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Regulatory Affairs Sr Manager

hace 2 meses


Madrid, España Vantage Oleochemicals, Inc A tiempo completo

Regulatory Affairs Sr Manager page is loaded Regulatory Affairs Sr Manager Apply locations Remote - Spain time type Full time posted on Posted 7 Days Ago job requisition id R-1516 Vantage is a leading supplier of naturally derived specialty ingredients and formulations that cater to the evolving needs of industrial and consumer markets. Through our chemistries, our customer focus and our global footprint, we are ENABLING TOMORROW'S SOLUTIONS TODAY.
As a company on the move, you'll be working as part of a collaborative team and getting to know the cultural diversity of our world. We learn from each other to constantly improve, adapt and iterate. We value the voice and talent of our colleagues by empowering them to drive their unique ideas to completion. We're convinced that exceptionally motivated employees produce outstanding results. Most importantly, we know you're going to like it here. For more information visit: www.vantagegrp.com or LinkedIn/vantage
The Role
POSITION SUMMARY
Regulatory Affairs Senior Manager is responsible for leading the regulatory strategy and managing the regulatory compliance in EMEA (Europe, Middle East & Africa). This position will report directly to the Director of Global Regulatory Affairs. The person will be responsible for personal care, cosmetic and performance solutions product regulatory compliance in Europe and lead a team of up to three people across Europe.
POSITION SCOPE
Responsible for regional regulatory compliance in EMEA.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Key responsibilities include, but are not limited to the following:
Manage a team of specialists responsible for regulatory compliance and issue management to ensure products are compliant on the marketplace.

Subject matter expert (SME) for EU REACH submissions including analytical, non-vertebrate, and vertebrate testing endpoints. Familiarity with Harmonized Tariff Schedule (HTS), Country of Origin (COO), Nagoya Protocol, and similar local, Member State regulatory requirements.

Lead and enhance the regulatory program to enable the business with optimal processes, and operating procedures to ensure Vantage solutions comply with applicable regulations and anticipate regulatory changes. Create, review, and publish product-relevant documents such as SDS's, PCN (poison control notification), and CLP (classification, labeling, and packaging), regulatory data sheets.

Monitor, interpret, assess, and develop compliance strategies to address emerging regulations that impact our capability to manufacture, market, distribute, import, or export our solutions in domestic and global markets. Act as a regulatory representative with internal/external customers, communicating regulatory requirements and the impact of regulations to the teams.

Conduct regulatory assessments of chemical substances, monitor and support commercialization and marketing initiatives including safety and claims substantiation.

Point of contact for internal stakeholders and external customers for all regional regulatory inquiries.

Note: The duties listed above are not all inclusive and may be subject to periodic updating or revision.
The Ideal Candidate
Desired Background
15 years' experience with a bachelor's degree, 10 years for a Ph.D. or MS in a field of science (cosmetic chemistry, biochemistry, toxicology, or relevant fields) is preferred.

Demonstrated expertise in European and UK regulatory frameworks including but not limited to EU and UK REACH programs.

Knowledge, Skills & Talents
More specifically, we would seek the following attributes and competencies for the position:
Strong knowledge of ECHA (European Chemicals Agency), SCCS (Scientific Committee on Consumer Safety), and various market requirements for cosmetic and performance chemical ingredients.

Active participation and potential leadership in relevant trade associations is highly desirable.

Management experience with an action orientation, and proactive ability to develop teams and manage with courage.

Knowledge of analytical, non-vertebrate, and vertebrate testing, as it relates to regulatory toxicology in GLP or fit-for-use conditions.

Proven success working in ambiguity, fostering collaborations in a fast-paced environment.

Ability to prioritize and create a sense of urgency to complete tasks under challenging conditions.

Excellent written and oral communication skills, especially detail-oriented and technical material, required.

About Us Vantage is a leading supplier of naturally derived specialty ingredients and formulations that cater to the evolving needs of industrial and consumer markets. Through our chemistries, our customer focus and our global footprint, we are Enabling Tomorrow's Solutions Today.
As a company on the move, you'll be working as part of a collaborative team and getting to know the cultural diversity of our world. We learn from each other to constantly improve, adapt and iterate. We value the voice and talent of our colleagues by empowering them to drive their unique ideas to completion. We're convinced that exceptionally motivated employees produce outstanding results. Most importantly, we know you're going to like it here.

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