GRÜNENTHAL

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:

Support of business development activities, including market research, database screenings, structured lead and opportunity tracking;
Coordination of conferences and trade fairs, this time the CPhI in Milano in October 2026, including appointment scheduling as well as logistical preparation and follow-up to ensure smooth participation and effective meetings;
Participation in external communication activities such as answering website requests, updates of website, orchestration of media plans, as well as operational management of social media posts and advertising campaigns;
Handling of some administrative tasks such as travel arrangements, expense reports, organization of team and customer meetings, follow-up on actions, powerpoint improvements.

What you'll bring to the table
To make the most of this role and truly thrive, you should have:

Degree in Management, Marketing or related fields
Good level of English and communication skills (B2/C1)
Self-confident, organized
Powerpoint, excel, ideally AI applications

Ti senti la persona giusta per questa posizione?
📩 Candidati presentandoti al nostro stand e consegnando il tuo CV direttamente agli hrs.
Ti aspettiamo l'8 maggio al Bio Pharma Day Milano, presso Superstudio Events!

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Supply Chain Stage

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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:

Processing & Analysis of the forecasts received from the customers;
Managing and planning of coded materials supplies;
Defining the delivery time of materials required for the execution of the Production plan;
Issuing Purchase Orders in accordance with MRP needs and monitoring of POs status;
Management of material reminder to suppliers, call off management;
Master Data maintenance and specifically of planning data (Lead time, MOQ, safety stock, safety lead time, reorder point, BOM, PV and Recipes);
Sharing rolling forecasts of purchasing requirements to suppliers;
Implementing and updating KPIs to monitor supplier performance, inventory level and obsolescence risks; take corrective actions to mitigate destruction risks.

What you'll bring to the table
To make the most of this role and truly thrive, you should have:

Bachelor's degree in Management Engineering or Business Administration;
English language (B2/C1);
Good knowledge of major computer tools (Office package: Word, Excel, PPT)
Relational skills and aptitude for working in cross-functional teams and aptitude for team-work

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Q.C. Compliance Specialist - LIMS Expert

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

You will work within the Quality Department as a Business Process Expert of LIMS
LIMS continuous implementation
Design specification, customization and configuration of LIMS in order to satisfy the business requirement
PQ validation tests of LIMS system
Setting of master data in LIMS
Support on LIMS relevant topics after go-live for all business departments
Support on LIMS relevant topics for all business departments
Workshops and daily meetings with cross functional and international teams
Training on Qualified Persons and QC analysts
Daily collaboration with Business Process Owners, Business Process Managers, IT consultants, and Project Managers to carry on the project
Support digital roadmap implementation on Quality Control project
Process mapping of Quality Control processes
Fit-gap analysis between processes in the headquarter and the local sites
Writing and reviewing of project documentation: flowcharts, Blueprint, SOPs, User Requirements, Risk Assessments, Validation documents

What you'll bring to the table
To make the most of this role and truly thrive, you should have:

Experience in a similar role, such as BPE or LIMS Key User within pharma companies
Familiarity with SAP QM Module is highly beneficial
Fluency in Italian and English
Previous experience in a pharmaceutical manufacturing site in Quality Control Department is beneficial
Excellent communication skills, Problem solver, agility, willing to work in a fast-paced environment
Knowledge of validation techniques (GMP; GAMP; WHO, CFR21…), risk management, data management, data integrity knowledges

Junior Analytical Development Analyst

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

Perform the execution of development, validation and optimization of chemical analytical methods on raw materials, semi-finished and finished products
Perform audits of Pharmacopoeia compendial methods
Perform the activities for the development / introduction of new analytical and instrumental technologies
Perform the validation and the monitoring processes for equipment cleaning validation
Perform analytical activities of process validations
Support in the preparation and review of analytical methods and operational procedures of competence.
Partner with internal (e.g. Production, Supply Chain, Engineering, Quality Assurance and Technology Transfer) and external stakeholders (e.g. Customers and Suppliers)

What you'll bring to the table
To make the most of this role and truly thrive, you should have:

Bachelor's degree preferably in science subject (biology, CTF, pharmacy, engineering).
Knowledge of analytical method and process validation.
Analytical/Problem Solving and Team Working attitude.
Fluent English (B2/C1)

QC Microbiology Analyst

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Country: Italy
City: Origgio (Varese)
Department: Global Operations & Production

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:

Microbiological analyses of release and/or stability of packaging materials, raw materials, semi-finished and finished products.
Microbiological analyses of environmental monitoring of the plant (water, air, surfaces, etc.).
Planned technological controls on the finished product in order to allow its release on the market by QPs.
Supporting the manager in the planning of analytical activities with the aim of optimising analysis times and laboratory efficiency.
Relevant analyses in compliance with GMP and company SOPs and analytical methods.
Recording of analytical results in company computer systems and correct filling in of related departmental forms.
Identification of technical/analytical problems, collaborating with your manager in their resolution.
Verifying product quality standards by critically evaluating analytical data and identifying out-of-specification, out-of-trend or deviations from standard procedural flows, reporting them promptly to the direct supervisor.
Maintenance of analytical instrumentation.
Supporting the Micro Lab Manager in drafting and managing laboratory documentation and in all team-related activities.

What you'll bring to the table

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

Bachelor's degree preferably in science subject (biology, CTF, pharmacy, engineering).
Ideal experience of at least 3 years as a laboratory analyst/laboratory technician in quality control in pharmaceutical manufacturing companies.
Instrumental Microbiological techniques.

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Documentation Specialist

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What the job looks like

Each day you'll enjoy a variety of challenges, such as:

Manufacturing GMP Documentation: Management of Events and Deviations, including Root Cause Analysis; CAPA management; handling of Complaints in collaboration with QA Operations (systems: MasterControl, LIMS, MES).
Collaboration with documentation team and bulk manufacturing supervisors, involvement of the production personnel and training management.
Managing Data Integrity compliance.
Updating and managing documentation in accordance with GMP regulations.
Support the analysis and review of product quality attributes (OPV; PQR using Minitab software and other statistical analysis tools).
Support in the review and modification of Production Department Master Batch Records (SAP system).

What you'll bring to the table

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

Master’s degree in Chemistry/Pharmacy/Biotechnology/CTF/Biology or related fields.
Knowledge of the English language (B2/C1).
Detail‑oriented, analytical skills and effective time‑management abilities to meet assigned deadlines.
A collaborative mindset and strong team spirit are essential to work efficiently with both the reference team and other departments.

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Packaging Engineer

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