Analyst; HPLC), Quality Control

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. Join a passionate team dedicated to developing and manufacturing life‑saving biopharmaceuticals.

The Analyst (HPLC), Quality Control will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment. This position requires a strong background in HPLC and supports/leads continuous improvement initiatives.

• Perform and review routine assays for HPLC and CE with strict adherence to written analytical test procedures.
• Perform aseptic sampling, visual inspection, gowning and working in clean room areas, 5S methodology.
• Review, revise and write test methods, standard operating procedures and perform trending analysis.
• In addition to performing QC testing, the Analyst may be designated as study lead for validation projects, investigations and method development projects.
• Other functions include writing study protocols and reports, training other analysts, and working with other departments in developing, revising and implementing QC procedures and policies.
• Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions.
• Participate in regulatory inspections to ensure laboratory is in compliance with current Good Manufacturing Practices.
• Demonstrate and provide evidence to FDA officials that the laboratory operations conform to code of federal regulation.
• Support continuous improvement initiatives by ensuring training relating to test methods and standard operating procedures are up to date to comply with current Good Manufacturing Practices.
• Utilize instruments software to perform calculations to minimize errors and eliminate time allocation for manual calculations.
• Perform other duties as assigned.

• BS in chemistry, biology or related field plus 2-4 years industry experience in a QC or analytical lab, or equivalent combination of education/experience.
• Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential.
• Strong HPLC, analytical biochemistry and chemistry experience.
• Experience with protein characterization, electrophoresis, chromatography (normal phase, reverse phase, size exclusion, ion exchange, etc), aseptic techniques, assay and validation/qualification.

This role is a full‑time onsite position. Days and hours of work are Monday through Friday, 8:00 am to 5:00 pm PST unless otherwise specified by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.

Compensation for this role is competitively structured, including 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 is $25.76 to $32.21 per hour annually depending on experience and qualifications.

• 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 clear and confident.
• You possess exceptional multitasking skills and an unparalleled attention to detail.
• You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors or suppliers.

This dynamic role requires regular activities such as sitting, standing and walking, with occasional tasks that involve lifting objects up to 25 pounds. The work environment may expose individuals to electrical shocks, toxic chemicals, vibrations or loud noise levels. Reasonable accommodations are available to enable individuals with different abilities to perform effectively. Visual acuity, including close, distance and color vision, is essential.