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Avid Bioservices

Manufacturing Associate, Downstream (Sunday - Wednesday)

Tustin · On-site$20 – $27
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About this role

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:
Join our dynamic team as a Manufacturing Associate, Downstream! In this role, you'll be a crucial part of our multi-product manufacturing facility, working in strict compliance with cGMP and Standard Operating Procedures. Your responsibilities will encompass various tasks, including production, meticulous documentation, report writing, materials procurement, and equipment scheduling. You'll be instrumental in ensuring the timely production and release of top-quality products. At our company, we value core principles such as Integrity, Adaptability, Innovation, Teamwork, and Passion, all united by a shared mission to enhance patients' lives through the consistent delivery of high-quality biopharmaceuticals. If you're ready to make a meaningful impact, apply now and be part of our journey!
  • Ensuring the timely setup of equipment and materials for each production run.
  • Planning and preparing all necessary resources for various processes and activities.
  • Operating and diligently maintaining BioProcess chromatography skids.
  • Proficiently handling the packing, unpacking, and cleaning of production-scale chromatography columns.
  • Executing antibody and enzyme purification techniques using Affinity chromatography, Size Exclusion chromatography, Ion Exchange chromatography, Hydrophobic Interaction, and Tangential Flow Filtration (TFF).
  • Conducting pH and conductivity meter calibration and testing.
  • Managing product filtration processes, including sterile filtration, ultrafiltration, and viral filtration.
  • Demonstrating exceptional aseptic techniques with precise, deliberate movements.
  • Participating in product filling, including aseptic processing and media fill qualifications.
  • Upholding the cleanliness and maintenance of cleanroom facilities and equipment.
  • Monitoring and controlling raw material inventory levels.
  • Ensuring compliance with Good Manufacturing Practices (GMP) documentation standards.
  • Taking the initiative to revise and initiate Batch Production Records, Standard Operation Procedures, study protocols, and reports.
  • Leading and managing independent projects as assigned, contributing to the overall success of the manufacturing team.
  • Skillfully preparing media and buffer solutions critical for production processes.
  • Conducting manual cleaning of small parts and equipment to maintain hygiene and efficiency.
  • Performing thorough filter integrity testing using specialized equipment like the Sartocheck 3/4 Filter Integrity Tester.
  • Operating and ensuring the proper maintenance of the ARS Frontier Autoclave.
Minimum Qualifications:
  • 2+ years of related experience and/or training; or equivalent combination of education and experience.
Preferred Qualifications:
  • Bachelor’s or Associate degree (A.A.) with a preference for Biology or Chemistry emphasis.
  • 2+ years of experience with large-scale liquid chromatography columns or similar equipment.
  • 1+ years of related experience in the life sciences industry.
  • Proficiency in working within a GMP production environment with aseptic techniques.
  • Capability to gown for a class 10,000 cleanroom environment and work under aseptic conditions in a class 100 environment.
Position Type/Expected Hours of Work:
This role is a full-time position with a Sunday through Wednesday schedule, working 10 hours each day (4 days x 10 hours), with operating hours from 7:00am to 6:00pm. During the initial training period, working days and hours will be Monday through Friday 7:00am to 4:00pm.
Compensation:
We offer competitive compensation packages for this role, including a base salary, equity grants, 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 $21.53 - $26.92 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
We understand the importance of attracting and retaining top talent. The expected base pay range for this position is ($21.53 - $26.92 hourly) plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being.
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.

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.

Founded2002
Team Size201-500 employees
WorkspaceOn-site
IndustryPharmaceutical Manufacturing
Location
Tustin, California, United States
Websiteavidbio.com
LinkedInLinkedIn

Top Benefits

  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • 401(k) Matching
  • Paid Time Off
  • Equity Grants
  • Performance-based Bonuses

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