Analyst (In-Process), Quality Control (Flex)
About this role
- Perform basic compendial test methods without supervision and with strict adherence to written protocols, analyze data and report results.
- Formulate buffers and reagents for the purpose of performing test methods.
- Write and revise test methods and procedures.
- Perform aseptic sampling, endotoxin, pH, conductivity, osmolality, A280 and endotoxin by LAL.
- Perform water testing and raw material sampling and testing.
- Perform QC testing for lot release, stability, development/validation projects, and investigations.
- Other functions include writing study protocols and reports.
- Work with other departments in developing, revising and implementing QC procedures and policies.
- Should be aware of company cGMPs as well as industry regulations that apply to all job functions.
- Perform sample pick up and sample locating without supervision and with strict adherence to written protocols.
- Other duties as assigned.
- Bachelor’s degree or 2-4+ years of biotech industry experience working in a QC or analytical lab.
- Must have experience with analytical testing, writing reports, GMPs, and regulatory audits.
- Experience with most, if not all the methodologies listed above.
- Experience with basic maintenance and troubleshooting of analytical instrumentation is highly desirable.
- This is a full-time position operating Wednesday through Saturday on a 4x10(4 days x 10 hours) schedule.
- Will have an adaptable schedule to accommodate operational and scheduling demands.
- Availability needed for overtime and weekend shifts as necessary.
- 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
Tired of cold applications?
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Know someone who'd be great for this?