Avid Bioservices
Scientist I, Process Development Viral Vector (Analytical Development)
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:
Step into the realm of groundbreaking biotechnology as a
Scientist I, Process Development Viral Vector (Analytical Development) . Unleash the power of scientific and methods development concepts to propel the testing and characterization of viral vector processes and products to new heights. Lead the charge in developing cutting-edge assays for identity, potency, purity, safety, and stability, and actively contributing to transferring these assays to Quality Control. Your unwavering commitment to scientific excellence and thirst for knowledge will position you as a trailblazer, shaping the future of process development and leaving an indelible mark on the scientific literature. Join us in revolutionizing the world of biotechnology and be part of a team that's rewriting the rules of possibility.Design and execute suitable experimental setups related to assay development and/or tech transfer. Analyze the outcome of such studies to draw meaningful conclusions to establish these assays. Utilize state-of-the-art methods, approaches, and tests related to viral vector production and purification.Participate in troubleshooting assays related to viral vector and residual testing and interact with the team to identify solutions to Analytical Development challenges.Operate and troubleshoot essential testing equipment and determine methods and procedures on new assignments.Document data and findings for traceability and regulatory requirements and update management on project status and progress.Provide support to Associate Scientists. Work with Quality Control to facilitate the transfer of assays that will be used to support CGMP production and purification of viral vectors.Write technical protocols and reports, and implement PD and manufacturing SOPs, BPRs.Comply with all safety policies, practices, and procedures, reporting all unsafe activities to your supervisor and/or Human Resources, participating in proactive team efforts to achieve departmental and company goals, perform other duties as assigned by the Company, and participating in regulatory and client audits.Minimum Qualifications:
Bachelor’s degree in biology, Biochemistry, Chemistry, or equivalent scientific field.4+ years of hands-on experience in testing viral vectors, proteins, or large molecules.Proficiency in aseptic techniques and cell-based assays.Hands-on experience with PCR.Strong knowledge of assay development, experimental design, and data analysis.Experience in working with Quality Control.Preferred Qualifications:
Master’s degree in biology, Biochemistry, Chemistry, or equivalent scientific field.Hands-on experience with additional analytical techniques like ELISA, HPLC, SDS-PAGE, Western Blotting, and MALDS.Ability to troubleshoot and optimize viral vector and residual testing assays.Familiarity with regulatory requirements and data integrity.Experience in working with Quality Control.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 analytical methods while ensuring their integrity and quality.Your troubleshooting skills are top-notch, enabling you to quickly identify, analyze, and resolve challenges related to operational aspects of analytical approaches.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, colleagues, 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 $101,300-$135,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.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. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
#J-18808-Ljbffr
Step into the realm of groundbreaking biotechnology as a
Scientist I, Process Development Viral Vector (Analytical Development) . Unleash the power of scientific and methods development concepts to propel the testing and characterization of viral vector processes and products to new heights. Lead the charge in developing cutting-edge assays for identity, potency, purity, safety, and stability, and actively contributing to transferring these assays to Quality Control. Your unwavering commitment to scientific excellence and thirst for knowledge will position you as a trailblazer, shaping the future of process development and leaving an indelible mark on the scientific literature. Join us in revolutionizing the world of biotechnology and be part of a team that's rewriting the rules of possibility.Design and execute suitable experimental setups related to assay development and/or tech transfer. Analyze the outcome of such studies to draw meaningful conclusions to establish these assays. Utilize state-of-the-art methods, approaches, and tests related to viral vector production and purification.Participate in troubleshooting assays related to viral vector and residual testing and interact with the team to identify solutions to Analytical Development challenges.Operate and troubleshoot essential testing equipment and determine methods and procedures on new assignments.Document data and findings for traceability and regulatory requirements and update management on project status and progress.Provide support to Associate Scientists. Work with Quality Control to facilitate the transfer of assays that will be used to support CGMP production and purification of viral vectors.Write technical protocols and reports, and implement PD and manufacturing SOPs, BPRs.Comply with all safety policies, practices, and procedures, reporting all unsafe activities to your supervisor and/or Human Resources, participating in proactive team efforts to achieve departmental and company goals, perform other duties as assigned by the Company, and participating in regulatory and client audits.Minimum Qualifications:
Bachelor’s degree in biology, Biochemistry, Chemistry, or equivalent scientific field.4+ years of hands-on experience in testing viral vectors, proteins, or large molecules.Proficiency in aseptic techniques and cell-based assays.Hands-on experience with PCR.Strong knowledge of assay development, experimental design, and data analysis.Experience in working with Quality Control.Preferred Qualifications:
Master’s degree in biology, Biochemistry, Chemistry, or equivalent scientific field.Hands-on experience with additional analytical techniques like ELISA, HPLC, SDS-PAGE, Western Blotting, and MALDS.Ability to troubleshoot and optimize viral vector and residual testing assays.Familiarity with regulatory requirements and data integrity.Experience in working with Quality Control.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 analytical methods while ensuring their integrity and quality.Your troubleshooting skills are top-notch, enabling you to quickly identify, analyze, and resolve challenges related to operational aspects of analytical approaches.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, colleagues, 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 $101,300-$135,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.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. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
#J-18808-Ljbffr