Lavori attuali relativi a Stability Support - Parma - Gsk


  • Parma, Italia Chiesi Farmaceutici A tempo pieno

    **Data**:11 set 2024**Dipartimento**:Corporate Quality Operations**Team**:Quality**Tipo Lavoro**:Dipendente**Tipologia Contratto**:Tempo indeterminato**Località**:Parma, IT**_Chi siamo_** - Con sede a Parma, in Italia, Chiesi è un gruppo farmaceutico e sanitario internazionale focalizzato sulla Ricerca, con oltre 85 anni di esperienza, che opera in 31...


  • Parma, Italia Chiesi Group A tempo pieno

    Chi siamo Con sede a Parma, in Italia, Chiesi è un gruppo farmaceutico e sanitario internazionale focalizzato sulla Ricerca, con oltre 85 anni di esperienza, che opera in 31 paesi con più di 7.000 dipendenti (Gruppo Chiesi). Per realizzare la sua missione di migliorare la qualità della vita delle persone, agendo responsabilmente nei confronti...


  • Parma, Italia Novasyte A tempo pieno

    On behalf of our Client a global pharmaceutical company, IQVIA is looking for a CTS Packaging Packer, based in Parma or surrounding areas. RESPONSIBILITIES: - Packaging and labelling of non-clinical studies and stability clinical trial material - Contributes to the evaluation for the definition of packaging specifications of materials for clinic,...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    ScopoIl Laboratorio di Stabilità è un'unità cruciale del dipartimento Corporate Quality Operations, responsabile della gestione delle analisi di stabilità dei prodotti Corporate (pMDI e DPI) realizzati presso gli stabilimenti di Parma, Blois e Santana de Parnaiba.Responsabilità principali• Coordinare gli analisti del laboratorio per monitorare e...

  • Analytical Scientist

    6 giorni fa


    Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    About the RoleWe are seeking an experienced Analytical Scientist to join our team at Chiesi Group. As an Analytical Scientist, you will play a key role in the design, monitoring, and data elaboration of analytical development studies relevant to inhalation (pMDIs/DPI) and/or biological drug products.Main ResponsibilitiesSupport to CTS releaseStudy Monitor of...

  • Analytical Scientist

    2 settimane fa


    Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    About the RoleWe are seeking an experienced Analytical Scientist to join our team at Chiesi Group. As an Analytical Scientist, you will play a key role in the design, monitoring, and data elaboration of analytical development studies relevant to inhalation products and/or biological drug products.Main ResponsibilitiesSupport the development of analytical...

  • Analytical Scientist

    1 settimana fa


    Parma, Emilia-Romagna, Italia Chiesi A tempo pieno

    About UsChiesi is a global pharmaceutical and healthcare group with a rich history of innovation and a commitment to improving people's quality of life. With over 85 years of experience, we operate in 31 countries and have a team of over 7,000 employees. Our mission is to act responsibly towards society and the environment, and we strive to achieve this...


  • Parma, Emilia-Romagna, Italia Chiesi A tempo pieno

    About ChiesiChiesi is a global pharmaceutical and healthcare group with over 85 years of experience, operating in 31 countries with more than 7,000 employees. Our mission is to improve people's quality of life by acting responsibly towards society and the environment.Our Research & Development TeamOur R&D team is a fundamental asset for the business, divided...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Who we are looking for Purpose We are seeking a skilled professional to design, oversee, and analyze analytical development studies pertinent to inhalation (pMDIs/DPI) and/or biological drug formulations. Key Responsibilities Provide support for CTS release processes. Act as Study Monitor for analytical method development initiatives. Oversee...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Who we are looking for Purpose We are seeking a skilled professional to design, oversee, and analyze analytical development studies pertinent to inhalation (pMDIs/DPI) and/or biological drug formulations. Key Responsibilities Provide support for CTS release processes. Act as Study Monitor for analytical method development initiatives. Oversee...


  • Parma, Emilia-Romagna, Italia Chiesi A tempo pieno

    About UsChiesi is a leading international pharmaceutical and healthcare company with a rich history of innovation and a strong commitment to improving people's quality of life. With over 85 years of experience, we operate in 31 countries and employ over 7,000 talented individuals worldwide.Our MissionWe strive to achieve our mission by researching,...


  • Parma, Italia Chiesi Group A tempo pieno

    Who we are looking for Purpose Design, monitor and data elaboration of analytical development studies relevant to inhalation (pMDIs/DPI) and/or biological drug products  Main Responsibilities Support to CTS release. Study Monitor of analytical method development studies. Study Monitor of analytical method validation/transfer...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Who we are looking for Purpose Responsible for the design, oversight, and data analysis of analytical development studies pertinent to inhalation (pMDIs/DPI) and/or biological medicinal products. Key Responsibilities Assist in the release of CTS. Monitor analytical method development studies. Oversee analytical method validation and transfer...

  • Analytical Scientist

    2 settimane fa


    Parma, Emilia-Romagna, Italia Chiesi Farmaceutici A tempo pieno

    About Chiesi FarmaceuticiChiesi is a leading international pharmaceutical and healthcare group with over 85 years of experience, operating in 31 countries with more than 7,000 employees. We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social and environmental standards.We believe that the...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Who we are looking for Purpose Responsible for the design, oversight, and analysis of studies related to analytical development for inhalation (pMDIs/DPI) and/or biological pharmaceutical products. Key Responsibilities Facilitate CTS release processes. Oversee analytical method development studies. Manage analytical method validation and transfer...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Who we are looking for Purpose Responsible for the design, oversight, and analysis of studies related to analytical development for inhalation (pMDIs/DPI) and/or biological pharmaceutical products. Key Responsibilities Facilitate CTS release processes. Oversee analytical method development studies. Manage analytical method validation and transfer...


  • Provincia di Parma, Emilia-Romagna, Italia Davines Italia spa A tempo pieno

    The Davines Group, founded in Parma in 1983, specializes in professional cosmetic products under the brands Davines for haircare and [ comfort zone ] for skincare. Led by Chairman Davide Bollati and CEO Anthony Molet, the Group is headquartered in Parma at the Davines Group Village, alongside which stand the Scientific Garden and EROC - European Regenerative...

  • Analytical Scientist

    3 settimane fa


    Parma, Emilia-Romagna, Italia Chiesi A tempo pieno

    About UsChiesi is a leading international pharmaceutical and healthcare company with a rich history of innovation and a strong commitment to improving people's quality of life. With over 85 years of experience, we operate in 31 countries and employ over 7,000 talented individuals worldwide.Our MissionWe strive to achieve our mission by researching,...

  • Analytical Scientist

    2 settimane fa


    Parma, Italia Chiesi Farmaceutici A tempo pieno

    Date: 17 Aug 2024 Department: GTD Global Technical Development Team: RD, Pharmacovigilance Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 31 countries with more...

  • Analytical Scientist

    2 settimane fa


    Parma, Italia Chiesi Farmaceutici A tempo pieno

    Date: 17 Aug 2024Department: GTD Global Technical DevelopmentTeam: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 31 countries with more...

Stability Support

3 mesi fa


Parma, Italia Gsk A tempo pieno

Site Name: Italy - Parma
Posted Date: Jun 20 2024
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 Lo Stability Support & Product Lyfe Cycle Lead si occuperà di guidare una squadra di circa 10 persone per raggiungere gli obiettivi di perfomance ed innovation prefissati, assicurando l'aderenza agli standard di sicurezza, qualità, conformità GMP e di miglioramento continuo. Viene inoltre richiesta una buona capacità ed attitudine allo sviluppo delle capacità individuali e di gruppo del team supervisionato, fornendo coaching e creando opportunità per il potenziamento delle competenze.
Il ruolo prevede un impegno nell'utilizzo degli strumenti GPS (Glaxo Production System) per facilitare il team nella gestione del lavoro, delle deviazioni e della CAPA.  Il ruolo prevede inoltre di supportare le ispezioni per gli argomenti di competenza e di mantenere relazioni efficaci con tutte le altre funzioni aziendali per raggiungere soluzioni tempestive e definitive ai problemi.
Il ruolo prevede inoltre la coordinazione del team per il completamento delle attività del progetto LES (Laboratory Enterprise System) nonché di supportare sia la fase di deployment (attualmente in finalizzazione) che mantenimento del sistema.
In questo ruolo TU… Assicurerai il coordinamento di risorse che eseguono attività inerenti la gestione di studi di stabilità volti a garantire il rispetto delle specifiche a fine vita dei prodotti fabbricati nel site di Parma.
Assicurerai il coordinamento di risorse che gestiscono la documentazione di responsabilità del Quality Control (specifiche tecniche, metodi di analisi, review periodiche, analisi statistiche) durante tutto il ciclo di vita del prodotto (da introduzione a dismissione).
Lavorerai con il LES Program Business Change Lead e con il team LES centrale al fine di facilitare e guidare il cambiamento nelle aree di laboratorio interessate, a seguito dell'implementazione del nuovo sistema LES ed al relativo mantenimento nel tempo.
Assicurerai che le attività siano svolte in ottemperanza ai requisiti regolatori, di farmacopea e di gruppo, nel rispetto delle date concordate nei piani di site.
Assicurerai una presenza attiva nell'ambito della relazione con eventuali Stability Hub esterni al site
Evidenzierai bisogni organizzativi, carenze tecnologiche e concorre alla relativa implementazione.
Identificherai, analizzerai e mitigherai i rischi relativi all'area di lavoro seguendo i principi del nostro Sistema di Gestione dei Rischi (RMS).
Perchè TU? Qualifiche e Competenze Richieste: Laurea Magistrale in disciplina scientifica (CTF / Chimica / Biotecnologie)
Esperienza analitica di laboratorio
Esperienza in gestione di un team
Inglese scritto e parlato fluente
Buone capacità di utilizzo di strumenti informatici (Excel, Power Point)
Qualifiche e Competenze Preferite: Buona capacità di relazione interpersonali
Closing Date for Applications – June 30th, 2024. 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.
#Hybrid
Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at ******** (US Toll Free) or +******** (outside US).
GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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 GSK's Transparency Reporting For the Record site.