Director, PV Quality Management

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.comAs 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: QualityJob Sub Function: Business Process QualityJob Category:People LeaderAll Job Posting Locations:Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of AmericaJob Description:Johnson & Johnson is recruiting for a Director, PV Quality Management located in Titusville, NJ, Raritan, NJ, Beerse, Belgium, High Wycombe, UK, Maidenhead, UK, Allschwil, Switzerland or Schaffhausen, Switzerland.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 note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):Belgium - Requisition Number: R-075920UK - Requisition Number: R-075915Switzerland - Requisition Number: 075918Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.Innovative Medicine Quality Systems (IMQS) is responsible for the Innovative Medicine Quality Management Systems (QMS) and GxP Process Ownership, and is the Global Process Owner for Quality Management Processes. IMQS ensures foundational governance through quality performance management, and alignment with regulatory requirements and emerging industry expectations. The IMQS-Process and Data Management (PDM) team, part of the IMQS organization, specifically focuses on and partners with the R&D and Pharmacovigilance and intensively collaborates with key partners including R&D Quality, Johnson & Johnson Enterprise Innovation (JJEI), the Therapeutic Areas (TA), Global Development (GD), Global Regulatory Affairs (GRA), and the Global Medical Organization (OCMO/GMS) along the development process, from discovery, pre-clinical, clinical, launch to post-approval activities. The IMQS-PDM team is responsible for GxP Quality Management System, GxP Personnel Qualification and Training by providing compliant, easy accessible process content, and for making learning tailored to the moment-of-need and at the point-of-use.As Director, Pharmacovigilance Quality Management, you lead a global team of PV Quality Management experts (PVQM experts) overseeing the end-to-end delivery of process, qualification and training in the IMQS supported QMS framework. You enable dedicated Business Partners to conduct R&D/Medical Safety in an efficient and compliant way, resulting in programs that allow for seamless registration of the J&J innovative products. You set the vision and strategy for process and personnel qualification management in collaboration with senior leaders in R&D functions.You are the single point of contact for senior management with business partners where you are responsible for roll out and training of the overall applicable quality framework. As an owner of the E2E procedural framework you are responsible for overall development of the PVQM strategy and ensuring Quality-by-Design principles are instigated in all PVQM deliverables. You are a member of the IMQS-PDM LT and collaborate with the other PDM Leads, the PDM Head and other positions in R&D to ensure an efficient and compliant QMS is delivered.You play a strategic and operational role in coordinating the work of the PPQM team in a respective business unit. Where applicable, you will work in close collaboration with the business partners managing the delivery of the end-to-end connected business processes, applicable documentation and supportive training to implement quality procedural content and personnel qualification programs supporting the business partner objectives.You manage staff for process/qualification/training design and keep abreast of all PVQM needs, new materials, methods and digital/data science and automation techniques tailored to the business needs. As department head, you develop functional programs for PVQM staff and identify developmental needs including preparing personnel for more responsible positions and increasing effectiveness in present assignments.Tasks/Duties/ResponsibilitiesMap, analyze, develop, and implement compliant and efficient end-to-end processes and related training and qualification as part of the GxP/GPvP Quality Management FrameworkRepresent IMQS-PDM and serve as a champion to key (pre)clinical, OCMO (Office of Chief Medical Officer) and Global/Local Medical Safety, Therapeutic Area and other business partners and stakeholders. Conduit between business partners, quality groups and governance to ensure the GxP/GPvP Quality Framework evolves with the business and regulatory requirements and needs, including changes, CAPA, investigational/inspectional requests.Implementation of the transformation roadmap of PDM towards data-centric content and qualification management, and the internal first-time-right end-to-end process from request to effective process/qualification material.Lead and manage a team of PVQM ExpertsOther responsibilitiesLeadership or support of projects, meetings, etc. as directed by the Head of Process and Data Management. Independence/AutonomyThis leader will act independently and with high impact to drive results and organizational performance. They will seek guidance only as needed on new assignments and understand the sense of urgency related to activities. They will develop and implement strategies related to job description core areas.The leader is expected to lead and be proactive in setting priorities to achieve IMQS goals and objectives.Required Minimum Education: Master’s degree in Science or Business Required Years of Related Experience: A minimum of 12 years’ experience in a medium to large scale matrix organization, including a minimum of 10 years of experience in a pharmaceutical/device compliance-related field and/or equivalent time and experience in a related healthcare R&D area is required. A minimum of 5 years’ experience in the field of Medical Safety/Pharmacovigilance, process design, training design or related field is required.Required Knowledge, Skills and Abilities:The ability to communicate well, both in oral and written form (in English) and using a variety of media, is required.Demonstrated competencies include industriousness, self-awareness, adaptability, attention to detail and a high capacity for teamwork. Is required.The role requires strong knowledge of worldwide (pre)clinical safety compliance regulations and guidelines, along with broad exposure to the array of regulatory and legal requirements within the life science industry.Working conditions require resolution of complex problems within tight timelines.This leader will be responsible for making decisions regarding business issues, strategic support, and organizational development, as required by business urgency and organizational growth. The scope is across R&D Quality, the OCMO (Office of Chief Medical Officer) and Global/Local Medical Safety, and various R&D functions, and requires significant collaboration, alignment and influencing.Leadership experience and skills:Strong personal leadership with demonstrated competency interfacing with senior leadersStrong networking and relationship-building skillsA proven track record of leading and developing people in a matrixed organizational set-upStrong organizational and people change leadership and management skillsAbility to create an open and inviting environmentAbility to embrace generational differencesAbility to operate in a virtual environmentProven business acumenStrong understanding of the digital and data science landscapeExceptional written and verbal communication skillsTechnology experience and skills:Proficiency with MS365 softwareProficiency with Project Management softwarePreferred Knowledge, Skills and Abilities:Technology experience and skills:Proficiency with Process Value Stream mapping and analyzing software (preferred)Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via , internal employees contact AskGS to be directed to your accommodation resource.#LI-HybridRequired Skills:Preferred Skills:The anticipated base pay range for this position is :$150,000.00 - $258,750.00Additional Description for Pay Transparency:Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).This position is eligible to participate in the Company’s long-term incentive program.Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:Vacation –120 hours per calendar yearSick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar yearHoliday pay, including Floating Holidays –13 days per calendar yearWork, Personal and Family Time - up to 40 hours per calendar yearParental Leave – 480 hours within one year of the birth/adoption/foster care of a childBereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar yearCaregiver Leave – 80 hours in a 52-week rolling period10 daysVolunteer Leave – 32 hours per calendar yearMilitary Spouse Time-Off – 80 hours per calendar yearFor additional general information on Company benefits, please go to: - Titusville, New Jersey, United States of America; Raritan, New Jersey, United States of AmericaType: Full time