Project Manager - Engineering

Description

Job Summary: We are seeking a Project Engineer focused on Automation and Systems to plan, implement, and validate projects, ensuring regulatory compliance and quality. Key Highlights: 1. Lead automation and continuous improvement projects 2. Develop, optimize, and validate pharmaceutical production processes 3. Ensure compliance with regulations and quality standards **Description:** ---------------- We are looking for a professional to work as a Project Engineer with a focus on Automation and Systems. The candidate will be responsible for planning, specifying, implementing, and validating automation/electrical projects, ensuring regulatory compliance, technical quality, cost control, and adherence to schedules. **Position:** Project Manager \- Engineering **Salary:** BRL 6,350.00 per month \+ BRL 1,800.00 in flexible benefits per month **Employment Type:** CLT (Consolidation of Labor Laws) **Work Mode:** Hybrid in São José dos Campos – SP **Standard CLT Benefits:** **Health and Dental Insurance:** Bradesco, with no employee contribution or co-payment, extendable to direct dependents at differentiated rates; **Mobility Allowance:** BRL 200.00 per month; **Meal Voucher:** BRL 27.55 per day; **AS2 Academy:** BRL 500.00 per year for training and certifications; **Flexible CLT Benefits:** **Education Allowance:** BRL 350.00 per month; **Health/Wellness Allowance:** BRL 1,050.00 per month; **Culture Allowance:** BRL 400.00 per month; Best of all, this package grows with you and your career, tailored according to your position. **Requirements:** * Bachelor’s degree in Electrical Engineering, Control and Automation Engineering, Mechatronics, or related fields. * Project management skills and experience using project management tools (e.g., MS Project or similar). * Advanced English proficiency; * Skills in negotiation, conflict resolution, strategic planning, and assertive communication. **Key Responsibilities:** * Project Management: Plan, execute, and monitor continuous improvement and automation projects, leading multidisciplinary teams, managing suppliers and contracts, and tracking CAPEX, schedules, risks, and deliverables from technical definition through commissioning (FAT/SAT). * Process Development: Design, optimize, and validate pharmaceutical production processes, analyzing data and conducting tests to ensure operational efficiency. * Execute and document URS, FRS, and SDS; conduct meetings with users and stakeholders to gather and analyze requirements; specify equipment and software; and manage validation activities (IQ/OQ/PQ) by developing protocols, executing tests, and issuing reports. * Prepare technical documentation and project reports, ensuring process compliance with ANVISA regulations, Good Manufacturing Practices (GMP), and quality standards such as GMP, GAMP 5, and 21 CFR Part 11\. * Collaborate closely with Quality, Research & Development, and Production departments to facilitate cross-departmental communication for implementing improvements. * Conduct training on new processes and technologies, promoting team awareness of safe and efficient practices. **If you’re excited about this challenge, join us!**