20BLOC
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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. Job Title: Bioprocess and Facility Engineer 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. Minimum 5 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. 20bloc is an equal opportunity employer. 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 Seniority level
Seniority level Not Applicable Employment type
Employment type Full-time Job function
Referrals increase your chances of interviewing at 20BLOC by 2x Inferred from the description for this job
Medical insurance Vision insurance 401(k) Get notified about new Facilities Engineer jobs in
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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. Job Title: Bioprocess and Facility Engineer 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. Minimum 5 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. 20bloc is an equal opportunity employer. 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 Seniority level
Seniority level Not Applicable Employment type
Employment type Full-time Job function
Referrals increase your chances of interviewing at 20BLOC by 2x Inferred from the description for this job
Medical insurance Vision insurance 401(k) Get notified about new Facilities Engineer jobs in
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