Secondary Process Improvement Specialist
GSK
This listing was originally posted on GSK's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moWe 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:
In accordo con il/la proprio/a responsabile, coordina le attività tecniche e organizzative finalizzate ad assicurare lo sviluppo degli impianti e dei processi per le operazioni di confezionamento, stoccaggio e logistica, con l’obiettivo di adattarne le capacità ai requisiti di mercato e garantire il miglioramento continuo delle performance.
Assicura il rispetto dei parametri produttivi, qualitativi e di sicurezza, contribuendo al raggiungimento degli obiettivi aziendali, interfacciandosi con altri stakeholder interni quali Ingegneria, MSAT, Asettico e Supply Chain.
In this role, you will:
Attraverso analisi FMEA (analisi dei modi e degli effetti di guasto), elabora e propone le soluzioni tecniche necessarie per il miglioramento continuo dei processi produttivi, con l’obiettivo di migliorarne efficienza, produttività e qualità del prodotto finito.
Collabora nella gestione dei Rapporti di Deviazione, facilitando l’identificazione delle cause e delle azioni correttive e preventive. Gestisce le Change Request tecniche e i CAPA per le sue aree di competenza.
Gestisce la creazione e definizioni di specifiche tecniche e funzionali di materiali ed equipment, assicurando il rispetto delle cGMP, delle richieste commerciali e delle iniziative del sito produttivo.
Partecipa alle attività e programmi cross-funzionali e interdipartimentali, inclusi progetti atti a sviluppare nuove produzioni o investigazioni di anomalie e criticità di funzionamento. Supporta inoltre le attività di installazione e validazione di apparecchiature e processi.
Durante le ispezioni regolatorie partecipa per le aree di competenza e collabora, se necessario, alla preparazione o revisione di dossier regolatori e documentazione GMP.
È infine responsabile del rispetto delle normative in materia di Sicurezza, Ambiente e Salute.
Siamo alla ricerca di professionisti con le seguenti competenze:
Laurea in Ingegneria
Esperienza in ruoli analoghi; su processi produttivi, preferibilmente packaging
Conoscenza delle GMP
Esperienza in analisi dati con competenze intermedie (tool statistici)
Buona conoscenza della lingua inglese (scritta e parlata) - Italiano fluente
Le seguenti competenze non sono necessarie; se non le possedete, vi invitiamo comunque a candidarvi:
Forte capacità analitica (lettura dati e identificazione root cause)
Approccio pratico e operativo su problematiche ingegneristiche
Flessibilità e capacità di apprendere rapidamente
Ottime capacità comunicative (interazione a diversi livelli organizzativi, es. value stream lead)
È considerato un plus la conoscenza delle metodologie di Lean Manufacturing e TPM
Accountability e buone capacità organizzative
Closing date for applications: 1 giugno 2026
Please note that relocation support cannot be provided; therefore, only candidates who are already based in the indicated country can be considered.
What we offer:
Permanent contract in a very Inclusive environment
Smart Working up to 50%
Flexible Benefits
Company Healthcare Plan
Integrative pension fund
Employee Assistance Programme
Prevention services and vaccination clinic
Tax assistance
Local nursery agreement
Postal service, laundry, shoe repair and tailoring
On site canteens and coffee corners
Free company bikes and shuttle
Closing date for applications: 1 giugno 2026
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?
Uniting science, technology and talent to get ahead of disease together.
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.
Should you require any specific adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on ita-inclusion.recruitment@gsk.com.
Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.
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/
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