QA Systems Specialist

Gr?nenthal GmbH; Varese; In loco; EUR 45.000 - 65.000; Tempo pieno

Vantaggi offerti da questo lavoro

Performance-based annual bonus

Descrizione del lavoro

Grünenthal GmbH is seeking a Quality Assurance professional to join their team in Varese, Italy. The role involves managing change controls, participating in training execution, and overseeing compliance with quality standards.

Candidates should have a degree in Scientific disciplines and 3–5 years of relevant experience in the pharmaceutical industry. Grünenthal promotes collaboration and offers performance-based bonuses and equal employment opportunities.

Competenze

• 3–5 years of experience in Quality Assurance positions within the pharmaceutical sector.
• Knowledge of local and international legal/regulatory requirements and GMP standards.
• Competency in communication and interfaces management.

Mansioni

• Management of change controls.
• Participation in planning and execution of site trainings.
• Issuance and revision of Product Quality Review (PQR).
• Participation in management of regulatory aspects to maintain required manufacturing licenses.
• Collection of site KPIs.

Conoscenze

Change control management

Communication skills

Knowledge of GMP standards

Risk assessment management

Formazione

Degree in Scientific disciplines

Descrizione del lavoro

Department: Global Operations & Production

Job ID: 45317

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

• management of change controls
• participation in planning and execution of site trainings
• issuance and revision of Product Quality Review (PQR)
• participation in planning and execution of self-inspections together with CAPA management
• revision of Master Batch Records
• issuance of process validation protocols and reports
• participation in risk assessment management
• cooperation in the revision of qualification and validation documentation
• overview on Quality Agreement with customers
• participation in management of regulatory aspects to maintain required manufacturing licenses
• collection of site KPIs

What you'll bring to the table

• degree in Scientific disciplines
• 3–5 years of experience in Quality Assurance positions within the pharmaceutical sector
• knowledge of the local and international legal/regulatory requirements and GMP standards
• competency in communication and interfaces management

Our pay ranges are based on an objective, gender-neutral job evaluation system. The final salary offered is determined based on factors like, but not limited to, relevant education, skills, experience, certifications, geographic location, and business or organizational needs. Your compensation package will include a performance-based annual bonus.

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.