Qa Process Specialist

QA Process Specialist
Salary : €33,700 - 54,395 yearly

Azienda : Johnson Tipo Lavoro : Full Time Italy JobCopilot will tailor your resume and auto-fill the application

Descrizione Lavoro - QA Process Specialist
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. 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:

Quality

Job Sub Function:

Quality Control

Job Category:

Business Enablement/Support

All Job Posting Locations:

Latina, Italy

Job Description:

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.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for QA Process Specialist to be in Borgo San Michele – Latina.

Purpose :

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 Process Specialist, you will:

Manage complex investigations ensuring compliance with GMP, regulatory, and company requirements.

Act as Quality Leader in the approval of investigations and contribute to the definition of investigation strategies.

Act as Escalation Lead, facilitating the escalation process in accordance with company procedures.

Serve as a tutor for new hires in investigation training, supporting them through proper planning until full autonomy is achieved; coordinate the team during support activities to operational departments on the shop floor.

Act as backup in the Quality Oversight process for Production and Quality Control departments, contributing to strengthening the site's compliance status: execution of controls defined in the annual plan, coordination of periodic meetings with management to evaluate results, trends, and improvement opportunities.

Ensure a constant presence in operational areas, providing support in training personnel on new regulations and ensuring that all procedures and work instructions are aligned with the applicable quality system.

Act as Quality point of reference for projects related to LCM products, serving as the first point of contact for the technical department and interfacing with all involved global functions.

May act as backup in the management of NPI projects.

Qualifications / Requirements:

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.

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.

Here's what you can expect:

Application review: We'll carefully review your CV to see how your skills and experience align with the role.

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