Life Sciences | Production Supervisor

ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and detail-oriented Production Supervisor.ALTEN GroupWithin 30 years, ALTEN has become leader in both outsourced Engineering and IT Enterprise Services. ALTEN, composed of 54,000 employees (88% engineers), carries out complex and highly technical projects throughout the value chain of 6,500 clients, the most prestigious companies in all sectors of industry, services and telecommunications. We work with key actors in the Aeronautics & Space, Defense & Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications and Services sectors.Do you want to work in exciting projects at renowned clients? At ALTEN we believe that knowing and meeting the expectations of our consultants is a key factor in our success. Our consultants make the difference. Do you want to make the difference too?We are seeking a Production Supervisor with strong experience in pharmaceutical manufacturing to coordinate and oversee daily production activities in compliance with GMP regulations. This role involves managing teams, ensuring production documentation accuracy, and guaranteeing the quality and efficiency of manufacturing operations.Key Responsibilities:Plan, coordinate, and supervise production activities, ensuring adherence to timelines, quality, and safety standards.Prepare, review, and approve batch documentation and other GMP-related records.Lead and monitor inspection and packaging teams, ensuring all operations meet compliance and performance goals.Oversee labeling and documentation printing activities as part of production workflows.Ensure proper planning and control of production materials, PPE, and equipment availability.Collaborate with cross-functional departments (Quality, Engineering, and Planning) to ensure smooth production flow.Identify opportunities for process improvement, operational efficiency, and team performance optimization.Qualifications:Bachelor’s degree in a Pharmaceutical-related field.2–3 years of professional experience in pharmaceutical production or a similar regulated environment.Strong knowledge of GMP principles and production documentation processes.Experience in batch review and team coordination within packaging or inspection activities.Proficiency in MS Excel and familiarity with SAP is a plus.Excellent communication, organization, and problem-solving skills.Location: Lisbon, Portugal (Hybrid).Why Join Us? Possibility to work with cutting-edge technology in the Life Sciences industryCollaborative and dynamic work environmentPossibility to join a top-leading company in the industryContinuous trainingsPossibility to join different and interesting projectsIf you want to embrace in a new and challenging opportunity and are excited about the opportunity to contribute to our team, we want to hear from you! Please submit your resume and cover letter detailing your relevant experience and qualifications.