Technical Sales Leader - Single Use Solutions

The Opportunity: . Applications / Technical Sales Manager Avantor Fluid Handling (AFH) : Single-Use Solutions | Bioprocessing & Sterile Injectable Manufacturing Business: Avantor Fluid Handling (AFH), Single-Use Solutions Role level : Senior technical sales / applications leadership; 15+ years experience Primary focus : Customer solution development, technical positioning, application support, and team leadership Industry coverage: Biopharma, biotech, vaccines, biologicals, CDMOs, and sterile injectable pharmaceutical manufacturing Regulated-market exposure: US FDA, EMA, MHRA, PMDA, and other ICH-regulated markets The Opportunity Avantor Fluid Handling (AFH) offers customized Single-Use Solutions that cater to the unique needs of biopharmaceutical and pharmaceutical manufacturers throughout the process workflow. Our solutions include single-use assemblies, fluid handling systems, and associated hardware designed to support critical manufacturing operations. The role of an Applications / Technical Sales Manager is pivotal in creating impactful solutions for our customers. With deep process knowledge, technical expertise, and commercial acumen, the individual will lead a team of Application Specialists and deliver innovative solutions that address the unique application needs of clients across biopharmaceutical, vaccine, biological, and sterile injectable pharmaceutical manufacturing environments. What We're Looking For Education Bachelor’s or Master’s degree in Life Sciences such as Biology, Molecular Biology, Microbiology, Immunology, Biochemistry, Biotechnology, Biopharmaceutical Engineering, Chemical Engineering, or related disciplines. Experience 15+ years of industry experience in Biopharmaceuticals, Biotechnology, Vaccines, Biologicals, and/or Sterile Pharmaceutical Manufacturing. Strong knowledge across bioprocessing and pharmaceutical manufacturing workflows, including upstream processing, downstream processing, formulation, buffer/media preparation, sterile manufacturing, and fill-finish operations. Experience working with external customers within the Biotech, Biologicals, Life Sciences, Vaccine, and/or Injectable Pharmaceutical industries. Experience supporting customers supplying products to highly regulated markets such as the United States, Europe, Japan, and other ICH-regulated regions. Strong understanding of customer manufacturing processes, technical challenges, material requirements, and evolving industry expectations. Regulatory & Compliance Knowledge Strong understanding of regulatory and compliance requirements applicable to single-use technologies used in biopharmaceutical and pharmaceutical manufacturing. Working knowledge of Extractables & Leachables (E&L), supplier qualification programs, GMP/cGMP expectations, change control, quality risk management, sterility assurance, contamination control, validation requirements, and regulatory expectations from US FDA, EMA, MHRA, PMDA, and other global agencies. Awareness of BPOG Single-Use guidance and USP / ISO standards relevant to single-use systems, fluid contact materials, sterilization, biocompatibility, and particulate control. Personal Attributes Purpose-driven, with passion for discovery and determination to overcome challenges that advance life-changing science. Customer-focused, solution-oriented, and able to convert technical insight into meaningful business impact. Strong leadership, communication, influencing, and cross-functional collaboration skills. Who You Are A Subject Matter Expert (SME) who partners closely with commercial teams, product managers, quality teams, and R&D scientists to achieve business objectives. Possess deep understanding of bioprocessing workflows and/or sterile pharmaceutical manufacturing operations. Strong understanding of customer technical challenges, process requirements, material requirements, and regulatory expectations. Capable of engaging effectively with stakeholders across Process Development, Manufacturing, Engineering, Validation, Quality Assurance, Quality Control, Regulatory Affairs, Supply Chain, and Procurement. Demonstrated project management and execution skills, with the ability to manage and prioritize multiple technical engagements and strategic opportunities. Able to develop and maintain strong technical relationships with targeted key accounts. Passionate about driving innovation and continuously improving AFH products, solutions, and service offerings. Possess strong knowledge of regulatory expectations associated with single-use assemblies, fluid handling systems, and critical process components used in regulated manufacturing environments. How You Will Thrive and Create an Impact Play a key role in identifying, qualifying, and prioritizing project opportunities, ensuring effective support for both internal and external customers. Contribute to the technical positioning of AFH products within customer manufacturing processes and influence strategic decision-making. Improve the quality, competitiveness, and value proposition of AFH products and service offerings. Gather, compile, and analyze Voice of Customer (VOC) insights to identify unmet needs and create differentiated solutions. Develop a deep understanding of the competitive landscape and emerging market trends to guide future product and service development. Stay current with industry, technology, and regulatory developments and communicate insights across the organization. Support local and global sales processes, strategic account management initiatives, and business growth objectives. Build and maintain strong technical relationships with key stakeholders and decision-makers within strategic customer accounts. Provide technical and regulatory guidance regarding implementation, qualification, validation, and lifecycle management of single-use systems. Support customer discussions related to supplier qualification, extractables and leachables assessments, contamination control strategies, particulate risk management, sterilization validation, and change management processes. Collaborate with Quality, Regulatory Affairs, Product Management, Operations, and R&D teams to ensure AFH solutions align with current and evolving regulations and standards. Participate in customer audits, technical reviews, product evaluations, and qualification activities as required. Support both biopharmaceutical and sterile pharmaceutical manufacturing customers in achieving compliance, operational excellence, and process optimization. Preferred Industry Experience Candidates with experience supporting leading biopharmaceutical, vaccine, CDMO, biologics, and sterile injectable pharmaceutical manufacturers supplying regulated markets such as US FDA, EMA, MHRA, PMDA, and other ICH-regulated regions will be highly preferred. Biopharma / Biotech Applications Sterile Injectable / Regulated Pharma Applications Monoclonal antibodies (mAbs) VaccinesRecombinant proteins Cell & gene therapies Plasma products CDMO biologics manufacturing Aseptic / fill-finish operations Sterile injectables Small Volume Parenterals (SVPs) Large Volume Parenterals (LVPs) Complex generic injectables US & EU regulated-market supply Success Profile Ideal Candidate Profile The ideal candidate combines deep bioprocessing and pharmaceutical manufacturing expertise, strong understanding of single-use technologies, knowledge of regulatory and quality requirements for regulated markets, proven technical sales and key account management experience, leadership capability to build high-performing technical teams, and the ability to translate customer needs into commercially successful solutions. DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. Privacy Policy: We will use the personal information that you have submitted to us in order to consider your application for the relevant role. Your privacy is important to us. 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