Process Technologist

GlaxoSmithKline; Parma; Ibrido; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

Una azienda biopharma globale cerca un professionista per supportare tecnicamente i processi produttivi a Parma. Il ruolo richiede una Laurea Magistrale in scienze e esperienza nel settore. Offriamo un contratto permanente con benefici flessibili e un modello di lavoro ibrido. La scadenza per le candidature è fissata per l'8 ottobre 2025.

Servizi

Piano sanitario aziendale

Fondo pensione integrativo

Programma di assistenza ai dipendenti

Canteen aziendale

Competenze

• Laurea Magistrale in Ingegneria Chimica o di processo.
• Esperienza nel settore Manufacturing, preferibilmente farmaceutico.
• Buona conoscenza dell'italiano e dell'inglese (parlato e scritto).

Mansioni

• Proporre progetti di miglioramento per i processi.
• Supportare la validazione di prodotto/processo.
• Gestire anomalie nei processi produttivi.

Conoscenze

Laurea Magistrale in discipline scientifiche

Esperienza in ruolo analogo

Buona conoscenza dell'italiano e dell'inglese

Formazione

Laurea in Ingegneria Chimica o equivalenti

Strumenti

Strumenti statistici

Pacchetto Office

Descrizione del lavoro

Overview

Site Name: Italy - Parma

Posted Date: Sep 24 2025

Job Description

We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.

We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK

Scope

È il supporto tecnico per il processo ed il prodotto nei reparti produttivi, garantendone il continuo miglioramento attraverso il troubleshooting e problem solving (RCA member). Svolge i ruoli di investigation lead e DE owner ad hoc. Supporta il team NPI nella introduzione dei nuovi prodotti per gli aspetti tecnologici. Supporta in campo i reparti produttivi.

In this role you will

• Propone progetti di miglioramento/process understanding per i processi esistenti.
• Supporta la convalida di prodotto/processo sia a seguito di change sia per introduzione di NPI.
• Supporta l’unità di Change Control nella stesura della documentazione tecnica limitatamente alla sua area di responsabilità.
• Puo’ dare supporto agli enti preposti nelle fasi di IQ/OQ di alcuni equipment
• Ha conoscenza dei prodotti nell’ambito della Dose Form di competenza
• Individua eventuali progetti di miglioramento da un punto di vista produttivo, sia per incrementare la robustezza che la produttività dei processi. Inoltre, garantisce il monitoraggio continuo dei parametri/attributi critici dei prodotti, mantenendoli sotto controllo ed evidenziando eventuali azioni correttive.
• Definisce le golden CAPA
• Promuove il Problem Solving/Troubleshooting
• Supporta il reparto produttivo e l’unità OQ nella gestione delle anomalie riscontrate nei processi produttivi (RCA sme )
• Agisce da Investigation lead e DE owner ad hoc
• E’ responsabile delle quality review di reparto
• Utilizza tutti gli strumenti OE e statistici per l’analisi dei dati e la valutazione degli scenari
• Rispetta e promuove le norme gmp, di data integrity e alcoa.

Why you?

Qualifications & Skills

We are looking for professionals with these required skills to achieve our goals:

• Laurea Magistrale in discipline scientifiche (i.e. Ingegneria Chimica o di processo, chimica industriale o equivalente, farmacia, ctf, biotecnologie.)
• Esperienza in ruolo analogo, proveniente da area tecnica, da contesti Manufacturing, preferibilmente Farmaceutici.
• Buona conoscenza dell\'italiano e dell\'inglese (scritto e parlato)

Preferred Qualifications & Skills

If you have the following characteristics, it would be a plus:

• Conoscenze di Lean Manufacturing.
• Uso di strumenti statistici.
• Conoscenza delle norme GMP, data integrity e alcoa.
• Conoscenza degli equipment e dei processi in uso in ambito pharma.
• Conoscenza del pacchetto office.

What We Offer

• Permanent contract in a very Inclusive environment
• Flexible Benefits
• Company Healthcare Plan
• Integrative pension fund
• Employee Assistance Programme
• Sustainable Mobility Programme
• Company canteen
• Performance Reward

Closing Date for Applications – 8th October 2025

Please note that relocation support cannot be provided; therefore, only candidates who are already based in the indicated country can be considered.

Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.

Why GSK?

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or [phone] (outside US).

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK\'s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/