Johnson & Johnson
Job title:
Principal Engineer MSAT Materials
Company:
Johnson & Johnson
Job 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 https://www.jnj.comJob Function:
Supply Chain EngineeringJob Sub Function:
Process EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Leiden, South Holland, NetherlandsJob Description:Johnson & Johnson is hiring for a Principal Engineer – MSAT Material Sciences! This position is located in Leiden, Netherlands.Are you interested in joining a team that is positively impacting patients’ lives by ensuring efficient and effective manufacturing of our biopharmaceutical products? Apply now for this exciting chance to build and lead our MSAT Materials team!Within the J&J Innovative Medicine Manufacturing Sciences and Technology (MSAT) Biotherapeutics Drug Substance team, the MSAT Material Principal Engineer will be responsible for the lifecycle management and scientific understanding of raw materials used in the manufacturing of biotherapeutic drug substances and drug products.Key Responsibilities:
- Lifecycle Management (LCM) raw material control strategies including supplier/material reliability, specification management, and critical material attribute monitoring
- Partner with MSAT drug substance and drug product operational teams for raw material-related manufacturing investigations and risk assessments
- Lead multidisciplinary product sub-team teams for raw material readiness in support of new product introduction, technical transfer, and commercial manufacturing operations
- Interpret and implement industry and regulatory guidance for raw materials, ensuring compliance with GMP, quality, and scientific principles
- Author, review, and approve raw material sections of regulatory documents for global filing updates of Janssen biotherapeutics drugs
- Leverage networking and influencing skills to ensure good collaboration with partners in MSAT, Therapeutic Development & Supply (TDS), Value Chain Management (VCM), Quality, and Regulatory
Qualifications:Education:
- Minimum of a Bachelor’s or equivalent University degree required; Master’s or focused degree preferred in Chemistry, Biology, Materials Science, Engineering, Pharmacy/Pharmaceutics, or related field
Experience and Skills:Required:
- Minimum 6 years of relevant work experience
- Knowledgeable of material structure/function in biopharmaceutical manufacturing and formulations
- Leading projects and collaborations with global teams for technology transfers and other supply-chain projects
- Excellent written and oral communication skills and ability to influence peers, superiors, and partners, while collaborating within a cross-functional team
- Excellent interpersonal skills with the ability to adapt effectively to manage a growing portfolio
- Motivated, self-starter able to work independently with demonstrated problem solving skills
Preferred:
- Competency and experience in quality investigations and deviations, material change risk assessments, regulatory questions and submissions
- Experience, training, or certification in Lean, Six Sigma, or Process Excellence tools & methodologies
Other:
- May require up to 10% domestic and international travel, depending on business needs and work location
Expected salary
Location
Leiden, Zuid-Holland
Job date
Thu, 17 Apr 2025 22:35:50 GMT
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