Associate Scientist, Analytical Development

avidbio; Tustin (CA); On-site; USD 91,300 - 100,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

401(k) matching

Paid time off

Performance-based bonuses

Job summary

Avidbio in Tustin, California is seeking an Associate Scientist in Analytical Development. This role involves developing ELISA, HPLC, and cell-based methods while collaborating with scientific teams and external clients.

The successful candidate should hold a BS degree and have over 5 years of experience in the biotech industry, specifically in analytical testing. The position offers competitive compensation, career growth, and a supportive work environment.

Qualifications

• 5+ years of biotech industry experience working in a QC or analytical lab.
• Experience with GMPs and regulatory audits required.
• Ability to perform and review routine wet chemistry and analytical methods.

Responsibilities

• Perform and review routine wet chemistry, ELISA, and cell-based immunoassays.
• Develop, review, and revise test methods and SOPs.
• Support continuous improvement initiatives.

Skills

Analytical testing

HPLC

ELISA

Cell-based assays

Protein characterization

Statistical analysis

Education

BS degree in Biochemistry, Chemistry, Biology or related field

Tools

HPLC

Electrophoresis (SDS-PAGE/CE)

Laboratory equipment

Job description

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 Associate Scientist, Analytical Development will have the opportunity to focus on developing cell-based, ELISA, HPLC, and/or CE methods and will work alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. This position offers the chance to interface with Quality Control as methods are transferred into that group for cGMP testing, as well as to interface with external clients. The Associate Scientist will perform testing and sampling to support validation, process development, and stability studies in a non-GMP and GMP environment. They will have a substantial understanding of the job and apply knowledge and skills to complete a wide range of tasks, as well as support and lead continuous improvement initiatives.

Key Responsibilities

• Perform and review routine wet chemistry/ELISA/cell-based immunoassays, electrophoresis (SDS-PAGE/CE) and/or HPLC.
• Must use scientific reasoning when making decisions regarding the quality of the data reported. Expected to research/gather information without supervision and to make scientifically sound decisions based on knowledge and experience.
• May train/supervise the experimental work of more junior analysts and may be a member of interdepartmental/tech transfer teams.
• Develop, review, revise and write test methods, standard operating procedures and may perform trending analysis. May be designated as study lead for validation projects, investigations, and method development projects.
• Previous experience in either HPLC, CE or Potency/ELISA assay methodologies is required.
• Knowledge of company cGMPs as well as industry regulations that apply to job functions. Participate in regulatory inspections.
• Support continuous improvement initiatives.
• Other tasks as assigned.

Minimum Qualifications

• BS degree in Biochemistry, Chemistry, Biology or a related field is required.
• 5+ years of biotech industry experience working in a QC or analytical lab.
• Previous experience with analytical testing and equipment utilizing analytical biochemistry methods, writing reports/procedures/specifications, GMPs and regulatory audits required.
• HPLC, CE, or Potency/ELISA experience is essential.
• Should also have experience with protein characterization, electrophoresis, chromatography, and assay validation/qualification.

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 $91,300 to $100,000 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 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.