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JOB DETAILS

Sr. Project Manager - CDMO, Pharmaceutical Manufacturing

CompanyLTS Lohmann Therapy
LocationWest St. Paul
Work ModeOn Site
PostedSeptember 11, 2026
About The Company
At LTS, our purpose drives everything we do: We CARE for patients, our partners , employees and communities, we CREATE innovative drug delivery solutions, and we DELIVER high-quality products to global markets with an exceptional track record in commercial manufacturing. As a global CDMO, we offer end-to-end development and manufacturing services for pharmaceutical and biotech companies. Our technology portfolio spans transdermal patches, oral thin films, nasal and sterile (drug delivery systems) dosage forms , wearable drug delivery devices as well as microneedle array patches. With over 40 commercial products and 50+ active development programs, we combine deep expertise with patient-centric innovation to advance small molecules, biologics, and vaccines. Operating from five global sites in the US, Germany and Israel and a representative office in China, LTS powers the future of drug delivery.
About the Role





About the Company

LTS Lohmann Therapy Systems is a global leader in transdermal and oral thin‑film drug delivery technologies. Our teams have pioneered breakthroughs such as the first contraceptive patch, nicotine patch, oral active ingredient film, and Parkinson’s patch. When you join LTS, you become part of a team that continues to shape the future of patient care and bring life‑changing therapies to market.

At LTS, our purpose drives everything we do: We CARE. We CREATE. We DELIVER. We’re committed to fostering an employee experience that reflects our innovation — supportive, collaborative, and empowering. Across our New Jersey and Minnesota locations, you’ll work alongside knowledgeable experts on diverse projects in an environment where every day is different and your contributions truly matter

Senior Project Manager- CDMO, Pharmaceutical Manufacturing


Position Overview:

LTS is seeking a Senior Project Manager to lead complex development and commercial programs from initiation through closeout. In this highly visible role, you will partner with internal teams, external customers, and cross-functional stakeholders to keep programs on time, within scope, and aligned to quality expectations in a pharmaceutical/GMP manufacturing environment.


This position is based in West St. Paul, MN and is hybrid eligible after the introductory period is complete.

Schedule: Monday–Friday, 8:00 AM–4:30 PM


What You’ll Do:

  • Lead senior-level project management activities across program initiation, planning, execution, control, and closeout.
  • Manage complex customer-facing programs to successful delivery, balancing timelines, scope, quality, risk, cost, and stakeholder expectations.
  • Serve as a trusted point of contact for development and commercial programs, providing high-quality customer service and clear communication.
  • Communicate project status, risks, decisions, and next steps to internal and external stakeholders in a timely, professional manner.
  • Influence and lead cross-functional teams to align priorities, resolve issues, and drive accountability for committed deliverables.
  • Apply LTS project management methodologies and tools, including timelines, agendas, meeting notes, action logs, risk tracking, and project task lists.
  • Identify critical path activities, proactively assess timeline impacts, and escalate significant risks or business relationship concerns.
  • Resolve program-related issues involving statements of work, billing, material inventory, material ordering and disposition, customer complaints, and change-of-scope items.
  • Partner with accounting, supply chain, process engineering, purchasing, manufacturing, and other functions to support purchase orders, invoices, work orders, ERP requirements, and resource planning.
  • Facilitate phase gate reviews, customer visits, audits, and project meetings while helping teams navigate competing priorities.
  • Support product packaging, design-related customer requests, and out-of-scope work proposals as needed.

 

What You’ll Bring:

  • Bachelor’s degree in engineering, operations management, a science-related field, or equivalent relevant experience.
  • 5+ years of project management experience, including leadership of complex, cross-functional programs.
  • 5+ years of experience in a pharmaceutical, GMP manufacturing, CDMO, or similarly regulated environment.
  • Demonstrated ability to use project management methodologies and tools to manage schedules, scope, action items, risks, and stakeholder communication.
  • Ability to clearly communicate complex technical and scientific topics to technical and non-technical audiences.
  • Proficiency with Microsoft Office applications, including Word, Excel and Project.
  • Strong communication, organization, time management, interpersonal influence, and conflict resolution skills.


Preferred Qualifications:

  • Expert level proficiency with MS Project.
  • Project Management Professional Certification (PMP).
  • Lean Six Sigma Green Belt or Black Belt certification.
  • Exposure to SAP ERP is very helpful.


LTS is an equal opportunity employer. Employment with LTS is at will, and this job posting does not constitute a contract of employment.


Key Skills
Project ManagementPharmaceutical ManufacturingGMPCDMOCross-functional LeadershipRisk ManagementStakeholder ManagementMS ProjectSupply ChainProcess EngineeringERPSAPLean Six SigmaCommunicationTime ManagementConflict Resolution
Categories
Management & LeadershipManufacturingHealthcareEngineeringScience & Research
Job Information
📋Core Responsibilities
The Senior Project Manager will lead complex development and commercial programs from initiation through closeout within a pharmaceutical GMP environment. They will partner with cross-functional teams and external customers to ensure projects remain on time, within scope, and aligned with quality expectations.
📋Job Type
full time
💰Salary Range
$90,000 - $120,000
📊Experience Level
5-10
💼Company Size
134
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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