Who we are: 20bloc, Inc. (www.20bloc.com) is an early-stage biopharma company creating breakthrough protein-based drugs to save lives. We are developing a safe and effective hemoglobin-based oxygen carrier for first response, organ preservation and oxygen therapy. We value and encourage innovations through robust information exchange, hard work, and team interaction. We are collaborative, we are intellectual, we are hands-on.
Position Overview: We are seeking an experienced Bioprocess and Facility Engineer with a strong background in biopharmaceuticals to facilitate and oversee project development and progress from initiation to completion. The ideal candidate will possess a blend of project management skills, engineering expertise, client management capabilities and a deep understanding of biopharma processes. This role is critical in ensuring that results meet or exceed expectations - delivered on time, within scope, and aligned with industry regulations.
Key responsibilities:
- Develop comprehensive project plans outlining scope, goals, deliverables, timelines, resource allocation, and critical path using appropriate project management tools and software.
- Document project activities, obstacles, costs, and results and provide summarized project plan documentation to functional coordinators and other stakeholders as needed.
- Monitor project progress and adjust plans as needed to ensure successful delivery.
- Conduct risk analyses to reduce and mitigate unforeseen obstacles.
- Communicate project status, risks, and issues to stakeholders and senior management.
- Design, optimize, and scale up biopharmaceutical processes, ensuring compliance with industry standards.
- Manage technical and non-technical workstreams within the organization such as process development, optimization, and other technical workstreams; and oversight of new facility build out for cGMP pilot plant and management of external partners.
Requirements:
- Bachelor’s degree in bioprocess engineering, chemical engineering or biological sciences.
- 5-10 years of experience in project management and process engineering within the biopharma industry.
- Proven track record of managing complex projects from initiation to completion and demonstrated proficiency with industry-standard project manager tools and software.
- Strong understanding of biopharmaceutical manufacturing processes and GMP regulatory requirements.
- Familiarity with facility and process validation activities in regulated environments preferred.
- Excellent verbal and written communication, leadership, and problem-solving skills.
This position provides an excellent opportunity for a highly motivated, collaborative individual to apply their skills and experience in an early-stage biopharma company with room for advancement while contributing to the development of a groundbreaking therapeutic protein product.
We offer a comprehensive benefits package which includes:
- Medical, dental and vision plans
- 120 hours paid time off (PTO)
- 12 paid holidays annually
- 401(k) U.S. retirement savings plan
- Employee assistance program
20bloc is an equal opportunity employer and values diversity. We provide the same opportunities disregarding race, religion, color, national origin, gender, gender identification, sexual orientation, age, marital status, veteran status, or disability status.
