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Biomanaufacturing Associate III

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 building the manufacturing operations team at our BaseCamp facility.  The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AAV) Lentivirus (LV) and mRNAs.  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. 

 

Here’s What You’ll Do:

  • Routine right-first-time cGMP manufacturing of viral vectors and mRNA including but not limited to upstream, downstream, and aseptic fill finish and processing.
  • Perform manufacturing/operations start-up 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 viral vectors and mRNA.
  • Work effectively with cross functional teams comprised of process sciences, development, facilities & engineering, tech ops, quality control, quality assurance, to ensure right-first-time technology transfer
  • Work closely 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.

 

Requirements:

  • Bachelor’s degree in biological science(s) field or related engineering w/4-8 years of experience in cGMP biotech manufacturing preferred.
  • High school equivalency w/6-10 years of experience in cGMP biotech manufacturing.
  • 4-8 years of experience in cGMP biotech manufacturing.
  • 2-6 years of Cell Therapy/Viral Vector/mRNA manufacturing experience.
  • 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.
  • Willingness to cross-train in cell therapy manufacturing.

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, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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Average salary estimate

$95000 / YEARLY (est.)
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$80000K
$110000K

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What You Should Know About Biomanaufacturing Associate III, ElevateBio

Join ElevateBio as a Biomanufacturing Associate III and be part of an exciting journey in the world of cell and gene therapy! Located in Waltham, Massachusetts, ElevateBio is a forward-thinking company committed to transforming medicine through cutting-edge technologies. In this role, you will be a part of our dynamic manufacturing operations team at our state-of-the-art BaseCamp facility. Your primary responsibility will be the routine cGMP manufacturing of various cell and gene therapy products, including CAR-Ts, iPSCs, and mRNAs. We’re looking for a motivated self-starter who is eager to embrace new technologies and contribute to our mission. As you work closely with cross-functional teams, you will engage in a variety of tasks ranging from authoring SOPs and preparing batch records to resolving quality assurance issues. You will play a key role in driving continuous improvement and ensuring the highest standards of safety and quality in our processes. Your expertise in aseptic techniques and your hands-on experience in biotech manufacturing will help us maintain our commitment to excellence. ElevateBio offers a vibrant environment where you can grow your skills and make a real impact on the future of therapies that will change lives. Join us and help power the creation of life-transforming cell and gene therapies at a pace the world deserves.

Frequently Asked Questions (FAQs) for Biomanaufacturing Associate III Role at ElevateBio
What are the responsibilities of a Biomanufacturing Associate III at ElevateBio?

As a Biomanufacturing Associate III at ElevateBio, your key responsibilities will include routine cGMP manufacturing of cell and gene therapies, ensuring processes such as upstream, downstream, and aseptic fill finish are executed right-first-time. Additionally, you'll author SOPs and batch records, oversee material management, and collaborate with various teams to ensure seamless technology transfers.

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What qualifications are required for the Biomanufacturing Associate III position at ElevateBio?

To qualify for the Biomanufacturing Associate III position at ElevateBio, you should possess a Bachelor’s degree in a biological science or related engineering, along with 4-8 years of cGMP biotech manufacturing experience. Alternatively, candidates with a high school equivalency and 6-10 years of relevant experience are also encouraged to apply. Experience in cell therapy, viral vector, or mRNA manufacturing is highly desirable.

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How does ElevateBio prioritize safety and quality in its manufacturing processes?

Safety and quality are at the forefront of ElevateBio's operations. As a Biomanufacturing Associate III, you'll be committed to maintaining the highest standards in cGMP manufacturing. This includes strict adherence to safety protocols, thorough quality assurance measures, and regular audits to identify and rectify any deviations promptly, ensuring the best outcomes for colleagues and patients alike.

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In what ways does ElevateBio promote professional growth for a Biomanufacturing Associate III?

ElevateBio promotes a culture of continuous improvement and professional development. As a Biomanufacturing Associate III, you will have opportunities to create training materials, engage in cross-training, and participate in teams focused on process enhancement. The company invests in the skill sets of its employees to ensure they are equipped to handle emerging technologies and methodologies in biotechnology.

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What is the work environment like for a Biomanufacturing Associate III at ElevateBio?

The work environment at ElevateBio for a Biomanufacturing Associate III is vibrant and collaborative. You'll work at our cutting-edge BaseCamp facility, where teamwork across various disciplines is essential. The dynamic atmosphere encourages innovation, adherence to best practices, and a focused approach to achieving therapeutic breakthroughs for patients.

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Common Interview Questions for Biomanaufacturing Associate III
Can you describe your experience with cGMP manufacturing processes?

When answering this question, highlight specific roles you've held and the types of products you manufactured under cGMP standards. Discuss any challenges you faced and how you successfully overcame them, emphasizing your attention to detail and commitment to quality.

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What strategies do you use to ensure compliance with safety and quality standards?

To answer this question effectively, explain the processes you follow, such as regular audits, training, and documentation practices. Provide examples of situations where you identified potential risks and took proactive measures to enhance safety and quality in the manufacturing process.

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How do you approach cross-functional team collaboration?

Discuss your experience working with teams from different departments. Emphasize your communication skills and provide an example of a time when effective collaboration led to successful project outcomes, focusing on how you managed to align goals across diverse teams.

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What experience do you have with aseptic techniques and processes?

Share specific training or certifications related to aseptic techniques. Describe how you've applied these techniques in previous roles, especially in your handling of sensitive products and maintaining sterile conditions.

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Can you explain your process for writing SOPs and batch records?

When addressing this question, detail your methodical approach to creating SOPs and batch records. Discuss how you ensure clarity and compliance, as well as any experiences you have had where your documentation led to improved processes.

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What tools or technologies have you used in previous biotech manufacturing roles?

Be specific about the tools, software applications, or equipment you've worked with. Mention any relevant experience you have with data management or process automation that contributes to efficiency in a biotech manufacturing environment.

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How do you handle unexpected problems during the manufacturing process?

Talk about your method for identifying issues quickly, analyzing root causes, and implementing corrective actions. Provide a scenario where you successfully resolved an unexpected issue and what techniques you used to minimize disruption.

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What motivates you to work in the biotech industry?

Convey your passion for biotechnology and how it intertwines with your skills and interests. Share personal stories or examples that demonstrate your commitment to making a positive impact on patients' lives through work in this field.

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Describe a time when you contributed to a project involving process improvement.

Use the STAR (Situation, Task, Action, Result) technique to discuss a specific project. Focus on your role in identifying areas for improvement, the initiatives you took, and the positive outcomes that resulted from your contributions.

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What do you consider the most challenging aspect of working in cGMP manufacturing?

Reflect on the complexities of compliance, the high stakes involved in maintaining quality, and the fast-paced nature of biotech manufacturing. Share your strategies for coping with these challenges and maintaining a focused, productive work environment.

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Full-time, on-site
DATE POSTED
January 8, 2025

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