Associate Scientist, Analytical Development
About this role
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.
- 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 have also have experience with protein characterization, electrophoresis, chromatography, and assay validation/qualification.
- 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.
Company at a glance
Avid Bioservices is a biologics CDMO and partner focused on delivering quality, speed, and predictability from DNA to CGMP.
We support biotech and pharma companies across the full development lifecycle, with integrated capabilities in cell line development, process development, and CGMP manufacturing for clinical and commercial supply.
Our platforms are intentionally aligned from early development through manufacturing, enabling seamless tech transfer and reducing risk as programs scale.
Our approach is built on predictable delivery. We combine rapid timelines with disciplined execution, giving our partners confidence in both speed and outcomes.
With transparent communication and strong program management, our teams operate as an extension of our clients - ensuring clarity, accountability, and momentum at every stage.
Quality underpins everything we do. We have a strong regulatory track record and a commitment to operational excellence that enables consistent, reliable results from early-phase programs through commercial production.
Our U.S.-based facilities provide a trusted, scalable manufacturing environment.
At Avid, our services are designed to solve a single problem: how to move biologics programs forward quickly and reliably without compromising quality. By aligning our capabilities, platforms, and teams around that goal, we help our partners accelerate development and deliver therapies to patients with confidence.
Top Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- 401(k) Matching
- Paid Time Off
- Performance-based Bonuses
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