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Experience in pharmaceutical/biopharmaceutical industry. Experience in cGMP environment, including commissioning, qualification and validation. Well-developed communication skills, both verbal and written. Should have demonstrated experience managing teams consisting of internal staff, supervising engineering and construction activities, and preparing turnover documentation and as-built drawings. Based on level, demonstrated project controls skills such as estimating, scheduling and cost reporting. Larger projects may require earned value/progress tracking systems. Leadership skills. Proficient with Microsoft Office products (Excel, Word, PowerPoint, etc.) Lead and manage all aspects of assigned complex projects that support improvements to the biologics operations.
- Bachelor’s Degree with experience in a Pharmaceutical Industry and related
- regulatory, engineering, and construction techniques.
- Experience working in cGMP biotech environment and with GDP Practices.