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This information is not specified in the job description.
The position requires full-time on-site client presence.
A Bachelor’s Degree in Life Science, Engineering, or related discipline is required, or equivalent work experience in CQV engineering, cGMP facility start-up, project management, or comparable military experience. Candidates must also be authorized to work full-time in the US without sponsorship.
The company features a dynamic, high-performing team of vibrant professionals passionate about innovation, high-quality work, and patient impact in a fast-paced environment. They emphasize a Patient Focused and People First Mission with opportunities for professional development and philanthropy.
Strong candidates thrive in fast-paced environments, are detail-oriented with natural leadership qualities, live in the job posting area, are willing to travel significantly, and have hands-on experience in engineering life cycles, validation, and GxP practices.
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.