Life Science Consultant, Supply Chain

Advanced Accelerator Applications AAA a Novartis Company; Piemonte; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A global consultancy firm is looking for a Supply Chain Consultant to join their team in Ivrea, Italy. The role requires a Master's degree and 2–3 years experience in a GMP environment within the pharmaceutical industry. Proficiency in English and Italian is essential. This position offers an unlimited full employment contract with an excellent remuneration package and benefits in a diverse, people-oriented culture.

Servizi

Flat hierarchies and responsibility from the beginning

People-oriented culture

Diversity and inclusion focused environment

Flexible working hours

Involvement in global conferences

Individual professional development

Competenze

• Minimum 2–3 years of working experience in a GMP environment (Supply Chain Operations).
• Able to manage multiple tasks and work to tight deadlines.
• Attention to detail and accuracy.

Mansioni

• Writing User Requirement Specifications (URS) and reviewing Functional Specifications (FS).
• Verification and alignment of Master data.
• Training Key Users on site.

Conoscenze

Fluent in English

Native Italian speaker

Strong organizational skills

Problem-solving skills

Formazione

Master's degree in Science, Engineering, Operations, Pharmacy or equivalent

Descrizione del lavoro

Job Post has been updated successfully

Life Science Consultant, Supply Chain  [Turin, 10024], Piedmont - Italy | Posted - 24 / 04 / 23

We are looking for enthusiasts to join a strategic partner and global Life Science network that focuses on quality and regulated industries. Headquartered in Basel, Switzerland with subsidiaries across Europe and Asia, we help pharmaceutical companies implement progressive technologies and best practices.

Location : Ivrea, Italy

Start Date : As soon as Possible

We are a consultancy firm that provides custom solutions to pharmaceutical companies worldwide. We are currently looking for a Supply Chain Consultant to join our team on a permanent basis to implement a cloud‑based customized solution in Supply Chain for our client in Ivrea, Italy.

Major Accountabilities

• Business Validation Deliverables: Writing of User Requirement Specifications (URS); aligning with stakeholders on site; reviewing Functional Specifications (FS); reviewing and executing Operational Qualification (OQ) and Performance Qualification (PQ)
• Data Management / Cleansing: Verification and alignment of Master data
• Training: Training Key Users on site
• Standard Operating Procedure (SOP) Writing
• Leading communication between Key Users on site and IT

Minimum qualifications and Experience

Education

Master's degree in Science, Engineering, Operations, Pharmacy or equivalent

Language

Fluent in English – written & spoken

Native Italian speaker

Work experience

Minimum 2–3 years of working experience in a GMP environment (Supply Chain Operations) within the pharmaceutical industry

Experience working within a complex environment

• Able to manage multiple tasks and work to tight deadlines
• Creative, structured, open‑minded for new ideas, and agile drive

Soft Skills

• Strong organisational and time management skills
• Able to work independently and as part of a team
• Must have strong problem‑solving skills
• Attention to detail and accuracy
• Quick learner, keen to learn new skills

We offer great benefits

• Flat hierarchies and responsibility from the beginning
• People‑oriented culture
• Diversity and inclusion focused environment
• Global client projects in a multinational environment
• Flexible working hours and home‑office
• Involvement in global conferences
• Individual professional development, training, and coaching

Unlimited full employment contract

Excellent remuneration package consisting of a competitive salary plus a substantial bonus

Contact

If you have the necessary background and experience and would like to join a small team responsible for a truly global operation, then please send your application to recruiting(at)kvalito.ch including your:

• CV, cover letter and supporting documents (i.e., diplomas, certificates, references)
• Availability – earliest start date
• Salary expectations
• Location preference

We are looking forward to your application.

Your KVALITO Team.