What are the responsibilities and job description for the Production Director position at KYDA Partners Ltd?
Director of Production
Location: San Antonio, TX (On-Site) Relocation assistance available
Schedule: Monday–Friday, 8:30 AM – 5:00 PM
Reports To: Senior Director of Production
Job Type: Full-Time | Exempt
Lead Innovation in Advanced Tissue Manufacturing!
KYDA Partners is working with a leading biomedical organization seeking a Director of Production (Cadaveric) to oversee manufacturing operations, drive efficiency, and ensure compliance with industry regulations. This role is pivotal in scaling production processes, integrating innovative technologies, and leading a high-performing team to support company growth.
Key Responsibilities:
- Strategic Leadership: Provide oversight and execution of long-term production strategies to align with corporate goals and expansion plans.
- Operational Excellence: Optimize manufacturing workflows, enhance scalability, and improve efficiency across all cadaveric tissue production operations.
- Compliance & Quality: Ensure strict adherence to FDA, AATB, ISO, cGMP/CGTP standards, implementing best practices to maintain quality and regulatory compliance.
- Team Development: Manage, mentor, and develop production leadership teams, ensuring strong performance, accountability, and continuous improvement.
- Process Innovation: Collaborate with R&D, Quality, Regulatory, and Supply Chain teams to transition new product innovations into full-scale production.
- Financial Management: Oversee departmental budgeting, cost control, and resource allocation to maintain profitability and operational efficiency.
- Workforce Planning: Ensure adequate staffing, training, and development programs to support production demands and business objectives.
- Performance Monitoring: Track production metrics, report findings to executive leadership, and drive data-driven decision-making.
What You Bring:
- 5 years of leadership experience in manufacturing, with at least 5 years in tissue processing, biomedical, or life sciences production.
- Strong expertise in FDA 21 CFR 1271, 21 CFR 820, AATB, ISO, and other regulatory standards.
- Proven ability to scale operations, optimize workflows, and implement process improvements.
- Strong background in financial planning, budgeting, and cost control.
- Experience leading cross-functional teams and collaborating with executive leadership.
- Proficiency in Microsoft Office, technical writing, and project management.
- Exceptional communication, leadership, and problem-solving skills.
Why Join?
- Make an impact in a cutting-edge, rapidly growing biomedical organization.
- Lead high-level operations with executive influence and strategic decision-making.
- Work with an innovative team driving advancements in regenerative medicine.
- Competitive compensation and professional growth opportunities.
Ready to lead and innovate? Apply today!