1

Senior Development Manager Jobs in Santa Rosa, CA

Sr. R&D Engineer

Santa Rosa, CA ยท On-site

$114K - $156K/yr

In this role, you'll provide advanced technical leadership to support the lifecycle management ... In addition, the Sr. R&D Engineer contributes to the design and development of next-generation ...

Sr. R&D Engineer

Santa Rosa, CA ยท On-site

$114K - $156K/yr

In this role, you'll provide advanced technical leadership to support the lifecycle management ... In addition, the Sr. R&D Engineer contributes to the design and development of next-generation ...

Senior Software Development Engineer

Bodega Bay, CA ยท On-site

$145K - $191K/yr

Release and Deployment Management: You define and evolve the deployment strategy to ensure rapid ... This ensures data-driven development and organizational efficiency, keeping the engineering team ...

New

Release and Deployment Management: You define and evolve the deployment strategy to ensure rapid ... This ensures data-driven development and organizational efficiency, keeping the engineering team ...

New

Senior Retirement Manager

Sonoma, CA ยท On-site

$184K - $230K/yr

The Senior Manager administers the Retirement Committee, collaborates closely with internal ERISA ... Professional Development * Stays current on legislative and regulatory trends; champions HRIS tools ...

Senior Retirement Manager

Santa Rosa, CA ยท On-site

$184K - $230K/yr

The Senior Manager administers the Retirement Committee, collaborates closely with internal ERISA ... Professional Development * Stays current on legislative and regulatory trends; champions HRIS tools ...

Senior Product Manager

Bodega Bay, CA

$150K - $198K/yr

... Senior Product Manager to drive consumer engagement, delight, and monetization from an online ... Analytical - 3+ years of experience using a rapid, test, and learn product development process to ...

Senior Sales Associate

Napa, CA ยท On-site

$30 - $33/hr

About Discovery Management Group Discovery Management Group leads one of the nation's most purpose ... We continually aspire and invest in learning and development opportunities that support our team ...

next page

Showing results 1-20

Senior Development Manager information

See Santa Rosa, CA salary details

$49.7K

$158.5K

$243.3K

How much do senior development manager jobs pay per year?

As of Jun 24, 2026, the average yearly pay for senior development manager in Santa Rosa, CA is $158,472.00, according to ZipRecruiter salary data. Most workers in this role earn between $123,000.00 and $188,600.00 per year, depending on experience, location, and employer.

What is the difference between Senior Development Manager vs Software Development Manager?

AspectSenior Development ManagerSoftware Development Manager
Required CredentialsBachelor's/Master's in Computer Science or related field; extensive experience in software developmentBachelor's/Master's in Computer Science or related field; experience in software project management
Work EnvironmentOversees multiple development teams, strategic planning, cross-department collaborationManages software development teams, focuses on project delivery and technical leadership
Employer & Industry UsageTech companies, software firms, IT departmentsSoftware companies, tech startups, IT divisions
Common Search & ComparisonOften compared with Software Development Manager regarding leadership scope and seniority

The main difference is that a Senior Development Manager typically has broader strategic responsibilities and oversees multiple teams or projects, while a Software Development Manager focuses more on managing software projects and technical teams. Both roles require similar technical credentials but differ in scope and seniority.

What is the highest salary of BDM?

The highest salary for a Business Development Manager (BDM) can vary widely depending on industry, experience, and location, but senior BDMs in large organizations or high-demand sectors can earn over $120,000 annually, often supplemented with bonuses and commissions. Compensation typically increases with proven sales success, strategic skills, and leadership responsibilities.

What is the role of a senior development manager?

A senior development manager oversees software or product development teams, manages project timelines, allocates resources, and ensures the delivery of high-quality solutions. They often coordinate with stakeholders, implement development processes, and may use project management tools like Agile or Scrum to meet organizational goals.

How does a Senior Development Manager typically collaborate with cross-functional teams to ensure project success?

A Senior Development Manager regularly works with product managers, designers, quality assurance, and operations teams to align project goals and timelines. They facilitate communication between these groups, resolve blockers, and ensure that technical solutions meet both business requirements and user needs. This role often involves leading strategic planning sessions, coordinating sprints, and conducting regular check-ins to monitor progress and adjust priorities. Effective collaboration is key to delivering projects on time and fostering a positive, high-performing team environment.

What jobs in the US pay 300,000 a year?

Senior Development Managers, especially in technology, finance, or large corporations, can earn $300,000 or more annually, often including bonuses and stock options. High-level executive roles such as CTOs or VP of Engineering also frequently reach this compensation level, typically requiring extensive experience, leadership skills, and advanced technical knowledge.

What is a Senior Development Manager?

A Senior Development Manager is a leadership professional responsible for overseeing teams of developers or engineers, managing project timelines, and ensuring the successful delivery of software or product development projects. They play a key role in strategic planning, resource allocation, and mentoring junior staff. Senior Development Managers collaborate with stakeholders to define project goals, ensure quality standards, and drive continuous improvement within the development process. Their experience enables them to bridge the gap between technical teams and business objectives, ensuring that projects align with organizational goals.

What are the key skills and qualifications needed to thrive as a Senior Development Manager, and why are they important?

To thrive as a Senior Development Manager, you need extensive experience in software development, project management, and leadership, often supported by a degree in computer science or a related field. Familiarity with agile methodologies, version control systems like Git, and tools such as JIRA or Azure DevOps is typically required. Exceptional communication, team-building, and strategic thinking skills help distinguish top performers in this role. These skills ensure effective project delivery, team motivation, and alignment with business goals in a dynamic technology environment.

What jobs pay 500,000 a year in the US?

Senior Development Managers in technology or software companies can reach annual compensation of $500,000 or more, especially with bonuses, stock options, and profit sharing. High-level executive roles such as CTOs or VP of Engineering also often exceed this salary level, typically requiring extensive experience, leadership skills, and advanced technical knowledge.
What job categories do people searching Senior Development Manager jobs in Santa Rosa, CA look for? The top searched job categories for Senior Development Manager jobs in Santa Rosa, CA are:
What cities near Santa Rosa, CA are hiring for Senior Development Manager jobs? Cities near Santa Rosa, CA with the most Senior Development Manager job openings:
Sr. R&D Engineer

Sr. R&D Engineer

Endologix

Santa Rosa, CA โ€ข On-site

$114K - $156K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago


Job description

Overview
Join our innovative, patient-focused Research & Development team as a Sr. R&D Engineer at Endologix!
WHO WE ARE:
Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training-supported by industry-leading clinical evidence. At Endologix, we're driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health.
What sets us apart is not just our technology, but our culture. At Endologix, we foster a forward-thinking, mission-driven environment where every team member plays a vital role in advancing patient care. Our core values guide how we operate. As for our people? We empower them with the tools, trust, and continuous learning they need to grow. If you're passionate about making a meaningful difference in healthcare, you'll find purpose and belonging here.
Our Core Values are the guiding principles informing our choices and actions, because our customers and patients depend on us:
  • Patient Outcomes Drive Us: We improve lives with every advancement we deliver.
  • Integrity Defines Us: We do what's right, stay transparent, prioritize quality, and own our actions.
  • Innovation Advances Us: We stay curious, adaptable, and push boundaries.
  • Boldness Propels Us: We take smart risks and are unafraid in our pursuit of excellence.
  • Collaboration Unites Us: We partner across teams and with physicians to drive exceptional results.

ABOUT THE ROLE:
We're looking for a Sr. R&D Engineer to join our Research & Development team. In this role, you'll provide advanced technical leadership to support the lifecycle management, enhancement, and sustaining engineering of commercially available stent grafts and catheter-based delivery systems. This role drives design improvements, evaluates product performance, and ensures compliance with regulatory and quality system requirements to support product safety, reliability, and patient outcomes.
In addition, the Sr. R&D Engineer contributes to the design and development of next-generation stent graft and delivery system technologies, supporting activities from concept and feasibility through verification, validation, and commercialization. Working cross-functionally with Quality, Regulatory, Manufacturing, Clinical, and physician partners, this role applies engineering expertise, analytical rigor, and sound judgment to solve complex technical challenges and advance Endologix's innovation and business objectives.
Responsibilities
WHAT YOU'LL DO:
  • Lead the development and execution of rigorous, science-based testing strategies, drafting comprehensive test plans (e.g., experimental design, statistical analyses) and detailed reports that ensure design robustness, regulatory compliance, and ultimately improved patient outcomes.
  • Conceptualize, develop, validate, and continuously refine test methods to support product design, verification and validation (V&V), and global regulatory submissions, demonstrating integrity through accurate, transparent, and defensible data practices.
  • Partner with New Product Development (NPD) teams to support component qualification and the creation and maintenance of Product Development Process (PDP) deliverables (e.g., Design Specifications, FMEAs, Traceability Matrices), ensuring alignment with quality system requirements and design control standards.
  • Document all work in accordance with GMPs, SOPs, and the company's quality system, maintaining audit readiness and full traceability in support of regulatory expectations and organizational integrity.
  • Provide technical leadership and clear direction while collaborating effectively with senior management, engineers, technicians, and cross-functional stakeholders to drive project milestones and successful commercialization.
  • Evaluate and influence designs for new products, product enhancements, components, assemblies, and tooling-balancing innovation with risk mitigation and manufacturability considerations.
  • Conduct thorough failure investigations, root cause analyses, and technical risk assessments to identify hazards and implement effective mitigations within Design and Process FMEAs.
  • Collaborate closely with R&D, Manufacturing, Regulatory, Quality, and Clinical teams to resolve complex technical issues, support sustaining engineering activities, and ensure continued product performance and safety in the field.
  • Proactively identify opportunities for product improvement, process optimization, and cost efficiencies while maintaining a bold yet thoughtful approach to risk and innovation.
  • Serve as a technical mentor to junior engineers and technicians, fostering a culture of curiosity, accountability, and continuous learning.
  • Engage with physician partners and external stakeholders, when appropriate, to ensure product designs reflect real-world clinical needs and deliver meaningful patient impact.
  • Perform additional responsibilities as assigned, supporting team objectives and advancing departmental and organizational goals.

Qualifications
WHAT YOU'LL BRING:
Education:
  • Bachelor's degree in Engineering discipline (Mechanical / Biomedical preferred) or equivalent experience.

Experience:
  • 5+ years of experience with a bachelor's degree, 3+ years of experience with a Master's degree, 15+ years of experience without an advanced degree.
  • Experience in medical device manufacturing, development, testing, or designing, GMP, FDA, and ISO requirements and experience writing protocols, test plans, test reports, design control regulation and experience with catheter and stents preferred.

Skills/Competencies:
  • Advanced Engineering Expertise: Strong foundation in mechanical and/or biomedical engineering principles with demonstrated experience in medical device design, verification and validation, and sustaining engineering activities.
  • Patient-Centered Design Mindset: Applies engineering rigor with a clear understanding that product performance, safety, and reliability directly impact patient outcomes; consistently prioritizes risk mitigation and clinical effectiveness.
  • Regulatory & Quality Systems Acumen: Deep working knowledge of FDA Quality System Regulations, ISO 13485, design controls, risk management (ISO 14971), and GMP requirements; demonstrates integrity through meticulous documentation and defensible data practices.
  • Experimental Design & Statistical Analysis: Proficiency in developing robust test strategies, applying statistical tools, interpreting complex datasets, and drawing sound technical conclusions to support regulatory submissions and engineering decisions.
  • Risk Assessment & Failure Analysis: Skilled in conducting FMEAs, root cause investigations, hazard analyses, and implementing effective corrective and preventive actions.
  • Innovation & Technical Curiosity: Demonstrates adaptability and creative problem-solving; challenges assumptions, explores new approaches, and advances product and process improvements while balancing technical and regulatory constraints.
  • Cross-Functional Collaboration: Effectively partners with R&D, Manufacturing, Quality, Regulatory, Clinical, and external stakeholders; fosters alignment and drives shared accountability for results.
  • Technical Leadership & Influence: Provides clear technical direction, mentors junior engineers and technicians, and confidently presents complex information to leadership and cross-functional teams.
  • Project & Time Management: Manages multiple priorities in a fast-paced development environment; delivers high-quality work within established timelines and project milestones.
  • Communication Excellence: Communicates technical concepts clearly and concisely in written reports, protocols, presentations, and cross-functional discussions.
  • Bold & Accountable Decision-Making: Exercises sound engineering judgment, takes thoughtful risks when appropriate, and owns outcomes with transparency and accountability.

WHAT WE OFFER:
At Endologix, we know that great work starts with great people - and people do their best when they feel valued and supported. That's why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You'll be part of a team that's making a real impact on patients' lives. When you join us, you're not just taking a job, you're building a meaningful career with a team that's invested in your success.
The compensation package includes:
  • Base salary of $100,000/yr-$115,000/yr
  • Discretionary bonus
  • Equity participation as approved by Board of Directors (4-year vesting schedule)
  • Comprehensive health, dental, and vision insurance plans
  • Flexible Health Savings Accounts (HSAs) and/or Flexible Spending Accounts (FSAs)
  • Generous paid time off (vacation, sick leave, holidays, and flexible time off that is available for Exempt employees)
  • 401(k) retirement plan with company match

Plus:
  • Employee wellness initiatives, mental health resources, and Employee Assistance Program (EAP)
  • Employee recognition programs and awards
  • Commuter benefits or transportation stipends

OUR COMMITMENT TO EQUAL OPPORTUNITY & VETERAN INCLUSION:
Endologix LLC is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. As a federal contractor, Endologix LLC is committed to taking affirmative action to recruit, employ, and advance in employment qualified individuals with disabilities and protected veterans.