Technical Operations Process Science and Validation Scientist

Kenvue; Val-de-Reuil; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading consumer products company in France is seeking a Technical Operations Process Science and Validation Scientist. This role requires a Bachelor’s Degree in a related scientific field and at least 2 years of industry experience in process development. Key responsibilities include supporting project tasks, resolving technical challenges, and collaborating with cross-functional teams. The ideal candidate will have strong analytical skills and technical writing proficiency. This position is fully onsite with minimal travel required.

Qualifications

• 2+ years of industry experience related to process development.
• Experience in Consumer and Personal Care industry preferred.
• GMP experience preferred.

Responsabilités

• Support execution of project tasks for New Product Introduction and improvements.
• Use scientific principles to resolve technical challenges.
• Prepare technical memos, analyze data, and recommend conclusions.
• Collaborate with Quality, Operations, and R&D teams.

Connaissances

Scientific principles

Technical writing

Analytical skills

Collaborative teamwork

Problem-solving

Formation

Bachelor’s Degree in Pharmacy, Chemistry, Engineering, or related scientific field

Outils

MS Word

Excel

Project software

Description du poste

Job Title

Technical Operations Process Science and Validation Scientist

Overview

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands—NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S®, and BAND-AID®. Science is our passion; care is our talent.

Who We Are

Our global team of ~22,000 people creates a culture where every voice matters. We are passionate about insights, innovation, and committed to delivering the best products to our customers.

Role Reports To

MS&T Process Science Leader

Location

Europe/Middle East/Africa – France, Normandy, Val-de-Reuil (Fully Onsite, 10% travel)

What You Will Do

The Technical Operations Scientist supports a broad range of consumer cosmetics, OTC drug products, and OTC monograph drug products. The role provides technical support in the design, development, and implementation of technical solutions for new product introductions and cost‑reduction initiatives.

Key Responsibilities

• Support execution of or lead small to moderately sized project tasks per established timeline, including technology transfer process for New Product Introduction, Product Improvements, and new raw material qualification.
• Use scientific principles to resolve technical challenges while articulating complex subject matter in clear, concise terms.
• Support the execution of the planned experimental design (sample collection, in‑process testing, sample management, etc.).
• Prepare technical memos, reports, analyze data, and recommend conclusions based on scientific rationale.
• Support or lead troubleshooting supply issues, global change control (GCC), root‑cause analysis, and remediation for technical‑related issues.
• Collaborate and work closely with Quality, Operations, and R&D teams to ensure seamless transitions through the new product and project development lifecycle.
• Effectively execute technical transfer and life cycle management initiatives.

Required Qualifications

• Bachelor’s Degree in Pharmacy, Chemistry, Engineering, or related scientific field.
• 2+ years of industry experience related to process development.
• Experience within the Consumer and Personal Care industry preferred. GMP experience preferred.

Additional Requirements

• Presence on site/shop floor is required; remote work must be agreed with the manager.

Desired Qualifications

• Knowledge of product characteristics, raw material performance, and customer needs.
• Knowledge of liquid/semi‑solid formulation development principles.
• Understanding of process equipment and in‑process control instruments.
• Process knowledge of mixing, filling, liquid dosage, solid dosage, packaging, scale‑up, technology transfer, and continued process verification.
• Knowledge of regulatory requirements for consumer cosmetic and OTC monograph drug products (FDA, MHRA, Health Canada, AIFA, etc.).
• Strong analytical and technical writing skills; proficiency in MS Word, Excel, and project software.

Equal Opportunity Employer

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.