Targeted expertise to support your regulatory monitoring and operations

Secondary packaging, serialization, repackaging, quality sorting: Cosmépharm manages every step with full control, under pharmaceutical supervision.

A partner for every stage of your value chain

At Cosmépharm, every product is the result of a rigorous process combining industrial expertise with pharmaceutical standards. Across our 15 production lines, our 45 employees apply strict protocols at every stage, from packaging through to final quality control.

Certified by the ANSM since 1988, we subject each batch to systematic quality checks prior to shipment, ensuring full compliance with current regulations in the cosmetic and pharmaceutical sectors.

"Each area of expertise is managed under pharmaceutical supervision, ensuring compliance and traceability at every stage."
Fabrice Gonin — Interim Responsible Pharmacist

A partner for every stage of your value chain

📦

Secondary packaging

Cartoning, leaflet insertion, labeling, batch and expiry date marking under GMP-compliant conditions.

🔐

Serialization & aggregation

FMD/DSCSA compliance, unit-level traceability, and data security.

🔄

Repackaging / rework

Market changes, compliance updates, and quality rework under controlled conditions.

🔬

Sorting & quality control

Visual inspection, compliance checks, and pharmaceutical batch release.

📋

Regulatory monitoring

Monitoring of regulatory and commercial developments in your market.

💊

Primary packaging

Cosmetics, food supplements — formulation and packaging.

We recrute

Professionals committed to quality

Joining Cosmépharm means becoming part of a team accustomed to GMP, ISO 22716, and ISO 13485 requirements—where documentary rigor and team spirit go hand in hand.

Operations
Packaging operator
Quality
Quality Assurance Technician
Supervision
Line Manager
Technical
Serialization Specialist
General application See in LinkedIn Varennes-sur-Allier (03) · CDI & CDD

A partner at every stage of your project

From initial assessment to post-production follow-up, Cosmépharm supports you with a dedicated contact and a proven methodology.

01

Feasibility study

Analysis of your specifications, regulatory constraints, volumes, and timelines.

02

Audit & qualification

Site visit, equipment validation, supplier qualification, and technical dossier.

03

Industrialisation

Machine trials, process validation, batch record preparation, and process fine-tuning.

04

Serial production

Packaging, serialization, quality control, and release under pharmaceutical supervision.

05

Monitoring & continuous improvement

Quality reporting, annual review, complaint management, and process optimization.

Nous tenons les délais que nous prenons

Petites et moyennes séries, décisions rapides, interlocuteur dédié — la réactivité est l'un de nos différenciateurs depuis près de 40 ans.

98 %
Taux de service
48 h
Délai de devis
4 sem
Démarrage moyen

A project related to our expertise?

Let’s talk. Response within 48 hours.