Senior Specialist Data Integrity / CSV 80-100%

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 https://www.jnj.com

Job Function:
Quality

Job Sub Function:
Quality Control

Job Category:
Professional

All Job Posting Locations:
CH008 Cilag AG, Schaffhausen

Job Description:

Senior Specialist Data Integrity / CSV (80-100%)

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 https://www.jnj.com

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.

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

We are seeking a passionate Senior Specialist, Data Integrity / CSV to champion the lifecycle management of laboratory equipment, enhance data governance practices, and contribute to lab automation.

Join our Site Quality Control team in Schaffhausen and make a difference in patients' lives globally.

Key Responsibilities:



* Laboratory Equipment & Software Qualification:


* Plan and coordinate qualification activities (in line with GMP and regulatory standards)


* Author comprehensive qualification lifecycle documents (e.g., Impact & Risk Assessments, URS, IOPQ protocols)


* Authoring and review of procedures (WIs, SOPs) related to data integrity and equipment lifecycle management


* Perform installation, configuration, testing, and troubleshooting on laboratory systems


* Data Integrity & Governance:


* Define requirements for new software solutions and analyze data/process flows


* Develop and oversee security, backup, and recovery strategies for laboratory systems (e.g., databases)


* Archive or migrate legacy system data


* Investigate data integrity issues and software non-conformities (CAPA)


* Cross-functional Collaboration:


* Act as a bridge between internal teams (Quality Control, R&D, IT) to ensure seamless integration of laboratory systems and data workflows.


* Collaborate effectively with external vendors for technical support, including manufacturer qual...