Air Liquide Logo

Air Liquide

Regulatory Specialist

Posted Yesterday
Be an Early Applicant
In-Office or Remote
Hiring Remotely in USA
90K-100K Annually
Mid level
In-Office or Remote
Hiring Remotely in USA
90K-100K Annually
Mid level
Manage global customer regulatory requests and portals (Salesforce, AODocs), monitor KPI metrics, maintain FDA and compliance documentation (including translations and expiration tracking), resolve quality complaints via VEEVA Vault, and coordinate with internal teams and external principals to secure required regulatory documentation for cosmetics and nutrition products.
The summary above was generated by AI
R10094604 Regulatory Specialist (Open)

Location:

Fairfield, NJ (Seppic) - Sales - North America zone

An Air Liquide Healthcare company, subsidiary of the Air Liquide group, Seppic has been designing, manufacturing, and marketing unique ingredients for over 75 years. These ingredients are used by consumers, patients, and professionals.

Worldwide, a vast team of talented women and men serve customers for health, well-being, and beauty of all. At Seppic, our vision is to help everyone enjoy a healthy life in a healthy environment.

How will you CONTRIBUTE and GROW?

At Airgas, we are committed to building a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.
Airgas is Hiring for a Regulatory Specialist in Fairfield, NJ

We are looking for you !

  • Pay - 90K-100K
  • Comprehensive Family Benefits: Airgas offers a full benefits package designed to support your whole life, including Medical, Dental, Vision, Life, AD&D, and Disability Insurance.

  • Support for Parents: We offer up to 14-week paid child birth benefits to support growing families.

  • Future Security: 401(k) Retirement Plan with company match, Tuition Assistance, Paid Holidays, Vacation, and Sick time.

  • Early Access: Your benefits start after just 30 days of employment.

Recruiter: Neelam Patel  / [email protected]  /  913.343.5762

The Regulatory Department at Seppic Inc. acts as a crucial link between scientific compliance and global market access, safeguarding portfolios while supporting commercial teams. By streamlining complex requirements into data-driven workflows, the team ensures adherence to evolving global standards and FDA mandates. This approach not only manages regulatory risk but also accelerates business momentum and provides the high-quality documentation customers rely on.

SEPPIC INC. is seeking a detail-oriented and proactive Regulatory Specialist to drive compliance excellence and streamline customer demand workflows for our growing Cosmetics and Nutrition divisions. Operating at the intersection of regulatory affairs and client relations, this role is critical to managing global documentation requests, ensuring adherence to FDA guidelines, and collaborating closely with internal stakeholders and external manufacturing principals. 

Key Areas of Impact
  • Customer Demand & Portal Management: Serve as the primary global gatekeeper for customer inquiries by leveraging Salesforce, AODocs, and external regulatory databases (e.g., PCPC, CIR, TSCA, EPA, Health Canada, and EWG).

  • Metrics & Reporting: Monitor response progress and maintain global KPI metrics through centralized reporting tools.

  • Compliance & FDA Oversight: Manage critical documentation, including FDA quality statements, expiration tracking, and English translations for distribution products.

  • Issue Resolution & Collaboration: Resolve customer quality complaints via VEEVA Vault, partnering with Sales and Customer Service to achieve a one-month resolution target.

  • Principal Relations: Cultivate external partnerships to efficiently secure documentation for non-standardized product requests.

  • Other duties and responsibilities in alignment with the role.

__________________Are you a MATCH?

Required Qualifications

  • Brings a strong foundation in regulatory affairs, ideally within the cosmetic or nutrition industries.

  • Systematic problem-solver who thrives on tracking critical quality metrics, navigating complex portals, and accelerating issue resolution.

Preferred Qualifications

  • Bachelor’s degree, Chemistry or Biology preferred.

Our Differences make our Performance


At Air Liquide, we are committed to build a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.


We welcome and consider applications from all qualified applicants, regardless of their background. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world.

Similar Jobs

4 Days Ago
Remote
USA
Expert/Leader
Expert/Leader
Information Technology • Professional Services • Biotech • Pharmaceutical
Lead regulatory strategy and submissions (primarily CMC, also clinical and non-clinical) for investigational and marketed products. Serve as RA lead on cross-functional teams, liaise with FDA and other health authorities, drive regulatory due diligence, and implement policies to ensure timely approvals and compliance with ICH, FDA, and EU guidelines.
4 Days Ago
In-Office or Remote
Junior
Junior
Information Technology • Professional Services • Biotech • Pharmaceutical
Support preparation, coordination, and review of domestic and international regulatory submissions and annual reports for drug/biologic programs. Ensure compliance with FDA/EMA/ICH guidelines, review promotional materials and clinical protocols, interact with agencies and vendors, assist with inspections and audits, update procedures, and manage regulatory tasks within project timelines and budgets.
Top Skills: Adobe AcrobatExcelMicrosoft PowerpointMicrosoft Word
7 Days Ago
Remote
2 Locations
143K-196K Annually
Senior level
143K-196K Annually
Senior level
Healthtech • Pharmaceutical • Manufacturing
Lead preparation and submission of 510(k) and other regulatory filings for SaMD. Develop and execute global regulatory strategies (US, EU MDR, Canada), review technical/software documentation, ensure regulatory compliance, and collaborate cross-functionally to integrate requirements into product development.
Top Skills: 510(K)Eu MdrIec 62304Samd

What you need to know about the Austin Tech Scene

Austin has a diverse and thriving tech ecosystem thanks to home-grown companies like Dell and major campuses for IBM, AMD and Apple. The state’s flagship university, the University of Texas at Austin, is known for its engineering school, and the city is known for its annual South by Southwest tech and media conference. Austin’s tech scene spans many verticals, but it’s particularly known for hardware, including semiconductors, as well as AI, biotechnology and cloud computing. And its food and music scene, low taxes and favorable climate has made the city a destination for tech workers from across the country.

Key Facts About Austin Tech

  • Number of Tech Workers: 180,500; 13.7% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Dell, IBM, AMD, Apple, Alphabet
  • Key Industries: Artificial intelligence, hardware, cloud computing, software, healthtech
  • Funding Landscape: $4.5 billion in VC funding in 2024 (Pitchbook)
  • Notable Investors: Live Oak Ventures, Austin Ventures, Hinge Capital, Gigafund, KdT Ventures, Next Coast Ventures, Silverton Partners
  • Research Centers and Universities: University of Texas, Southwestern University, Texas State University, Center for Complex Quantum Systems, Oden Institute for Computational Engineering and Sciences, Texas Advanced Computing Center

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account