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Sr Scientist Biotherapeutics RD, Schaffhausen

Sr Scientist Biotherapeutics RD, Schaffhausen
Anzeigentext
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 Discovery&Pre-Clinical/Clinical Development

Job Sub Function Biotherapeutics R&D

Job Category Scientific/Technology

All Job Posting Locations Schaffhausen, Switzerland

Job Description The Device Methods Laboratory (DML) is a unique group within Johnson and Johnson Innovative Medicine responsible for the end-to-end development and testing of combination products, drug delivery systems and primary containers. Our wide range of responsibilities spans across early and late stages of clinical development including the support of technology transfers as well as cover product life cycle management such as the handling and resolution of global product quality device complaints. As a development lab that is embedded in the GMP environment within the global Research&Development organization we strive for innovative solutions in drug delivery and shape new visions for the development of medicines of tomorrow.

Your Responsibilities

Design experimental plans and serve as the analytical development expert on combination product testing, test method development and validation

Assume a leading role to advance the data insight-driven characterization of patient-focused parenteral drug delivery systems

Translate industry and international regulatory standards into the operational business to support the development and Life Cycle Management of combination products

Lead and execute device investigations and the handling of customer complaints and provide hands‑on expertise during troubleshooting

Ensure best scientific and GMP standards

Establish and cultivate strong relationships and independently liaise with cross‑functional teams, external partners and stakeholders

Support the preparation and review of technical reports and global regulatory submissions

Evaluate new and innovative technologies, methodologies and modalities to support science-based advancements

Your Profile For this position we are looking for a scientifically minded, flexible, and team-oriented person with the following skills:

Self‑employed and entrepreneurial working style

Curiosity and drive to deep dive into scientific questions

Excellence in analytical and problem‑solving skills, with attention to detail

Ability to make strategic recommendations

Strong project coordination and management skills

Committed to perform and thrive in a highly dynamic, fast‑paced environment

Motivated by achieving extraordinary goals creating cutting‑edge products for our patients

Team player with excellent communication skills at all levels

Strong knowledge of GMP

Fluent in English (oral and writing), German desired

PhD in Analytical Chemistry, Biochemistry, or related scientific discipline with minimum 2 years of experience in the pharmaceutical or biotech industry

Preferred Skills

Analytical Reasoning

Biochemistry

Chemistry

Manufacturing, and Control (CMC)

Coaching

Consulting

Critical Thinking

Drug Discovery Development

Emerging Technologies

Molecular Diagnostics

Pharmacogenetics

Pharmacovigilance

Process Improvements

Quality Assurance (QA)

Relationship Building

Research Documents

Scientific Research

Technologically Savvy

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