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Be an Early Applicant
Transforming the CDMO experience: Unrivaled expertise. Worldclass facilities. Exceptional quality. Personalized process.
The Role
Plans and executes analytical studies supporting biologics process and formulation development. Performs and interprets chromatography, electrophoresis, qPCR, plate-based, and protein characterization assays; investigates atypical results; troubleshoots instruments and methods; authors protocols and technical documentation; supports method development, qualification, and transfer; and presents findings to cross-functional teams.
Summary Generated by Built In
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:
The Research Associate, Process Analytics applies advanced scientific knowledge acquired through a specialized course of study to plan and execute analytical studies supporting cell line development, upstream and downstream process development, formulation development, process characterization, and other non-GMP studies. Working with limited day-to-day supervision, the role selects appropriate analytical approaches, interprets data, investigates atypical results, and recommends scientifically supported next steps. The Research Associate owns assigned analytical studies and serves as a technical resource to development teams.
Key Responsibilities:
- Plan and execute routine and non-routine analytical studies supporting cell line development, upstream and downstream process development, formulation development, process characterization, and other non-GMP studies.
- Select appropriate analytical methods, experimental conditions, controls, and data-analysis approaches within established program objectives.
- Execute and interpret assays such as HPLC or UPLC, icIEF, plate-based assays, residual DNA or qPCR, pH, osmolality, and SDS-PAGE, applying scientific judgment to evaluate results.
- Investigate atypical or unexpected results, assess data quality and validity, and recommend scientifically supported next steps.
- Troubleshoot routine method and instrument performance issues and determine appropriate technical resolutions within the role’s authority.
- Author and revise analytical protocols, methods, technical summaries, and investigation documentation to maintain data integrity and traceability.
- Support analytical method development, qualification, and transfer activities in partnership with Analytical Development.
- Present analytical conclusions and recommendations to Process Development and cross-functional project teams.
- Contribute to continuous improvement of analytical approaches, throughput, data quality, and turnaround time.
Minimum Qualifications:
- Bachelor's degree in biology, biochemistry, chemistry, biotechnology, pharmaceutical sciences, or a related scientific field, providing the advanced knowledge required to perform the analytical work.
- One or more years of relevant hands-on experience in process development, quality control, biologics characterization, or a related analytical laboratory, or equivalent experience gained through advanced scientific coursework or internships.
- Demonstrated ability to apply scientific principles to plan analytical work, interpret data, investigate atypical results, and recommend technical next steps.
- Hands-on experience with analytical biochemistry, chromatography, electrophoresis, protein characterization, or comparable biologics testing.
Preferred Qualifications:
- Experience with Waters chromatography systems and Empower software.
- Experience with Maurice, Compass, ELISA, qPCR, or comparable analytical platforms.
- Experience with analytical method development, qualification, or transfer.
Position Type/Expected Hours of Work:
This role is a full-time onsite position in Tustin, CA. Days and hours of work are Monday through Friday 8:00 a.m. to 5:00 p.m. unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, 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 $70,304 to $80,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
- You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
- Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
- You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
- You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
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 25 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.
Skills Required
- Bachelor’s degree in biology, biochemistry, chemistry, biotechnology, pharmaceutical sciences, or a related scientific field.
- One or more years of relevant hands-on experience in process development, quality control, biologics characterization, or a related analytical laboratory, or equivalent experience through advanced scientific coursework or internships.
- Ability to apply scientific principles to plan analytical work, interpret data, investigate atypical results, and recommend technical next steps.
- Hands-on experience with analytical biochemistry, chromatography, electrophoresis, protein characterization, or comparable biologics testing.
- Experience with Waters chromatography systems and Empower software.
- Experience with Maurice, Compass, ELISA, qPCR, or comparable analytical platforms.
- Experience with analytical method development, qualification, or transfer.
Avid Bioservices Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Avid Bioservices and has not been reviewed or approved by Avid Bioservices.
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Healthcare Strength — Health coverage includes medical, dental, and vision alongside life and disability insurance. Plan breadth is presented as solid, with health benefits frequently highlighted as a strong element of the package.
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Equity Value & Accessibility — An Employee Stock Purchase Plan with a discounted purchase feature and the availability of stock grants provide accessible ownership opportunities. These components add long-term value beyond base pay.
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Fair & Transparent Compensation — Pay ranges are posted for some roles, offering upfront clarity on expected compensation. This transparency supports clearer expectations during hiring.
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The Company
What We Do
Avid Bioservices is transforming the CDMO experience, with more than 30 years of unrivaled experience manufacturing biologics, and world-class mammalian protein facilities. We’ve produced more than 250 commercial batches, and 5 commercial products marketed in 90+ countries. For more than 10 years, we’ve maintained a flawless quality track record which we’re committed to uphold. We do it right the first time, which saves money and time. From early-stage to late-stage, concept to market, every part of our process is personalized. We’re your advocates, your trusted experts, your true partners.
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