22 set - Latina
Altro
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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.
Job Sub Function: Quality Control Business Enablement/Support About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. We are searching for the best talent for QA Assistant to be in Borgo San Michele – Latina.
For our manufacturing site in Borgo San Michele (Latina), we're looking for a permanent hire to join the Quality team. The role focuses on making sure our products fully comply with national and international pharmaceutical regulations, both in terms of quality control and documentation. You'll be part of the Quality Assurance team, helping ensure that processes and products meet GMP and internal quality standards.
This includes reviewing procedures and working with quality systems and tools. As a QA Assistant, you will: Act as Quality Leader/Quality Approver in the management of investigations, ensuring appropriate review and approval of records. Ensure that investigations are complete, that compliance and quality impact are properly assessed, and that appropriate corrections and corrective actions are defined and implemented.
Support the different site departments in resolving issues with potential quality impact and actively contribute to the definition of improvement actions. Contribute to the effectiveness and efficiency of the Quality System by monitoring departmental KPIs and implementing appropriate improvement actions where necessary. Actively participate in the department's preparation for Regulatory and Customer inspections and act as Subject Matter Expert (SME) during inspection execution.
Master's degree or diploma in a scientific field, or an equivalent combination of education and experience in the pharmaceutical industry. At least 2 years of experience in quality field in a pharmaceutical company, and experience as an investigator.
Excellent
English language skills. Good knowledge of Microsoft Office suite.
Administrative
Support ISO 9001 Quality Control (QC) Quality Control Testing Quality Systems Documentation Report Writing Administrative Support ISO 9001 Quality Control (QC) Quality Control Testing Quality Systems Documentation Report Writing The anticipated base pay range for this position is: €33,700.00 - €54,395.00 Benefits: An annual premio with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees' and companies' performance of the previous calendar year, or sales commissions. Vacation days Parental leave for a minimum of 12 weeks Caregiver leave Volunteer leave Well-being reimbursement Service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location's eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers. *Amounts and actual benefits may vary by location and are subject to change.
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