Manufacturing Science & Technology experts at Novartis

Târgu Mureș, , Romania -

Full Time

Start Date

Immediate

Expiry Date

07 Mar, 26

Salary

0.0

Posted On

07 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacy, Pharmaceutical Technology, Chemistry, Manufacturing Science, Technical Development, Quality, Process Validation, Statistical Data Analysis, Tech Transfer, Project Management, GMP, Risk Management, Documentation, Compliance, Cross-Functional Collaboration, Continuous Improvement

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary #LI-Onsite Location: Târgu Mureş, Romania This role is based in Târgu Mureş, Romania. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. Join Novartis and help ensure robust, compliant, and continuously improving manufacturing processes across the product lifecycle. As we actively map and assess the labour market, we are looking for Manufacturing Science & Technology Experts, that will own process knowledge, lead technology transfers and product launches, and drive validation strategies to keep our therapies safe, reliable, and inspection-ready. Job Description Key Responsibilities Maintain end-to-end process knowledge and lifecycle oversight for assigned products. Lead tech transfers and launch readiness activities, ensuring seamless scale-up and compliance. Develop and execute validation strategies (process, cleaning, packaging) aligned with cGMP and regulatory standards. Provide technical support, risk mitigation, and cross-functional collaboration to ensure business continuity and quality. Essential Requirements: BSc in Pharmacy, Pharmaceutical Technology, Chemistry, or an equivalent scientific degree; MSc desirable or equivalent experience. Fluent in English (oral and written). 2–3 years of experience in manufacturing, manufacturing science and technology (MS&T), technical development, or quality—ideally within GMP/GxP-regulated environments. Experience in GMP-regulated pharmaceutical manufacturing and MS&T. Strong skills in process validation, CPV, and statistical data analysis. Proven leadership in tech transfer and cross-functional project management. Excellent documentation and compliance mindset. Commitment to Diversity and Inclusion / EEO paragraph: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Skills Desired Assembly Language, Change Control, Chemical Engineering, Chemistry, Continual Improvement Process, Cost Reduction, Data Analytics, Electronic Components, General Hse Knowledge , Including Gdp, Knowledge Of Capa, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Pharmaceutics, Process and Cleaning Validation, Process Control, Process Engineering, Risk Management, Root Cause Analysis (RCA), Scheduler, Six Sigma, Sop (Standard Operating Procedure) Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

The Manufacturing Science & Technology Experts will maintain end-to-end process knowledge and lifecycle oversight for assigned products, lead technology transfers, and ensure compliance during product launches. They will also develop and execute validation strategies aligned with regulatory standards.