Global Talent Acquisition

hace 2 semanas

Argentona Barcelona provincia, España Beiersdorf Manuf. Argentona A tiempo completo

At Beiersdorf, we want to help people feel good about their skin - and our commitment goes far beyond caring for skin. For 140 years, we have developed innovative skin and body care products for well-known brands such as **NIVEA**, **Eucerin**, **La Prairie**, **Hansaplast**, and **Labello**. We act according to our purpose, **WE CARE BEYOND SKIN**, and take responsibility for our consumers, our employees, the environment, and society.

Behind every brand, product and accomplishment are our more than 20,000 employees worldwide. We live a culture of **inclusion**, **respect**, and **trust**, strongly aligned with our values**:CARE, COURAGE, SIMPLICITY**, and **TRUST**. We embrace diversity and are committed to equal opportunities for all.

**Your Tasks**:
As part of the Health Care Supply Chain Technology Team, the **Technology Development Engineer** will play a key role in driving technical implementation of new products and processes across Beiersdorf’s global healthcare supply network. This includes developing and scaling up production technologies such as **coating, converting, packaging**, and more, both internally and with Third-Party Manufacturers (TPMs).

Your responsibilities will include:

- Lead product and process development from pilot to industrial scale, including planning and executing trials, and ensuring smooth handover to operations.
- Define and implement technical and process standards with a strong focus on **Safety, Quality, Automation, Digitalization**, and **Lean Manufacturing**.
- Collaborate with local and global cross-functional teams to bring innovative healthcare solutions to the market efficiently.
- Manage equipment and process investments, ensuring regulatory compliance and validation (FAT, SAT, IQ, OQ, PQ).
- Support local engineering teams with **CAPEX planning** and continuous improvement initiatives.
- Conduct technical audits and assessments of TPMs, and guide them through **validation**, **trial execution**, and **production ramp-up**.
- Prepare and maintain technical documentation aligned with **medical device standards** (e.g., URS, SOPs, FMEAs, BOMs).
- Drive standardization of best practices to strengthen process reliability and operational excellence.

**Your Profile**:

- Master’s degree in **Engineering** (Industrial, Chemical, Mechanical, or similar) with a strong technical and business understanding.
- Professional experience in **Pharma**, **Medical Devices**, or **FMCG**, ideally in Production, Engineering or Project Management environments.
- Proven ability to lead technical projects in a global and cross-functional setup, with a strong performance and solution-oriented mindset.
- Solid knowledge of validation processes and regulatory requirements in the healthcare sector.
- Strong interpersonal and communication skills with the ability to work across cultures and disciplines.
- Fluent in **English** and **Spanish**; other languages are an asset.
- Willingness to travel occasionally based on project needs.

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