Development Services Capacity Planner

Development Services Capacity Planner United States, Portsmouth (New Hampshire) Location 100% on-site. Portsmouth, NH. Relocation assistance is available for eligible candidates and their families. The Development Services Capacity Planner optimizes laboratory operations by managing daily schedules, equipment usage, and maintenance. Additionally, this role oversees laboratory personnel, including technicians and interns, while ensuring study timelines are met. Ultimately, the planner drives continuous improvement initiatives to make overall laboratory workflows more efficient and productive. What you will get Competitive salary and comprehensive benefits package. Opportunities for career development and advancement. Supportive and collaborative team environment. Access to cutting-edge technology and tools. Commitment to employee well-being and safety. Inclusive workplace culture. Recognition and reward for your contributions. Responsibilities Integrated Scheduling: Develop and maintain aligned schedules for Cell Culture Development (CCD), Purification Development (PD), and Analytical Development (AD) to ensure visibility for both short- and long-term execution plans. Capacity Management: Review resource utilization, resolve potential over/under-capacity bottlenecks, and balance supply with demand. Collaboration & Alignment: Partner with the mammalian scheduling team, participate in manufacturing production schedule (MPS) meetings, and coordinate cross-functional (MSAT, IT, Engineering) ad-hoc work. Performance Tracking: Monitor and report On Time, In Full (OTIF) deliverables, and generate KPIs to identify negative scheduling trends. Equipment Lifecycle: Oversee the onboarding and decommissioning of lab instrumentation while maintaining accurate tracking systems (e.g., SAP). Contract Review: Review Master Service Agreements (MSA) and Statements of Work (SOW) for completeness and accuracy. Stakeholder Support: Collaborate with Commercial Development, customers, and internal teams to resolve contract comments and inquiries. Qualifications Bachelor’s Degree required (Biological Sciences or Biomedical/Chemical preferred) with 5+ years of biotech industry experience. Strong communication, technical writing, organizational, and interpersonal skills. The capacity to motivate and encourage others in the achievement of specific objectives. Familiarity with large scale manufacturing, cGMP and regulations. Able to shift priorities based on company needs and multitask on multiple projects. Ability to think critically and logically. Intermediate knowledge of scale up and mass transfer, bioreactor operation; intermediate understanding of filtration; basic knowledge of statistical analysis. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. Ready to shape the future of life sciences? Apply now. #J-18808-Ljbffr