Validation Engineer Salary in State of New York, USA

DESCRIPTIONAmazon Advertising seeks a Business Intelligence Engineer with strong analytical and technical skills to join the Deals and Third Party Ads Supply Finance team. In this role, you will play a crucial part in designing, developing, and maintaining business intelligence solutions for internal stakeholders within the Finance organization supporting third party ads supply and programmatic deals businesses. You will collaborate closely with stakeholders, understanding their unique business needs, and delivering impactful insights that drive success. To be successful in this role, you need to be a proven engineer, diligent task manager, communicator, and problem solver. Key job responsibilitiesThe successful candidate will be a self-starter who is comfortable with ambiguity; dives deep into data to find the root cause of problems, creates action plans to take advantage of business opportunities, is detail oriented and has the ability to work well with cross-functional teams including product development, sales, other finance teams, and senior leaders. Core Responsibilities • Build data pipelines to enable new metrics; Create and track key advertiser, publisher and supply metrics. • Build data systems that leverage diverse data sources to provide a comprehensive view of product adoption across all customer segments. • Conduct cohort level analyses; develop growth and retention monitoring dashboards. • Present findings and recommendations to business leadership. • Recognize and adopt best practices in reporting/ analysis: data integrity, test design, analysis, validation, and documentation. A day in the lifeIf you enjoy using analytical skills to shape strategy and build new initiatives from concept to full-scale operations this will be a good match. We are looking for a highly motivated individual to develop deep industry understanding, create key performance indicators, analyze monetization strategies to maximize revenue, and provide valuation guidance for feature roadmap prioritization and decision-making. This position will collaborate with business and finance stakeholders on a daily basis and will be providing business insights into key initiatives.About the teamThe Deals and Third Party Ads Supply Finance team is responsible for driving key mechanisms that support the rhythm of the ADSP Deals and Ads 3P Supply businesses. We generate insights to guide product and business development strategy. We also provide direct business partnership and ongoing business performance measurement support to senior leaders.We are open to hiring candidates to work out of one of the following locations:New York, NY, USA | Palo Alto, CA, USABASIC QUALIFICATIONS- Bachelor's degree in engineering, statistics, computer science, mathematics, or a related quantitative field- Experience with data querying or modeling with SQL- Experience in analyzing and interpreting data with Redshift, Oracle, NoSQL etc.- Experience gathering business requirements, using industry standard business intelligence tool(s) to extract data, formulate metrics and build reports- Experience with data visualization using Tableau, Quicksight, or similar tools- Experience building and maintaining basic data artifacts (e.g., ETL, data models, queries)PREFERRED QUALIFICATIONS- Knowledge of data modeling and data pipeline design- Experience with statistical analysis, co-relation analysis- Experience with scripting language (e.g., Python, Java, or R)Amazon is committed to a diverse and inclusive workplace. Amazon is an equal opportunity employer and does not discriminate on the basis of race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. For individuals with disabilities who would like to request an accommodation, please visit https://www.amazon.jobs/en/disability/us.Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $65,800/year in our lowest geographic market up to $165,600/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Amazon is a total compensation company. Dependent on the position offered, equity, sign-on payments, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits. For more information, please visit https://www.aboutamazon.com/workplace/employee-benefits. Applicants should apply via our internal or external career site.

Job DescriptionAs part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.How will you make an impact?Molding process engineers provide technical support for molding and assembly operations for current production product and for new product and process development. This role interacts with a large cross section of the Thermo Fisher Employee base inclusive of hourly line workers, equipment set up personnel, team leads, shift supervisors, quality engineers, tool room personnel, maintenance and site leadership.Key Responsibilities: Establish and optimize manufacturing processes, methods and procedures to assure product performance, quality and cost effectiveness.Troubleshoot production issues and keep production running to support customer requirements until corrective actions can be implemented. Partner with Set-up, Maintenance, Quality, Operators, and other groups as needed to accomplish this.Uses fact-based analysis to identify gaps (NCRs, systemic problems, etc.) and develop corrective and preventive actions to address. Responsible for overseeing the timely implementation of countermeasures.Identify and implement Continuous Improvement projects and/or general improvement projects, applying Lean methodologies and tools.Coordinate and direct investigations in new processes, materials and other related technologies, and provides training for the operation as needed.Support the research, evaluation and procurement of machines, tools, molds and other equipment required to meet production needs.Coordinate and complete the validation process for new molding processes, machines and equipment.Establish engineering tolerances and specifications.Provide technical assistance and expertise to manufacturing in problematic situations, implementing corrective action and providing training as required.Establish and maintain manufacturing specifications, i.e., BOM, routings, set up sheets and other related technical input and documentation.Develop optimized Decoupled molding process.Work with Tooling, Quality and Manufacturing Departments to debug and validate molds, maintaining optimized process.Interpret print for product requirements.Represent manufacturing engineering on New Product Development teams, ensuring new products that are brought to market are capable of being manufactured to accepted specifications.Work with New Product Development group to validate new products.Support NPD, such as with Process FMEA, Design FMEA, Process Flow Chart, and Control Plan / QCIPActively participates in daily Gemba walks, as well as other site meetings.Participates in Value Stream Key Performance Indicators (KPI) reviews.Prepares capital appropriation requests and is responsible for administering the approved project capital. Aids in the development and implementation of capital budget.Is responsible to manage and lead team projects as assigned.Acts as a Role Model Leader, with a positive attitude and a passion to achieve short- term and long-term goals.Learn and implement internal and external standard processes.Communicate with Marketing, Product Development, Industrial Design and Operations team members to resolve process, mold and equipment details that differ from product specifications. May coordinate and present manufacturing plans at design review meetings.Performs all job duties in a safe manner, consistent with the Code of Ethics and the 4-I Values, and follows all ISO standards, Company and site policies and guidelines, and regulatory or statutory requirements.Performs other duties and responsibilities, as needed.Minimum Requirements/Qualifications:Bachelor's degree in engineering (Mechanical, Chemical or Plastics Engineering preferred); Work experience may replace bachelor's degree.Prior manufacturing experience required. 5+ years working experience in a manufacturing environment with ISO quality standards strongly preferred.Technical depth in Blow Molding and/or Injection Molding strongly preferred. Experience with Tooling, Assembly/Test Automation and Clean Rooms a plus.Experience working closely with set-up and maintenance functions strongly preferred.SMED experience supporting mold and process requirements a plus.Ability to deliver fact- based decisions and apply a mentality for Lean Management, gaining Value Stream efficiencies and continuous improvement. Candidate should have experience in successfully driving continuous improvement.Ability to conduct critical analysis and assessments to develop action plans that ensure efficient, lean, and effective processes are in place to produce quality products.Ability to accurately and quickly assess a situation on the manufacturing floor and determine and implement corrective measures to maintain flow of production.Proficient in process auditing and Lean manufacturing techniques.Knowledgeable in advanced data collection, measuring, analysis, improvement and control.Strong ability to effectively use judgment and make decisions.Excellent prioritization, time management, and organizational skills.Excellent verbal and written communication skills.Ability to work effectively in a team environment.Ability to work effectively with people at all levels in an organization.Has working knowledge of other business functions (Quality, Supply Chain, Human Resources and Financial) in addition to Engineering and Manufacturing.Demonstrated ability to quickly learn technology systems and applications is required; proficiency in SAP and Microsoft Office Suite is preferred.Ability to travel as required, < 10% of the time.Working conditions require the ability to sit, stand, walk, bend, climb stairs, and work at a computer station and on manufacturing shop floor.Non-Negotiable Hiring Criteria: Prior manufacturing experience required.Ability to deliver fact-based decisions and apply a mentality for Lean Management.Strong ability to effectively use judgment and make decisions.Excellent prioritization, time management, and organizational skills.Ability to work effectively in a team environment.We offer competitive salary, an annual incentive bonus plan, and a range of other employee benefits!Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.comThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.Accessibility/Disability AccessJob Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.Compensation and BenefitsThe salary range estimated for this position based in New York is -.This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:A choice of national medical and dental plans, and a national vision plan, including health incentive programsEmployee assistance and family support programs, including commuter benefits and tuition reimbursementAt least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policyRetirement and savings programs, such as our competitive 401(k) U.S. retirement savings planEmployees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discountFor more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Job DescriptionAs part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.The Engineer III, Validation is responsible for assisting the validation team in supporting all site validation activities. This includes automation equipment, product transfers, new product development, and working as part of a cross-functional team responsible for sustaining change. The Validation Engineer is an active participant in the origination of design concepts and specifications, process/technology development, product verification/validation, project planning, and other applicable documentation while adhering to quality and manufacturing requirements.Job Description:Serve as the primary interface between Operations and Quality Assurance.Originate and assist in the preparation and approval of change orders related to the operation and improvement of manufacturing processes.Assist the validation team in maintaining the Site Validation Master Plan.Support development projects, transfer projects, process changes, and engineering projects to provide overall guidance as it relates to quality standards, inspection techniques and frequencies, statistical analysis, testing, validations, and risk assessments (FMEAs).Direct and oversee validation activities for Operations, Engineering, Quality Assurance, and other functional areas.Review, revise, and maintain site validation procedures, qualification protocols, and associated data in accordance with FDA and ISO requirements.Lead and/or assist in training of staff involved in validation activities.Assist Quality, Operations, and Engineering personnel during inspections or audits.Performs other duties as assigned by Staff Validation Engineer and direct manager.Required Qualifications:Bachelor's degree from a four-year college or university and 5+ years of relevant experience or in the pharmaceutical, medical device, or in-vitro diagnostics industry with progressively increasing responsibilities is required.Associate degree and 8+ years of relevant experience in the pharmaceutical, medical device, or in-vitro diagnostics industry.Preferred Qualifications:Knowledge of global regulatory and quality requirements associated with medical devices.Working knowledge of ISO 13485 and 21 CFR Part 820.Proficient in Microsoft Office Suite.Experience with formal problem solving in a team environment.Detail oriented with the ability to lead multiple projects and activities as assigned.Proficiency with various software platforms such as Minitab, Blue Mountain RAM, and Master Control is preferred.Excellent organizational, planning, communication, and follow-up skills.Physical Requirements:Normal office and manufacturing environment.Position may require frequent communication and walking to other areas in which designated PPE will be required.Position will require sitting and standing.Employee may occasionally lift and/or move up to 25 pounds.Knowledge, Skills & Abilities: Must be proficient on validation protocol development, technical writing, data analysis, and report generation. i.e.; IQ, OQ, PQ, FAT, SAT as an example.Must have knowledge of process + packaging equipment, and software validation principles and concepts.Must have high level of expertise concerning current validation principles and regulatory requirements.Strong understanding and proficiency in cleaning validation and cleaning process design.Must be proficient in statistical analysis and process control.Ability to influence and coordinate activities of personnel over which he/she has no direct authority.Must possess strong organizational skills.Ability to effectively communicate with all levels of the organization, from the General Manager to the production operators.Ability to resolve conflicts between requests for process change and the validation requirements for those processes.Proficiency with various software platforms such as Minitab, Blue Mountain RAM, and Master Control is preferred.Independent self-starter who is capable of planning schedules, controlling plans, and leading projects as assigned.Must ensure adherence to FDA and ISO requirements throughout the product life cycle.Develop and execute verification and validation plans and protocols associated with product/process quality according to FDA and ISO requirements.Ability to manage multiple projects simultaneously without supervision. This includes creating detailed and accurate project tasks and schedules, interfacing with project team members and support personnel, and solving project-related conflicts and issues.Strong working knowledge of design and process controls.Travel when required to support business projects as a validation representative.Knowledge of process and product risk assessments.Knowledge of global regulatory and quality requirements associated with medical devices.Working knowledge of ISO 13485 and 21 CFR Part 820.Experience with formal problem solving in a team environment.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.Apply today! http://jobs.thermofisher.comBenefits:We offer driven remuneration, annual incentive plan bonus scheme, healthcare, company pension/retirement, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Experience Level: Experienced HireCategories:Credit Analysis & ResearchLocation(s):7 World Trade Center, 250 Greenwich Street, New York, New York, 10007, US#efc-dnp#LI-DNI*nocb #ind-dnp#NoPDN Moody's is a developmental culture where we value candidates who are willing to grow. So, if you are excited about this opportunity but don't meet every single requirement, please apply! You may be a perfect fit for this role or other open roles.Moody's is a global integrated risk assessment firm that empowers organizations to make better decisions.At Moody's, we're taking action. We're hiring diverse talent and providing underrepresented groups with equitable opportunities in their careers. We're educating, empowering and elevating our people, and creating a workplace where each person can be their true selves, reach their full potential and thrive on every level. Learn more about our DE&I initiatives, employee development programs and view our annual DE&I Report at moodys.com/diversityEmployer: Moody's Investors Service, Inc.Title: Financial EngineerLocation: 7 World Trade Center, 250 Greenwich Street, New York, NY 10007Duties: Verify and enhance the financial models underlying Moody's credit rating methodologies. Build complex cash flow models using Moody's fixed income software for verification purpose. Implement model testing procedures and develop analytical projects to confirm the ability of financial models to assess credit risk. Build financial model prototypes, implement validation procedures, and assist with the implementation of new control processes for rating models and scorecards. Support in research and validation of projects. Collaborate with rating analysts, model development team and research groups. Design and implement procedures to verify financial models, including building replicas in programming languages such as Python, VBA and R. Convert detailed structured finance deal documents into programming scripts to model cash waterfall and calculate tranche ratings. Review and verify models, scorecards, and structured finance deals against their specification documents, which outlines their technical details.Requirements: Master's degree or foreign equivalent in Statistics, Financial Mathematics, or a closely related quantitative field plus three (3) years of experience as a Financial Analyst or in a related position. Must have experience or academic training with the following: performing financial and credit analysis; developing credit risk models and applying knowledge of financial quantitative methods and data analytics; applying knowledge of Probability, Statistics, Monte Carlo simulation, Regression analysis, and Time series models; utilizing data and programming tools, including VBA, Python, SQL, R.For US-based roles only: the anticipated hiring base salary range for this position is $88,670 to $154,600, depending on factors such as experience, education, level, skills, and location. This range is based on a full-time position. In addition to base salary, this role is eligible for incentive compensation. Moody's also offers a competitive benefits package, including not but limited to medical, dental, vision, parental leave, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, a discounted employee stock purchase plan, and tuition reimbursement.To apply please submit resume through careers.moodys.com, via e-mail at [email protected], or by mail to: Moody's Investors Service, Inc., Attn: HR Box 28, 7 World Trade Center, 250 Greenwich Street, New York, NY 10007. Please refer to Job Ref. 3527. For US-based roles only: the anticipated hiring base salary range for this position is $88,670 to $154,600 depending on factors such as experience, education, level, skills, and location. This range is based on a full-time position. In addition to base salary, this role may be eligible for a completion bonus. Moody's also offers insurance and a discounted employee stock purchase plan for limited duration employees.Moody's is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, gender, age, religion, national origin, citizen status, marital status, physical or mental disability, military or veteran status, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law. Moody's also provides reasonable accommodation to qualified individuals with disabilities or based on a sincerely held religious belief in accordance with applicable laws. If you need to inquire about a reasonable accommodation, or need assistance with completing the application process, please email [email protected]. This contact information is for accommodation requests only, and cannot be used to inquire about the status of applications.For San Francisco positions, qualified applicants with criminal histories will be considered for employment consistent with the requirements of the San Francisco Fair Chance Ordinance.This position may be considered a promotional opportunity, pursuant to the Colorado Equal Pay for Equal Work Act.Click here to view our full EEO policy statement. Click here for more information on your EEO rights under the law. Click here to view our Pay Transparency Nondiscrimination statement.Candidates for Moody's Corporation may be asked to disclose securities holdings pursuant to Moody's Policy for Securities Trading and the requirements of the position. Employment is contingent upon compliance with the Policy, including remediation of positions in those holdings as necessary.For more information on the Securities Trading Program, please refer to the STP Quick Reference guide on ComplianceNetPlease note: STP categories are assigned by the hiring teams and are subject to change over the course of an employee's tenure with Moody's.Moody's Corporation is a Government contractor subject to the Vietnam Era Veterans' Readjustment Assistance Act of 1974, as amended by the Jobs for Veterans Act of 2002, 38 U.S.C. 4212 (VEVRAA), which requires Government contractors to take affirmative action to employ and advance in employment: (1) disabled veterans; (2) recently separated veterans; (3) active duty wartime or campaign badge veterans; and (4) Armed Forces service medal veterans.VEVRAA Federal ContractorWe Request Priority Protected Veteran and Disabled Referrals for all of our locationsPlease contact Donna Hutchinson, Assistant Vice President, Talent Attraction for any questions regarding this listing.PDN-9bf2e0da-2a1b-4f23-bed5-3b6752fdb360

Job DescriptionAs part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.The Validation Staff Engineer is responsible for leading / assisting the validation team in supporting all site validation activities. This includes automation equipment, product transfers, new product development, and working as part of a cross-functional team responsible for sustaining change.The Validation Staff Engineer is an active participant in the origination of design concepts and specifications, process/technology development, product verification/validation, project planning, and other applicable documentation while adhering to quality and manufacturing requirements.Job Description:Serve as the primary interface between Operations and Quality Assurance.Originate and assist in the preparation and approval of change orders related to the operation and improvement of manufacturing processes.Assist the validation team in maintaining the Site Validation Master Plan.Support development projects, transfer projects, process changes, and engineering projects to provide overall guidance as it relates to quality standards, inspection techniques and frequencies, statistical analysis, testing, validations, and risk assessments (FMEAs).Direct and oversee validation activities for Operations, Engineering, Quality Assurance, and other functional areas.Review, revise, and maintain site validation procedures, qualification protocols, and associated data in accordance with FDA and ISO requirements.Lead and/or assist in training of staff involved in validation activities.Assist Quality, Operations, and Engineering personnel during inspections or audits.Performs other duties as assigned by Staff Validation Engineer and direct manager.Required Qualifications: Bachelor's degree from a four-year college or university and 10+ years of relevant experience or in the pharmaceutical, medical device, or in-vitro diagnostics industry with progressively increasing responsibilities is required.Associate degree and 15+ years of relevant experience in the pharmaceutical, medical device, or in-vitro diagnostics industry with progressively increasing responsibilities is required. Preferred Qualifications: Knowledge of global regulatory and quality requirements associated with medical devices.Working knowledge of ISO 13485 and 21 CFR Part 820.Experience with formal problem solving in a team environment.Detail oriented with the ability to lead multiple projects and activities as assigned.Proficiency in Microsoft Office products (i.e. Mini Tab, Excel, Outlook, PowerPoint, etc.).Previous medical device (Class II or Class III) experience required (from product development, validation engineering, sustaining engineering or manufacturing engineering).Must have good oral and written communication skills. This includes interfacing with external customers and internal Senior Management.Physical Requirements: Normal office and manufacturing environment.Position may require frequent communication and walking to other areas in which designated PPE will be required.Position will require sitting and standing.Employee may occasionally lift and/or move up to 25 pounds. Non-Negotiable Hiring Criteria: Must be proficient on validation protocol development, technical writing, data analysis, and report generation. i.e.; IQ, OQ, PQ, FAT, SAT as an example. Must have knowledge of process + packaging equipment, and software validation principles and concepts. Must have high level of expertise concerning current validation principles and regulatory requirements. Must be able to handle prioritization changes in a fast-paced environment. Strong understanding and proficiency in cleaning validation and cleaning process design. Must be proficient in statistical analysis and process control. Must be able to influence and coordinate activities of personnel over which he/she has no direct authority. Must possess strong organizational skills. Must be able to effectively communicate with all levels of the organization, from the General Manager to the production operators. Must be able to resolve conflicts between requests for process change and the validation requirements for those processes. Proficiency with various software platforms such as Minitab, Blue Mountain RAM, and Master Control is preferred. Independent self-starter who is capable of planning schedules, controlling plans, and leading projects as assigned. Must ensure adherence to FDA and ISO requirements throughout the product life cycle. Develop and execute verification and validation plans and protocols associated with product/process quality according to FDA and ISO requirements.Ability to manage multiple projects simultaneously without supervision. This includes creating detailed and accurate project tasks and schedules, interfacing with project team members and support personnel, and solving project-related conflicts and issues. Strong working knowledge of design and process controls. Travel when required to support business projects as a validation representative.Knowledge of process and product risk assessments.Knowledge of global regulatory and quality requirements associated with medical devices. Working knowledge of ISO 13485 and 21 CFR Part 820.Experience with formal problem solving in a team environment.Proficiency with various software platforms such as Minitab, Blue Mountain RAM, and Master Control is preferred.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.Apply today! http://jobs.thermofisher.comBenefits:We offer driven remuneration, annual incentive plan bonus scheme, healthcare, company pension/retirement, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Our client is seeking a manufacturing engineer to be responsible for designing, implementing, and optimizing manufacturing processes and systems in order to ensure efficient production and high-quality products. Their role involves analyzing production methods, identifying areas for improvement, and implementing strategies to enhance productivity, reduce costs, and maintain product quality.Job Function:Design, develop, and improve manufacturing processes, procedures, and layouts to achieve production goals.Identify and implement cost-effective process improvements, including automation, tooling upgrades, and workflow optimizations.Conduct time and motion studies, process flow analysis, and capacity planning to maximize efficiency and throughput.Collaborate with cross-functional teams, including design engineers and production managers, to ensure seamless integration of processes.Provide technical support and guidance to production teams to resolve manufacturing issues and achieve production targets.Investigate and troubleshoot process failures, quality problems, and equipment malfunctions, and implement corrective actions.Develop and maintain production documentation, including work instructions, process specifications, and standard operating procedures (SOPs).Perform root cause analysis and implement preventive measures to minimize production downtime and ensure product quality.Drive continuous improvement initiatives using Lean Manufacturing principles, such as 5S, Six Sigma, and Kaizen.Identify and eliminate waste, reduce variability, and streamline production processes to optimize productivity and reduce costs.Lead or participate in cross-functional teams to implement lean tools and techniques and foster a culture of continuous improvement.Conduct regular process audits and performance evaluations to track progress and identify areas for further improvement.Identify, evaluate, and recommend new equipment, tools, and technologies to improve manufacturing processes and capabilities.Collaborate with equipment vendors to ensure proper installation, commissioning, and validation of new equipment.Job Requirement:Bachelor's degree in engineering, preferably in mechanical, industrial, or manufacturing engineering.Strong knowledge of manufacturing processes, including machining, assembly, fabrication, and automation.Proficiency in process optimization, Lean Manufacturing, and quality improvement methodologies.Familiarity with CAD/CAM software and manufacturing simulation tools.Experience with statistical analysis, data-driven decision making, and process control techniques.Excellent problem-solving, analytical thinking, and decision-making skills.Strong communication and interpersonal skills

Location: REMOTESalary: $33.00 USD Hourly - $43.00 USD HourlyDescription: Our client is currently seeking a Engineer SeniorCandidates must have a minimum of 5 years of experience. Key words that should be in resumes: single use technologies, process engineering , and validation experiencewithin 100 miles of Cambridge, MA or Thousand Oaks, CA to be able to meet face to face with colleagues on occasion. This job will have the following responsibilities: Background in Single Use Technologies Background in Process Engineering Project management skills Validation experience Qualifications & Requirements: Bachelor's degree and 5 years of Engineering or Operations experience OR Master's degree and 3 years of Engineering or Operations experience OR Contact: [email protected] job and many more are available through The Judge Group. Find us on the web at www.judge.com

Location NY New York, United StatesSalary $110,000 - $150,000Industry Real estateJob DescriptionSkills: Electrical Systems, Revit or Catia, Architectural Engineering or Construction experienceQualifications: A degree in engineering or related field.Our team seeks a highly organized, detail-oriented professional who excels in precision design modeling of complex electrical systems, including wiring and wiring harnesses, electrical devices, lighting, and panel boards. If you are passionate about detailed high-quality engineering, have an in-depth understanding of electrical systems, and thrive in a collaborative/fast-paced setting, this role is for you.You will:• Join a diverse team of architects, manufacturing engineers, and industrial designers responsible for the design, development, and product validation of prefabricated MEP components.• Design and model intricate building electrical systems to a fabrication level of detail using advanced 3D modeling software.• Produce detailed shop drawings and comprehensive bill of materials for electrical, fire alarm, and low voltage systems.• Create work instructions, assembly drawings for customers which may include suppliers of combined products as well as the internal modular assembly process.• Coordinate effectively with various teams to ensure seamless integration of electrical system components and supporting elements built into products and coordinated with overall building projects.• Apply your experience in systems design, possibly gained in adjacent industries, to innovate and improve existing electrical solutions.• Maintain rigorous attention to detail in all aspects of work, from planning to execution.• Assist in defining product requirements, standardized data sheets, and specifications.• Develop test criteria in support of data sheets and for work instruction inclusion.• Support Supply Chain in the development of qualifying criteria for vendor bid sheets.• Review of shop drawings and submittals received from suppliers and fabricators.• Research innovative materials, connections, and processes while keeping up with standard construction products and staying informed about new materials, code changes, and current industry trends.• Maintain high standards of productivity, quality work, and collaboration.• Develop innovative ways to seek the integration of electrical components into sub assembly components.You are:• Exceptionally detail-oriented with a knack for precision in every aspect of your work.• Adept in using advanced 3D modeling software for electrical systems design.• A proactive communicator capable of working effectively within a team and across departments.• Innovatively minded, always seeking to improve and streamline processes and designs.• Substantially experienced in electrical engineering, particularly proven in a subcontractor role specializing in building component coordination and detailing of means & methods. Adjacent industry professions highly regarded.• Knowledgeable and experienced in designing and modeling electrical systems, including lighting, power distribution, controls, fire alarm, low voltage systems, & support hanger detailing.• Familiar with building codes and regulations and persistent in the examination of design against the building code and other relevant jurisdictional constraints.• Experienced working on mid to high-rise multi-family projects or large-scale facilities or complex componentry.• A problem solver, enabling you to quickly and creatively solve technical challenges inherent in modular construction and in the interface with conventional construction towards the development of high-resolution solutions.• Highly self-motivated, flexible, and resourceful.You have:• A degree in engineering or related field.• A minimum of 7 years experience is required.• Modular construction or prefabrication experience.• Strong leadership, written & verbal communication, and organizational skills.Benefits• Medical, Dental, and Vision Benefits• 20 PTO days per year, plus holidays• Free One Medical and virtual healthcare services, including Health Advocate and Teladoc• Commuter Benefits• FSA and HSA• 401k

Validation Staff Engineer - Medical DeviceDirect Hire (No C2C)Location: Middletown, VA 22645Salary: $120,000 -130,000 + Full Benefits Package and Bonus PotentialOverview: Our client is looking for a Validation Staff Engineer located in Middletown, VA. Their customers globally rely on their extensive range of products and services from life-saving medicines to lab essentials to next-generation instruments. The operations team leverages PPI (Practical Process Improvement Business System) to manufacture and produce these products and continuously improve productivity and quality all while contributing to the Mission - to enable our customers to make the world healthier, cleaner, and safer.Responsibilities:Responsible for leading / assisting the validation team in supporting all site validation activities. This includes automation equipment, product transfers, new product development, and working as part of a cross-functional team responsible for sustaining change. An active participant in the origination of design concepts and specifications, process/technology development, product verification/validation, project planning, and other applicable documentation while adhering to quality and manufacturing requirements.Serve as the primary interface between Operations and Quality Assurance.Originate and assist in the preparation and approval of change orders related to the operation and improvement of manufacturing processes.Assist the validation team in maintaining the Site Validation Master Plan.Support development projects, transfer projects, process changes, and engineering projects to provide overall guidance as it relates to quality standards, inspection techniques and FMEADirect and oversee validation activities for Operations, Engineering, Quality Assurance, and other functional areas.Review, revise, and maintain site validation procedures, qualification protocols, and associated data in accordance with FDA and ISO requirements.Lead and/or assist in training of staff involved in validation activities.Assist Quality, Operations, and Engineering personnel during inspections or audits.Requirements:Bachelor degree from a four-year college or university and 5+ years of relevant experience or in the pharmaceutical, medical device, or in-vitro diagnostics industry with progressively increasing responsibilities.Or Associate degree and 10+ years of relevant experience in the pharmaceutical, medical device, or in-vitro diagnostics industry with progressively increasing responsibilities is required.Must be proficient on validation protocol development, technical writing, data analysis, and report generation. i.e.; IQ, OQ, PQ, FAT, SAT as an example.Must have knowledge of process + packaging equipment, and software validation principles and concepts.Must have high level of expertise concerning current validation principles and regulatory requirements.Strong understanding and proficiency in cleaning validation and cleaning process design.Must be proficient in statistical analysis and process control.Must be able to resolve conflicts between requests for process change and the validation requirements for those processes.Independent self-starter capable of planning schedules, controlling plans, and leading projects as assigned.Must ensure adherence to FDA and ISO requirements throughout the product life cycle.Develop and execute verification and validation plans and protocols associated with product/process quality according to FDA and ISO requirements.ability to manage multiple projects simultaneously without supervision. This includes creating detailed and accurate project tasks and schedules, interfacing with project team members and support personnel, and solving project-related conflicts and issues.Strong working knowledge of design and process controls.Knowledge of global regulatory and quality requirements associated with medical devices. Working knowledge of ISO 13485 and 21 CFR Part 820.Preferred Qualifications:Proficiency in Microsoft Office products (i.e. Mini Tab, Excel, Outlook, PowerPoint, etc.).Working knowledge of ISO 13485 and 21 CFR Part 820.Knowledge of global regulatory and quality requirements associated with medical devices.Previous medical device (Class II or Class III) experience required (from product development, validation engineering, sustaining engineering or manufacturing engineering).Proficiency with various software platforms such as Minitab, Blue Mountain RAM, and Master Control is preferred.Client is not able to provide H1B sponsorship right now but may be available in the future

We are looking for a Manufacturing Engineer with a genuine passion for excellence and a desire to work in a fast-paced, entrepreneurial company.Overview: This role will be responsible for helping us implement manufacturing processes that result in high-quality products. The ideal candidate will have a good knowledge of tool design and fabrication methods. Other necessary manufacturing engineer skills include project management ability, commitment to quality, and familiarity with safety and environmental standards. If you're also inventive and meticulous, we'd like to meet you. Ultimately, you'll be the one to ensure our production lines work efficiently and effectively to satisfy our customers.Job Responsibilities:Evaluate manufacturing processes based on quality criteria, such as efficiency and speed. Provide technical assessment and validation review/approval for engineering and process changes.Requires the ability to troubleshoot systemic issues, develop, organize, analyze, and present interpretation of results regarding operational issues or Engineering projects, and apply advanced engineering principles to the design and implementation of new or modified system or processes.Offer production support and troubleshooting assistance to Production Staff, Design Engineering, R&D Engineering and Maintenance.Creation of Work Instructions and support the Design/R&D teams with optimizing designs for DFM principles. Train staff in new and existing processes.Develop and test effective automated and manual systems. Support manufacturing team for process improvements, assess proper tooling, and implement applicable certifications based on customer requirements.Aid in the development of BOM creation and optimize kitting operations.Creation and maintenance of PFEMA, DFEMA & Process Control Plans for both hand build and automation lines.Find ways to reduce costs and maximize quality. Utilize Lean Manufacturing Tools such as Root Cause Analysis, Gemba and Poka-Yoke to continually improve manufacturing operations.Ensure that manufacturing procedures follow safety and environmental regulations.QualificationsPrevious experience as a manufacturing engineer or similar roleDegree in Engineering; post-graduate degree is a plus, however recent graduates welcomeKnowledge of manufacturing processes, fabrication methods and tool designFamiliarity with manufacturing equipment and quality assurance techniquesMust have a thorough knowledge of manufacturing processes, quality systems, engineering design and start-up fundamentals, regulatory agency expectations and industry trends.Experience with regulated environments (i.e. cGMP, FDA, ISO 13485, OSHA, EPA) is essential.Commitment to health and safety standards and environmental regulationsMust be able to work independently as well as with teams, organize and manage projects by defining milestones, budgets, and schedules; prepare regulatory summaries and present validation to regulatory authorities.Salary:$70-80K, depending on experience and qualifications