Lavori attuali relativi a Sterile Business Unit Process Specialist - Parma - GlaxoSmithKline


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  • Parma, Italia Glaxosmithkline A tempo pieno

    OverviewSite Name: Italy - ParmaPosted Date: JanWe 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;...


  • Parma, Italia Gsk A tempo pieno

    Un'azienda biopharma globale cerca un referente tecnico per garantire la sicurezza e la qualità del processo produttivo.Richiesta una laurea in materie tecnico/scientifiche e almeno 3 anni di esperienza nei processi farmaceutici.L'accettazione nel ruolo prevede anche esperienze in produzioni sterili e competenze di technical writing.Offriamo un contratto...

  • Unit People

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    Parma, Italia IKEA A tempo pieno

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  • Process Engineer

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    Parma, Italia agap2 Italia A tempo pieno

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  • Tecnologo dei processi

    4 settimane fa


    parma, Italia agap2 Italia A tempo pieno

    1) Il tuo ruolo ⚙️- Gestire e ottimizzare processi produttivi farmaceutici su impianti sterili- Supportare lo sviluppo e la validazione di nuovi processi e prodotti- Garantire la conformità alle normative GMP e agli standard qualitativi- Collaborare con team multidisciplinari per la risoluzione di criticità di processo2) Le tue mansioni- Supervisione...

  • Tecnologo dei processi

    3 settimane fa


    Parma, Italia Agap2 Italia A tempo pieno

    1) Il tuo ruolo ⚙️ Gestire e ottimizzare processi produttivi farmaceutici su impianti sterili Supportare lo sviluppo e la validazione di nuovi processi e prodotti Garantire la conformità alle normative GMP e agli standard qualitativi Collaborare con team multidisciplinari per la risoluzione di criticità di processo 2) Le tue mansioni Supervisione...

  • Preparatore Sterile

    2 settimane fa


    Parma, Italia GSK A tempo pieno

    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...

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    Parma, Italia GSK A tempo pieno

    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...


  • parma, Italia Sidel A tempo pieno

    Contract Type: PermanentCountry: ITALYLocation: ParmaYour opportunityWithin the Innovation (R&D) team, the position of Business process management specialist on Product lifecycle and Enabling Processes offers a dynamic environment to utilize and expand your expertise in process management and contributes to the continuous improvement and digital...

Sterile Business Unit Process Specialist

7 ore fa


Parma, Italia GlaxoSmithKline A tempo pieno

OverviewSite Name: Italy - ParmaPosted Date: Jan 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 | GSKResponsibilitiesSvolge il ruolo di referente tecnico per gli aspetti di sicurezza e qualità legati al processo produttivo.Individua, promuove e gestisce attività/progetti di miglioramento continuo legati sia al processo che alla documentazione (es. Master Batch Document, SOP).Viene coinvolto/a come referente tecnico nelle valutazioni di impatto per change o progetti (es. NPI) o per investigazioni.Mantiene aggiornata la documentazione tecnica di reparto e viene coinvolto/a come referente tecnico per le review periodiche dei documenti.In questo ruolo, TU:Gestione documentazione tecnica di reparto (es. Review allarmi critici, Data process mapping, ATRD, review periodica AT, QR, Risk Assessment EHS).Coinvolgimento come SME per progetti o NPI e valutazioni di impact assessment legati al processo di change.Coinvolgimento come SME per investigazioni legate a deviazioni tecniche o per la definizione di CAPA.Analisi e gestione di Process or Documentation Improvement (coinvolgimento nei processi di Quality, Waste o Safety TOP 3).Coinvolgimento nell’oversight di processo come supporto tecnico.Supporto tecnico al Process Expert per aggiornamento o emissioni nuove SOP o metodi.Coinvolgimento come SME per ispezioni.Why You?Basic Qualifications & SkillsSiamo alla ricerca di persone con le seguenti competenze per raggiungere i nostri obiettivi:Laurea in materie Tecnico/Scientifiche o Ingegneria (es. Chimica e Tecnologia Farmaceutiche, Ingegneria Chimica, Chimica ecc)Conoscenza minima di 3 anni di processi farmaceuticiEsperienze di Produzioni SteriliConoscenza dei processi produttivi e impianti, anche in ambiti diversi dal farmaceuticoConoscenza della lingua Inglese (scritto e parlato)Technical WritingPreferred Qualifications & SkillsLe seguenti competenze non sono necessarie; se non le possedete, vi invitiamo comunque a candidarvi:Comunicazione efficaceBuone capacità collaborative all’interno di team multifunzionaliWhat we offerPermanent contract in a very Inclusive environmentFlexible BenefitsCompany Healthcare PlanIntegrative pension fundEmployee Assistance ProgrammeSustainable mobility programmeCompany canteenPerformance RewardClosing date for applications: 12 febbraio 2026Please 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 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 noticesGSK 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