field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

Straumann Group Position Title: Process Improvement &amp; Technology Engineer Co-Op Location/s: Andover (MA), United States Job Category: Manufacturing Company: STUM - Straumann US / Manufacturing Description: #ChangeMakers Ready to make an impact? We develop, manufacture, and supply dental implants, clear aligners, instruments, CADCAM prosthetics and biomaterials for use in esthetic dentistry, tooth replacement and restoration solutions or to prevent tooth loss. We empower our employees to perform and make an impact, to question the status quo, to drive change, to stay ahead of the competition. From the first Dental Implant in 1974 to the latest Digital Solution – we do things differently than others We deliver innovation based on evidence. This is part of our employer culture as well as an exceptional team spirit that truly encourages diversity and a powerful “can-do” attitude. #WeChangeDentistry every day. Be part of it. Straumann SummaryStraumann Manufacturing produces dental implants and associated parts at high volume. There are many different processes required to turn raw titanium into a dental implant with correct dimensional features, proper surface finishing, and appropriate packaging. The co-op program has been in place for a number of years, and we pride ourselves in giving the co-op student responsibility in a hands-on apprentice type-learning environment.Position SummaryYou will be challenged with a process improvement project, working both independently and as part of a team. You will report to the Director of Process Improvement and Technology and will function as a direct report engineer.Tasks:Participate in process improvement activities in the following areas<ul><li>CNC Machining</li><li>Automation</li><li>Statistical Process Control (SPC)</li><li>Laser Marking</li><li>Packaging / Labeling</li><li>Anodizing</li><li>Surface Treatment</li></ul>Data Analysis / Technology<ul><li>Collect and analyze Gauge Repeatability and Reproducibility (GR&amp;R) information</li><li>Update documentation through Engineering Change Order (ECO) process</li><li>Validation of New Processes</li></ul><h2>Work Environment &amp; Physical Demands:</h2><ul><li>Sit/stand for 8 hours</li></ul><h2>Minimum Qualifications:</h2><ul><li>Enrolled in an engineering degree program at a college or university</li></ul><h2>Preferred Qualifications:</h2><ul><li>Mechanical aptitude</li><li>Ability to get along well with others</li><li>High degree of attention to detail</li><li>Effective verbal and written communication skills</li><li>Analytical problem solving skills</li><li>CAD</li></ul> Additional Information: Whether you’re looking to build your career, improve your health, or brighten your SMILE, we offer generous benefits to help you achieve your goals. • Very Competitive total compensation plans (some positions include discretionary bonus, or Performance Share Units). • A 401(K) plan to help you plan for your future with an employer match • Great health, dental and vision insurance packages to fit your needs to ensure you’re happy and healthy. Straumann contributes a healthy portion towards employees’ premium. • Generous PTO allowance - plenty of time to recharge those batteries! Please understand that we do not need external support by recruiting agencies and consultants to fill this vacancy. Thank you for respecting this. Videos To Watch <a href="https://yccccccccccccccccccccccoutu.be/3lq5BLAvIdQ" target="_blank">https://youtu.be/3lq5BLAvIdQ</a> All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.Employment Type: Contract Alternative Locations: United States : Andover (MA) Travel Percentage: 0% Requisition ID: 14672 Equal Opportunity and Affirmative Action Employer (US applicants only) Straumann Group is an equal opportunity employer and will not discriminate against any employee or applicant for employment on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national origin, age, veteran status, or disability unrelated to job requirements. Straumann Group will take affirmative action to ensure that qualified applicants are employed and that employees are treated without regard to their race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran and disability status. In compliance with U.S. Department of Labor Executive Order 11246, Section 503 of the Rehabilitation Act, and Section 4212 of the Vietnam Era Readjustment Assistance Act, Straumann Group has developed and maintains an affirmative action program and plan. <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/EEOisthelaw-EnglishAccessibleformat-1648736178550.pdf" target="_blank">EEO is the Law - English Acccessible Version</a> <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/EEOisthelaw-English-1634312377644.pdf" target="_blank">EEO is the Law - English</a> <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/EEOisthelaw-Spanish-1634312378469.pdf" target="_blank">EEO is the Law - Spanish</a> <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/EEOisthelawSuppliment-1634312379241.pdf" target="_blank">EEO is the Law - Supplement</a> <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/E-Verify_Participation_Poster_ES-1634312375995.pdf" target="_blank">E-Verify Participation</a> <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/IER_RighttoWorkPoster-1634312379752.pdf" target="_blank">IER Right to</a><a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/IER_RighttoWorkPoster-1634312379752.pdf" target="_blank"> Work</a> <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/PayTransparencyNondiscriminationPoster-1634312380754.pdf" target="_blank">Pay Transparency Nondiscrimination</a> <a href="https://cdn.phenompeople.com/CareerConnectResources/STGRGLOBAL/documents/StraumannGroupEEO-AAPolicy-1634312381283.pdf" target="_blank">Straumann Group EEO-AA Policy</a> PI244261007

Process Improvement & Technology Engineer Co-Op

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status. Bedford, MA Full time REQ-6726 Job Title:Process Engineer - Metal MembraneJob Description:Position Summary: Our team supplies critical materials to the ultra-high purity semiconductor market. Our technology enables the latest chip technology and its applications, including IoT, AI, machine learning, and 5G. Specifically, we make products that filter and purify process chemistries used in semi-processing. Demand for our products is rising rapidly and we are looking for someone who can help us meet the needs of our customers.As part of Entegris’ Manufacturing Operations team, the Process Engineer will work closely with the production team to drive initiatives to increase output, reduce scrap and rework, eliminate waste, improve overall efficiency, and ensure quality and safety are built into processes at every step.This position is a 1st shift full-time position.Responsibilities: <ul><li>Develop, lead, and implement projects that improve operational efficiency to deliver savings that support corporate objectives, such as on-time delivery, productivity, scrap reduction, etc.</li><li>Maintain a presence in the manufacturing area to provide sustaining manufacturing support. Resolve day-to-day production/process issues. Drives issues to root cause.</li><li>Will be area owner in assembly and work closely with operators, other engineers, R&amp;D, NPI, and quality team.</li><li>Assist in the creation of CAD designs using software such as SolidWorks or CATIA.</li><li>Improve maturity of process data and apply statistical methods to develop a deeper understanding of our process with the goal of achieving higher yields and efficiency</li><li>Support the development of lean manufacturing processes, continuous improvement, standard work, problem solving, value stream mapping, training, and employee involvement</li><li>Apply manufacturing best practices to drive safety, quality, reliability, and predictability into everything we do.</li><li>Work with teams to identify problems, analyze information, and develop and implement process solutions.</li><li>Assist in directing and controlling processes in accordance with defined policies and procedures</li></ul>Qualifications and Preferred Skills: <ul><li>Bachelor’s degree in chemical or mechanical engineering or related discipline.&nbsp; </li></ul><ul><li>1-3 years’ experience working in a manufacturing or clean room environment. </li></ul><ul><li>Motivated and self-directed team player with good interpersonal skills. </li></ul><ul><li>Must have ability to reach out, communicate and influence personnel at all levels within the organization. </li></ul><ul><li>Demonstrated hands on problem solving utilizing good engineering principles. </li></ul>Physical Requirements: <ul><li>Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus. </li></ul><ul><li>Ability to lift and/or move up to 30 pounds. </li></ul><ul><li>Use hands to finger, handle, or feel; reach with hands and arms and you must be able to move throughout the department/facility. </li></ul><ul><li>Able to stoop, kneel, crouch, or crawl. </li></ul><ul><li>Work Environment: </li></ul><ul><li>The work environment characteristics described are representative of those an employee encounters while performing the essential functions of this job. </li></ul><ul><li>This is a manufacturing environment. It involves exposure to moving mechanical parts, risk of electrical shock and moderate to high noise levels. </li></ul><ul><li>Wearing safety glasses and Nitrile Gloves are also required. </li></ul><ul><li>Other safety garments or protection may need to be worn, depending on the nature of the work area. </li></ul><ul><li>Exposure to metal powders, isopropyl alcohol, and Di water. </li></ul> At Entegris, we want you to be part of our culture, which values your unique talents, skills, and experiences. We believe what we do is as important as how we do it.People at our company bring their true selves to work, and are appreciated not only for what they do, but for who they are. This plus the technical complexity of our products and solutions means you can be sure your work is both challenging and changing the world for the better. PI243695601

Process Engineer - Metal Membrane

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status. Bedford, MA Full time REQ-6531 Job Title:Quality EngineerJob Description:The Role: Our site in Bedford is seeking a Quality Engineer to join our team! The Quality Engineer will work with our team Quality Engineers and Process Engineers supporting the Bedford, MA site. Our site manufactures Ultra-high molecular weight polyethylene (UPE) membrane and Metal Membrane products. Production is focused on the Semi-conductor and Life Science industries. We are looking for a versatile engineer that can interpret customer requirements and provide the necessary leadership to ensure the site meets its’ quality and business objectives. The position will require a balancing of delegation and hands on participation as determined by the team members experience levels and training. This is a dynamic position that requires a partnership with all key functions. Our ideal engineer can look forward to working with a talented multi-disciplined team. We expect that you will collaborate, share, and be ready to learn in a team that partners closely with its customers and stakeholders. This position has the opportunity to be hybrid: 3 days on-site, 2 days working remotely What You’ll Do: <ul><li>Be a high contributor in advancing the Entegris Way quality mindset. </li></ul><ul><li>Working with the functions, the successful candidate will find solutions to complex problems, enhancing our fully data-driven, risk-based thinking culture. </li></ul><ul><li>Provide work guidance and mentorship to junior Quality Engineers </li></ul><ul><li>Provide leadership to the Change Control Management Board (CCMB) – establish continuity and ownership to ensure changes are made methodically in support of our quality requirements, with subject matter experts’ input. </li></ul><ul><li>Develop Verification &amp; Qualification (V&amp;Q) requirements to ensure customer requirements and manufacturing capabilities are aligned. </li></ul><ul><li>Act as the site (MC) focal point on quality related issues and involve appropriate site functions to address concerns. </li></ul><ul><li>Support and participate in a Continuous Improvement environment, always ensuring the highest standards are maintained. </li></ul><ul><li>Work both independently and on a team. Lead with influence across multi-disciplined teams to achieve quality initiatives. </li></ul><ul><li>Be an active member of all external and internal audits. </li></ul><ul><li>Work with external customers in responding to quality issues. </li></ul><ul><li>Ensure compliance with our quality management systems. </li></ul><ul><li>Continue to drive SPC across multiple manufacturing cells </li></ul><ul><li>Be ready to learn. Entegris is committed to continual learning. </li></ul><ul><li>Complete tasks as assigned in support of business objectives. </li></ul><ul><li>Be a hands-on Engineer ready to go out on the production floor and learn the process from beginning to end. </li></ul><ul><li>Be a key contributor to solving problems. </li></ul>What We Seek: <ul><li>The ability to analyze requirements and prioritize actions in support of the objectives. </li></ul><ul><li>A collaborative leader that inspires cross-functional teams, prioritizing and driving for execution </li></ul><ul><li>Can take on assignments with broad objectives where guidance is provided on critical issues only. </li></ul><ul><li>Demonstrated application of risk-based thinking and root cause analysis. </li></ul><ul><li>Demonstrated experience with Six Sigma and statistical methods. </li></ul>Your success will be measured by: <ul><li>Achieving the best possible outcome with integrity and collaborative leadership, building a cohesive team </li></ul><ul><li>Taking responsibility for self and team and delivering to commitments. Focusing on team success and assuming accountability for team results. </li></ul><ul><li>Naturally using common toolsets/resources to get things done. Open to trying new methods. </li></ul><ul><li>Executing consistently and finding ways to add new value. </li></ul>Qualifications: <ul><li>Minimally a bachelor’s degree in chemical engineering, material science, mechanical engineering, industrial engineering or related field.</li></ul><ul><li>Minimal 3 years of experience in a manufacturing environment with a significant amount of that time focusing on quality and / or continuous improvement related initiatives. </li></ul>Outstanding Candidates Will Have: <ul><li>A strong willingness to learn, and heavy interest in the semiconductor industry</li><li>Ability to work well in a cross-functional capacity</li></ul>What We Offer: At Entegris, we invest in providing opportunity to our employees and promote from within. The new hire in this role will have the potential to grow and create relationships across the organization and be recognized for demonstrated success and adherence to company PACE values. Our total rewards package goes above and beyond just a paycheck. Whether you’re looking to build your career, improve your health, or protect your wealth, we offer generous benefits to help you achieve your goals. <ul><li>Generous 401(K) plan with an impressive employer match </li></ul><ul><li>Excellent health, dental and vision insurance packages to fit your needs </li></ul><ul><li>Flexible work schedule and 11 paid holidays a year </li></ul><ul><li>Paid time off (PTO) policy that empowers you to take the time you need to recharge </li></ul><ul><li>Education assistance to support your learning journey </li></ul><ul><li>Values-driven culture with colleagues that rally around People, Accountability, Creativity and Excellence. </li></ul>At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status. Entegris strongly encourages all of its employees to be vaccinated against COVID-19. At Entegris, COVID-19 vaccination is preferred but not required at this time. At Entegris, we want you to be part of our culture, which values your unique talents, skills, and experiences. We believe what we do is as important as how we do it.People at our company bring their true selves to work, and are appreciated not only for what they do, but for who they are. This plus the technical complexity of our products and solutions means you can be sure your work is both challenging and changing the world for the better. PI243648832

Quality Engineer

ALL4 LLC Description:Job DescriptionALL4 is seeking a Staff Engineer/Staff Scientist for our Boston Office, located in Marlborough, MA. An ALL4 Staff Engineer/Staff Scientist is a technical staff member who shares our vision and passion for helping our clients succeed. They are self-motivated, coachable individuals interested in developing their technical and regulatory knowledge to enable the efficient completion of environmental projects. This individual will enjoy challenging environmental work, create their own professional path, and make a tangible contribution to a growing, employee-centric company. They will join a team of environmental professionals that are well-versed in complex air quality permitting, compliance, and multi-media projects, and who are committed to furthering our mission of being a globally recognized consulting company shaping environmental responsibility and creating distinction for employees, clients, and partners. Requirements:Duties &amp; Responsibilities<ul><li>Consistently deliver quality and timely work products to project team.</li><li>Review state and federal environmental regulations and expand environmental consulting knowledge.</li><li>Efficiently provide accurate technical calculations, effective written communication, and utilization of spreadsheets and databases to contribute to project deliverables.</li><li>Prepare technical reports in support of environmental permits.</li><li>Provide direct project support to colleagues of varying career levels.</li><li>Demonstrate strong analytical and technical skills; coordinate with team members the review of project deliverables to ensure project compliance with ALL4's quality assurance procedures.</li><li>Exhibit ALL4's core values in all transactions both internally and externally.</li><li>Meet billable hour and utilization targets.</li></ul>Qualifications<ul><li>Engineering or applicable environmental/science degree and an interest in environmental consulting.</li><li>Strong organizational, technical calculation, and analytical skills.</li><li>Ability to meet deadlines by independently managing priorities and workflows.</li><li>Commitment to excellence and ALL4's core values; openness to personal growth and coaching.</li><li>Creative thinking with complex problem-solving skills.</li><li>Excellent communication and interpersonal skills, including strong document production skills (proficiency in Word and Excel) and technical writing ability.</li><li>Acute attention to detail.</li><li>Basic chemistry knowledge.</li></ul>About ALL4ALL4 provides consulting services that span challenges encountered within industrial EHS programs. Our strategic services include air quality, chemical reporting and management, digital solutions, environmental, social, and governance, investigation and remediation, occupational health and safety, waste management, and water quality. ALL4 has offices and remote staff members in 27 U.S. states as well as in Calgary and Toronto, Canada, Madrid, Spain, Columbia, Mexico, and Brazil. The company has office locations in the metro areas of Philadelphia, PA (headquarters); Rancho Cucamonga, CA; Atlanta, GA; Louisville/Lexington, KY; Boston, MA; Raleigh, NC; Houston, TX; Bellingham, WA; and Washington, DC. ALL4 provides strategic consulting services to numerous heavily regulated industries across the country, including pulp and paper, food and beverage, consumer products, cement, chemical/pharmaceutical, waste management, power, oil and gas, and automotive. ALL4 has been consistently recognized as a Best Place to Work both regionally and nationally – growing in personnel, culture, and environmental disciplines. For more information, visit <a href="https://all4inc.us18.list-manage.com/track/click?u=efc96fd27b80aa1bfc20910af&amp;id=328aa7e1e0&amp;e=36aaea98f0" target="_blank">https://www.all4inc.com/</a> and connect with ALL4 on LinkedIn, Facebook, X, and Instagram. ALL4 is an Equal Opportunity Employer. We value diversity and do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, age, national origin, veteran status, disability status, or any other applicable characteristics protected by law. All employment is decided based on qualifications, merit, and business need. PI243600546

Staff Engineer/Staff Scientist - Boston Office

Equal Employment Opportunity/M/F/disability/protected veteran status Azzur Group Azzur is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever-changing healthcare field while simultaneously and organically exuding Azzur’s core values: Put Others First, Courage to Take Action, Take Personal Responsibility and Have Fun!Responsibilities: <ul><li>Lead and oversee the commissioning, qualification, and validation activities related to pharmaceutical manufacturing and facility systems, including process equipment, utilities, HVAC, cleanrooms, and automation systems. </li><li>Develop and execute validation protocols (IQ, OQ, PQ) and associated documentation, ensuring compliance with regulatory requirements and industry standards. </li><li>Conduct risk assessments and impact assessments to determine the criticality of systems and equipment, identifying areas that require validation and ensuring appropriate validation strategies are implemented. </li><li>Provide technical expertise and guidance to cross-functional teams on validation requirements, best practices, and compliance issues. </li><li>Collaborate with internal stakeholders, including Quality Assurance, Engineering, Manufacturing, and Regulatory Affairs, to ensure alignment and adherence to validation procedures and timelines. </li><li>Perform qualification activities, including equipment installation, operational testing, performance testing, and cleaning validation. </li><li>Analyze validation data, generate validation reports, and document any deviations or non-conformances, implementing corrective and preventive actions as needed. </li><li>Stay up-to-date with current regulations, industry trends, and technological advancements related to validation practices, ensuring compliance and suggesting process improvements when appropriate. </li><li>Participate in regulatory inspections and audits, providing support and documentation as required. </li><li>Mentor and provide guidance to junior validation engineers, promoting professional development and knowledge sharing within the team. </li></ul> Qualifications and Experience: <ul><li>Bachelor's degree in Engineering, Pharmaceutical Sciences, or a related field. </li><li>Minimum of 8-10 years of experience in commissioning, qualification, and validation activities within the pharmaceutical or biotech industry. </li><li>In-depth knowledge of regulatory guidelines and requirements, including FDA, EMA, and ICH guidelines. </li><li>Strong understanding of validation methodologies, such as risk-based validation, process validation, cleaning validation, and computer systems validation. </li><li>Experience in authoring and executing validation protocols (IQ, OQ, PQ) and generating associated documentation. </li><li>Proficient in utilizing validation tools, software, and statistical analysis methods. </li><li>Excellent problem-solving skills and attention to detail, with the ability to analyze complex data sets and identify trends or deviations. </li><li>Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and present validation findings to stakeholders. </li><li>Experience working in a GMP-regulated environment, with knowledge of cGMP principles and industry best practices. </li><li>Professional certifications such as Certified Validation Professional (CVP) or Certified Quality Engineer (CQE) are desirable. </li><li>Experience with custom equipment validation a huge plus. </li></ul>#LI-AH1 Do What You LoveAt Azzur, we look for talented individuals who take pride in the work they do. We foster employee growth by encouraging our employees to focus on doing what they love and what they do best. PI243227488

Senior Validation Engineer

Equal Employment Opportunity/M/F/disability/protected veteran status Azzur Group Azzur is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever-changing healthcare field while simultaneously and organically exuding Azzur’s core values: Put Others First, Courage to Take Action, Take Personal Responsibility and Have Fun!Responsibilities: <ul><li>Lead and oversee the commissioning, qualification, and validation activities related to pharmaceutical manufacturing and facility systems, including process equipment, utilities, HVAC, cleanrooms, and automation systems. </li><li>Develop and execute validation protocols (IQ, OQ, PQ) and associated documentation, ensuring compliance with regulatory requirements and industry standards. </li><li>Conduct risk assessments and impact assessments to determine the criticality of systems and equipment, identifying areas that require validation and ensuring appropriate validation strategies are implemented. </li><li>Provide technical expertise and guidance to cross-functional teams on validation requirements, best practices, and compliance issues. </li><li>Collaborate with internal stakeholders, including Quality Assurance, Engineering, Manufacturing, and Regulatory Affairs, to ensure alignment and adherence to validation procedures and timelines. </li><li>Perform qualification activities, including equipment installation, operational testing, performance testing, and cleaning validation. </li><li>Analyze validation data, generate validation reports, and document any deviations or non-conformances, implementing corrective and preventive actions as needed. </li><li>Stay up-to-date with current regulations, industry trends, and technological advancements related to validation practices, ensuring compliance and suggesting process improvements when appropriate. </li><li>Participate in regulatory inspections and audits, providing support and documentation as required. </li><li>Mentor and provide guidance to junior validation engineers, promoting professional development and knowledge sharing within the team. </li></ul> Qualifications and Experience: <ul><li>Bachelor's degree in Engineering, Pharmaceutical Sciences, or a related field. </li><li>Minimum of 8-10 years of experience in commissioning, qualification, and validation activities within the pharmaceutical or biotech industry. </li><li>In-depth knowledge of regulatory guidelines and requirements, including FDA, EMA, and ICH guidelines. </li><li>Strong understanding of validation methodologies, such as risk-based validation, process validation, cleaning validation, and computer systems validation. </li><li>Experience in authoring and executing validation protocols (IQ, OQ, PQ) and generating associated documentation. </li><li>Proficient in utilizing validation tools, software, and statistical analysis methods. </li><li>Excellent problem-solving skills and attention to detail, with the ability to analyze complex data sets and identify trends or deviations. </li><li>Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and present validation findings to stakeholders. </li><li>Experience working in a GMP-regulated environment, with knowledge of cGMP principles and industry best practices. </li><li>Professional certifications such as Certified Validation Professional (CVP) or Certified Quality Engineer (CQE) are desirable. </li><li>Experience with custom equipment validation a huge plus. </li></ul>#LI-AH1 Do What You LoveAt Azzur, we look for talented individuals who take pride in the work they do. We foster employee growth by encouraging our employees to focus on doing what they love and what they do best. PI243227509

Project Engineer- Water US-MA-Reading Job ID: 2023-2914 Type: Regular Full-Time # of Openings: 1 Category: Engineering Reading, MA Overview Innovative and reliable for more than a century, Weston &amp; Sampson strives to make the world a better place through interdisciplinary design, engineering, and environmental services. An employee-owned company (ESOP) of more than 725 professionals, we are seeking talented technical and professional individuals to join our growing firm. Dedicated to improving quality of life for both our clients and our employees, we offer opportunities to collaborate on meaningful projects that transform the environment, with a team that respects and values your ideas. Weston &amp; Sampson offers a flexible work environment, competitive compensation, excellent benefits, and dynamic career growth, in an equitable and welcoming corporate culture that embraces diverse perspectives and experiences and recognizes people for their contributions.Weston &amp; Sampson is an Equal Opportunity Employer. We embrace the rich perspectives and experiences that arise from people of different races, ethnicities, cultures, sexual orientation, gender identities, ages, socio-economic statuses, abilities, and religions, as well as valuable insight from other untapped groups without our Weston &amp; Sampson family and the communities we serve. Your world is always changing, and so are we. Join us as we grow: <a href="https://www.westonandsampson.com/join-our-team/" target="_blank">https://www.westonandsampson.com/join-our-team/</a>#midlevelprofessionals Responsibilities Weston &amp; Sampson is currently seeking a Project Engineer with 2-5 years of experience to work with our Water group in our Reading, MA office. Qualifications What you’ll do:<ul><li>Preparing water utility designs including preparation of plans and specifications for permitting and construction for water treatment, pump station, storage, and water main projects</li><li>Familiar with water system planning and assessment, hydraulic modeling, design and construction administration for water supply, treatment and distribution systems </li><li>Dealing with multiple projects and clients along with managing technical, budgetary and client aspects of projects</li><li>Flexible workload, diverse project files, and working well with multiple staff members including delegating work to entry level staff</li></ul>What you will bring:<ul><li>Bachelor’s or Master's degree in Civil/Environmental Engineering</li><li>Experience with AutoCAD, Civil 3D, GIS, REVIT (preferred)</li><li>PE is preferred or ability to become licensed within twelve (12) months</li><li>Strong writing and verbal communications skills</li><li>Strong work ethic</li><li>Valid driver’s license</li></ul>#LI-Hybrid PI243083292

Project Engineer- Water

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status. Billerica, MA Full time Posted 2 Days Ago REQ-6558 Job Title:Senior Project EngineerJob Description: At Entegris, we want you to be part of our culture, which values your unique talents, skills, and experiences. We believe what we do is as important as how we do it.People at our company bring their true selves to work, and are appreciated not only for what they do, but for who they are. This plus the technical complexity of our products and solutions means you can be sure your work is both challenging and changing the world for the better. PI243035543

Senior Project Engineer

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status. Bedford, MA Full time Posted 2 Days Ago REQ-6555 Job Title:Production EngineerJob Description:Entegris is currently seeking a talented and innovative&nbsp;Production&nbsp;Engineer who will own sustaining and quality assurance activities for manufacturing products and lead continuous improvement projects to drive process efficiency and reduce product variation. The Engineer will work closely with various business functions to support manufacturing processes and resolve customer product quality inquiries.PRIMARY RESPONSIBILITIES AND DUTIES<ul><li>Sustain productivity and quality levels of the manufacturing process. Activities include dispositioning of non-conforming materials (raw materials, intermediates, and finished goods), establishing/reviewing/updating SPC/SQC control limits, maintaining FMEAs and Control Plans, and participating in customer quality and ISO audits. </li></ul><ul><li>Production Eng will be ultimately responsible for the product quality from Incoming to finished goods. </li></ul><ul><li>Drive productivity in the manufacturing process by identifying opportunities and implementing solutions to improve safety, quality, productivity, yield, and cost. </li></ul><ul><li>Reduce variation in product and process parameters by identifying key contributors to variation and implementing effective control systems and enhanced manufacturing processes. </li></ul><ul><li>Make data-driven decisions to improve product quality, efficiency, and throughput. </li></ul><ul><li>Lead root cause investigations of manufacturing out-of-control conditions by fixing equipment and processes, observing, and performing experiments, locating the source of problems, and implementing permanent effective corrective actions. </li></ul><ul><li>Act as the process specialist, create work instructions, OJTS, and training requirements for processes and for new processes, lead training for Operators and submit signed OJTs to supervisors. </li></ul><ul><li>Develop and execute the Design of Experiment trials, manage new product scale-ups, and lead new equipment installations &amp; qualifications as dictated by business needs. </li></ul><ul><li>Support machine breakdown resolution by providing guidance and hands-on assistance to remedy and correct issues. </li></ul><ul><li>Sustain and develop incoming inspection for Raw material, in-process and outgoing inspection for manufacturing released products. </li></ul><ul><li>Identify KPIV and OVs for raw material and maintain the SPC charts, RFCs, and disposition for the raw material. </li></ul><ul><li>Support Material Engineer (SQE) for non-conformance in RM or external processing. </li></ul><ul><li>Own the Metrology for released products in Manufacturing along with performing MSA on a needed basis. </li></ul><ul><li>Lead Metrology continuous improvement. </li></ul><ul><li>Work with Plant Quality Engineer to support customer complaints, escalations, and excursions. </li></ul><ul><li>Perform OCAP for customer ship to control limits. </li></ul><ul><li>Support plant quality and customer quality with Customer requests and FAs. </li></ul><ul><li>Support CQE with Customer PCS reviews. </li></ul><ul><li>Support NPD with release to manufacturing and training. </li></ul><ul><li>Own BCP for metrology and manufacturing tools. </li></ul><ul><li>Lead excursions in the production line, and communicate to stakeholders in a timely manner. </li></ul><ul><li>Follow change control requirements. </li></ul>MINIMUM QUALIFICATIONS At Entegris, we want you to be part of our culture, which values your unique talents, skills, and experiences. We believe what we do is as important as how we do it.People at our company bring their true selves to work, and are appreciated not only for what they do, but for who they are. This plus the technical complexity of our products and solutions means you can be sure your work is both challenging and changing the world for the better. PI243035597

9 Engineering Jobs in Massachusetts