Supply Chain Project Manager

11200 Hudson Rd, Woodbury, MN 55129, USA

Posted Thursday, February 12, 2026 at 6:00 AM

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

This is a great opportunity as a Supply Chain Project Manager will be responsible for managing a variety of large, cross‑functional projects critical to our strategic objectives and the success of the business. The key responsibilities include managing the full project lifecycle, developing and maintaining project plans, timelines, and budgets, identifying and mitigating project risks, communicating project status to stakeholders, leading and motivating cross‑functional project teams, and driving continuous improvement in project management processes.

• Manage the full project lifecycle, including initiation, planning, execution, monitoring and control, and closure.
• Develop and maintain charters, project plans, timelines, budgets, and resource allocations.
• Identify and mitigate project risks, issues, and dependencies.
• Communicate project status, progress, and issues to stakeholders at all levels of the organization.
• Lead and motivate cross‑functional project teams to deliver results on time and within budget.
• Drive continuous improvement in project management processes, tools, and methodologies.
• Ensure compliance with GMP and other regulatory requirements.

• A bachelor's degree in a relevant field (such as business, engineering, or project management).
• LSSBB or LSSGB Certification
• At least 7 years of experience in project management, with a track record of successfully delivering complex projects on time and within budget.
• Experience managing cross‑functional project teams, including coordinating activities across multiple departments and geographies.
• Strong project management skills, including the ability to develop and maintain project plans, timelines, and budgets, as well as identify and mitigate risks and issues
• Excellent communication and stakeholder management skills, with the ability to build relationships with stakeholders at all levels of the organization.
• A demonstrated ability to work in a fast‑paced, dynamic environment and manage multiple projects simultaneously.

• PMP certification.
• Experience working in a regulated industry, such as medical device, pharmaceuticals, or biotechnology.
• Experience managing technology transfer projects for a contract design and manufacturing organization (CDMO).

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, & Vision, Health Savings Accounts, Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and 401k Benefits, etc.).

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!