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Stage in Quality Assurance

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  • Job title Stage in Quality Assurance
  • Function Career Programs
  • Sub function Non-LDP Intern/Co-Op
  • Category Intern/Co-Op, Non-LDP Intern/Co-Op (C)
  • Location Latina / Italy
  • Date posted
  • Requisition number R-073713
  • Work pattern Hybrid Work

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Latina, Italy

Job Description:

For the production site of Borgo San Michele (Latina), we are looking for 2 interns for the Quality Assurance Department.

The interns will be supporting the activities aimed at ensuring that the quality of the products align 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.

Activities:

The intern will be trained and will be supporting:

  • The 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.

  • The activities aimed at the execution and definition of the necessary control activities and related operating procedures.

  • The Identification of opportunities to improve current compliance with GMP requirements in the various plant processes.

  • The Interaction and collaboration with the various company departments to support a flawless review process.

  • The management of documentation and product samples.

Requirements:

  • Master's Degree in Pharmaceutical Chemistry and Technology, Pharmacy, Chemistry, Biology or Engineering.

  • Proficency in Italian.

  • Fluency in English.

  • Good knowledge of the MS Office package.

As this position is posted in a country that is subject to EU pay transparency requirements, the Talent Acquisition team will provide pay range information on request and to candidates invited to an interview.

Required Skills:

Preferred Skills:

The anticipated pay range and benefits for this position is:

opzione B indennità di stage fissa 950 euro al mese

Stage in Quality Assurance

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