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Transforming the CDMO experience: Unrivaled expertise. Worldclass facilities. Exceptional quality. Personalized process.
The Role
Performs in-process quality control testing and sampling in a GMP biopharmaceutical manufacturing environment. Responsibilities include compendial testing, buffer and reagent preparation, aseptic sampling, endotoxin and water testing, raw material analysis, lot release, stability and validation testing, investigations, data reporting, procedure development, and analytical instrument troubleshooting.
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 Quality Control In-Process Analyst will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment for the Quality Control In-Process team.
- 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.
Minimum Qualifications:
- 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.
Position Type/Expected Hours of Work:
- This is a full-time position operating Sunday through Wednesday 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.
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 $25.77 to $32.21 hourly, 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.
Skills Required
- Bachelor's degree or 2-4+ years of biotech industry experience in a QC or analytical laboratory
- Experience with analytical testing
- Experience writing reports
- Experience with GMPs
- Experience with regulatory audits
- Experience with most or all listed methodologies, including aseptic sampling, endotoxin, pH, conductivity, osmolality, A280, water testing, and raw material testing
- Experience with basic maintenance and troubleshooting of analytical instrumentation
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.
