SVP of Pharmaceutical Sciences - Jurata Thin Film : Job Details

About Jurata Thin Film:

Jurata Thin Film is a pioneering company dedicated to revolutionizing drug delivery through innovative thin film technologies. Our mission is to enhance patient and animal care and access by developing cutting-edge, thermostable formulations that eliminate the need for injections and cold-chain distribution. We are driven by science, a passion for excellence, a commitment to quality, and a relentless pursuit of innovation.

Our Values:

Innovation: We embrace creativity and encourage the development of novel solutions to meet the evolving needs of the healthcare industry.

Integrity: We conduct our business with the highest ethical standards, ensuring transparency and accountability in all our actions.

Collaboration: We believe in the power of teamwork and foster a culture of open communication and mutual respect.

Excellence: We strive for excellence in everything we do, from research and development to external collaborations and beyond.

Equitable Access: We are simplifying the manufacturing, distribution, storage, and delivery of vaccines and biologics, enabling access of life-saving therapies to everyone person and animal who needs them around the world.

Position Overview:

Our company is seeking a highly strategic and experienced Senior Vice President of Pharmaceutical Sciences to join our executive leadership team. This pivotal role will be responsible for leading and overseeing our innovative drug delivery platform based on our proprietary technology for animal and human health. The successful candidate will play a crucial role in platform advancement through all stages of development, from early research to commercialization. You will develop and execute global strategies for our development programs, ensuring alignment with regulatory requirements worldwide. You will lead cross-functional teams in formulation science, analytical development, and drug product manufacturing. This role requires a visionary leader with extensive experience in biopharmaceutical development, regulatory affairs, and a proven track record of successfully bringing complex products to market using novel drug delivery technologies. You will be responsible for building and mentoring high-performing teams, collaborating cross-functionally and representing the company to external partners and regulatory authorities. Your leadership will be instrumental in shaping our portfolio strategy, driving technological advancements, and ultimately delivering innovative therapies with improved bioavailability and efficacy to patients worldwide.

Key Responsibilities:

As the Senior Vice President, you will play a pivotal role in shaping our company's future in the rapidly evolving field of biologics. The SVP will oversee R&D, Drug Product Design and Analytical Development. This executive position demands a visionary leader with extensive expertise in formulation science, analytical development, and research for a diverse range of biological products and drug delivery modalities.

Strategic Leadership

Develop and execute the company's formulation strategy for vaccines and biologics, including virus, antibody, bacteria, enzyme, mRNA LNP, and plasmids for both animal and human applications

Enhance the company's overall scientific vision and long-term research strategy, aligning it with business objectives

Lead the expansion of our novel thermostable liquid and film formulation platforms, driving innovation in drug delivery systems

Represent the company at high-level meetings with clients, collaborators, NGOs, investors, and the Board of Directors

Lead the company's intellectual property strategy, working closely with legal teams to protect proprietary technologies and innovations

Portfolio Management and Development

Build and lead world-class formulation, analytical, and research teams prioritizing projects based on scientific merit and market potential

Manage the allocation of resources across different research programs and therapeutic areas

Ensure the success of direct reports and manage multiple parallel activities to meet project timelines and milestones

Foster a culture of scientific excellence and innovation within the organization

Develop and implement key performance indicators (KPIs) to measure and track scientific progress and impact

Scientific Advisory Board Management

Establish and manage a Scientific Advisory Board comprised of leading experts in relevant fields.

Leverage the advisory board's expertise to inform research directions and validate scientific approaches

Technical Expertise

Develop formulation platforms based on a deep understanding of liquid and lyophilized formulation development and physical/chemical stability of proteins and how process-related stress impacts product quality

Oversee the development of comprehensive data packages supporting commercial formulation/process development and characterization

Guide the analytical team in developing new methods for formulation characterization and manufacturing quality control

Direct research efforts to expand the formulation platform and support mechanism of action (MOA) studies

External Partnerships

Establish and nurture strategic partnerships with academic institutions, research organizations, and industry collaborators

Lead scientific due diligence efforts for potential licensing opportunities, and collaborative ventures

Cross-functional Collaboration

Work closely with client stakeholders, analytical development, manufacturing, supply chain, quality, and regulatory affairs teams

Support GMP manufacturing initiatives, including technology transfer, campaign analysis, and risk assessments

Provide scientific guidance on regulatory submissions and interactions with regulatory agencies and ensure compliance with evolving regulatory requirements

Oversee the development and implementation of good laboratory practices and quality control and assurance protocols for scientific operations

Innovation and Continuous Improvement

Identify emerging scientific trends and technologies to maintain the company's competitive edge in biologics development

Apply sophisticated statistical/analytical techniques and leverage statistical analysis software for data-driven decision-making

Lead initiatives to demonstrate the value of Juratas thin film technology for delivery of multiple therapeutic modalities and expand the company's technological capabilities

Lead the company's intellectual property strategy, working closely with legal teams to protect proprietary technologies and innovations

Communication and Representation

Effectively communicate progress, milestones, and departmental needs to company stakeholders

Represent the company at high-profile scientific and partnering conferences and industry events to enhance its scientific reputation

Talent Development and Mentorship

Implement programs to attract, develop, and retain top scientific talent

Mentor junior scientists and foster a culture of continuous learning and professional development within the scientific community

Qualifications

Educational Background:

Masters degree in Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics, or a related field and 20 years of formulation experience OR

Ph.D. in Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics, or a related field OR PharmD with minimum 15 years therapeutic industry formulation experience

The ideal candidate will possess:

Ph.D. in a relevant scientific field such as Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics with extensive experience in biologics development

A minimum of 15 years experience in the biotechnology industry with deep experience in formulation development of liquid and lyophilized products and commercial process development at top-tier organizations

Experience in parenteral and other routes of administration (patches, microneedles, gels, intranasal)

Significant leadership experience in senior-level positions

Proven track record of successfully managing teams to design and develop products

Strong leadership skills with the ability to inspire and mentor diverse teams

Deep understanding of regulatory requirements in biologics manufacturing

Excellent communication skills and the ability to influence at all levels of the organization

Willingness to travel internationally and domestically (up to 15% of the time)

Why Join Jurata Thin Film?

At Jurata, you will have the opportunity to be part of a dynamic and innovative team dedicated to making a difference in the healthcare industry. We offer a collaborative and supportive work environment, competitive compensation, and benefits packages, and the chance to contribute to the development of transformative products that improve the lives of humans and animals throughout the world.

The annual salary range for this role in the U.S. is commensurate with experience and based on industry standard surveys.

Jurata Thin Film offers a comprehensive employee benefits package, including a Retirement and Savings Plan with company contributions, group medical, dental, and vision coverage, life and disability insurance, and flexible spending accounts.

A discretionary annual bonus program

Stock-based long-term incentives

Applicants must be authorized to work for any employer in U.S. We are unable to sponsor or take over sponsorship at this time. We do not accept unsolicited resumes from agencies or recruiters.