Senior Director, Technical Manufacturing

Senior Director, Technical Manufacturing

Welcome to the forefront of innovation in cutting edge patient-centered treatments. We are seeking the best and brightest to join our high-performing organization as a Senior Director, Technical Manufacturing. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. If you are looking for a career accelerator, driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, Project Farma wants you to join our team.

Responsibilities

• As a Senior Technical Manufacturing Director, you will play a strategic leadership role with focus on business development and organizational growth while ensuring project delivery via your own billability. You will also focus on training, mentoring, and coaching teams in the evolution and continued operational excellence of Project Farma’s practice areas. Success requires technical expertise combined with business acumen, advanced people- and team-building skills, and a consulting mindset to deliver technical and business solutions.

About you

How will you spend your days as a Senior Director, Technical Manufacturing?

Examples of our core services within the life science space include Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance.

Required

Benefits

Who are we?

We are Project Farma, the leading advanced therapy technical operations consulting company in the life science industry. We are patient-focused, people-first, and committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook supports partners across the life science space with project management, validation, engineering, quality / compliance, and consulting services.

Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs.

Equality and compliance : Precision is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, national origin, age, disability, veteran status or other protected characteristics. If you require a reasonable accommodation to complete any part of the application process, please contact us.

This description intentionally excludes extraneous application forms and policy disclosures not pertinent to the role. For candidate privacy information, please refer to our privacy notices as applicable.

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