Director Manufacturing Strategy

Overview

The Director of Manufacturing Strategy will play a pivotal role in shaping and executing the manufacturing strategy for Iovance. This role focuses on leading and overseeing high-priority strategic and operational projects and initiatives that shape the future of Iovance, including capacity expansions, process and operational improvements, technology upgrades, and other critical projects aligned with the company’s business goals. The Director will work closely with senior leadership and cross-functional teams to ensure the successful delivery of these strategic projects to meet the company growth objectives in context of evolving market demands and regulatory requirements,

The Director of Manufacturing Strategy will work in a dynamic, fast-paced environment, collaborating closely with a range of internal and external stakeholders. Occasional travel may be required to manufacturing facilities, supplier sites, and partner locations.

Essential Functions and Responsibilities:

Strategic Planning & Execution:

•         Lead and manage the planning, execution, and delivery of strategic projects that align with the company’s long-term goals.

•         Develop project roadmaps for key initiatives, including new capacity expansion, manufacturing facility setups, process optimization, technology integration, operational efficiencies, and COGS reduction.

•         Lead and manage cross-functional teams and act as the primary point of contact for strategic projects, ensuring alignment across all stakeholders and facilitating decision-making at all levels.

•         Prioritize projects based on business impact, regulatory requirements, and market needs, ensuring that the company remains agile and competitive.

•         Continuously assess and recommend improvements to processes, technology, and infrastructure to enhance efficiency, reduce costs, and improve product quality.

Project Management:

•         Oversee the planning, execution, and monitoring of key projects from inception to completion.

•         Ensure that projects are delivered on time, within budget, and in compliance with regulatory standards and company policies.

•         Act as a liaison between various departments, ensuring timely and effective communication and coordination across teams involved in manufacturing projects.

•         Develop and manage budgets for projects, ensuring alignment with company financial goals and objectives.

•         Monitor financial performance of projects, identifying areas for cost optimization without compromising quality or timelines.

•         Ensure projects comply with all applicable regulations, standards, and best practices (e.g., GMP, FDA, EMA).

•         Work closely with quality assurance teams to ensure product integrity, safety, and efficacy throughout the manufacturing process.

•         Identify potential risks and implement strategies to mitigate.

Innovation & Technology:

•         Stay abreast of technological advancements in manufacturing and the biopharmaceutical industry to drive innovation.

•         Identify opportunities to implement cutting-edge technologies that support scalability and cost-effectiveness.

Stakeholder Management:

•         Build and maintain relationships with internal stakeholders, including senior leadership, Manufacturing, Quality, R&D, Clinical, and Commercial teams.

•         Serve as a primary point of contact for key external stakeholders, including suppliers, regulatory bodies, and partners.

•         Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.

•         Perform miscellaneous duties as assigned.

Education, Skills, and Knowledge

•         Education: Bachelor’s degree in engineering, Life Sciences, Chemistry, Biochemistry, or a related field. Advanced degree (Master’s or PhD) preferred.

•         Experience: At least 10-15 years of experience in manufacturing or operations management within the biopharmaceutical or related industry, with at least 5 years in a leadership or strategic role.

•         Experience in strategic management consulting is preferred.

•         Strong knowledge of biopharmaceutical manufacturing processes, technologies, and regulatory requirements (GMP, FDA, EMA).

•         Proven project management skills with the ability to manage multiple initiatives simultaneously.

•         Excellent leadership, communication, and interpersonal skills.

•         Strong analytical and problem-solving abilities.

•         Experience in managing cross-functional teams and collaborating with multiple departments.

•         Financial acumen and experience managing project budgets.

•         Strategic thinking with a focus on continuous improvement and innovation.

The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodation may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request accommodation. 

Physical Demands and Activities Required

• Must be able to remain in a stationary position standing or sitting for prolonged periods of time. 
• Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects.
• Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading.  
• This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers.
• Must be able to communicate with others to exchange information.

Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines

Work Environment

This job works in a professional office environment and a manufacturing lab setting. Potential exposure to latex, bleach, loud noise, lab equipment hazards, strong odors, and chemical/biochemical is possible.  Requires operating standard office equipment and keyboards.

The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.

Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact careers@iovance.com.

By voluntarily providing information and clicking “Submit Application”, you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice. 

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