Product Manager - CPV_Hybrid_Tampa, Florida, USA

ValGenesis · Tampa Bay, FL

Company

ValGenesis

Location

Tampa Bay, FL

Type

Full Time

Job Description

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, Tampa, Florida office


Key Responsabilities:

• 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).


Only candidates based in Tampa, Florida, USA aligned with the requirements presented will be considered



Headquartered in South San Francisco, since 2005 we’ve grown into a global organization with offices around the world. ValGenesis is the global market leader and fastest-growing provider of digital validation software for life science companies. We are proud to partner with 30 of the top 50 global pharmaceutical and biotech companies.

Our SaaS platform and flagship product, Validation Lifecycle Management System (VLMS), is the first enterprise software solution to fully electronically manage the validation process lifecycle, accelerating time to market, reducing manufacturing costs, and increasing quality and regulatory compliance for our customers. As a first mover supporting the pharmaceutical, biotech, and medical device industries, ValGenesis is pioneering innovation over web, mobile, IoT, and AR channels. For more, see the Paperless Validation Software Solution ValGenesis video.


ValGenesis is an equal-opportunity employer. All qualified applicants will be considered for employment without regard to race, age, national origin, religion, marital status, sexual orientation, ancestry, color, gender identity/expression, family/medical care leave, genetic information, medical condition, physical/mental disability, political affiliation, status as a protected veteran, status as a person with a disability, or other characteristics protected by laws or regulations.

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Date Posted

11/17/2023

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