More jobs:
Manager, Advanced R&D
Job in
Irvine, Orange County, California, 92713, USA
Listed on 2026-10-04
Listing for:
Advanced Sterilization Products, Inc.
Full Time
position Listed on 2026-10-04
Job specializations:
-
Research/Development
Regulatory Compliance Specialist -
Management
Regulatory Compliance Specialist
Job Description & How to Apply Below
Communicate program progress, risks, and opportunities to leadership and relevant external stakeholders.
Key Responsibilities Lead and execute complex scientific research, method development, and analysis across single or multiple scientific disciplines to generate high‑quality, reliable data supporting program objectives.
Lead a high-performing scientific team, setting clear expectations, developing talent, and ensuring delivery of high‑quality, compliant scientific work.
Plan and conduct technically challenging research programs from feasibility through validated outcomes, interpreting data and translating findings into actionable insights.
Develop, validate, and transfer analytical, chemical, or microbiological methods while ensuring robust documentation and adherence to applicable standards.
Collaborate closely with cross‑functional teams and external partners to provide scientific expertise, influence project direction, and ensure alignment with business, quality, and compliance needs.
Lead laboratory operations including equipment qualification, data review, technical reporting, and maintenance of a compliant scientific environment.
Provide formal guidance and mentoring of lower level scientists, review technical work, and contribute to building a high‑performing scientific team.
Drive continuous improvement by identifying opportunities to enhance scientific processes, methodologies, and data quality.
Education and Experience Requirements Master’s degree in Chemistry, Microbiology, Biochemistry, or related scientific field with minimum 8 years of experience in a regulated scientific or laboratory environment.
PhD with equivalent experience preferred.
Minimum 2 years of experience leading or supervising scientific or technical staff.
Role and Competencies Requirements Knowledge of regulatory and quality requirements including FDA, ISO, and laboratory compliance expectations.
Proficiency in relevant laboratory and scientific techniques and methodologies.
Ability to lead teams through coaching, clarity of expectations, and cross‑functional collaboration.
Strong experimental design, documentation, critical‑thinking, and problem‑solving skills.
Ability to manage multiple scientific initiatives with accountability for quality and compliance.
Domestic and international travel up to 20%.Fortive Corporation Overview Fortive's essential technology makes the world safer and more productive. We accelerate transformation in high-impact fields like workplace safety, build environments, and healthcare.
We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in healthcare sterilization, industrial safety, predictive maintenance, and other mission-critical solutions. We're a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to advanced technologies that help providers focus on exceptional patient care.
We are a diverse team 10,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven…
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