About the Role

Our client, a rapidly expanding pharmaceutical company with a integral reach, is looking for an innovative Industrial Engineer to focus on the design and optimization of manufacturing processes for pharmaceutical production. This is a fully remote position, offering unparalleled flexibility. The role is critical in ensuring that our production lines meet stringent regulatory requirements (GMP, FDA) while maximizing efficiency and minimizing costs. The ideal candidate will have specialized knowledge in pharmaceutical manufacturing, process validation, and sterile environments. You will be responsible for developing process flow diagrams, P&IDs;, and implementing scalable solutions that adhere to the highest industry standards. We seek a meticulous professional who thrives on complex challenges and can contribute significantly from a remote setting.

Key Responsibilities

- Design and optimize industrial processes for pharmaceutical manufacturing, including upstream and downstream operations.
- Develop detailed process flow diagrams, P&IDs;, and equipment specifications.
- Ensure all process designs comply with Good Manufacturing Practices (GMP) and other relevant regulatory standards.
- Collaborate with R&D;, quality assurance, and production teams to translate laboratory processes into scalable manufacturing operations.
- Perform process simulations and risk assessments (e.g., FMEA) to identify potential issues.
- Develop and execute process validation protocols (IQ, OQ, PQ).
- Optimize existing processes to improve yield, reduce cycle times, and enhance product quality.




- Source and evaluate new technologies and equipment suitable for pharmaceutical manufacturing.
- Analyze production data to identify trends and opportunities for continuous improvement.
- Provide technical support and troubleshooting for manufacturing issues remotely.

Requirements

- Bachelor's or Master's degree in Industrial Engineering, Chemical Engineering, or a related field with a strong focus on pharmaceutical processes.
- Minimum of 5 years of experience in industrial engineering within the pharmaceutical or biopharmaceutical industry.
- In-depth knowledge of GMP, FDA regulations, and validation principles (IQ/OQ/PQ).
- Experience with process design software and simulation tools.
- Excellent analytical, problem-solving, and documentation skills.
- Strong understanding of chemical or biological processes relevant to drug manufacturing.
- Exceptional remote communication and collaboration skills, with the ability to work effectively with cross-functional teams.
- Proven ability to manage projects and meet deadlines in a remote work environment.
- High level of autonomy and self-motivation.
- Proficiency in English is required for documentation and communication with international teams.

Benefits

- Fully remote work arrangement, offering excellent work-life balance.
- Highly competitive salary and potential for bonuses.
- Comprehensive health and wellness benefits package.
- Generous paid time off and company holidays.
- Opportunities for professional development, including conferences and certifications.
- Retirement savings plan.
- Be part of a cutting-edge company impacting global health.

📌 Ingeniero de Diseño de Procesos para Industria Farmacéutica (Santiago de Querétaro)
🏢 Placements24
📍 Santiago de Querétaro