Description
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 EngineeringJob Sub Function:
Process EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Beerse, Antwerp, Belgium, Latina, ItalyJob Description:
The Fellow, MSAT Synthetics Nitrosamines and Impurity Management is a scientific authority ensuring a robust strategy on Impurities potentially present in synthetic drug products, with a primary focus on the Nitrosamine Risk Assessment Strategy across the commercial synthetic portfolio.
The role provides technical and scientific continuity from late development through commercial manufacturing and across the commercial product lifecycle, ensuring that scientific intent, process architecture and regulatory commitments translate into resilient and supply‑reliable commercial execution and impurity control strategy.
Operating as an individual contributor, the Fellow influences through technical depth, platform and systems thinking, and mentorship.
Key Responsibilities:
1. Technical leadership
- Provide expert leadership in Impurity Management across the Synthetics portfolio.
- Drives risk assessments and regulatory controls for Impurities across Drug Substance and Drug Product. Deep knowledge of ICH Guidelines on Impurity Management.
- Initially focuses on Nitrosamines, later expert leadership on Impurities such as PFAS as well as Extractables & Leachables management across the commercial synthetic portfolio.
- Interacts with manufacturing and synthesis chemists as well as with formulation scientists and packaging engineers to optimize reaction parameters and/or adjust pharmaceutical compositions/packaging in view of Impurity Management.
- Interacts with analytical and safety experts in relation to control strategy development
- Serve as the global subject matter expert on degradation pathways, extractables/leachables, and impurity profiling
- Strengthen JJIM’s Impurity Management via intellectual property and scientific communications.
2. Portfolio & Stakeholder management
- Serve as trusted Synthetics DP technology advisor on MSAT Synthetics Technical Review Committee (TRC), partner closely with management and SME’s across Synthetics Development (pharmaceutical, chemical and analytical development), Toxicology, MSAT SM DS and DP, Global Engineering, Quality, Regulatory Affairs, Value Chain Management, and Supply Chain.
- Strongly link to Manufacturing Sites and Cleaning CoP/Fellow on the Impurity Management and Cleaning Validation Strategies (Impurity Carry-over).
- Ensure alignment between product portfolio needs, site capabilities, and value chain expectations.
- Act as a technical representative and innovative leader in relevant industry and regulatory fora.
- Function as mentor to partnering functions
3. Regulatory & CMC Technical Stewardship
- Serve as a senior technical reviewer and contributor for CMC sections related to Impurity Management and control strategies.
- Support inspections, health authority interactions, and lifecycle changes with clear, scientifically grounded justifications.
4. Commercialization and Life Cycle Management
- Serve as technical steward for the Impurity Management across the synthetic commercial product portfolio.
- Provide expert input on manufacturing technologies as well as packaging materials for both DS and DP from an Impurity Management point of view.
- Guide BP²AL-targets, driving towards a robust design together with a validated Impurity control strategy.
Provide technical guidance of post‑launch Impurity Management to enable commercial improvements
Required Skills:
Preferred Skills:
Agile Decision Making, Compliance Management, Consulting, Crisis Management, Design Mindset, Disruptive Innovations, Emerging Technologies, Lean Supply Chain Management, Managing Blended Teams, Operational Excellence, Process Control, Process Engineering, Product Costing, Program Management, Project Schedule, Science, Technology, Engineering, and Math (STEM) Application, Technical Credibility, Technical ResearchThe anticipated pay range for this position, in the primary posting location, is:
The anticipated pay ranges for additional locations are:
Belgium – The anticipated base pay range for this position is 119,200.00 - 237,900.00Benefits:
In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.
*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
