Lenti Investigations, Senior Supervisor

Overview

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 [_jnj.com_](https://www.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.

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/innov](https://www.jnj.com/innovative-medicine)ative-medicine.
We are searching for the best talent, **.** ​ Lentiviral Vector Senior Supervisor, This position is based in Raritan New Jersey..

Job Function:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Assembly

Job Category:

People Leader

Key Responsibilities:

• Carry out supervisory responsibilities in accordance with the organization’s policies and applicable laws.
• Carry out supervisory responsibilities in accordance with the organization’s policies and applicable laws.
• Interviewing, hiring, training employees, appraising performance, rewarding and disciplining employees, addressing complaints and resolving conflict.
• Manage quality system metrics for deviations. Evaluate, track, and trend deviations.
• Accountable for reporting of deviation metrics at site and cross-site levels. Support internal and external audits.
• Guides daily work activities of 10-15 direct reports within the investigations organization under LV operations.
• Work with Process Development team, Quality and Operations organization to successfully transfer process to cGMP facility to manufacture products.
• Review/approve documents as an investigations department subject matter expert (SME). Support investigation of nonconformances, CAPAs and change controls.
• Set priorities and manage work assignments.
• Maintain individual and investigation team training completion in a compliant state.
• Communicate both within team and across departments.
• Foster a culture of compliance and strong environmental, health, and safety performance. Promote a mindset of continuous improvement, problem solving, and prevention.

Key Proficiencies/Skills/Requirements:

• Strong knowledge of Lentiviral vector/ cell/gene therapy processing.
• Experience with ICH Q7 and/or 21 CFR parts 210, 211, 600, 601, and 610.
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint).
• Detailed knowledge and understanding of current Good Manufacturing Practices (cGMP) related to Lenti operations and ability to identify/remediate gaps in processes or systems is required.
• Detailed knowledge of compendial (USP, EP, JP, etc.) requirements and standards for manufacturing.
• Ability to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process.
• Ability to accommodate unplanned overtime (including nights and weekends).

Education: Experience:

ABachelor’sdegreewith 4 years of deviation investigations experience and aminimumoftwo (2)yearsrelatedsupervisoryexperience is required. A master’s degree is preferred.