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.

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.

Job Function:

Supply Chain Engineering

Job Sub Function:

Quality Engineering

Job Category:

People Leader

All Job Posting Locations:

Beerse, Antwerp, Belgium, Mumbai, Maharashtra, India, Schaffhausen, Switzerland

Job Description:

We are searching for the best talent for Director, Combination Product & Device, Product Quality Management (PQM) to join our Quality organization located in Beerse, Belgium; Schaffhausen, Switzerland; or Mumbai, India.

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):
 

United States - Requisition Number: R-068312
 

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

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
 

The Director, Combination Products & Device, PQM provides Quality Engineering & Quality Assurance leadership for dynamic portfolio of Drug-Device combination products in J&J Innovative Medicine. The scope spans end-to-end product cycle including new product development pipeline and lifecycle management of marketed combination products with emphasis on Design Control & Combination Product Quality Engineering. The Director, Combination Product & Device, PQM works on problems of diverse scope involving the application of global & regional combination product quality and compliance frameworks including 21 CFR Part 4, FDA QMSR, EU-MDR etc. The individual serves as a subject matter expert on global Combination Product Quality and Compliance aspects, provides quality oversight and guidance, training and consultation or medical device and combination products quality systems and quality requirements. The individual is acutely tuned into the external regulatory landscape, keep abreast of the latest trends and actively interact with and influences internal and external stakeholders.
 

Key Responsibilities

• Provide strategic direction for the Johnson & Johnson Innovative Medicine Combination Product & Device Development initiatives while ensuring design control procedures are harmonized, integrated, understood & executed by key business partners across multiple departments and sites.
• Drive innovative thinking along with a disciplined approach for the rapid, compliant, high-quality development, transfer and lifecycle management of new drug device combination products across multiple sites while ensuring business and regulatory requirements are achieved.
• Take ownership of achieving and maintaining a robust compliance profile for Durg Device Combination Products across the JJIM development and supply chain sites. This includes proactive identification of risks, driving mitigation/remediation activities and supporting inspection readiness activities.
• Provide functional management to a team of Quality Engineers supporting new product development and lifecycle management of drug-device combination products.
• Act as a Combination Product & Device Quality Subject Matter Expert in global Health Authority inspections.
• Oversee the revision of site / functional procedures related to Combination Product Development Process & Design Control and provide training programs in the area of Combination Products.
• Act as a Qualified Trainer for the deployment of these and any other applicable training programs.
• Develop and apply advanced knowledge of advanced quantitative analysis, statistics, DoE etc. 
• Support asset evaluation for licensing and acquisitions activity.
• Carry out duties in compliance with all local, state, and federal and international regulations and guidelines including FDA, EMA, EPA, OSHA, and global health authorities as applicable.
   

Qualifications

• Bachelor’s degree in scientific or technical discipline is required. Master’s or PhD preferred.
• At least 15 years of experience in Pharmaceutical, Combination Product and/or Medical Device industry. Multifunctional background preferred
• Deep understanding of Combination products and associated regulatory and quality requirements
• Understanding of business & technical needs and can relate these to scientific concepts
• Experience with Quality Systems, ISO 13485, ISO 14971, EN 62366, cGMP, and ICH Requirements
• Knowledge of Devices, Biotech and/or Pharma Manufacturing required, particularly in Design Controls and Risk Management
• Demonstrated strong stakeholder management skills
• Prior leadership of and participation in projects across functions & sites
• Strong Project Management and Communication Skills
• Strong Decision-making skills:  Makes decisions independently on problems and methods.
• Excellent technical writing skills; experienced in SOPs, protocols, reports.
• Conflict Management and facilitation skills required.
• Fluent in English
• Ability to write routine technical & quality documents and correspondence or procedures using original, prescribed, or innovative techniques or styles.
• Ability to speak, present and/or respond before groups of customers, employees, Regulatory agencies, clients, and to address common inquiries.

#LI-Hybrid

 

 

Required Skills:

 

 

Preferred Skills:

Business Planning, Coaching, Controls Compliance, Developing Others, Fact-Based Decision Making, Give Feedback, Inclusive Leadership, Industry Analysis, ISO 9001, Leadership, Lean Supply Chain Management, Non-Conformance Reporting (NCR), Process Improvements, Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application