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Master online in Project Management

Johnson & Johnson > offerta di lavoro n. 239605

immagine: lavoro con Johnson & Johnson

Technician Qa

> 2105906806W

contratto
Assunzione alle dipendenze

durata
Tempo indeterminato

regime orario
Full time

luogo di lavoro
IT Lazio, Latina

area professionale
Qualità, Ambiente, Sicurezza

livello professionale
Junior

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Descrizione della posizione

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science -- bringing creative ideas, products and services to advance the health and well-being of people. We touch the lives of over a billion people every single day.

Are you ready to impact the world?

If you want to leave your personal mark and be valued for who you are, we offer an outstanding experience to graduates looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career.

Janssen spa represents the pharmaceutical sector of the Johnson & Johnson group and markets over 30 medicinal specialties pertaining to five different therapeutic areas with the aim of offering groundbreaking therapeutic solutions that meet high standards of efficacy and safety.

For the production site of Borgo San Michele (Latina) we are looking for one candidate to join the Quality Assurance Department as QA Technician (fixed term contract of 12 months). The profiles will help to manage and ensure that the quality of the products aligns with the current specifications and regulations ('Good Manufacturing Practices' or GMP) both from the point of view of control over the product itself and the documentation linked to it.

The Activities Included In The Role Include:

  • Review and approval of the preparatory documentation for production activities (Master Data: product codes, production recipes, etc.)
  • Review of the data produced in the phases of the pharmaceutical production process (Batch Record Review) in order to verify the compliance of the product with the regulatory and regulatory requirements in force and to allow the batches to be placed on the market;
  • Execution and definition of the necessary control activities and related operating procedures.
  • Identification of opportunities to improve current compliance with GMP requirements in the various plant processes;
  • Interaction and collaboration with the various company departments to support a flawless review process.


Qualifications

  • Master's Degree in Pharmaceutical Chemistry and Technology, Pharmacy, Chemistry, Biology or Engineering
  • Proficiency in English (B1 and above)
  • Good knowledge of the Office package.

 

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Avvertenze

La presente inserzione è pubblicata allo scopo esclusivo di raccogliere candidature in relazione ad opportunità di lavoro o formazione effettivamente esistenti presso la nostra azienda o presso società controllate o partecipate. È pertanto esclusa qualsiasi finalità di intermediazione. La ricerca è rivolta a candidati di entrambi i sessi (L.903/77). I dati saranno trattati ai sensi del Regolamento UE 2016/679.
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