Regulatory Senior Scientist

Our client is a leading manufacturers, marketers, and sellers of quality skin care, makeup, fragrance, and hair care products. The client is looking for a Senior Regulatory Scientist to join the growing team.

Job Title : Regulatory Senior Scientist

Job Type : Full-time, Day Shift

Research & Development

Competitive compensation package

JOB DESCRIPTION

Regulatory & Product Stewardship : 50%

• Responsible for liaising with other company R&D Groups to obtain technical data on formulas with a vision to ensure compliance.
• Initiates new regulatory review and ingredient label policies / SOPs to be adopted across all company brands
• Initiates formula policy reviews as needed.
• Oversees changes / corrections to regulatory reviews / ILNs that are made for regulatory reasons.
• Uses independent judgment when reviewing technical information based on established regulatory, safety and corporate practices.
• Collects and inputs information into appropriate reports, charts, spread sheets and provides weekly reviews for management.
• Leads RDS bi-weekly issues reviews with chemists related to ingredient label creation and formula regulatory review.

Cosmetovigilance US / CAN / LATAM : 50%

Management of key RDS functionalities to ensure global compliance of company ingredients, formulas and products. Takes part in designing formula regulatory review and ILN policies and SOPs supporting the Manager role independently and with little supervision. The leadership of the RDS bi-weekly global R&D alignment discussions. Reviews existing and new formulas for global regulatory compliance. This entails ensuring compliance of Raw Materials, components and sub-formulas working in collaboration with the Registration, RMM and R&D teams. Communicates and ensures execution of changes, if any, to team and management. Monitors formula changes assessing regulatory impact on company ingredient labels and registration.

Leads development of COVI and GVP work, supporting the rollout of mSafety globally. Establishes a COVI / GVP plan for Canada and the US. Collaborates with LATAM Manager to establish COVI in the region, as regulations are proposed. Participate in causality and expectedness assessments, interface with regulators and support the global team as we establish this new program. Keep updated with emerging regulations across the region. Supports global defense work on trade association committee and taskforces operating, mainly in Canada (CA / CME) and the US (PCPC) in collaboration with our global RA partners.

QUALIFICATIONS