Project Manager, On-Market Products - Pleasanton, CA at Calyxo

Pleasanton, California, United States -

Full Time

Start Date

Immediate

Expiry Date

16 Oct, 26

Salary

140000.0

Posted On

18 Jul, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Medical Device Development, Cross-functional Leadership, Risk Management, Waterfall Methodology, Scrum, FDA Submission Process, QMSR Requirements, JIRA, Monday.com, MS Office, Operational Support, Supply Chain Mitigation, Cost Reduction, Stakeholder Communication, Portfolio Planning

Industry

Medical Equipment Manufacturing

Description

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology. Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere. Summary: You will serve as Project Manager and play a leadership role in maintaining our kidney stone treatment systems, accountable for leading multi-disciplinary teams in operational and sustaining improvements. You will plan for long-view work, balance day-to-day issues as they arise, define schedules, share information widely with team members and stakeholders, and foster healthy, productive teams. You will help us pursue ‘No stone left behind’! Your experience in operations and sustaining support for devices and capital equipment will facilitate your success. Your excellent PM skills, predictive/waterfall and adaptive/scrum work management methods, collaborative approaches and attention to social cues will keep everyone engaged and productive. Work examples: CVAC device, CVAC vision system, sustaining improvements, cost reduction, supply chain mitigations. You have led work from idea to production cut-in. In This Role, You Will: Communicate with clarity and impact: Provide visibility on project progress, decisions, dependencies, risks, and timelines to teams and senior staff. Ensure transparency through excellent written and verbal communication. Develop and drive cross-functional alignment: Facilitate agreement among engineering, operations, supply chain, quality, commercial and regulatory on scope, priorities, and value delivery to achieve project objectives. Own execution: Lead planning and delivery of multiple, concurrent projects. Define objectives, success metrics, and guide internal and external contributors to execute effectively while adapting to changing conditions. Foster collaboration and trust: Build strong relationships across teams and levels to encourage knowledge sharing, accountability, and positive work habits. Enable technical delivery: Coordinate development activities. Manage prioritization, define “Done,” and lead planning and retrospectives for predictable delivery. Manage risks and remove obstacles: Anticipate challenges and eliminate barriers to progress. Apply structured risk-based decision-making, contingency planning, and trade-off analysis to maintain momentum. Champion process improvement: Contribute to evolving project management practices and tools tailored to organizational culture, driving efficiency and scalability. Support portfolio planning: Partner with stakeholders to forecast future project delivery, update routinely, and balance resource capacity against active programs, ensuring successful execution across multiple initiatives. Who You Will Report To: Director, Program Management, R&D Requirements: Education: BS Engineering/Science degree or equivalent required Minimum 5+ years total experience; medical device development experience strongly preferred Work location: Pleasanton, CA office Travel: ~10% Full-time employment Hard Skills: experience with operational support of on-market products, and development & cut-in of improvements for hardware, firmware & capital systems. Familiarity with FDA submission process, QMSR requirements. Proficiency in MS Office, Atlassian/JIRA, Monday.com and other PM tools. Soft skills: strong facilitation and communication skills across technical and executive audiences. Ability to lead cross-functional teams and influence without direct authority. Naturally accountable and organized. Physical requirements: Must be able to sit for up to 8 hours/day and operate standard office equipment. Compliance with relevant county, state, and Federal rules regarding vaccinations. What We Offer: At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself. We also offer an attractive compensation package, which includes: A competitive base salary $130,000 - $140,000 and variable incentive plan Stock options – ownership and a stake in growing a mission-driven company Employee benefits package that includes 401(k), healthcare insurance and paid vacation Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth. Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. Disclaimer: At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following: Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture. Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment. Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of firstname.lastname@calyxoinc.com. If you receive a request for information from any other domain, please contact us directly at info@calyxoinc.com to verify the legitimacy of the communication. We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.

Responsibilities

Lead multi-disciplinary teams in the operational and sustaining improvements of kidney stone treatment systems. Manage concurrent projects from idea to production, ensuring alignment across engineering, quality, and regulatory teams.