Ecolab Life Sciences, the world leader in resin‑based separation, purification, and extraction technologies, is seeking a Global Biopharma Regulatory Consultant to support our rapidly growing Bioprocessing division.
Ecolab’s high‑performance Purolite Resins are critical to the safe and effective manufacture of pharmaceutical and biopharmaceutical products. Our chromatography solutions help customers around the globe produce medicines and therapies with the highest levels of purity, quality, and safety. This is an exciting opportunity to contribute to a mission that truly helps make the world cleaner, safer, and healthier.
What's in it for you:
The Global Biopharma Regulatory Consultant will play a key role in supporting global biopharma customers with regulatory filings and interactions with governmental authorities. Working across multiple internal teams, geographic regions, and time zones, this role ensures customers receive accurate, timely, and compliant regulatory support.
You will collaborate closely with colleagues across Regulatory Affairs, Quality, R&D, Product Management, and Commercial teams to help biomanufacturers meet international regulatory standards. You will also engage with external stakeholders—including regulatory bodies—to support customer submissions and ensure global compliance.
About Ecolab Life Sciences
Ecolab Life Sciences is a global leader dedicated to helping biopharmaceutical manufacturers achieve excellence in safety, compliance, and operational performance. We deliver end‑to‑end solutions backed by deep scientific expertise and a strong commitment to patient safety.
Our work is grounded in a comprehensive understanding of global regulatory expectations and the rapidly evolving landscape of pharmaceutical production. By aligning innovative technologies with cGMP and international regulatory frameworks, we empower customers to operate confidently in highly regulated environments.
What You Will Do
Global CMC Leadership: Serve as a trusted strategic partner for Ecolab’s biopharma customers, providing expert guidance on filing strategies for chromatography and other downstream purification unit operations. Accelerate regulatory timelines and secure regulatory success for our customers through proactive, science-driven solutions.
Regulatory Excellence as a Growth Driver: Collaborate seamlessly with Sales, R&D, Quality, and Bioprocess Development teams—both internally and externally—to execute CMC regulatory strategies, reduce time-to-market, strengthen compliance, and enhance customer competitiveness.
Proactive Regulatory Foresight: Anticipate and influence evolving global regulations to design forward-looking CMC strategies. Support internal product development and bioprocess development initiatives to align with upcoming regulatory changes.
Strategic Alignment for Business Impact: Integrate regulatory planning with commercial objectives to deliver measurable customer value. Accelerate adoption of Ecolab’s downstream processing solutions, optimize regulatory pathways for customers, and fuel sustainable business growth.
Minimum Qualifications
Bachelor's degree and 10 years of experience
Extensive experience in CMC regulatory filing within biopharma with focus on downstream purification steps.
Proven ability to lead global regulatory strategies and influence industry standards.
Must be able to travel of at least 50%
Immigration sponsorship not available for this role
Preferred Qualifications:
More than 5+ years of demonstrated experience in authoring CMC content for IND/BLA or PACMP with FDA and European agencies
Advanced degree in Life Sciences related fields
Strong collaboration skills with commercial and technical teams.
Excellent communication and advocacy capabilities.
Annual or Hourly Compensation Range
Benefits
Ecolab strives to provide comprehensive and market-competitive benefits to meet the needs of our associates and their families. Click hereto see our benefits.
If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at jobs.ecolab.com/working-here.
Potential Customer Requirements Notice
To meet customer requirements and comply with local or state regulations, applicants for certain customer-facing roles may need to:
- Undergo additional background screens and/or drug/alcohol testing for customer credentialing.
- Be fully vaccinated for COVID-19, including a booster if eligible, unless a religious or medical accommodation is requested by the applicant and approved by Ecolab.
Americans with Disabilities Act (ADA)
Ecolab will provide reasonable accommodation (such as a qualified sign language interpreter or other personal assistance) with our application process upon request as to comply with applicable laws. If you have a disability and require accommodation assistance in this application process, please visit the Recruiting Support link in the footer of each page of our career website.
A trusted partner for millions of customers, Ecolab (ECL) is a global sustainability leader offering water, hygiene and infection prevention solutions and services that protect people and the resources vital to life. Building on a century of innovation, Ecolab has annual sales of $15 billion and more than 48,000 associates, Ecolab delivers comprehensive science-based solutions, data-driven insights and world-class service to advance food safety, maintain clean and safe environments, and optimize water and energy use, and improve operational efficiencies and sustainability for customers in the food, healthcare, life sciences, hospitality and industrial markets in more than 170 countries around the world.
When you come to work at Ecolab, you get to take on some of the world’s most meaningful challenges and have the opportunity to learn and grow, shape your career, make an impact and quickly see the importance of your work.
For more Ecolab news and information, visit www.ecolab.com. Follow us on Twitter @ecolab, Facebook at facebook.com/ecolab, LinkedIn at Ecolab or Instagram at Ecolab Inc. To explore career opportunities at Ecolab, visit jobs.ecolab.com.