Title: Scientist, Research & Development Hybrid locations North America, United States, New Jersey, Summit time type Full time Job Description: Kenvue is currently recruiting for a: Scientist, Research & Development What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role reports to: Manager Face Treatments R and D Location: North America, United States, New Jersey, Summit Work Location: Hybrid What you will do Kenvue is recruiting for a Scientist Skin Health & Beauty R&D, located in Summit, NJ The Scientist will support the product development of regional and global projects for the facial treatments category. They will work closely with their manager and team to understand how to build and improve our facial treatment pipeline initiatives. They will also partner closely with cross-functional partners to help assess risk and proactively solve obstacles to ensure successful new product launches. Responsibilities include formulation prototype development and batching for stability and aesthetic evaluation, attending project update meetings, maintaining organized documentation, drafting technical reports, and ensuring compliance with quality and regulatory standards. Excellent communication skills together with the ability to manage complexity are must-have prerequisites. Key Responsibilities He/she will develop facial treatment formulations and execute deliverables for regional and global projects while collaborating with cross functional partners to ensure all timeline deliverables are met. Responsibilities of the Scientist: - Formulate new products that incorporate consumer insights and align with the facial treatments brand strategy and pipeline with supervisor oversight. - Conduct Design of Experiments and formulation tasks inclusive of batching and stability. - Provide technical support for product lifecycle management, including post-commercialization support and troubleshooting technical issues. - Proactively identify project obstacles and technical risks, evaluating potential solutions to minimize impact through data-driven decision-making. - Define critical process parameters and collaborate with technical operation partners and manufacturing sites to establish process controls. - Collaborate with cross-functional project team to ensure all project deliverables are met on-time. - Prioritize tasks across projects to meet deliverables and update stakeholders of risks and product launch progress. - Maintain accurate and organized records of project documents, data, and materials. - Draft and complete technical documents, including development summary reports, specifications, and patent filings. - Adhere to established standards and processes (e.g., GDP, GLP) to ensure compliance with quality, safety, and regulatory requirements. Qualifications Required: - A minimum of a bachelor’s degree with a minimum of 2 years of experience OR a master’s degree with 0-1 years of experience is required. A degree in Chemistry, Chemical Engineering, Industrial Pharmacy, Material Science or other science or engineering discipline is preferred. - Ability to work cross-functionally in a team environment while being an individual contributor is required. - Technical writing skills that facilitate the creation of documents that are complete & accurate are required. - MS Office (Word and Excel) proficiency, excellent oral and written communication skills are required. - Effective presentations skills that are used to communicate clearly & informatively are required.​​​​​​​ Preferred: - Experience with consumer products, such as skin care, emulsions, cleansers, hair care, oral care, baby care and/or deodorant products - Good technical foundation of formulated products including emulsions, surfactants, suspensions, structured liquids and an understanding of material chemistry - Experience collaborating with external partners, manufacturing vendors, and suppliers. - Familiarity with cGMP and other regulatory requirements is helpful.​​​​​​​ Other: Must be proficient in the English language. This position is based Summit, NJ, and will require up to 10% travel both domestic and international Travel. What’s in it for you Annual base salary for new hires in this position ranges: $82.025,00 - $115.800,00 This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors. - Competitive Benefit Package* - Paid Company Holidays, Paid Vacation, Volunteer Time & More! - Learning & Development Opportunities - Kenvuer Impact Networks - This list could vary based on location/region *Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit 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. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Title: Field Applications Scientist Location: Philadelphia, PA Job Description: Full-time Description The Field Applications Scientist (FAS) provides technical and troubleshooting support to customers of MaxCyte’s Scalable Transfection Systems, with primary focus on cell therapy and protein production/expression but will work with customers in multiple application areas. The FAS partners with customers to identify and implement solutions for process improvements throughout the transfection workflow, including pre- and post-electroporation. Working closely with potential and current customers, the FAS is responsible for conducting product demonstrations, end-user training and troubleshooting, both during the evaluation phase and post-sale. This position participates in trade shows and contributes to the publication of scientific and marketing documentation related to the use and applications of MaxCyte’s technology. The FAS will partner with customers from feasibility through scale-up—optimizing pre- and post-electroporation workflows, troubleshooting in real time, and translating complex data into clear recommendations. You will also play a key role in pre-sales, helping identify high-potential projects and educating customers on off-target risk assessments for cell & gene therapy, highlighting our SeQure Services portfolio. Territory: Southeast Region Preferred Locations: Philadelphia, Washington D.C area, Raleigh/Durham area. Customer Engagement & Pre-Sales - Partner with the Regional BDM to support existing customers and introduce MaxCyte technology and SeQure Services to new accounts. - Conduct onsite/virtual product demonstrations and end-user training during evaluations and post-sale. - Collaborate with Sales to prospect and qualify opportunities, assess technical fit, and craft evaluation plans (success criteria, milestones, data-review cadence). Applications & Troubleshooting - Integrate MaxCyte technology and SeQure Services into customer workflows; diagnose issues and recommend solutions. - Analyze customer data and recommend next steps; guide scale-up and tech transfer to manufacturing-relevant workflows. - Optimize pre- and post-transfection/electroporation steps to improve viability, editing efficiency, and reproducibility. - Provide scientific consultation on cell models (e.g., primary/T cells), payloads (RNP, mRNA, plasmid), delivery parameters, and post-edit workflows. - Develop SOPs, quick-start guides, and best-practice resources. Technical Operations - Perform installations, customer training, instrument calibrations, and preventive maintenance, and IQ/OQ at customer sites. Coordinate/execute software and firmware updates and upgrades. Communication & Enablement - Present technical and product content at conferences, seminars/webinars, and customer visits. - Contribute to application notes, posters, and scientific/marketing materials. - Share technical updates internally and contribute to team/department meetings. Collaboration & Continuous Improvement - Work cross-functionally with the global FAS team, Product Management, R&D, Service, Sales, and Quality to ensure customer success. - Recommend and help implement process improvements; identify new applications for MaxCyte technology. Voice of Customer & Market Intelligence - Capture field insights, competitive activity, and emerging use cases (e.g., CRISPR off-target assessment, AAV/LNP workflows) and relay them to Product/R&D. - Conduct literature reviews and identify key opinion leaders in major application areas. Documentation & Follow-Through - Record interactions, experimental designs, results, and outcomes in CRM; ensure timely follow-up and resolution to maintain high customer satisfaction Requirements - MS or PhD in bioengineering, cell biology, molecular biology, biochemistry or related field. - Recent hands-on experience in mammalian cell culture essential (primary cells/T cells preferred). - 3+ years in one or more: genome editing (e.g., CRISPR/Cas9), cell therapy development, immunology, protein/viral expression, or process development. Experience in large scale cell culture and/or high throughput cell-based screening would be beneficial. - Practical knowledge of on-/off-target assessment workflows and analytics is a strong plus. - Demonstrated troubleshooting ability and experimental design/data interpretation skills. - Customer-facing experience (FAS, applications, technical support, or similar) preferred. Robust trouble shooting skills. - Confident communicator—able to present to scientific and executive audiences; strong writing and documentation discipline. - Core competencies: Scientific rigor with a solution-oriented, hands-on mindset. Clear, audience-appropriate communication and teaching. Cross-functional collaboration (Sales, Product, Service, Marketing). Organization, ownership, and reliable follow-through. - Comfortable with CRM (e.g., SFDC), standard data analysis tools, and documentation best practices. - ·Entrepreneurial mindset: Proven ability to thrive in an entrepreneurial, high-growth environment, demonstrating strategic thinking, problem-solving, and self-motivation. - Customer-centric leadership: Builds and maintains strong customer relationships, demonstrating passion for the company’s mission and solutions. - Ability to travel ~ 50-70% within territory, occasional conferences/customer visits outside territory. - Work Setup: Field-based with regular onsite customer engagements; close alignment with Sales and the global FAS team. MaxCyte offers a base salary, annual bonus, and equity. MaxCyte also offers a comprehensive benefits package including health, dental, vision, life, and disability insurance and generous time off, MaxCyte is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status

Role Description Forming part of the Biotechnology segment at Danaher, the Manufacturing Science and Technology (MSAT) Scientist II for Cytiva is responsible for providing technical pre and post-sale support for the integration of Cytiva filtration technologies into customer processes in collaboration with the commercial team and R&D. This position is part of the EU Filtration Customer Success (FCS) team and will be fully remote. In this role, you will have the opportunity to: - Application of Cytiva Bioprocess filtration products (normal and tangential flow filtration) to create process solutions. - Conduct feasibility assessments, technical consultations, training and bench trials at customers. - Maintain close customer contact during projects, involving travel to customer sites for technical meetings or to perform test work. - Give technical presentations and update customers on project status. - Provide technical consultation involving scale up/scale down testing plans and data review, sizing and compatibility recommendations, troubleshooting customer technical issues, and field investigations. - Maintain an up-to-date knowledge of current regulatory trends, issues, and guidelines relating to the products being supported. Qualifications - Bachelor’s Degree in a relevant field; Master’s Degree in life science, Chemical or Biological Engineering preferred. - 3+ years of experience in the Biopharmaceutical industry, preferably in MSAT or PD role. - Technical support experience. - Fluent English and good communication skills. - Advanced proficiency in German is considered an advantage. Requirements - Valid driving licence. - You are willing and able to travel up to 50%, primarily within Europe. - Ability to travel weekly for customer support located mainly in central, north, and east Europe. Benefits - Annual salary starting from EUR 60,000 gross per annum, depending on qualifications and experience. - Eligible for a bonus. - Comprehensive and competitive benefit programs, including voluntary pension contributions. - Flexible working time and remote working arrangements.

• Maintain the project website and portals to ensure accuracy and timeliness of information. • Upload final and draft protocols, accrual reports, announcements, communications, other documents, and videos to the project website. • Monitor the ACTG User Support Help Desk. • Provide peer review and word processing support to project staff. • Monitor project communications mailbox and distribute messages. • Schedule and send meeting invitations for community calls and in-person meetings. • Collaborate with the Community Coordinator on surveys and polls. • Attend and support community meetings as needed. • Monitor the ACTG Community Support mailbox and assist with responses and resolutions. • Draft and distribute community communications. • Oversee preparation of the quarterly community newsletter.