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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.

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.

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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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:

• 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.

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.

 
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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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:

• Be part of Global Operations multidisciplinary group dealing with plant engineering, automation and applications.
• 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.
• Dynamic interaction with internal and external customers to drive innovation.

What you'll bring to the table

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

• University degree Biotechnologies, Engineering, IT or comparable.
• Minimum 3 years-experienced with validation, CSV in Pharma or comparable.
• An experience in a coordination role (e.g. project manager, coordinator, team leader) would be beneficial.
• Knowledge of validation techniques (GMP; GAMP; WHO, CFR21…), risk management, data management, data integrity knowledges.
• OPEX problem solving techniques is beneficial.
• Interpersonal understanding, communication skills, leadership attitude.
• 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.

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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