Qualification & Validation Specialist - Pharma

Our people in **Manufacturing & Global Operations** share two priorities: getting things done and making things better. If you’re a dynamic person with a positive mindset, you’ll fit in well here. It’s an international team with a powerful spirit of collaboration. Together, we make sure our products meet the highest standards of quality by constantly searching for ways to improve at every stage of our value chain - from the raw materials we buy through to the logistics network that brings our medicines to patients. Join our team and help us make an even bigger contribution to Grünenthal’s future.

**What the job looks like**
Each day you'll enjoy a variety of challenges, such as:

- Dynamic interaction with internal and external customers to drive innovation
- Support digital roadmap implementation and engineering/production project
- Application of global engineering standards, best practices to the manufacturing sites
- Provide scientific engineering solutions to problems in Global Manufacturing with focus on operations excellence and KPI satisfaction
- Taking care of utilities/equipment/computerized System Validation lifecycle (e2e)
- Support in managing the inventory of computerized systems of the plant, undertake an evaluation of the risk and propose mitigations
- Ensure top-level helpdesk of ERP (i.e. SAP), MES, serialisation and/or computerized systems of competence

**What you'll bring to the table**

To make the most of this role and truly thrive, you should have:

- University degree Biotechnologies, Engineering or comparable
- Experienced with validation, CSV in Pharma or comparable (at least 2 years)
- Risk management, data management, data integrity knowledges
- Knowledge of ERP system is beneficial
- Knowledge of validation techniques (GMP; GAMP; WHO, CFR21 )
- OPEX problem solving techniques is beneficial
- Interpersonal understanding and communication skills
- Fluency in business English.

Grünenthal offers equal employment opportunities. Recruitment will take place without distinction with regard to religion, gender, sexual orientation, age, origin, disability or other relevant categories.

La ricerca è rivolta ad ambo i sessi (Legge 903/77 e 125/91). Si richiede esplicito consenso al trattamento dei dati personali (ex D.Lgs 196/03 e GDPR - Reg.UE. 2016/679).

Contratto di lavoro: Tempo pieno, Tempo indeterminato

Retribuzione: €35.000,00 - €45.000,00 all'anno

Benefit:

- Buoni pasto
- Mensa aziendale

Disponibilità:

- Dal lunedì al venerdì

Retribuzione supplementare:

- Bonus annuale
- Maggiorazione lavoro notturno
- Premio di produzione
- Quattordicesima