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.

Ready to apply Before you do, make sure to read all the details pertaining to this job in the description below. 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 You thrive in a fast-paced, dynamic environment. You embody high-caliber leadership qualities and excel in your field. You have knowledge in change management, strategic decision making, and people management in an agile environment. You live in the area where this job is posted or are willing to relocate. You have a philanthropic drive and will embody our Patient Focused and People First Mission through involvement in professional development and philanthropic opportunities. How will you spend your days as a Senior Director, Technical Manufacturing? Role is primarily client-facing and includes billable work to ensure timely delivery of innovative solutions while staying current with market and technology trends. Identify and develop resources within the practice area to ensure high expertise, performance, and client focus. Lead business development activities and support organizational growth. Change Management: anticipate impact, communicate the need for change, and implement change aligned with strategic goals. Strategic Prioritization and Decision Making: evaluate options, risks, and align with the organization's strategy and market trends. Agility: navigate and lead in an ambiguous, dynamic environment, driving value creation. People Management: build partnerships, hold team members to high standards, develop strengths, and provide mentorship. 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 Bachelor’s or Master’s Degree in Life Science, Engineering, or related discipline and/or comparable experience. Typically 8–12 years of advanced therapy, life science, pharmaceutical, or biotech experience. Typically 8–12 years of managing high-performing teams. Minimum of 7 years business development, lead generation, or sales experience. Willingness to travel as required to support project and business needs. Benefits Competitive salary based on experience Aggressive bonus structure Medical, Dental, and Vision insurance from day one 401k Plan with company match Paid Time Off and Company Paid Holidays Company Paid Maternity and Parental Leave Continuing Education Assistance 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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