Avid Bioservices
Scientist II, Process Development Viral Vector
Avid Bioservices, Costa Mesa, California, United States, 92626
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
Join us as a
Scientist II, Process Development Viral Vector , where you'll harness scientific and engineering concepts to drive viral vector production with mammalian and insect cells. Your role as a lab bench scientist encompasses cell culture and viral vector production, participation in process scale-up, optimization, technology transfer, and process characterization efforts. You'll be an integral part of both client and internal programs. Make your mark in the world of cutting-edge science and innovation.
Cultivate mammalian and insect cell lines for viral vector production using various bioreactor systems and cell culture techniques, ensuring strict aseptic conditions.Design, execute and analyze well-designed experiments, translating data into meaningful insights that drive process improvements and innovation. Actively engage in supporting both client and internal programs, contributing your expertise to drive successful outcomes.Excel in troubleshooting complex upstream process issues, proactively developing innovative solutions to overcome upstream challenges and optimize performance.Operate and troubleshoot essential process equipment, while also pioneering methods and procedures for novel assignments.Maintain comprehensive and accurate documentation of data and findings to ensure traceability and regulatory compliance, while regularly updating management on project status and progress.Exhibit strong technical writing skills, creating detailed technical protocols, Process Development reports, user requirements, SOPs, and other essential documents.Provide valuable guidance and mentorship to Associate Scientists and Laboratory interns, fostering their growth and development.Prioritize safety by adhering to all policies, practices, and procedures, promptly reporting any unsafe activities, actively participating in collaborative team efforts to achieve departmental and company goals, and flexibly performing additional duties as assigned.Minimum Qualifications:
Bachelor’s degree in biology, Biochemistry, Immunology, Virology, biomedical engineering or an equivalent scientific field, or a combination of education and experience that demonstrates the necessary knowledge and skills.5+ years of relevant and hands-on experience in viral vector, protein, or large molecule production.Advanced hands-on experience with various mammalian and insect cell lines, both adherent and suspension cultures, all executed with stringent aseptic technique.Proven experience with midsize and large-size single-use bioreactors to produce viral vectors through transfection and/or infection.Extensive hands-on experience with benchtop and pilot scale bioreactors for suspension cultures, including proficiency in scale-up and optimization for viral vector production.Proficiency in working with multi-layer vessels for adherent cultures, demonstrating hands-on experience.Understanding of regulatory requirements and cGMP compliance in bioprocess development.Ability to lead projects, mentor junior staff, and collaborate cross-functionally to drive innovation and process improvements.Preferred Qualifications:
Master’s degree in biology, Biochemistry, Immunology, Virology, biomedical engineering or an equivalent scientific field, or a combination of education and experience that demonstrates the necessary knowledge and skills.Familiarity with microcarriers is desired and will be considered an asset.Who you are:
You are a highly independent and proactive scientist, able to design and execute experiments with minimal supervision while ensuring the highest standards of quality and reproducibility.Your written and verbal communication skills are exceptional, enabling you to craft clear, concise, and detailed batch records, protocols, and reports.You bring a proactive mindset, always seeking ways to optimize upstream processes while ensuring their integrity and quality.Your troubleshooting skills are top-notch, enabling you to quickly identify, analyze, and resolve challenges across various upstream unit operations.You thrive in a fast-paced environment, multitasking with unparalleled attention to detail to keep everything running smoothly.While you are independent, you are also a strong team player who collaborates effectively, leveraging teamwork to drive innovation and success.You excel at building relationships, fostering a positive and collaborative environment with team members, clients, vendors, and suppliers.Position Type/Expected Hours of Work:
This role is a full-time position with working days of Monday through Friday, unless otherwise stated by Supervisor. Must have the ability to work overtime, weekends and/or holidays when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, equity grants, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $109,700-$146,300 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
We understand the importance of attracting and retaining top talent. The expected base pay range for this position is ($109,700-$146,300) plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training.
Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting.#J-18808-Ljbffr
Your Role:
Join us as a
Scientist II, Process Development Viral Vector , where you'll harness scientific and engineering concepts to drive viral vector production with mammalian and insect cells. Your role as a lab bench scientist encompasses cell culture and viral vector production, participation in process scale-up, optimization, technology transfer, and process characterization efforts. You'll be an integral part of both client and internal programs. Make your mark in the world of cutting-edge science and innovation.
Cultivate mammalian and insect cell lines for viral vector production using various bioreactor systems and cell culture techniques, ensuring strict aseptic conditions.Design, execute and analyze well-designed experiments, translating data into meaningful insights that drive process improvements and innovation. Actively engage in supporting both client and internal programs, contributing your expertise to drive successful outcomes.Excel in troubleshooting complex upstream process issues, proactively developing innovative solutions to overcome upstream challenges and optimize performance.Operate and troubleshoot essential process equipment, while also pioneering methods and procedures for novel assignments.Maintain comprehensive and accurate documentation of data and findings to ensure traceability and regulatory compliance, while regularly updating management on project status and progress.Exhibit strong technical writing skills, creating detailed technical protocols, Process Development reports, user requirements, SOPs, and other essential documents.Provide valuable guidance and mentorship to Associate Scientists and Laboratory interns, fostering their growth and development.Prioritize safety by adhering to all policies, practices, and procedures, promptly reporting any unsafe activities, actively participating in collaborative team efforts to achieve departmental and company goals, and flexibly performing additional duties as assigned.Minimum Qualifications:
Bachelor’s degree in biology, Biochemistry, Immunology, Virology, biomedical engineering or an equivalent scientific field, or a combination of education and experience that demonstrates the necessary knowledge and skills.5+ years of relevant and hands-on experience in viral vector, protein, or large molecule production.Advanced hands-on experience with various mammalian and insect cell lines, both adherent and suspension cultures, all executed with stringent aseptic technique.Proven experience with midsize and large-size single-use bioreactors to produce viral vectors through transfection and/or infection.Extensive hands-on experience with benchtop and pilot scale bioreactors for suspension cultures, including proficiency in scale-up and optimization for viral vector production.Proficiency in working with multi-layer vessels for adherent cultures, demonstrating hands-on experience.Understanding of regulatory requirements and cGMP compliance in bioprocess development.Ability to lead projects, mentor junior staff, and collaborate cross-functionally to drive innovation and process improvements.Preferred Qualifications:
Master’s degree in biology, Biochemistry, Immunology, Virology, biomedical engineering or an equivalent scientific field, or a combination of education and experience that demonstrates the necessary knowledge and skills.Familiarity with microcarriers is desired and will be considered an asset.Who you are:
You are a highly independent and proactive scientist, able to design and execute experiments with minimal supervision while ensuring the highest standards of quality and reproducibility.Your written and verbal communication skills are exceptional, enabling you to craft clear, concise, and detailed batch records, protocols, and reports.You bring a proactive mindset, always seeking ways to optimize upstream processes while ensuring their integrity and quality.Your troubleshooting skills are top-notch, enabling you to quickly identify, analyze, and resolve challenges across various upstream unit operations.You thrive in a fast-paced environment, multitasking with unparalleled attention to detail to keep everything running smoothly.While you are independent, you are also a strong team player who collaborates effectively, leveraging teamwork to drive innovation and success.You excel at building relationships, fostering a positive and collaborative environment with team members, clients, vendors, and suppliers.Position Type/Expected Hours of Work:
This role is a full-time position with working days of Monday through Friday, unless otherwise stated by Supervisor. Must have the ability to work overtime, weekends and/or holidays when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, equity grants, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $109,700-$146,300 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
We understand the importance of attracting and retaining top talent. The expected base pay range for this position is ($109,700-$146,300) plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training.
Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting.#J-18808-Ljbffr