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Cosmetic Technical Manager

56400Cb1-3A2C-4233-9A2C-7E10Be65Cc00

Cape Town

On-site

ZAR 200 000 - 300 000

Full time

Today
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Job summary

A well-established manufacturing business in Cape Town seeks an experienced Technical Manager to oversee the R&D, Technical, Regulatory, and Quality systems functions for personal care and cosmetic products. The ideal candidate will have a background in scientific disciplines, extensive experience in the FMCG sector, and a strong grasp of regulatory requirements. This role offers a competitive remuneration package, reflective of expertise and experience.

Qualifications

  • Minimum 4–6 years' experience in cosmetic or personal care product development.
  • Strong working knowledge of CTFA guidelines and local cosmetic regulations.
  • Experience managing GMP, QMS, and audit compliance.

Responsibilities

  • Lead the R&D function with accountability for innovation pipeline delivery.
  • Provide oversight and performance management of R&D and QC laboratories.
  • Act as the company's Regulatory Authority Representative.

Skills

Leadership
Regulatory knowledge
Project management
Technical reporting
Problem-solving

Education

BSc Chemistry
BTech Cosmetic Science
Job description

Technical Manager – Personal Care & Cosmetics

Location

Paarden Eiland, Cape Town

Industry

FMCG / Personal Care Manufacturing

Overview

A well-established manufacturing business supplying personal care and cosmetic FMCG products to major South African retailers is seeking an experienced Technical Manager to manage its R&D, Technical, Regulatory, and Quality systems functions.

Key Responsibilities
  • Research & Development Leadership
    • Lead the R&D function with accountability for innovation pipeline delivery, resource planning, performance management, and workflow prioritisation.
    • Translate marketing briefs into scientifically sound formulation strategies aligned with cost, performance, and brand objectives.
    • Establish and enforce best‑practice R&D standards, documentation, and laboratory processes.
    • Provide coaching and technical mentorship to Development & Research Chemist and laboratory staff.
    • Lead development of all new personal care products per approved briefs.
    • Ensure product files are opened and maintained with accurate, complete technical documentation.
    • Oversee raw material feasibility research, ingredient selection, and supplier evaluations.
    • Manage all required product testing, including stability, compatibility, challenge, dermatological, and user trials.
    • Liaise collaboratively with the Buyer and Development Chemist on raw material sourcing, alternatives, and risk mitigation.
    • Review and troubleshoot formulation challenges, deviations, or performance concerns.
    • Manage and approve raw material changes necessitated by supply or regulatory updates.
    • Own costings for all new products and cost optimisation initiatives, reviewing and approving changes in costings arising from fluctuations or supply issues.
    • Ensure preparation and external distribution of professionally presented samples for testing and evaluation.
    • Ensure QC receives final product standards and written specifications once pilot batches are approved.
    • Deliver final, compliant ingredient listings for artwork.
    • Coordinate artwork approval with all stakeholders and ensure alignment with regulations.
    • Approve and sign off manufacturing instructions and final product standard before handover to Production and Quality.
  • Laboratory Oversight (R&D Laboratory & QC Laboratory)
    • Provide leadership and performance oversight to R&D and QC teams.
    • Ensure alignment between laboratory capabilities and company growth plans.
    • Develop training plans, SOPs, and competency matrices for laboratory staff.
    • Drive a culture of scientific excellence, accuracy, and continuous improvement.
    • Ensure all new products undergo required testing including stability, compatibility, challenge etc.; review and sign off results.
    • Ensure claims validation processes are followed and that all required user trial, clinical and other necessary testing is complete with validated results.
    • Approve final formulas and ensure accurate documentation on the system, including weekly test results and manufacturing instructions.
    • Provide oversight, guidance and performance management of the QC laboratory.
  • Regulatory Affairs Management
    • Act as the company's Regulatory Authority Representative, both locally and internationally.
    • Lead regulatory intelligence activities, ensuring proactive identification of changes impacting formulations, artwork, and compliance.
    • Ensure team adherence to documentation standards and regulatory SOPs.
    • Provide regulatory guidance to cross‑functional teams.
    • Maintain and update all product files and flag future changes due to regulatory or supply risks.
    • Create new product files according to internal procedure and keep all existing product files current.
  • Manufacturing Support & Scale‑Up
    • Strengthen cross‑functional collaboration between Technical and Production teams.
    • Drive continuous improvement initiatives in scale‑up, batch consistency, and technical issue resolution.
    • Support the development of technical training for Production teams.
    • Support Manufacturing in troubleshooting technical issues during production batches.
    • Recommend necessary formula or process adjustments.
    • Ensure final approval of Production Standards.
  • Compliance, Governance & Quality Management Systems
    • Own the end‑to‑end QMS structure, ensuring alignment with business objectives, retailer requirements, and global best practices.
    • Lead audits (internal & external) and drive corrective / preventative actions (CAPA).
    • Ensure robust systems for complaints handling, traceability, and documentation control.
    • Maintain alignment with CTFA, EU / UK cosmetics regulations, and all local legal requirements.
    • Manage the full complaints‑handling system, root‑cause investigations, CAPA, and reporting.
    • Set GMP standards, internal audit schedules, and oversee all GMP audits.
    • Communicate retailer, licensor, and regulatory requirements across the organisation.
    • Provide training on continuous improvement methods and regulatory updates.
    • Oversee regulatory compliance, artwork changes, legal updates, environmental regulations, and cross‑department training and communication.
  • Export Regulatory Management
    • Lead export regulatory strategy across multiple regions.
    • Manage liaison with external consultants or regulatory specialists for international compliance.
    • Coordinate product or artwork changes required for export market compliance.
    • Prepare, issue, and verify export documentation.
  • Leadership & Soft Skills Expectations
    • Strong leadership with the ability to coach and develop technical teams.
    • Excellent cross‑functional communication and stakeholder engagement.
    • Strong project management, prioritisation, and organisational skills.
    • High level of scientific rigor, problem‑solving capability, and decision‑making.
    • Ability to interpret complex regulatory frameworks and translate them into business‑friendly processes.
    • Continuous improvement mindset with strong attention to detail.
Remuneration

Remuneration : R… monthly depending on experience

Requirements
  • BSc Chemistry, BTech Cosmetic Science, or equivalent scientific degree.
  • Cosmetology or Advanced Diploma in Cosmetic Science.
  • Minimum 4–6 years' experience in cosmetic or personal care product development, R&D, technical operations, or regulatory affairs within the South African FMCG sector.
  • Strong working knowledge of CTFA guidelines, local cosmetic regulations, and the Consumer Protection Act (CPA).
  • Experience managing or contributing to GMP, QMS, and audit compliance in a South African manufacturing environment.
  • Hands‑on experience in laboratory oversight, stability testing, microbiological requirements, and product safety compliance.
  • Strong project management, documentation, and technical reporting skills.
  • Ability to work effectively with cross‑functional teams, including Marketing, Production, Procurement, and Quality.
  • Excellent communication skills, with the ability to present technical information clearly to internal and external stakeholders.
  • High attention to detail, strong problem‑solving abilities, and a continuous improvement mindset.
  • Willingness to stay up to date with EU cosmetic regulations and interpret the impact for the South African market.
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