Job Description
Job Description
Job Title : Manufacturing Engineering Manager
Department / Division : Engineering
Reports to : Sr. Director Technical Services
About LTS :
LTS Lohmann Therapy Systems is a premier, global Contract Development and Manufacturing Organization (CDMO) and partner the pharma industry trusts most to deliver innovative oral, transdermal, and intradermal drug delivery systems. From concept to market, launch to lifecycle management, we deliver single source oral and transdermal drug delivery solutions that power partners’ market advantage. Every one of our 1,000 plus members of the LTS family, across three continents, is focused on utilizing our collective strength and innovation to explore new therapeutic opportunities, maximize partner value and improve patient outcomes.
We Care.
We Create.
We Deliver.
Job Summary
LTS is seeking a dynamic and results-driven Manufacturing Engineering Manager to lead and optimize our pharmaceutical manufacturing processes. You will be instrumental in driving continuous improvement initiatives, mentoring our production teams, and ensuring operational excellence while maintaining the highest quality and compliance standards. This is an exciting opportunity to lead impactful projects and contribute to the advancement of life-changing therapies.
This is a full time, mostly onsite located in West St. Paul MN.
Hybrid potential after initial probationally period, up to 2 days / weekWe do not offer relocation assistance for this role : Candidates with existing plans to move to the Twin Cities, MN area, may be considered.What You Will Do :
Lead Process Improvement : Identify, analyze, and implement process improvements within pharmaceutical manufacturing operations.Cross-Functional Collaboration : Work closely with R&D, Production, Quality, and other teams to ensure process efficiency, consistency, and compliance.Drive Continuous Improvement (CI) : Implement Lean Manufacturing, Six Sigma, and other CI methodologies to streamline operations, reduce waste, and enhance productivity.Foster a Culture of CI : Develop and drive a culture of continuous improvement within the manufacturing department.Optimize Equipment Performance : Lead CI initiatives to optimize equipment performance, reduce downtime, and increase throughput while maintaining high-quality standards.Data-Driven Problem Solving : Utilize data-driven approaches, including process control, root cause analysis, and failure modes, to improve manufacturing processes.Team Leadership & Mentoring : Provide leadership, mentoring, and training to production and engineering teams.Promote Best Practices : Champion best practices in process execution, quality, and safety.Team Development : Support the development of team members' skills and competencies.Project Management : Lead and manage engineering projects focused on process enhancements, equipment upgrades, and manufacturing system improvements.Regulatory Compliance : Ensure all manufacturing processes meet cGMP, FDA, EMEA, and other relevant regulatory and safety requirements.Quality Assurance Collaboration : Collaborate with the Quality Assurance team to investigate and resolve manufacturing discrepancies, deviations, and CAPAs.SOP Development : Develop and implement standard operating procedures (SOPs).Data Analysis & Reporting : Analyze manufacturing data to identify trends and provide regular reports to senior management.Cross-Departmental Interaction : Interact with sales, operations, and project managers to resolve problems and provide solutions.Qualifications :
Bachelor’s degree in Engineering, Pharmaceutical Sciences, or a related field. Master’s degree or equivalent is a plus.Minimum of 5 years of engineering management (leading teams) experience in the pharmaceutical or related manufacturing industry, with a focus on process and continuous improvement.Proven experience leading and mentoring teams in a regulated manufacturing environment.Strong background in process engineering, Lean, Six Sigma, and CI methodologies.In-depth knowledge of cGMP, FDA regulations, and other industry standards.Excellent problem-solving, analytical, and project management skills.Strong communication and interpersonal skills.Preferred Qualifications :
Certifications in Six Sigma, Lean Manufacturing (Black Belt or Green Belt).Experience with pharmaceutical equipment and systems (automated manufacturing, packaging lines).Familiarity with computerized systems and software for manufacturing process control (SCADA, MES, SAP).Join our team and be a part of a company dedicated to improving patient lives through innovative drug delivery solutions. Apply today!
LTS is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
