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Engineering/Architecture Salary in Framingham, MA

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Engineering/Architecture Salary in Framingham, MA

115 000 $ Average monthly salary

Average salary in branch "Engineering/Architecture" in the last 12 months in Framingham

Currency: USD Year: 2024
The bar chart shows the change in the average wages in Framingham.

Popular professions rating in the category "Engineering/Architecture in Framingham" in 2024 year

Currency: USD
Mechanical Engineer is the most popular profession in Framingham in the category Engineering/Architecture. According to our Site the number of vacancies is 1. The average salary of the profession of Mechanical Engineer is 115000 usd

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Principal Embedded Security Engineer, Consumer Software
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You know the moment. It's the first notes of that song you love, the intro to your favorite movie, or simply the sound of someone you love saying "hello." It's in these moments that sound matters most. At Bose, we believe sound is the most powerful force on earth. We've dedicated ourselves to improving it for nearly 60 years. And we're passionate down to our bones about making whatever you're listening to a little more magical. The engineering team at Bose is a thriving, passionate, deeply skilled team of professionals from a broad range of disciplines and experiences, who share a common goal-to create products that provide transformative sound experiences.Job Description About BoseYou know the moment. It's the first notes of that song you love, the intro to your favorite movie, or simply the sound of someone you love saying "hello". It's in these moments that sound matters most. At Bose, we believe sound is the most powerful force on earth. 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Senior Embedded Security Engineer, Consumer Software
Bose Corporation, Framingham
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Process Engineer Coop
DPS Group Global, Framingham
PROCESS ENGINEER COOPJOB SUMMARYThe Process Engineering Co-op will be work closely with the Process Engineering Discipline at DPS in the effort to provide our clients with the process engineering designs for a variety of life-science projects. DPS is a global consulting, engineering and construction management company, serving high-tech industries around the world. We have industry experts in key locations in Europe, the Middle East, Asia, and the US, bringing world-class resources and the latest innovative technologies to every project. In New England, DPS primary focus is on Architecture, Engineering, Construction, and Validation related to designing and building of life-science manufacturing facilities. The Process Engineering Discipline works closely with our clients to define their process, capture the key elements in design documents like process flow diagrams (PFDs) and piping and instrument diagrams (P&IDs), and developing equipment specifications and 3D piping diagrams for the procurement and construction phases of the project.The Process Engineering Co-op will be delegated tasks of increasing responsibility during the six month assignment. Early tasks may have some administrative or training basis, but all will help the Co-op to understand the process by which a client's goals are realized into a final design that is constructible and functional. This Co-op assignment will also utilize a rotation of learning in the other disciplines of the design phase (Architecture, Mechanical, Electrical, Plumbing/Fire-protection, Instrument & Controls, Quality) as well as the Project Management, Construction, and Commissioning/Qualification/Validation (CQV) departments. KEY COMPETENCIES & RESPONSIBILITIES• The chosen candidate must have an interest in the technical aspects of the pharmaceutical / biotech / novel therapeutics manufacturing process.• Self-motivated individual who has a thirst for learning• Pump / hydraulic system principles• Basic thermodynamic operationsJOB REQUIREMENTS• Candidate for Chemical Engineering B.S. with at least one previous Co-op assignment• Preferred Co-op experience in the Life Sciences industry• Good oral communication skills• Work individually and as a team• Learn new skills through a variety of platforms• MS Office, especially Excel• PDF editor (i.e. Bluebeam)
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DPS Group Global, Framingham
DPS Group is hiring for Spring Coops in all Engineering and Architecture disciplines.Positions commence in January, 2024 for a period of 3, 4, or 6 months.
Principal Manufacturing Compliance Engineer
Sanofi, Framingham
Principal Manufacturing Compliance Engineer owns and ensures a robust investigations process, uses expert knowledge of compliance and GXP manufacturing processes to manage investigations, improvement initiatives, and major projects within manufacturing operations.Core ResponsibilitiesPractice and promotes safe work habits and adheres to Sanofi's safety procedures and guidelines.Lead and perform investigations, CAPAs and Change Controls (CCRs)for on-time closure and supporting Annual Product Reviews.Provide guidance and direction to team to drive complex investigation close outs, determine root cause and implement appropriate Corrective and Preventative Action.Utilize manufacturing process knowledge and investigation skill sets to identify and resolve manufacturing issues, improve process operations, and affect positive change.Represent Manufacturing Compliance Engineer team on cross-functional teams involved in the design and implementation of new or updated quality systems in accordance with the corporate standards, regulatory standards, cGMP, and industry standards.Actively participate and provide input and feedback to cross functional teams to ensure alignment on investigations and identified corrective and preventative actions.Escalate to management when investigations pose risk shipment or release and impact to department and site metrics.Maintain and report applicable department or organizational metricsRoutinely perform trend and statistical analysis as required to identify continuous improvement opportunities within manufacturing functional groupsWork to develop strategy and action plans for improving the system where opportunities are identified.Lead and actively participate in cross-functional continuous improvement projects with Manufacturing, Engineering, Validation, Quality Assurance, Quality Control, Facilities, Metrology, and Manufacturing Technical Services.Recognize and act on potential compliance issues and opportunities for process changes/improvement.Provide front room support during regulatory inspectionsRepresent investigation team during internal and external GxP audits.Partner with cross functional teams and team members, direct and indirect management chain to ensure the following:Participate in timely completion of investigation, deviations and CAPAFacilitation, Collaboration, completion, and active follow-upSupport investigation team to ensure site Key Performance Indicators (KPIs) are consistently metUse experience and knowledge of manufacturing functional areas to propose continuous improvements to deliver efficiency gains.Assess customer needs and provides effective solutions through regular analysis of data and information reported from a broad variety of sources.Routinely assess progress made against Key Performance indicators to reach individual and team goals.Sensitive to the broader work environment and fosters relationships with partners, experts from other functions and customers in order to achieve tactical objectives.Monitor Quality Systems (e.g., investigations and CAPAs) activities to ensure compliance with company and regulatory standards.Assist with Quality Management Review (QMR)/Quality Council.Support Corporate Compliance initiatives.*Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs.Leadership QualificationsAn ongoing commitment to conducting our global business according to the highest legal and ethical standards and to continually pursue excellence in the development and delivery of all our products and services. This includes:Adhering to all applicable laws and regulations of the places in which we conduct business, as well as our own Company policies and procedures.Being honest and treating people with respect and courtesy.Constantly striving to make Sanofi's a great place to work and a company respected for the quality of its people and products.Acting as role models for our fellow employees by acting responsibly, fairly and honestly in our dealings and exercising sound judgment in performing our jobs.Leading People:Sanofi's leaders are courageous motivators that inspire, build, and retain highly effective teams while managing for high performance and developing others.Leading the Business:Sanofi's leaders are effective at operating in an evolving, complex, and dynamic environment, providing clear direction and instruction to direct reports, and continuously looking internally and externally for best practices and areas for improvement.Delivering to Customers:Sanofi's leaders understand patient and customer needs and build relationships to meet manufacturing goals while continuously improving operations by setting high standards for the team so they may perform to a level of excellence.Basic Qualifications:Bachelor's degree in Sciences, Technical, Engineering or Advanced degree with 8 years in a cGXP manufacturing environment or a Master's degree in Sciences, Technical, Engineering or Advanced degree and 3 years of experience in cGXP manufacturing environment.Experience in troubleshooting, investigation, and root cause analysis in a cGMP environmentProficiency with critical thinking and technical writingThorough knowledge and understanding of the technical and commercial aspects of pharmaceutical API products, Current Good Manufacturing Practices {part of GxP}, validation principles, and applicable regulationsExtensive experience with Quality Management Systems.Ability to learn and operate various enterprise systems including LIMS, SAP, OSI/PI, EMS, BMS, is requiredRegardless of format, able to carry all technical communications which will allow the end-user, specifically QA personnel and regulatory inspectors, to arrive at the intended conclusions.Knowledge of GXP regulations and guidance.Ability to effectively coach and train employees.Demonstrate high-level of communication for cross-functionally and across levels, including timely identification of potential sources of conflict and resolve independently or escalate to stakeholders promptly.Excellent verbal and written communication skills, with the ability to share vision, direction, and data with colleagues across all levels and in a wide range of different work groupsStrong ability to balances the speed of delivering work with quality and shows commitment to make improvements in both aspectsDemonstrate a high degree of engagement and involvement in all job-related activities. Catalyst for selecting methods, techniques and evaluation criteria for obtaining results. Mentor junior members of team on technical topics. May potentially be a Qualified Trainer on investigation processPreferred QualificationsBachelor's degree in Biology, Chemistry, Biochemistry, Chemical Engineering.Operations experience in one or more of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation.Keeps tasks (deviations, CAPA, or CCR) on schedule, tracks them carefully, and delivers results on time; seeks assistance to solve a problem quickly to adhere to on-time deliveryExperience with project managementExperience in supervisory teamsAbility to lead staff in absence to people managerSpecial Working ConditionsAbility to gown and gain entry to manufacturing areas.Ability to work off shift hours, seldom, to support product releaseSanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.Learn more about Sanofi M&S: https://www.youtube.com/watch?v=_xz_sSanXhc#GD-SG#LI-GZPursue progress, discover extraordinaryBetter is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!