About Valgenesis:We're a rapidly growing global SaaS company that helps life-science organizations bring lifesaving products to market with increased quality and reduced ecological impact. Our customers include 30 of the top 50 global pharma and biotech companies. We lead our market through innovation and by delivering value over web, mobile, IoT, AR channels and consulting services.Workplace type: Hybrid, Lisbon officeKey Responsibilities:Spearhead the strategy, vision, and roadmap for ValGenesis Process Insight, ensuring alignment with market needs and company objectives.Collaborate with cross-functional teams to guide products from conception through launch, ensuring deadlines and performance metrics are met.Be the advocate and subject matter expert on CPV, GMP, and relevant industry regulations.Understand and analyze market trends, customer feedback, and competitor offerings to identify opportunities and threats.Lead efforts to promote and differentiate ValGenesis Process Insight in the marketplace.Establish and nurture relationships with key stakeholders, industry experts, and customers.Ensure product adherence to industry standards and regulatory requirements, including GMP.Mentor and develop junior product team members, fostering a culture of excellence and continuous learning.Technical Aptitudes:Proficient in working with data analytics, statistical analysis, and predictive modeling to analyze and interpret complex data sets related to process validation and verification.Strong understanding and experience with parameter definition, control, and monitoring within CPV products.Solid grasp of data management principles, including data acquisition, cleansing, and transformation.Experience with model validation, tuning, and analytics to drive product improvements and ensure accuracy and compliance.Familiar with modern data visualization tools and techniques to represent data in a meaningful and accessible manner.Technical experience with software development, systems integration, and platform configuration is desirable.Ability to collaborate with technical teams, clearly communicate requirements, and guide the development of solutions aligned with CPV and GMP standards.Continuous learning and adaptation to emerging technologies and methodologies that enhance CPV product performance and compliance.Qualifications:Knowledge of SDLC is preferred but not required.Bachelor's degree with mathematics, statistical modeling.Minimum 5 years in the life sciences, GxP or related sector, with a demonstrable track record in CPV working with process and tools.In-depth understanding of GMP and other relevant regulatory frameworks.Excellent leadership, communication, and interpersonal skills.Ability to travel as needed.Proficiency in English (additional languages are a plus).Please kindly submit your CV in English.Only candidates based in Lisbon, Portugal aligned with the requirements presented will be considered.#J-18808-Ljbffr
