R&D & Regulatory Affairs Manager
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Key skills for this role
Role Overview
Lead cosmetic product development, technical delivery, and regulatory readiness for safe, stable, effective, and commercially viable products.
Own formulation development, innovation, product registration, regulatory intelligence, Halal and COSMOS compliance, and transfer of approved formulations to commercial manufacturing.
Provide formulation, safety, claims, and regulatory expertise for complaints and post-market reviews.
Key Skills for This Role
Full Job Posting
Job Purpose
Lead cosmetic product development, technical delivery, and regulatory readiness for safe, stable, effective, and commercially viable products.
Own formulation development, innovation, product registration, regulatory intelligence, Halal and COSMOS compliance, and transfer of approved formulations to commercial manufacturing.
Provide formulation, safety, claims, and regulatory expertise for complaints and post-market reviews.
Product Development and Innovation
- Develop and modify formulations against approved briefs, brand positioning, consumer needs, cost targets, and market requirements.
- Manage the R&D pipeline from brief and feasibility through prototypes, testing, approval, scale-up, and launch.
- Lead reformulation, value engineering, and continuous product improvement without compromising safety, quality, performance, or registration status.
- Apply expertise in ingredients, preservation, compatibility, processing, sensory performance, and foreseeable product risks.
Regulatory and Compliance
- Monitor cosmetic regulations in the UAE, KSA, and other target markets and translate changes into actions for R&D, Marketing, QA/QC, and Supply Chain.
- Assess formulas, ingredients, labels, artwork, and claims for regulatory and scientific acceptability.
- Own product registration dossiers, submissions, renewals, variations, authority queries, and market-by-market compliance tracking.
- Coordinate Halal and COSMOS certification compliance, documentation, renewals, audit evidence, and assigned corrective actions.
- Ensure claims are supported by scientific, stability, safety, or performance evidence throughout the product lifecycle.
Safety, Testing, and Technical Qualification
- Define stability, packaging compatibility, challenge or microbiological, safety, and efficacy testing plans based on product and market risk.
- Interpret results, investigate adverse trends, and recommend scientifically justified shelf life, storage conditions, and specifications.
- Define technical requirements for ingredients and packaging and assess suitability, compatibility, sustainability, and regulatory status.
- Partner with QA/QC and Procurement on supplier and material qualification while maintaining technical specifications and change control.
Scale-Up and Manufacturing Support
- Plan and supervise pilot and commercial trials and translate laboratory formulas into robust, repeatable manufacturing processes.
- Define manufacturing instructions, critical process parameters, in-process controls, and acceptance criteria.
- Lead technical troubleshooting and complete formal handover to Production and QA/QC while preserving QA/QC independence over batch release.
Documentation and External Projects
- Control master formulas, specifications, development history, raw-material data, samples, test reports, and product information files.
- Protect formulation know-how, confidential information, and assigned intellectual property, including technical packages for contract-manufacturing clients.
- Govern external laboratories, consultants, contract clients, and development partners against agreed briefs, samples, changes, and deliverables.
Complaints and Team Leadership
- Assess complaints and quality events for formulation, ingredient, safety, claims, or regulatory implications and provide technical conclusions.
- Support investigations, trend review, CAPA, recall assessments, and market-withdrawal decisions with formulation and regulatory input.
- Manage concurrent NPD, reformulation, and contract-manufacturing projects against timeline, scope, cost, MOQ, capacity, and margin expectations.
- Set objectives, allocate workload, review technical output, coach team members, and build specialist and succession capability.
Qualifications and Experience
- Bachelor’s degree in cosmetic science, chemistry, pharmacy, or a closely related discipline.
- Typically 7–10 years of cosmetic or personal-care R&D experience, including formulation, scale-up, and regulatory exposure.
- At least 2–3 years leading people or major projects.
- Experience with stability, compatibility, microbiological or challenge testing, technical dossiers, claims support, and product registration in the UAE and/or KSA.
- Halal and/or COSMOS compliance, certification, or audit coordination experience is strongly preferred.
- Strong project management, scientific writing, data interpretation, stakeholder management, and commercial judgment.
Decision Rights and Interfaces
The manager recommends formulation approval, shelf life, technical specifications, testing strategy, and regulatory readiness.
The manager may stop or delay technical progression when safety, stability, regulatory, or evidence requirements are unmet.
The manager does not independently release batches, approve quality concessions, or override a QA/QC hold.
Key interfaces include Marketing, QA/QC, Production, Procurement, Packaging, Supply Chain, authorities, laboratories, and contract-manufacturing clients.
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