This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
We are seeking a Technical Project Manager with a strong engineering background and proven project management experience to lead initiatives involving control systems, data acquisition, and pharmaceutical manufacturing processes. This role supports late-stage development, technical transfer, and commercialization, with a focus on execution, compliance, and client engagement.
Job Responsibility:
Lead technical projects from initiation through completion, ensuring alignment with scope, schedule, and budget
Develop and maintain project plans, risk assessments, and resource strategies
Coordinate cross-functional teams across R&D, Quality, Regulatory, and Operations
Ensure compliance with GMP, FDA, and regulatory requirements
Oversee design, implementation, and optimization of control systems and data acquisition platforms
Support technical transfer activities for pharmaceutical manufacturing programs
Guide system integration, testing, and validation efforts
Apply Quality by Design (QbD) principles and statistical tools (DoE, FMEA, Gage R&R)
Serve as the primary point of contact for clients throughout the project lifecycle
Lead project kick-offs, technical reviews, and issue resolution
Clearly communicate technical concepts to internal and external stakeholders
Support client audits and regulatory inspections
Identify opportunities to improve process robustness, product quality, and efficiency
Contribute to Lean initiatives and best practice implementation
Requirements:
Bachelor's or Master's degree in Engineering (Chemical, Mechanical, Electrical, Biomedical, or related)
PMP certification (or equivalent) required
7 years of experience in pharmaceutical manufacturing
Experience managing technical projects in regulated or CDMO environments
Strong background in control systems, automation, and data acquisition
Knowledge of cGMP and regulatory requirements
Excellent communication, leadership, and stakeholder management skills
Nice to have:
Experience with transdermal patch or inhalation (MDI) manufacturing processes
Familiarity with coating, laminating, die-cutting, or filling/crimping operations
Experience supporting CMC documentation for regulatory submissions (NDA/ANDA)
Lean Six Sigma or continuous improvement certification