Job Description
Qualifications
The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards
Bachelor’s degree in biological science(s) field or related engineering with 4-6 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies
2+ years of experience in people leading and/or project leadership
Experience with some or all of the following: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV, or other biologics
Outstanding communication skills (verbal and written)
Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word
Demonstrate proficiency in aseptic technique and/or processing
Ability to function in dynamic environment and balance multiple priorities simultaneously
Shift requirements may be subject to change based on processing needs
Employee will frequently stand, walk, bend, stretch for extended periods
Routinely carry up to 25 pounds and up to 50 pounds
Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE
Routine repetitive use of arms/wrist/hands
Ability to work nights, weekends, holidays as needed to support business needs
Ability to don job-specific PPE
Responsibilities
ElevateBio is looking for a dynamic individual to join and, contribute to leading the manufacturing operations team at our BaseCamp facility
The incumbent will supervise routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as autologous/allogenic cell therapies and other advance therapies including mRNA and/or Lentiviral Vector (LLV)
Lead right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection
Lead manufacturing/operations tech transfer activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management
Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc
Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products
Work effectively with cross functional teams comprised of process sciences, development, facilities & engineering, MSAT, quality control, quality assurance, to ensure right-first-time technology transfer
Work with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls
Commitment to the highest safety and quality standards in service of our colleagues and patients
Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities
Proactively identify opportunities for improvements in process, safety, quality, and cost
Be integral in providing hands-on technical, organizational, and leadership expertise to the manufacturing department including but not limited to equipment selection, SOPs, batch records, reports, risk assessments, material ordering/management
Ensure the safety of assigned areas and work practices in accordance with EHS program
Ensure JHA (Job Hazard Analysis) are reviewed regularly, and pre-job briefs are in place prior to execution
Provide daily management oversight for the team and ensure process are executed with cGMP
Recruit and develop staff, maintain, and report department metrics to drive operational improvement
Balance and priorities daily production demands to ensure right first-time execution
8-hour day shifts, Monday through Friday
Must be available to support overtime on weekdays, weekends and holidays as driven by production schedule and requirements
Job description
ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine. Our integrated technologies model offers turnkey scale and biotechnological capabilities to power genetic medicines processes, programs, and companies to their full potential.
The Role
ElevateBio is looking for a dynamic individual to join and, contribute to leading the manufacturing operations team at our BaseCamp facility. The incumbent will supervise routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as autologous/allogenic cell therapies and other advance therapies including mRNA and/or Lentiviral Vector (LLV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.
Here’s What You’ll Do
• Lead right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.
• Lead manufacturing/operations tech transfer activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.
• Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.
• Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.
• Work effectively with cross functional teams comprised of process sciences, development, facilities & engineering, MSAT, quality control, quality assurance, to ensure right-first-time technology transfer.
• Work with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.
• Commitment to the highest safety and quality standards in service of our colleagues and patients.
• Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.
• Proactively identify opportunities for improvements in process, safety, quality, and cost.
• Be integral in providing hands-on technical, organizational, and leadership expertise to the manufacturing department including but not limited to equipment selection, SOPs, batch records, reports, risk assessments, material ordering/management.
• Ensure the safety of assigned areas and work practices in accordance with EHS program. Ensure JHA (Job Hazard Analysis) are reviewed regularly, and pre-job briefs are in place prior to execution.
• Provide daily management oversight for the team and ensure process are executed with cGMP.
• Recruit and develop staff, maintain, and report department metrics to drive operational improvement.
• Balance and priorities daily production demands to ensure right first-time execution.
Requirements
• Bachelor’s degree in biological science(s) field or related engineering with 4-6 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.
• 2+ years of experience in people leading and/or project leadership.
• Experience with some or all of the following: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV, or other biologics.
• Advanced understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system, a plus.
• Outstanding communication skills (verbal and written).
• Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word.
• Demonstrate proficiency in aseptic technique and/or processing.
• Ability to function in dynamic environment and balance multiple priorities simultaneously.
• Work Schedule:
• 8-hour day shifts, Monday through Friday.
• Must be available to support overtime on weekdays, weekends and holidays as driven by production schedule and requirements.
• Shift requirements may be subject to change based on processing needs.
• Physical Requirements:
• Employee will frequently stand, walk, bend, stretch for extended periods.
• Routinely carry up to 25 pounds and up to 50 pounds.
• Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.
• Routine repetitive use of arms/wrist/hands.
• Ability to work nights, weekends, holidays as needed to support business needs.
• Ability to don job-specific PPE.
Why Join ElevateBio?
ElevateBio is a technology-driven company built to power transformative genetic medicines today and for many decades to come. The Company commercializes its enabling technologies, manufacturing capabilities, and industry-leading expertise through partnerships to accelerate development across a breadth of therapeutic approaches and modalities. The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp®, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
We aim to be the dominant engine inside the world’s greatest scientific advancements harnessing human cells and genes to alter disease.
Our Mission
To power the creation of life-transforming cell and gene therapies, at a speed the world deserves.
Our Vision
We seek to be the world’s most indispensable cell and gene therapy technology company, redefining how companies operate, how products are created and how disease is treated.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, ****** orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards
Bachelor’s degree in biological science(s) field or related engineering with 4-6 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies
2+ years of experience in people leading and/or project leadership
Experience with some or all of the following: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV, or other biologics
Outstanding communication skills (verbal and written)
Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word
Demonstrate proficiency in aseptic technique and/or processing
Ability to function in dynamic environment and balance multiple priorities simultaneously
Shift requirements may be subject to change based on processing needs
Employee will frequently stand, walk, bend, stretch for extended periods
Routinely carry up to 25 pounds and up to 50 pounds
Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE
Routine repetitive use of arms/wrist/hands
Ability to work nights, weekends, holidays as needed to support business needs
Ability to don job-specific PPE
Responsibilities
ElevateBio is looking for a dynamic individual to join and, contribute to leading the manufacturing operations team at our BaseCamp facility
The incumbent will supervise routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as autologous/allogenic cell therapies and other advance therapies including mRNA and/or Lentiviral Vector (LLV)
Lead right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection
Lead manufacturing/operations tech transfer activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management
Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc
Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products
Work effectively with cross functional teams comprised of process sciences, development, facilities & engineering, MSAT, quality control, quality assurance, to ensure right-first-time technology transfer
Work with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls
Commitment to the highest safety and quality standards in service of our colleagues and patients
Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities
Proactively identify opportunities for improvements in process, safety, quality, and cost
Be integral in providing hands-on technical, organizational, and leadership expertise to the manufacturing department including but not limited to equipment selection, SOPs, batch records, reports, risk assessments, material ordering/management
Ensure the safety of assigned areas and work practices in accordance with EHS program
Ensure JHA (Job Hazard Analysis) are reviewed regularly, and pre-job briefs are in place prior to execution
Provide daily management oversight for the team and ensure process are executed with cGMP
Recruit and develop staff, maintain, and report department metrics to drive operational improvement
Balance and priorities daily production demands to ensure right first-time execution
8-hour day shifts, Monday through Friday
Must be available to support overtime on weekdays, weekends and holidays as driven by production schedule and requirements
Job description
ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine. Our integrated technologies model offers turnkey scale and biotechnological capabilities to power genetic medicines processes, programs, and companies to their full potential.
The Role
ElevateBio is looking for a dynamic individual to join and, contribute to leading the manufacturing operations team at our BaseCamp facility. The incumbent will supervise routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as autologous/allogenic cell therapies and other advance therapies including mRNA and/or Lentiviral Vector (LLV). The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.
Here’s What You’ll Do
• Lead right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.
• Lead manufacturing/operations tech transfer activities including but not limited to authoring SOPs, batch records, reports, risk assessments, material ordering/management.
• Provide constructive input on teams for the selection and set-up of equipment, process and material flows, etc.
• Create and maintain training materials and curricula that support continuous improvement in the cGMP manufacture of cell therapy products.
• Work effectively with cross functional teams comprised of process sciences, development, facilities & engineering, MSAT, quality control, quality assurance, to ensure right-first-time technology transfer.
• Work with Quality Assurance and Process Sciences to proactively resolve issues such as deviations, CAPAs, Change Controls.
• Commitment to the highest safety and quality standards in service of our colleagues and patients.
• Generate and manage batch records, run reports, batch data, etc. for manufacturing and scale-up activities.
• Proactively identify opportunities for improvements in process, safety, quality, and cost.
• Be integral in providing hands-on technical, organizational, and leadership expertise to the manufacturing department including but not limited to equipment selection, SOPs, batch records, reports, risk assessments, material ordering/management.
• Ensure the safety of assigned areas and work practices in accordance with EHS program. Ensure JHA (Job Hazard Analysis) are reviewed regularly, and pre-job briefs are in place prior to execution.
• Provide daily management oversight for the team and ensure process are executed with cGMP.
• Recruit and develop staff, maintain, and report department metrics to drive operational improvement.
• Balance and priorities daily production demands to ensure right first-time execution.
Requirements
• Bachelor’s degree in biological science(s) field or related engineering with 4-6 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies.
• 2+ years of experience in people leading and/or project leadership.
• Experience with some or all of the following: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV, or other biologics.
• Advanced understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system, a plus.
• Outstanding communication skills (verbal and written).
• Excellent computer and word processing skills including Microsoft Excel, PowerPoint, and Word.
• Demonstrate proficiency in aseptic technique and/or processing.
• Ability to function in dynamic environment and balance multiple priorities simultaneously.
• Work Schedule:
• 8-hour day shifts, Monday through Friday.
• Must be available to support overtime on weekdays, weekends and holidays as driven by production schedule and requirements.
• Shift requirements may be subject to change based on processing needs.
• Physical Requirements:
• Employee will frequently stand, walk, bend, stretch for extended periods.
• Routinely carry up to 25 pounds and up to 50 pounds.
• Routinely push, pull, bend, kneel, twist, and climb step ladders while wearing PPE.
• Routine repetitive use of arms/wrist/hands.
• Ability to work nights, weekends, holidays as needed to support business needs.
• Ability to don job-specific PPE.
Why Join ElevateBio?
ElevateBio is a technology-driven company built to power transformative genetic medicines today and for many decades to come. The Company commercializes its enabling technologies, manufacturing capabilities, and industry-leading expertise through partnerships to accelerate development across a breadth of therapeutic approaches and modalities. The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp®, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
We aim to be the dominant engine inside the world’s greatest scientific advancements harnessing human cells and genes to alter disease.
Our Mission
To power the creation of life-transforming cell and gene therapies, at a speed the world deserves.
Our Vision
We seek to be the world’s most indispensable cell and gene therapy technology company, redefining how companies operate, how products are created and how disease is treated.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, ****** orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
💡 Quick Summary
Seeking a career-building opportunity? The Supervisor| Cell Therapy Manufacturing position is now open for candidates interested in the Manufacturing Jobs sector. This role in Waltham offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Manufacturing Jobs is a plus.
