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At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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
Supply Chain Engineering
Job Sub Function
Process Engineering
Job Category
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America, Ringaskiddy, Cork, Ireland
Job Description
About Innovative Medicine
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/innovative-medicine
We are searching for the best talent for a Director, MSAT Validation & Digital that can be in either Raritan, NJ or Cork, Ireland.
An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
Please 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):
USA - Requisition Number: R-020408
Ireland – Requisition Number: R-020846
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Purpose
We are seeking a dynamic and innovative Director, MSAT Validation & Digital to spearhead the development and implementation of advanced strategies for validation, automated processing, and digital data capabilities. The successful candidate will focus on advancing and automating critical compliance functions across Advanced Therapies Supply Chain. This role demands a forward-thinking professional with expertise in validation processes and digital transformation who can drive strategic initiatives that elevate compliance and operational efficiency.
Key Responsibilities
Strategic Development:
* Lead the design and implementation of advanced validation strategies and frameworks to ensure compliance with regulatory standards.
* Identify opportunities for process automation and digital solutions that enhance validation and compliance functions.
Automation & Digital Integration
* Develop and deploy automated processing tools to streamline validation workflows, ensuring accuracy and efficiency.
* Collaborate with IT and data management teams to integrate digital capabilities into existing compliance frameworks.
Data Management
* Establish protocols for data integrity, quality assurance, and validation to support compliance objectives.
* Utilize advanced analytics and data visualization techniques to monitor validation processes and compliance metrics.
Core Competency Development
* Enhance organizational capabilities in validation and compliance through training, support, and resource development.
* Mentor and develop a team of validation and compliance professionals, fostering a culture of continuous improvement.
Stakeholder Collaboration
* Work closely with cross-functional teams, including Quality Assurance, Regulatory Affairs, and IT, to align validation activities with overall business goals.
* Communicate effectively with stakeholders at all levels to convey validation strategies, progress, and outcomes.
Regulatory Compliance
* Stay abreast of industry regulations and standards, ensuring all validation processes align with current requirements.
* Lead inspections and audits related to validation processes to ensure compliance readiness.
Qualifications
Required:
* Bachelor’s degree in Science, Engineering, Computer Science, or a related field; Master's degree preferred, with 10-12 years of experience.
* Proven experience in validation processes, automation, and digital transformation, preferably within a regulated industry.
* Strong understanding of compliance requirements and regulatory frameworks.
* Proficiency in data analytics tools and automated validation software.
* Excellent project management skills, with the ability to lead and prioritize multiple initiatives.
* Strong analytical and problem-solving skills with attention to detail.
* Exceptional communication and interpersonal skills.
Preferred Skills
* Familiarity with industry standards such as GMP, GDP, and ISO.
* Experience with programming languages and database management.
* Knowledge of machine learning and advanced data processing techniques.
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 and 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, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
Seniority level
* Seniority level
Not Applicable
Employment type
* Employment type
Full-time
Job function
* Job function
Marketing and Sales
* Industries
Pharmaceutical Manufacturing
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