Sr. Scientist Proteins AD

h3Job Function: /h3 pDiscovery Pre-Clinical/Clinical Development /p h3Job Sub Function: /h3 pBiotherapeutics RD /p h3Job Category: /h3 pScientific/Technology /p h3All Job Posting Locations: /h3 pSchaffhausen, Switzerland /p h3Job Description: /h3 h3Job Description: /h3 pThe Container Closure Integrity (CCI) team is a development laboratory within the global Research Development organization and operates in the GMP environment of Johnson Johnson Innovative Medicine Supply Chain (IMSC). As part of Analytical Development, we provide end-to-end support for biologics and advanced therapy products, including antibodies, cell and gene therapies, and antibody-drug conjugates, across therapeutic areas including oncology, immunology, and neuroscience. We work closely with RD and IMSC partners in an international, dynamic, and collaborative environment. /p pTo strengthen our team, we are seeking a Senior Scientist to lead projects for early- and late-phase development programs and commercial products. You will help advance our center of excellence (CoE) for container closure integrity testing (CCIT) of primary containers, sterile barrier integrity testing (SBIT) of devices and residual seal force testing (RSF), expand laboratory capabilities, and deliver robust, compliant analytical strategies and analytical procedures in a GMP-regulated development environment. Following comprehensive on-the-job training, you will coordinate projects, lead method development, validation, and transfer activities, support investigations, contribute to regulatory submissions, and provide analytical support for marketed products. /p h3Your Responsibilities: /h3 ul liAssume a leading role in project coordination, development and validation of CCIT, SBIT and related assays for a variety of container closure systems (CCS) and devices for cell and gene therapy, antibody, and antibody-drug conjugate programs, representing the CCI team across JJ Innovative Medicine. /li liCoordinate method development, validation, and transfer activities in accordance with internal guidance and health authority expectations. /li liProvide timely scientific support for investigations and other high-priority stakeholder requests with short turnaround times. /li liAlign project plans, deliverables, timelines, and risks with internal and external partners. /li liRepresent the CCI team in project meetings as a subject matter expert. /li liAuthor scientifically sound technical documents, including study and validation protocols, reports. /li liCompile, interpret, and communicate analytical data to support project decisions, investigations, and regulatory deliverables. /li liDevelop an end-to-end understanding of business processes and propose improvements that increase quality and efficiency. /li liEvaluate emerging technologies and translate promising approaches into fit-for-purpose laboratory capabilities. /li liContribute to an inclusive, team-oriented environment and collaborate respectfully with partners and colleagues. /li /ul h3Qualifications /h3 pWe are looking for a scientifically minded, flexible, and collaborative professional with the following qualifications: /p ul liIndependent, accountable, and entrepreneurial working style. /li liScientific curiosity and the ability to investigate complex questions in depth. /li liStrong analytical reasoning, project coordination, communication, and presentation skills. /li liExperience with container closure systems, such as vials, prefilled syringes or cartridges, bags, or devices such as needle-based injection systems and on-body delivery systems are advantageous. /li liExperience in the pharmaceutical industry or another GMP-regulated environment, with knowledge of GMP requirements for analytical laboratories, is preferred. /li liExcellent written and spoken English; German language skills are desirable. /li liMaster’s degree with at least five years of relevant experience, or PhD with at least two years of relevant experience, in life sciences, materials science, analytical development, pharmaceutical development, or a related field. /li /ul pWe offer a varied and impactful role in a dynamic, international environment, with strong infrastructure and opportunities for professional growth. /p h3Required Skills: /h3 h3Preferred Skills: /h3 pAnalytical Development, Coaching, Critical Thinking, GMP Compliance, Project Coordination, Regulatory Documentation, Scientific Writing, Head Space Analysis, Helium Leak Detection, CCIT at Frozen conditions, Residual Seal Force Testing, Stakeholder Communication, CMC, Investigation, Emerging Technologies, Process Improvement, Quality Assurance, Relationship Building, Technologically Savvy /p h3Job Function: /h3 pDiscovery Pre-Clinical/Clinical Development /p h3Job Sub Function: /h3 pDPDS, TDS Proteins AD /p h3Job Category: /h3 pScientific/Technology /p h3Primary Job Posting Location: /h3 pSchaffhausen, Switzerland /p h3Additional Job Posting Locations: /h3 h3Legal Entity Name: /h3 p8562-Cilag AG Legal Entity /p h3Pay Grade: /h3 p26 /p h3Required Skills: /h3 h3Preferred Skills: /h3 pAnalytical 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 /p #J-18808-Ljbffr