Qa Associate Batch Record Review
Johnson & Johnson is currently seeking a QA Associate Batch Record Review to join our team located in Latina, Italy.
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. 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.
What you will be doing:
For the production site of Borgo San Michele (Latina), we are looking for one candidate for a Fixed Term employment in the Quality Assurance Department. The profile 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.
What impact you will also have:
Review of the data produced in the phases of the pharmaceutical production process (Batch Record Review) to verify the compliance of the product with the regulatory requirements 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 We would love to hear from you if you have the following requirements:
Master's Degree in Pharmaceutical Chemistry and Technology, Pharmacy, Chemistry, Biology, or Engineering; Proficiency in English; Good knowledge of the office package.
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