ASSOCIATE SCIENTIST

Description

Position Summary: Associate Scientist responsible for leading high-impact projects, new product introductions, and technology transfers, applying scientific methodologies and tools. Key Highlights: 1. Lead high-impact projects and new product introductions. 2. Collaborate cross-functionally with scientific and engineering perspectives. 3. Support technical problem resolution and continuous improvement initiatives. At Johnson \& Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson \& Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson \& Johnson, we respect the diversity and dignity of our employees and recognize their merit. **Job Function:** Discovery \& Pre\-Clinical/Clinical Development**Job Sub Function:** Chemical Research**Job Category:** Scientific/Technology**All Job Posting Locations:** Huejotzingo, Puebla, Mexico**Job Description:** * **About Innovative Medicine** Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our scientific advances. Visionary individuals like you work in life-saving teams developing tomorrow’s medicines. Join our team in developing treatments, finding cures, and pioneering the journey from lab to life—while empowering patients every step of the way. Learn more at https://www.jnj.com/innovative\-medicine **We are seeking top talent for the Associate Scientist position located in Puebla – Mexico.** **Purpose:** The Associate Scientist is responsible for effectively leading and executing high-impact projects, new product introductions, line extensions, and technology transfers, as well as programs focused on core business processes—including adherence to Master Validation Plans and validation lifecycle management. Additionally, the scientist is responsible for effectively collaborating as part of a team and applying required tactics and tools to their process with scientific and engineering rigor—aligned with organizational quality and safety requirements. **Key Responsibilities:** * Execute new product introductions, line extensions, technology transfers, Process Performance Qualification (PPQ) projects, continuous process verification, and site manufacturing process changes. * Manage projects end-to-end—from technical and financial feasibility assessments, execution control against project plans, budget oversight, and timely communication of potential risks and mitigation strategies. * Support team members and other departments in resolving technical process issues, conducting research, and implementing improvement initiatives. * Participate in developing or updating the site’s Master Validation Plan and relevant Validation Plans, as well as associated procedures, work instructions, and other technical documents. * Participate in evaluating Johnson \& Johnson corporate procedures and work instructions related to site Technical Operations processes and their implementation. * Develop and update documentation related to processes or studies to be executed. * Submit SAP master data requests for creation, deletion, or updates. * Work is performed primarily in controlled manufacturing areas and office spaces. * Personal protective equipment (PPE) is required per site EHS\&S guidelines. * Travel requirement: < 5%. * Education: Bachelor’s degree in Pharmaceutical Chemistry, Biology, Biochemical Engineering, Chemical Engineering, Biotechnology Engineering, Industrial Engineering, or related field. * English language proficiency: Advanced. * Experience: Minimum 5 years in pharmaceuticals, food, or chemical industries (production, projects, safety, quality systems). * Software proficiency: Microsoft Office, Minitab, SAP query tools. * People management experience: Preferred. * Knowledge: * Regulatory experience: NOM\-059\-SSA1, NOM\-073\-SSA1, 21 CFR 211. * Pharmaceutical technology (manufacturing of solid, liquid, and semi-solid dosage forms). * Packaging technology (primary and secondary filling). * Project management (PMI, FPX, Agile methodologies or equivalents). * Six Sigma, Lean Manufacturing, Statistical Analysis, and Design of Experiments training. * Intermediate/advanced Minitab usage. * Licenses and certifications: * Project Management training (FPX, Agile methodologies or equivalents). * Six Sigma, Lean Manufacturing, Statistical Analysis, and Design of Experiments training. * **Qualifications** **/** **Requirements:** **Required Skills:** **Preferred Skills:** Analytical Reasoning, Chemistry, Data Analysis, Data Reporting, Drug Discovery Development, Execution Focus, Innovation, Interdisciplinary Work, Laboratory Experiments, Process Oriented, Quantitative Research, Research Ethics, Research Informatics, Scientific Evaluation, Scientific Research, Technical Writing, Technologically Savvy