FAREVA

About the Company

Since the company was founded in 1990, our objective at Fareva has always been to offer customers impeccable service by providing tailored R&D, production and packaging facilities which fully satisfy their needs. Clearly Fareva has obviously changed a lot since it began: the company has grown, adapted its technologies, developed its expertise, and expanded its fields of business. But in spite of these changes, we have never strayed from the initial ambition of the family business created in the Ardèche region of France: to answer our client demands.

Nowadays, FAREVA is one of the world’s leading subcontractors in the Industrial & Household, Cosmetics and Pharmaceuticals fields.

In 2023: FAREVA is present on 3 continents, 13 countries around the world and represents 13,000+ employees, 41 production sites for a turnover of €2,2 Billion.

Listed Jobs

Company Name

FAREVA

Job Title

Ingénieur composants/Ingénieure composants

Job Description

**Job Title:** Component Engineer (Packaging) **Role Summary:** Lead and manage projects related to primary, secondary, and tertiary packaging components for sterile pharmaceutical manufacturing. Serve as the technical liaison between suppliers and internal stakeholders, ensuring compliance with GMP/ICH standards and driving continuous improvement in packaging quality and performance. **Expectations:** - Deliver functional, compliant packaging solutions meeting customer and regulatory requirements. - Identify, investigate, and resolve packaging-related quality issues. - Maintain up‑to‑date specifications and documentation for all packaging materials. **Key Responsibilities:** - Develop, qualify, and update packaging specifications (primary, secondary, tertiary) in line with quality standards. - Act as the technical contact for suppliers, driving component development, optimization, and defect resolution. - Investigate non‑conformances, root causes, and implement corrective actions on sites and with suppliers. - Interface with internal teams (QC, production, supply, purchasing, QA) and act as a subject‑matter expert in risk and change management. - Manage packaging change processes, aligning with facility procedures and regulatory expectations. - Draft and update documents (procedures, work instructions, technical rationales, records). - Ensure adherence to GMP, cGMP, ISO regulations, and respond to regulatory or client inquiries. - Participate in regulatory audit preparations and post‑audit follow‑ups. - Conduct technical surveillance and keep abreast of industry advances in packaging technologies. **Required Skills:** - Deep knowledge of pharmaceutical packaging systems and production lines. - Strong analytical and problem‑solving abilities for packaging failure investigations. - Excellent written communication for technical reports, specifications, and SOPs. - Proficiency in risk assessment (QRA) and change impact analysis. - Familiarity with GMP, cGMP, ISO 13485/9001, and relevant quality standards. - Ability to synthesize information quickly and focus on actionable solutions. - Team collaboration and effective cross‑functional communication. **Required Education & Certifications:** - Master’s (Bac+5) in Packaging, Pharmaceutical Engineering, or Quality Management. - Certification in GMP or a related quality assurance discipline is advantageous.

Riom, France

On site

31-10-2025