11 Engineers jobs in Shelton

Join to apply for the Project Management/PMP Tutor role at Varsity Tutors, a Nerdy Company 2 days ago Be among the first 25 applicants Join to apply for the Project Management/PMP Tutor role at Varsity Tutors, a Nerdy Company The Varsity Tutors Live Learning Platform has thousands of students looking for online Project Management/PMP tutors nationally. As a tutor on the Varsity Tutors Platform, you’ll have the flexibility to set your own schedule, earn competitive rates, and make a real impact on students’ learning journeys—all from the comfort of your home. Why Join Our Platform? Base contract rates start at $18/hour and increase for specialized subjects. Plus, you’ll earn incrementally higher pay for each session with the same student—reaching up to $0/hour. Get paid up to twice per week, ensuring fast and reliable compensation for the tutoring sessions you conduct and invoice. Set your own hours and tutor as much as you’d like. Tutor remotely using our purpose-built Live Learning Platform—no commuting required. Get matched with students best-suited to your teaching style and expertise. Our AI-powered Tutor Copilot enhances your sessions with real-time instructional support, lesson generation, and engagement features—helping you save prep time and focus on impactful teaching. We handle the logistics—you just invoice for your tutoring sessions, and we take care of payments. What We Look For In a Tutor Strong communication skills and a friendly, engaging teaching style. Expertise in Project Management/PMP and the ability to explain concepts clearly. Ability to personalize lessons and adapt to different learning styles. Priority given to those with tutoring experience, teaching experience, and graduate-level education. Ways To Connect With Students 1-on-1 Online Tutoring - Provide personalized instruction to individual students. Instant Tutoring - Accept on-demand tutoring requests whenever you’re available. About Varsity Tutors And 1-on-1 Online Tutoring Our mission is to transform the way people learn by leveraging advanced technology, AI, and the latest in learning science to create personalized learning experiences. Through 1-on-1 Online Tutoring, students receive customized instruction that helps them achieve their learning goals. Our platform is designed to match students with the right tutors, fostering better outcomes and a passion for learning. Please note: Varsity Tutors does not currently contract with tutors in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New Hampshire, North Dakota, Vermont, West Virginia, or Puerto Rico. Please note: Varsity Tutors does not contract in: Alaska, California, Delaware, Hawaii, Maine, New Hampshire, North Dakota, Vermont, West Virginia or Puerto Rico. Seniority level Seniority level Entry level Employment type Employment type Full-time Job function Job function Project Management and Information Technology Industries Technology, Information and Internet Referrals increase your chances of interviewing at Varsity Tutors, a Nerdy Company by 2x Get notified about new Project Management Specialist jobs in Norwalk, CT . Port Washington, NY $101,100.0 - 158,950.00 1 week ago Shelton, CT 80,000.00- 105,000.00 4 days ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

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We anticipate the application window for this opening will close on - 9 Aug 2025

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

At Medtronic you can begin a lifelong career of exploration and innovation, while helping champion healthcare access and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

You will be a key member of the Post Market Development - Compliance PMO within the Surgical Operating Unit, focused specifically on ensuring the Surgical product portfolio maintains compliance with MDR Regulations. This role will be the primary liaison with our Clinical organization to integrate deliverables into the broader Compliance roadmap and planning activities.

In this role, you will:

• Ensure Compliance: Collaborate with Clinical, Quality, and Regulatory teams to develop an annual plan for MDR compliance deliverables.
• Manage Projects: Oversee projects through the Change Development Process to implement critical compliance needs across the Surgical product portfolio.
• Shape Processes: Help develop scalable processes and governance models for Compliance PMO to enable timely and efficient execution.
• Drive Lifecycle Success: Ensure product safety, efficacy, cost-effectiveness, and market readiness throughout the product lifecycle.
  
  

• Lead cross-functional teams to evaluate, develop, and manage lifecycle projects for products and processes
• Manage the operational aspects of projects, including planning, scheduling, and status reporting
• Monitor project progress, identifying risks, and implementing solutions to meet business goals
• Manage project financials, including forecasting and tracking of accruals and actuals
• Manage stakeholder communications and ensuring alignment to project/program objectives
• Develop or co-develop processes and tools to track project progress and ensure compliance within assigned areas.
• Gather, plan, and manage requirements to ensure they meet demands of the projects key stakeholders.
• Communicate with stakeholders and obtain stakeholder engagement to ensure the end products or processes address business needs effectively.
  
  

• Bachelors Degree and minimum of 4 years of relevant experience OR advanced degree with a minimum of 2 years of relevant experience
• 2+ years of experience working in a cross-functional, matrixed organization.
• 2+ years leading projects of increasing complexity
• 2+ years of experience with budget management or financial tracking within projects
• Proven ability to form strong relationships with key cross-functional partners
  
  

• Knowledge in product development and commercialization in the medical device industry
• PMP or PgMP certification
• Strong knowledge of MDR regulations and its implications for Clinical and Quality
• Proven experience managing projects within compliance, particularly related to MDR or similar regulations.
• 2+ years leading stakeholder communications across various peer and leadership levels of an organization
• Experience with advanced scheduling and resource management tools like Microsoft Project and/or Resource First/PDWare
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Project Management and Information Technology
• Industries Medical Equipment Manufacturing, Hospitals and Health Care, and Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Medtronic by 2x

Oxford, CT 120,000.00- 150,000.00 2 weeks ago

Rocky Hill, CT 85,000.00- 115,000.00 2 weeks ago

Wallingford, CT 140,000.00- 390,000.00 2 weeks ago

Waterbury, CT 130,000.00- 160,000.00 2 days ago

Waterbury, CT 150,000.00- 200,000.00 3 weeks ago

New Haven, CT 68,000.00- 120,500.00 3 days ago

New Haven, CT 68,000.00- 120,500.00 4 days ago

Newington, CT 55,000.00- 65,000.00 1 week ago

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At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to do our work. We're working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This is an onsite role located at our North Haven, CT site.

At the intersection of healthcare innovation and project management expertise, we invite you to lead the charge in ensuring customer satisfaction design integrity, and impeccable quality across each milestone. The Principal Product Development Project Management Specialist will support the Core Surgical Innovations (CSI) business in an on-site position based out of North Haven, CT.

We seek out and hire a diverse workforce at every level: We need fresh ideas and inclusive insights to continue to be an innovative industry leader that's why we make it a point to seek out, attract and develop employees who are patient-centric, passionate, and who represent the same wide variety of life experiences as our patients.

As a Principal Product Development Project Management Specialist, you will lead a variety of new product development projects centered around next generation Core Surgical Innovations technologies. This pivotal role will lead cross functional teams through our product development process, from concept development through launch, delivering novel solutions to our patients and customers. The role has high visibility, with regular presentations to the executive leadership team to communicate project status, schedule, risks, and other key program metrics.

Responsibilities may include the following and other duties may be assigned:

• Lead multifaceted cross-functional teams, encompassing design, development, verification, validation, documentation. Guide them through the product development journey, ensuring project success and aligning with business objectives.
• Develop and uphold project plans, schedules, risk registers, budgets, and resource allocation for designated projects. Champion timely and effective communication, continuously updating stakeholders on the project's advancement.
• Manage project meetings, meticulously document meeting minutes and pivotal decisions, and diligently track action items.
• Foster harmony between the project team, the business, and other stakeholders. Integrate input early in process development and quality planning.
• Establish robust channels for both formal and informal communication, relaying accurate and current information to all stakeholders.
• Organize and guide a diverse array of distributed, cross-functional resources toward triumphant outcomes.
• Serve as the primary liaison for prominent leaders and stakeholders spanning the organization.
• Engage stakeholders, ensuring their involvement in shaping end products and processes that effectively address business challenges.
• Contribute to project prioritization decisions by offering data-driven insights and analysis derived from ongoing and previous projects.
• Reviews status of projects and budgets; manages schedules and prepares status reports.
• Monitors the project from initiation through delivery.
• Assesses project issues and develops resolutions to meet productivity, quality, and client-satisfaction goals and objectives

Minimum job requirements:

• Bachelor's degree and 7+ years managing technical related projects OR: an advanced degree and 5 years of experience managing technical related projects

Nice to have:

• Master's degree in engineering and/or scientific discipline, or MBA
• PMP Certification or other PMI certification
• Experience with ProChain scheduling methodology
• Expert skills with managing project plan, scope, schedule, budget, and risk register
• Agile Software Development certification, including SAFe
• Lean/Six Sigma Certification
• Expert skills in JIRA, JAMA, Polarion, PowerBI tools
• Experience leading diverse and complex projects and programs and coordinating multiple teams to execute concurrent, interdependent projects.
• Knowledge of medical device R&D, product development, and clinical/regulatory procedures; including identifying use conditions, developing requirements, and implementing risk management activities like failure mode analysis
• Excellent written and oral communication skills and able to influence all customers (both internal and external) on issues that impact the business and its technical service and product strategies
• Expert active listening skills with a keen awareness for various messaging styles; and polished ability to tailor delivery to a broad range of audiences
• Exceptional influencing and interpersonal skills, negotiating; managing change; goal setting; planning and organizing teamwork; ability to address difficult situations; conflict resolution; resource constraint and problem solving.
• Experience participating in internal and external audits as a Subject Matter Expert
• Comprehensive knowledge of medical device standards and regulations (e.g., IEC 60601, IEC 62304, ISO 14971, ISO 13485).

Physical job requirements:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For office roles: while performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the work conditions and physical requirements that may be specific to each role.

Benefits & compensation:

Medtronic offers a competitive salary and flexible benefits package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD): $142,400.00 - $213,600.00. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.