Scientist Pharma Prod RD

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

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Job Description:

Join us as a Allround LIMS analyst and be at the forefront of the redesign of elims processes ranging from end user training, sample management, set up of products specifications and stability protocols in LIMS with the goal to contributing to a strong end to end quality control of clinical pharmaceutical products. We offer an opportunity to learn and shape all the different processes that run on elims, starting from the delivered documents, the samples that are documented up until the final testing certificates and reports.

We invite you to be a part in redefining the future of Synthetic Molecule Analytical Development in by joining the new vibrant Technology and Transformation Alliances (TNT) team where you be surrounded by passionate scientist and your contributions can truly make a difference!

Primary responsibilities:

• Interpretation of analytical product specifications and stability protocols.
• User training and support for LIMS related to sample management, data entry and data review of internal and external labs.
• Review and improve quality procedures related to system use and master data set up, author new procedures if requires
• Setup of static master data in LIMS of pharmaceutical materials for clinical release and stability (API, intermediates, drug product, …)

Qualifications

Education:

• Bachelor degree in analytical sciences or a related relevant field with a minimum of 3 years of professional experience required

Required:

• Relevant experience in Labvantage ELIMS
• An analytical quality mindset with the ability to handle multiple issues and requests with a can-do attitude
• Relevant knowledge of specifications and stability protocols as key documents driving LIMS activities
• Demonstrated ability to operate successfully in a GMP lab environment
• Ability to work and collaborate effectively in hybrid workplace, both virtually as globally.

Preferred:

• Relevant experience in sample management, master data and/or user management in LIMS
• Experience working in healthcare or another regulated industry
• Proficiency and affinity to other lab systems is a plus: Empower, ELN, …
• A record of effective collaboration with diverse personalities and backgrounds