
Caring for the world, one person at a time.
Material Science Engineer
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:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Gent, East Flanders, Belgium
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 htps://www.jnj.com/innovative-medicine
We are seeking a proactive and hands-on Material Science Engineer to join our Manufacturing Science & Technology (MSAT) organization in Ghent. In this role, you will be responsible for New Material Introduction, defining and maintaining the Material Control Strategy, and driving continuous process improvements across both clinical and commercial CAR-T manufacturing.
The ideal candidate combines strong material science expertise with structured project management skills and thrives in a GMP-regulated environment. You will act as key interface between Operations, Quality, Procurement and external suppliers to ensure material robustness, compliance and process reliability.
Key Responsibilities:
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Leads the introduction of new materials in alignment with business and regulatory requirements.
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Define and implement material qualification strategies for use in GMP manufacturing processes.
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Develop and optimize material-related control strategies to ensure process robustness and product quality.
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Author, review and approve material characterization protocols, reports and risk assessments in preparation for material qualification and process validation.
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Support material release laboratories with technical expertise and lead in-depth supplier investigations in case of non-conformances.
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Contribute to quality systems by supporting Deviations, Investigations, Change Controls, CAPAs, Root Cause Analyses and FMEAs.
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Establish and improve procedures (SOPs, Working Instructions) to enhance operational performance and compliance.
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Implements or proposes alterations, modifications or replacements of existing supplies to improve process reliability and reduce overall equipment lifecycle costs and process downtime.
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Provide structured and timely project updates to stakeholders and senior leadership.
Qualifications:
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Master’s degree in Biotechnology, Chemistry, Engineering, Life Sciences, or a related scientific discipline.
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Minimum 3 years of experience in the pharmaceutical or biopharmaceutical industry.
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Experience in GMP-regulated clinical and/or commercial manufacturing environments.
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Good understanding of material science, process equipment, manufacturing processing and computerized systems within a pharmaceutical manufacturing environment
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Strong knowledge of change control processes
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Strong communication skills with the ability to engage effectively across all organizational levels.
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Strong organizational and prioritization skills in a fast-paced and evolving environment.
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
Here’s what you can expect:
- Application review:
We’ll carefully review your CV to see how your skills and experience align with the role.
- Getting to know you:
If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
- Staying informed:
We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
- Final steps:
For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.
Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA
Required Skills: Preferred Skills:
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Johnson & Johnson 소개

Johnson & Johnson
PublicJohnson & Johnson (J&J) is an American multinational pharmaceutical, biotechnology, and medical technologies corporation headquartered in New Brunswick, New Jersey, and publicly traded on the New York Stock Exchange.
10,001+
직원 수
New Brunswick
본사 위치
$400B
기업 가치
리뷰
2개 리뷰
3.3
2개 리뷰
워라밸
4.0
보상
2.5
문화
2.5
커리어
2.0
경영진
2.0
65%
지인 추천률
장점
Good work-life balance
Strong R&D environment
Potential for fulfilling work
단점
Significant pay cuts
Employees feel unimportant
Unclear role expectations
연봉 정보
2,250개 데이터
Junior/L3
Senior/L5
Junior/L3 · Analyst
177개 리포트
$93,472
총 연봉
기본급
$85,723
주식
-
보너스
$7,749
$59,968
$146,648
면접 후기
후기 6개
난이도
3.0
/ 5
소요 기간
14-28주
면접 과정
1
Application Review
2
HR Screen
3
Personality/Assessment Test
4
Virtual/Video Interview
5
Hiring Manager Interview
6
Offer
자주 나오는 질문
Behavioral/STAR
Technical Knowledge
Culture Fit
Past Experience
최근 소식
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1w ago
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·
1w ago
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·
1w ago




