedies for questionable products. Routes parts to other operations according to work instructions. Participate in various types of audits (product, process, equipment, department) in relation to adherence to Safety and Quality Processes. Performs other related duties as assigned. Requirements High School diploma or equivalent required. Technical school education with a mathematics emphasis preferred. One to two years of quality control experience in a manufacturing environment preferred. Ability to interpret technical documents such as drawings, specifications, and procedures. Ability to understand the products and processes being inspected. Ability to use measuring tools and electronic inspection equipment. Thorough attention to detail. Excellent verbal and written communication skills. Excellent teamwork and collaboration skills. High level of manual dexterity. Outstanding mathematical skills and analytical abilities. Proficient in Microsoft Office Suite or related software as needed to complete reports. All qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other legally protected status. Annualized Salary: $41,600-$52,000 per year ($20-25 per hour) Schedule: Monday-Friday, 8:00 AM-4:30 PM Benefits Solid Sealing Technology offers comprehensive benefits for full-time positions, and many begin on first day of employment. Generous Holidays, Vacation and Paid Sick Leave Health, Dental and Vision Insurance Employer-funded Health Reimbursement Account (HRA) Matched 401k Retirement Savings Plan Profit Sharing and Bonuses Group Life Insurance and optional Voluntary Life Insurance Disability Insurance Health Flexible Savings Account (FSA) Dependent Care Assistance Plan An Employee Assistance Program (EAP) Full access to on-site Fitness Center and recreational facilities (Watervliet Arsenal)

The Reporting and Change Control Analyst supports large-scale, multi-workstream projects by managing project status reporting, documentation quality, RAID tracking, and change control activities. This role partners closely with project managers and workstream leads to ensure accurate reporting, timely follow-up, and adherence to governance standards. Key Responsibilities * Coordinate and compile bi-weekly project status reports across multiple teams * Review status reports for accuracy, completeness, and consistency * Perform quality assurance checks using established templates and checklists * Prepare and distribute meeting minutes and action items * Track, manage, and follow up on project action items * Maintain and update RAID (Risks, Assumptions, Issues, Dependencies) logs * Produce and distribute weekly RAID summary reports * Support change control processes, including ticket validation and approval tracking * Act as a point of contact for documentation accuracy and reporting timelines Requirements * Strong proficiency in Microsoft Excel, PowerPoint, and Word * Excellent organizational, time management, and attention-to-detail skills * Strong written and verbal communication abilities * Experience managing and tracking project documentation * Ability to work independently and collaboratively in a team environment * Experience with status reporting and action item tracking Preferred Qualifications * Experience supporting PMO or project management environments * Familiarity with Jira, Microsoft Project, Smartsheet, or similar tools * Knowledge of RAID log management * Experience supporting change control processes * Exposure to IT, technology, or consulting projects * Experience with quality assurance or validation checklists Deliverables * Project Status Reports * RAID Logs and Weekly RAID Reports Additional Information * 80% remote; onsite attendance required when requested Physical Requirements & Environmental Conditions: An employee must meet these physical demands to successfully perform the essential functions of this role. The employee is regularly required to sit, talk, hear, and utilize technology tools such as a laptop computer for extended periods of time. Specific vision abilities include close vision and the ability to adjust focus. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Briljent is a solutions-based company. Solutions come from creative ideas; ideas come from being creative with differences. Briljent believes diversity and inclusion are critical to the success of the company. Employment is based on merit and professional qualifications. We do not discriminate against any employee or applicant on the basis of race, creed, color, religion, gender, sexual orientation, national origin, disability, age, veteran status, marital status, or any other status protected by applicable law.

The Reporting and Change Control Analyst supports large-scale, multi-workstream projects by managing project status reporting, documentation quality, RAID tracking, and change control activities. This role partners closely with project managers and workstream leads to ensure accurate reporting, timely follow-up, and adherence to governance standards. Key Responsibilities Coordinate and compile bi-weekly project status reports across multiple teams Review status reports for accuracy, completeness, and consistency Perform quality assurance checks using established templates and checklists Prepare and distribute meeting minutes and action items Track, manage, and follow up on project action items Maintain and update RAID (Risks, Assumptions, Issues, Dependencies) logs Produce and distribute weekly RAID summary reports Support change control processes, including ticket validation and approval tracking Act as a point of contact for documentation accuracy and reporting timelines Requirements Strong proficiency in Microsoft Excel, PowerPoint, and Word Excellent organizational, time management, and attention-to-detail skills Strong written and verbal communication abilities Experience managing and tracking project documentation Ability to work independently and collaboratively in a team environment Experience with status reporting and action item tracking Preferred Qualifications Experience supporting PMO or project management environments Familiarity with Jira, Microsoft Project, Smartsheet, or similar tools Knowledge of RAID log management Experience supporting change control processes Exposure to IT, technology, or consulting projects Experience with quality assurance or validation checklists Deliverables Project Status Reports RAID Logs and Weekly RAID Reports Additional Information 80% remote; onsite attendance required when requested Physical Requirements & Environmental Conditions: An employee must meet these physical demands to successfully perform the essential functions of this role. The employee is regularly required to sit, talk, hear, and utilize technology tools such as a laptop computer for extended periods of time. Specific vision abilities include close vision and the ability to adjust focus. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Briljent is a solutions-based company. Solutions come from creative ideas; ideas come from being creative with differences. Briljent believes diversity and inclusion are critical to the success of the company. Employment is based on merit and professional qualifications. We do not discriminate against any employee or applicant on the basis of race, creed, color, religion, gender, sexual orientation, national origin, disability, age, veteran status, marital status, or any other status protected by applicable law.

Job Title:Summer 2026 Quality Control InternSummary:As a Quality Control Intern, you will support high-impact initiatives that drive continuous improvement across our Waterford, NY site. From optimizing lab methods and mapping processes to contributing to certification efforts and strategic planning, you will collaborate with experts and gain hands-on experience in shaping the future of quality operations.Responsibilities Include: Complete Quality Risk Assessment and Process Mapping for a minimum of 3 Waterford Assets including process mapping. Test method optimization under direction of Quality Chemist. Complete trend analysis on defect data to identify continuous improvement opportunities. Formulate solutions and improvement plan. Support of IATF Certification and GLIMS project teams Benchmark and evaluate external test labs to develop scope of business plan to sell a selection of Quality tests externally. MES for the Lab, work with Lean Techs, pilot a portion of the upcoming rollout / changes. Work on 5 year CapEx plan for the labs, put together all of the separate documents into a single plan. Turn into a working file for future reference. Develop technician training plan for new lab technicians onboarding to Quality Control Laboratories. Qualifications: The following are required for the role Pursuing an undergraduate degree in Chemistry, Engineering, Biology, or a related technical discipline. Attention to detail - ability to document new processes and procedures. Self-starter - Proactively identify new opportunities to drive efficiencies in Quality and Service at Waterford, NY site. Computer skills including Excel and Powerpoint. Minitab or other statistical analysis tool preferred. Knowledge of Basic statistics and/or successful completion of university-level mathematics courses. Prior experience training or teaching technical topics to small groups considered a plus. Program Qualifications: The candidate must be actively enrolled in an undergraduate or graduate program at the time of application and for at least one semester following the conclusion of the internship. The candidate is expected to be available 40 hours a week for a period of 10-12 weeks between the months of May and August. What We Offer:Base Pay Range: $22.00 - $26.00 The base salary offered is determined by factors including but not limited to education, experience, skill sets, and geography. If you are interested in this position, we'd ask that you apply! #BePartoftheSolution At Momentive, we value your well-being and offer competitive total rewards and development programs. Our inclusive culture fosters a strong sense of belonging and provides diverse career opportunities to help you unleash your full potential. Together, through innovative problem-solving and collaboration, we strive to create sustainable solutions that make a meaningful impact. Join our Momentive team to open a bright future. Refer to the Hiring Process tab on our Careers page for a detailed description on the physical job requirements. About Us: Momentive is a premier global advanced materials company with a cutting-edge focus on silicones and specialty products. We deliver solutions designed to help propel our customer's products forward-products that have a profound impact on all aspects of life, around the clock and from living rooms to outer space. With every innovation, Momentive creates a more sustainable future. Our vast product portfolio is made up of advanced silicones and specialty solutions that play an essential role in driving performance across a multitude of industries, including agriculture, automotive, aerospace, electronics, energy, healthcare, personal care, consumer products, building and construction, and more. Momentive believes a diverse workforce empowers our people, strengthens our business, and contributes to a sustainable world. We are proud to be an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by law. To be considered for this position candidates are required to submit an application for employment and be of legal working age as defined by local law. An offer may be conditioned upon the successful completion of pre-employment conditions, as applicable, and subject to applicable laws and regulations. Note to third parties: Momentive is not seeking or accepting any unsolicited assistance from search and selection firms or employment agencies at this time.

Responsible for the inspection of raw materials and finished goods (including medical products) using manual, visual, measurement and/or test equipment following company established procedures. Complete required documentation to record quality inspections results. Provide disposition for the inspected product and ensure adequate inventory control. Ensure compliance with established quality procedures and company policy. Job Description MAJOR RESPONSIBILITIES: Perform in-process inspection and testing of finished goods and/or raw materials manufactured by or for Medline Industries. Read and understand company procedures for specific materials inspections. Complete inspection documentation per applicable inspection procedures. Identify errors and omissions for correction. Operate test equipment and perform simple measurement activities per applicable standard operating procedures. Equipment may include tools such as a ruler, caliper, micrometer, scales, etc. Read and understand company procedures for specific test equipment operation. Identify defects and initiate non-conforming material reports during in-process and final inspections per pre-established company policy or Accepted Quality Limits (AQL). Communicate effectively with business partners such as quality assurance, warehouse, maintenance, and/or manufacturing groups. Commutation includes but is not limited to inspection defects, issuance of non-conforming reports, inspection prioritization or any concerns associated to the product quality. Verify and/or approve line start-up and equipment applicable requirements per company-established procedures when applicable. Education: High School Diploma or equivalent. Work Experience At least 1 year of quality control experience in a regulated industry. Knowledge / Skills / Abilities: Basic math skills including fractional to decimal conversions. Position requires:- Working in hot and cold environments and at heights. Sitting, walking or standing for prolonged periods, with frequent bending and kneeling. Ability to lift up to 50 lbs. Ability to prioritize quickly in a fast paced manufacturing environment. Ability to process all relevant details, understanding and prioritizing their importance and drawing concise conclusions. Basic knowledge of Microsoft Office Suite (Outlook, Word, Excel, etc.). Basic knowledge of quality regulations such as GMP, GDP, ISO, or 21CFR 820, 210 - 211. PREFERRED JOB REQUIREMENTS: At least 1 year of quality control experience in medical device and/or drug manufacturing setting. Ability to read, write, speak, and understand English. Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization. The anticipated salary range for this position: $17.00 - $23.75 Hourly The actual salary will vary based on applicant's location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold. Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here. Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

Job ID 251330 Posted 16-Jan-2026 Service line PJM Segment Role type Full-time Areas of Interest Building Surveying/Consultancy, Construction, Consulting **About the role** The Facility Condition Assessments (FCA) Team at CBRE | Turner & Townsend Inc. is currently seeking a detail-oriented individual who will ensure that the deliverables are accurate, consistent, and conform to the standards and guidelines for the facility condition assessments, capital planning, and asset management reports established by the Building Consultancy group. Primary duties include identifying content issues, developing and enforcing quality standards, and collaborating with teams to provide various client deliverables in a timely manner. **What you'll do** + Data Assessment: Review facility condition and asset data for content, structure, and quality, and identify anomalies and inconsistencies. Must have fluency of the English language, as it relates to grammar, punctuation, and spelling. Must be able to compare data criteria/fields for content, agreement, and technical accuracy. + Standards Adherence: Collaborate with team members to ensure that the comprehensive quality standards and metrics (e.g., accuracy, completeness, timeliness) are met. Must be able to switch between sets of rules pertaining to each client and project. + Data Cleansing and Resolution: Identify and rectify errors, inconsistencies, and redundancies within facility condition assessment and asset datasets. + Monitoring and Reporting: Evaluate and provide corrective action of data quality, create reports for facility capital planning engagements. + Process Improvement: Recommend changes to existing processes, entry, and deliverable workflow. Must be a team player and not afraid to ask questions. Must be comfortable in a fast-paced, high-volume setting and managing projects and deadlines. **What you'll need** + We will provide reasonable accommodations that may be made to enable individuals with disabilities. To perform this job optimally, an individual must be able to perform each crucial duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. + Associate's degree (AA/AS), College Diploma, or equivalent preferred. Minimum of three years of related experience in addition to education. Consideration will be given to a person with 5 years of related experience, regardless of whether they hold a degree. Experience in the Architecture, Engineering, and Construction field is preferred. + Experience with Microsoft Office Suite products. + Applicants must be currently authorized to work in the United States without the need for visa sponsorship now or in the future. **Additional Skills** + Ability to write in a clear and concise, coherent way using appropriate grammar, spelling, punctuation, and style. Adapt writing style for different audiences, purposes, and formats. + Ability to edit technical documents in a detailed and accurate manner to ensure deliverables are professional and presentable. + Ability to comprehend and interpret instructions, short correspondence, and memos and ask clarifying questions to ensure understanding. Must be detail-oriented and observant + Requires basic knowledge of financial terms and principles. Ability to calculate simple figures such as percentages. + Must have a basic understanding of architectural, mechanical, and electrical equipment and features, and some familiarity with industry standards and language. **Disclaimer:** _Please be advised that effective January 1, 2025, CBRE Project Management and Turner & Townsend will be consolidated into a single global business entity. As a candidate applying for a position, you should be aware that while your initial employment may be with CBRE Project Management, you will subsequently transfer to the newly formed entity that encompasses both organizations._ Turner & Townsend carefully considers multiple factors to determine compensation, including a candidate's education, training, and experience. The minimum salary for this position is $50,000 annually and the maximum salary for this position is $70,000 annually. The compensation that is offered to a successful candidate will depend on the candidate's skills, qualifications, and experience. Successful candidates will also be eligible for a discretionary bonus based on Turner & Townsend's applicable benefit program. This role will provide the following benefits: 401(K), Dental insurance, Health insurance, Life insurance, and Vision insurance. **Equal Employment Opportunity:** CBRE has a long-standing commitment to providing equal employment opportunity to all qualified applicants regardless of race, color, religion, national origin, sex, sexual orientation, gender identity, pregnancy, age, citizenship, marital status, disability, veteran status, political belief, or any other basis protected by applicable law. **Candidate Accommodations:** CBRE values the differences of all current and prospective employees and recognizes how every employee contributes to our company's success. CBRE provides reasonable accommodations in job application procedures for individuals with disabilities. If you require assistance due to a disability in the application or recruitment process, please submit a request via email at recruitingaccommodations@cbre.com or via telephone at *************** (U.S.) and *************** (Canada). CBRE, Inc. is an Equal Opportunity and Affirmative Action Employer (Women/Minorities/Persons with Disabilities/US Veterans)

Are you detail-oriented, passionate about quality, and looking for a hands-on role in a fast-paced environment? Repligen's Clifton Park facility is looking for a Quality Inspector I to join our 2nd shift team and play a vital role in ensuring our products meet the highest standards. Make a global impact-join Repligen. We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No matter your role or background, at Repligen, you will play a key part in shaping some of the most innovative and life-changing therapies in the world. We foster a culture of purpose, collaboration, and shared success-where every voice matters and every contribution drives progress. Join us! 2nd shift: 2:00pm-10:30pm, M-F Responsibilities What You'll Do: Inspect products against acceptance criteria to maintain high-quality standards. Work closely with manufacturing teams to identify and resolve quality issues. Read and interpret engineering drawings, specifications, and purchase orders. Accurately document inspection results using Microsoft Office and other software. Use precision measurement tools like calipers and pin gauges. Operate in an ISO 7 cleanroom while following strict gowning procedures. Support additional quality-related functions as needed. Qualifications What You Bring: High School Diploma or equivalent (required); Bachelor's degree in science or relevant experience preferred. Experience in Quality Assurance (QA) or Quality Control (QC) is a plus. Strong attention to detail and ability to work in a structured environment. Proficiency in basic math, measurements, and testing equipment. Experience in a cleanroom environment is highly desirable. Medical device or medical manufacturing experience is preferred. What Repligen Offers Our mission is to inspire advances in bioprocessing as a trusted partner in the production of biologic drugs that improve human health worldwide. Focused on cost and process efficiencies, we deliver innovative technologies and solutions that help set new standards in bioprocessing. The estimated base salary range for this role, based in the United States of America is $21/Hr.- $23/Hr. Compensation decisions are dependent on several factors including, but not limited to an individual's qualifications, location, internal equity, and alignment with market data. Additionally, employees are eligible to participate in one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits such as paid time off, health/dental/vision, retirement benefits and flexible spending accounts. All compensation and benefits information will be confirmed in writing at the time of offer.

JLA International, a Leader in Food Safety, is now accepting applications for a Microbiology Laboratory Analyst position at its facility in Albany, GA. Ideal candidates will possess the following: * A BS or BA in Microbiology or a related field (required) * Proficiency with data entry and computer applications * Ability to multitask and work in a fast-paced environment * Strong written and verbal communication skills * Strong attention to detail * Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. This is a full-time position and is eligible for standard benefits after a brief waiting period. The laboratory operates weekends, so candidates must be willing to work occasional weekends. Due to exposure to various food allergens in the laboratory environment, applicants with moderate to severe food allergies are discouraged from