SENIOR PRINCIPAL MANUFACTURING SCIENTIST - MSAT MATERIALS
Descrizione dell'offerta di lavoro
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.
nj.
om/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
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 Material Sciences team! Within the J&J Innovative Medicine Manufacturing Sciences and Technology (MSAT) Large Molecule Drug Substance team, the new Material Sciences team is expanding in order to strengthen connectivity to and experience within raw materials used in our broad biotherapeutics portfolio.
The Senior Principal Scientist will be responsible for raw materials and process contact materials control strategies in connection with product quality, value and ensure regulatory compliance.
Key Responsibilities.
Owner of Lifecycle Management (LCM) raw material control strategy 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 8 years of relevant work experience Experience in operationalizing CMC technical requirements in the manufacturing environment Understanding of raw material functionality and stability in the biotherapeutics manufacturing process Experience leading or managing projects and/or business process improvements 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.
Good knowledge of pharmaceutical quality requirements, FDA and EMA regulations related to raw materials 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 Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.
areers.
nj.
om.
#LI-MV2 #LI-Hybrid
Dettagli dell'offerta
- Imprecisato
- Tutta l'Italia
- Imprecisato - Imprecisato
- 12/10/2024
- 10/01/2025
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