# Sr. Program Manager at Lonza

Lonza is hiring a Sr. Program Manager in Houston, United States. Level rates it Little AI ●○○○; you can [apply on Lonza](https://jobsbylevel.com/go/6177609d-5687-4935-80ff-f6bd69a00a93?utm_medium=ai-agent).

AI Level 1, AI centrality 38 out of 100. US - Houston, TX.

## Details

- Company: [Lonza](https://jobsbylevel.com/companies/lonza)
- AI level: AI Level 1 (score 38 out of 100)
- Location: US - Houston, TX
- Posted: October 20, 2026
- Apply: https://jobsbylevel.com/go/6177609d-5687-4935-80ff-f6bd69a00a93?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=sr-program-manager-at-lonza-6d7cfd

## Description

Sr. Program Manager Houston, TX The actual location of this job is in Houston, TX, US. Relocation assistance is available for eligible candidates and their families, if needed. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. A variety of benefits dependent on role and location. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits . What you will do: Be the interface between the Customer and Lonza to ensure execution and delivery according to Lonza and the Customer’s expectations Understand the Customer’s needs and represent their interests by acting as their advocate on-site Use all PM Standard Work processes to effectively manage projects Fully accountable for all operational aspects in leading and motivating cross-functional project teams to deliver on all scope objectives with the highest level of quality Manages the financial aspects of assigned programs. Actions include but not limiting to forecasting, invoicing, and revenue recognition. Ensure Customer satisfaction throughout the life of the program through collaborative relationship management with AM/Sales Act as PM Peer during Onboarding of new individuals Develop and share best practices in PM tools and methodologies at local level Ensure adherence to Global Program and Project Center of Excellence (PPM CoE) Standards, including maintenance of data integrity excellence in Planview. What we are looking for: Required: 3-5 years in managing clinical development and GMP manufacturing. Candidates must demonstrate experience managing programs that involve both clinical-stage development and manufacturing operations. Demonstrated manufacturing experience within a CDMO or biopharmaceutical environment , including cross-functional coordination of GMP manufacturing, process development, technology transfer, scale-up, manufacturing readiness, and product supply. Experience managing programs spanning pre-clinical development through clinical manufacturing and commercial manufacturing, including coordination of technical, quality, regulatory, and operational deliverables. Experience building, managing and owning cross-functional integrated timelines 10+ Years of experience in the life sciences, biotechnology, or CDMO industry, inclusive of 4–5 years of experience in Program Management Bachelor's Degree in Life Sciences, Biotechnology, Engineering, or related field Matrix Management Ability to engage with individuals over whom you have no direct control, to form a cohesive team around a set of common project objectives. Ensure a robust project governance is in place and provide clarity of roles, responsibilities & expectations of everyone associated with the project. Demonstrate motivational skills and ability to build robust, long-lasting relationships, developing rapport and trust within the project teams. Demonstrate a positive attitude fostering open dialogue and two-way communication within the team. Lead cross-functional teams across Cell and Gene Therapy development, clinical operations, process development, manufacturing, Quality Assurance, Quality Control, Regulatory Affairs, Supply Chain, and commercial functions. Drive alignment between clinical development objectives and manufacturing execution, ensuring clinical supply requirements, production schedules, technical milestones, and quality deliverables are effectively coordinated. Partner with manufacturing leadership and technical teams to ensure program commitments are aligned with production capacity, resource availability, equipment readiness, and operational priorities. Organization Skills Ability to successfully plan, organize and control all activities and

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/sr-program-manager-at-lonza-6d7cfd

Source: https://jobsbylevel.com/jobs/sr-program-manager-at-lonza-6d7cfd

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