Project Manager & Process Scientist – Self Care / OTC

Project Manager & Process Scientist – Self Care / OTC

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

Director Support to Marketed Products – OTC

Lieu :

Europe/Middle East/Africa, Sweden, Skane, Helsingborg

Lieu de travail :

Hybride

Ce que tu vas faire

This hybrid role integrates  project management with technical process‑science to support the introduction, lifecycle management, and continued compliance of Self‑Care / OTC products destined for the China market. The position coordinates  cross functional global projects, regulatory and change control activities, and provides hands‑on technical operations support, including formulation and manufacturing process expertise for solids, liquids, and gum‑based products.

The role supports delivering technically robust, compliant, and cost‑effective solutions, maintaining global alignment, and supporting expansion of existing products into new markets.

Key Responsibilities

1. Project & Portfolio Support

• Support new product introduction (NPI) projects for Self‑Care/OTC products imported from Europe into China.
• Coordinate lifecycle management (LCM) projects, including formulation changes, raw‑material qualifications, process optimization, packaging updates, and regulatory‑driven revisions.
• Contribute to global change control (GCC) and China‑specific change management to ensure timely approvals and regulatory compliance.
• Support introduction of existing products into new markets, ensuring technical readiness and regulatory alignment.
• Support scenario planning, risk analysis, and decision optimization for project strategies.
• Support project budgeting includes technical, regulatory, and financial considerations.

2. Technical Operations & Process Science

• Support Technical Operations activities for the qualification of alternative APIs, raw materials, and primary packaging for existing products.
• Support validation strategies (process, cleaning, packaging, material changes) for new products, new markets, or changes to existing processes.
• Support validation, characterization, and stability study protocols and reports.
• Partner with Production and Quality to develop or update batch manufacturing records (BMRs), packaging records, and batch documentation.
• Liase with production teams for new processes, validation batches, and technology transfer activities.
• Follow validation batches on the shop floor; collect and assess samples per protocol.
• Support manufacturing process troubleshooting, deviation investigations, and identification of corrective and preventive actions (CAPA).
• Ensure all activities comply with cGMP, internal Quality Systems, and China‑specific regulatory requirements.

3. Regulatory, Quality & Compliance Support

• Translate Chinese regulatory insights and requirements into clear technical actions for global teams.
• Prepare technical documentation to support registration filings, including process descriptions, risk assessments, and validation packages.
• Provide Technical Operations support for post‑approval variations, site changes, material substitutions, and market expansions.
• Ensure structured risk‑management integration across technical and project activities.

4. Cross‑Functional & Cross‑Cultural Collaboration

• Serve as the technical and project interface between China stakeholders and global teams (EMEA & APAC).
• Collaborate with external manufacturing partners, raw‑material suppliers, and packaging vendors.
• Navigate cross‑cultural interactions effectively, demonstrating transparency, respect, and strong stakeholder management.
• Communicate clearly and consistently with all stakeholders, ensuring visibility of risks, progress, and alignment needs.

Qualifications & Experience

Required

• Bachelor’s degree or above in Pharmacy, Chemistry, Chemical Engineering, or related field.
• 5+ years of experience in pharmaceutical process development, product development, or drug product manufacturing.
• Strong experience in process validation, including cleaning validation.
• Project management experience with the ability to manage multiple priorities and cross‑functional workstreams.
• Solid understanding of quality systems, GMP, regulatory expectations, and technical risk management.
• Strong analytical, scenario‑planning, and structured problem‑solving skills.
• Excellent verbal and written English; Mandarin is an advantage.

Desired

• Broad experience with solid, liquid, and gum‑based dosage forms.
• Knowledge of formulation science, process equipment, packaging systems, and scale‑up considerations.
• Strong shop‑floor presence; hands‑on, flexible, and proactive working style.
• Ability to influence without authority; strong leadership and team‑collaboration skills.
• Ability to work independently while managing multiple projects concurrently.
• Strong statistical literacy (e.g., DoE, SPC, validation statistics).
• Excellent presentation and communication skills.
• Financial and business acumen enabling integration of technical and commercial perspectives.

Key Competencies

• Project Management & Cross‑Functional Collaboration Skills
• Process Validation & Technical Operations
• Manufacturing & Regulatory Knowledge
• Problem‑Solving, Creativity & Risk‑Based Thinking
• Cross‑Cultural Communication & Collaboration
• Business & Financial Acumen

 

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