Continuous Improvement Engineer

Overview Continuous Improvement Engineer in Springfield, MO. Build your future at Curia, where our work has the power to save lives. The Continuous Improvement Engineer is a key driver of engineering excellence and operational performance at our manufacturing site. This role leads high-impact process improvement initiatives, serves as the Engineering team’s CAPA lead, and partners with cross-functional teams to identify, execute, and sustain meaningful improvements across the facility. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives. Responsibilities Continuous Improvement & Engineering Excellence: Identify and prioritize improvement opportunities through data analysis, process observation, and cross-functional collaboration. Lead or support Lean and Six Sigma initiatives (Kaizen events, value stream mapping, DMAIC projects) that reduce waste, improve yield, and increase process reliability. Develop and maintain process documentation including SOPs, work instructions, and control plans to sustain improvement gains. Apply statistical methods and process capability analysis (Cp, Cpk, SPC) to monitor and improve manufacturing performance. Engineering Team CAPA Lead Serve as the Engineering team’s primary point of accountability for CAPA coordination, ensuring actions are assigned, tracked, and closed on time. Facilitate root cause analysis for engineering-related events using structured tools such as 5-Why, Fishbone, and FMEA. Partner with Quality Assurance to ensure CAPA documentation meets regulatory and site quality system requirements. Report CAPA status and trends to Engineering leadership; flag systemic issues and support corrective strategies. Quality Systems & Compliance Support site compliance with cGMP/GDP requirements; participate in internal audits and regulatory inspections as assigned. Author, review, and approve change control documentation in support of process and equipment changes. Collaborate with Quality Assurance on deviation investigations, risk assessments, and product complaints as applicable. Ensure all project and improvement activities are executed in alignment with site quality systems and applicable regulatory standards. Collaboration & Communication Serve as a resource and subject matter expert for teams navigating quality events and improvement initiatives. Present findings, project status, and recommendations to Engineering, Operations, and Quality leadership. Contribute to a culture of continuous improvement by coaching team members on CI tools and quality mindset. Good Manufacturing & Documentation Practices Requirements Quality is something we take pride in together. You’ll perform your work in alignment with cGMP requirements and Curia’s standards, which means: Perform all documentation in compliance with ALCOA++ principles and site SOPs. Adhere to applicable cGMP documents including SOPs, batch records, protocols, change controls, and controlled forms. Keep all required cGMP training current and escalate quality concerns along with proposed solutions to the Quality department. Qualifications B.S. in Engineering (Chemical, Electrical, Industrial or Mechanical Engineering preferred). 5 years of relevant engineering experience in a manufacturing environment. Experience supporting or coordinating CAPAs, deviations, or non-conformances in a regulated manufacturing environment. Proficiency with root cause analysis methodologies (5-Why, Fishbone, FTA, FMEA). Strong analytical and detail-oriented skills with the ability to interpret data and translate findings into actionable improvements. Effective written and verbal communication skills; ability to author clear technical documentation. Strong project management skills with the ability to manage multiple priorities and hold peers accountable to deadlines. Collaborative working style with the ability to influence without direct authority. Commitment to quality, continuous improvement, and doing what is right; consistent with the Curia Way. Other Qualifications Must pass a background check Must pass a drug screen May be required to pass Occupational Health Screening Preferred Experience in pharmaceutical manufacturing is strongly preferred Lean Six Sigma Green Belt or Black Belt certification strongly preferred. Familiarity with eQMS and document control platforms. Experience with statistical software (Minitab or equivalent) and SPC methodologies. Knowledge of 21 CFR Part 210/211 or other applicable GMP regulatory frameworks. ASQ Certified Quality Engineer (CQE) or equivalent certification a plus. Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer. #J-18808-Ljbffr