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Common questions about this position
The role requires you to currently live or be willing to live in the area where the job is posted, and involves working across various client sites/locations.
This information is not specified in the job description.
Candidates need to thrive in a fast-paced environment, be detail-oriented with natural leadership qualities, excel in leading teams, and have expertise in CQV engineering including commissioning, qualification, validation life cycles, project management, and life science industry knowledge.
Project Farma has a dynamic, high-performing team of vibrant professionals passionate about innovation, high-quality work, and patient impact, with a fast-paced environment, Patient Focused and People First Mission, and emphasis on professional development and philanthropy.
Strong candidates thrive in fast-paced settings, demonstrate natural leadership and detail-orientation, enjoy building teams and career development, love to travel for client sites, and align with the company's patient-focused mission.
Biomanufacturing services for cell and gene therapy
Project Farma specializes in biomanufacturing, focusing on cell and gene therapy. The company develops and implements strategies for advanced therapy facilities, helping clients create treatments that modify genes to address diseases. Their services encompass the entire lifecycle of biomanufacturing projects, including facility construction, validation, quality assurance, regulatory compliance, and automation. Project Farma distinguishes itself by offering comprehensive, turnkey solutions that ensure facilities meet Good Manufacturing Practices (GMP), which is essential for producing safe therapies. Their goal is to enhance patient outcomes through effective project execution and they also emphasize philanthropy and professional development within their team.