SENIOR PRODUCTION ANALYST

Description

Job Summary: Professional responsible for managing deviations, CAPA (Corrective and Preventive Actions), technical investigations, audits, and continuous improvement in pharmaceutical manufacturing. Key Highlights: 1. Join a diverse, inclusive, and flexible work culture. 2. Significant opportunities for personal development and professional advancement. 3. Impact millions and champion human progress in science and technology. Make your magic happen with us Are you ready to explore, break barriers, and make new discoveries? We know you have big plans—and so do we! Globally, we love innovating in science and technology to add value to people’s lives through our Healthcare, Life Science, and Electronics solutions. Together, we dream big and are relentless in caring for our rich mix of people, customers, patients, and the planet. That’s why we’re always seeking curious minds who envision the unimaginable alongside us. United As One for Patients: Our purpose in Healthcare is to help create, improve, and extend lives. We develop medicines, smart devices, and innovative technologies in therapeutic areas such as Oncology, Neurology, and Fertility. Our teams collaborate across all six continents with great passion and curiosity to support patients at every stage of life. Joining our Healthcare team means becoming part of a diverse, inclusive, and flexible work culture, with significant opportunities for personal development and professional advancement worldwide. **Your Role:** * Deviation and CAPA Management: Collect and analyze data to initiate deviations, manage change controls, and oversee CAPAs (Corrective and Preventive Actions). * Technical Investigations: Lead investigations of events and deviations (minor, major, and critical), identify root causes, and propose effective solutions. * Audits and Compliance: Review audit trails and actively participate in preparation for external audits and health authority inspections. * Production Monitoring: Monitor production processes in real time, ensuring strict adherence to applicable regulations and Good Manufacturing Practices (GMP). * Continuous Improvement: Lead small-scale optimization projects, supporting coordination in achieving KPIs (key performance indicators) and reducing market complaints. * Document Management: Ensure consistent updates of SOPs (Standard Operating Procedures), PPs, and other technical documents within the area. * Technical Representation: Deliver presentations in cross-functional meetings and provide technical accountability for assigned activities to health authorities. **Who You Are:** * Education: Bachelor’s degree completed (Pharmacy, Chemical Engineering, or Production Engineering). * Regulatory Knowledge: Proficiency in Good Manufacturing Practices (GMP) and current health regulations. * Advanced English proficiency. * Relevant experience in Quality, Manufacturing, Pharmaceutical Technology, and pharmaceutical industries. * Analytical Thinking: Ability to investigate complex deviations and analyze statistical data using logical reasoning. * Autonomy: Ability to deliver results responsibly and make sound technical decisions within your scope of authority. * Communication: Skill to clearly, objectively, and unambiguously report technical situations. **What We Offer:** We are curious minds from a wide range of backgrounds, perspectives, and life experiences. We believe this diversity drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for everyone to develop and grow at their own pace. Join us to build a culture of inclusion and belonging that impacts millions and empowers everyone to champion human progress! Apply now and become part of a team dedicated to Awakening Discovery and Elevating Humanity!