Qc Laboratory Analyst

Recordati Group; Aprilia; In loco; EUR 30.000 - 40.000; Tempo pieno

Descrizione del lavoro

Un'importante azienda farmaceutica conduce la ricerca di un 'Quality Control Laboratory Analyst'. Il candidato sarà responsabile dell'analisi di materiali e lotti, assicurando la qualità secondo le normative cGMP. È richiesta esperienza in laboratori di controllo qualità e familiarità con tecniche analitiche. L'ambiente di lavoro è inclusivo, promuovendo la diversità e le opportunità per tutti.

Servizi

Ambiente di lavoro diversificato

Opportunità di sviluppo professionale

Competenze

• Almeno 1 anno di esperienza in laboratori di controllo qualità, preferibilmente nelle aziende farmaceutiche.
• Conoscenza di cGMP e tecniche analitiche.
• Disponibilità a orari di lavoro flessibili.

Mansioni

• Eseguire analisi su materiali in arrivo e lotti secondo cGMP.
• Condurre studi di stabilità e analisi per indagini di qualità.

Conoscenze

Principi scientifici

Analisi qualitativa

Comunicazione in inglese

Formazione

Diploma di scuola superiore in chimica o Laurea in chimica

Strumenti

MS Excel

MS PowerPoint

MS Access

MS Word

EMPOWER

Descrizione del lavoro

With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical force, listed on the Italian stock exchange, with over 4,300 employees.

We are a group of like-minded, passionate individuals who go to extraordinary lengths for our partners, customers, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries.

At Recordati, our mantra is simple. We've always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest - we want to give people the opportunity to be the best version of themselves.

This drive will never stop. Together, we will always be reimagining tomorrow - with new ideas, new technologies and new innovations to fight diseases.

Recordati. Unlocking the full potential of life

• Job purpose

The Quality Control Laboratory Analyst reports to the Quality Control Laboratory Manager and collaborates with the Quality Control Supervisor who supervises the daily activities of the laboratory.

• Key responsibilities

The Quality Control Laboratory Analyst performs the analysis on incoming materials and batches according to cGMP; the activities include (but are no limited to) testing for :

• In-Process controls
• Raw materials, Intermediates and API batches
• Stability studies
• Analysis for quality investigations
• Required skills, qualifications and experience
• Chemistry High school certificate or Bachelor's degree, preferably in Chemistry or Pharmaceutical Chemistry
• Basic cGMP
• At least 1 year experience in Quality Control laboratory is preferred, specifically in pharmaceutical companies
• Working Knowledge of scientific principles for wide range of analytical techniques
• Understanding of EMPOWER is strongly preferred
• Routine use of MS Excel, MS PowerPoint, MS Access, and MS Word
• Good English speaking and comprehension is strongly preferred
• Available to adapt to flexible working hours

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.