Python Job: Data Specialist

JOB DESCRIPTION

Role: Quality Data Specialist

Location: Barnahely, Cork

Contract: Full Time/Permanent

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences

That is why we in Ireland are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”!

Job Summary

We are Currently recruiting for a Quality Data Specialist in our Ringaskiddy site.

The responsibilities & the impact YOU will have:

• Support GMP activities and provide oversight for processes relating to batch manufacture and release within the manufacturing facility.
• Provide GMP oversight and support to Automation processes, dashboards and solutions to assess compliance to Global and regulatory requirements.
• Accountable for Quality oversight of processes and procedures related to Data integrity, Computerised Systems & Automation compliance.
• Partner with Automation CSV, Engineering and Quality Control to ensure site procedures for computerized systems, data integrity and automation activities are in compliance with current standards.
• Provide Quality and cGMP input and oversight for all Data Management and Data Integrity activities.
• Provide support for the business using tools to ensure completed in a compliant manner.
• Lead the compliance activities to sustain and improve complex workflows and Tableau visualisations.
• Interrogate data analysis results and write technical summaries to support product quality and safety related discussions.
• Communicate with customers to develop an understanding of GMP standards as they apply to data analytics and ensure compliance and validation activities are included in project timelines.

We would love to hear from YOU, if you have the following essential requirements:

• Third level degree in Engineering, Science, or an IT discipline.
• Minimum of three years’ experience within a pharmaceutical or GMP regulated manufacturing environment.
• Ability to work individually or collaborate with cross-functional teams, as required.
• Familiarity with SIMCA, Tableau, Python, R studio desirable.

This is what awaits YOU at J&J:

This is an opportunity to work with a ground-breaking biomedicine operation and to be a member of a Johnson & Johnson company, with an excellent record in employee continuous professional development and business improvement.

We are passionate about our work; we play vital roles across a range of professional disciplines and care deeply about our customers and communities. At Johnson & Johnson our culture enables dynamic and impactful careers.

Whether you’re one of the people who already work here, or you’re considering joining the team, we offer:

• An opportunity to be part of a global market leader.
• A dynamic and inspiring working environment.
• Opportunities to work on challenging projects and assignments.
• Possibilities for further personal and professional development/education
• Excellent Benefits