QA Systems Specialist

Grünenthal Group; Origgio; In loco; EUR 37.000 - 40.000; Tempo pieno

Vantaggi offerti da questo lavoro

Performance-based annual bonus

Descrizione del lavoro

Grünenthal Group is seeking a Quality Assurance professional to manage change controls, planning training, and issuing Product Quality Reviews in Origgio, Italy. This role demands 3-5 years of relevant experience in the pharmaceutical sector.

Key qualifications include a degree in scientific disciplines and knowledge of GMP standards. The position offers a competitive salary between EUR 37,000 - 40,000 with performance-based bonuses. Join a collaborative international team dedicated to maintaining high-quality standards.

Competenze

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

Conoscenze

Quality Assurance experience

Knowledge of GMP standards

Communication skills

Fluent English

Formazione

Degree in Scientific disciplines

Descrizione del lavoro

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.

Pay range (full-time): EUR 37.000 - 40.000 €

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
• fluent English

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.