.png){kind=logo}
Manufacturing Associate supporting downstream biopharmaceutical production in a GMP, aseptic cleanroom environment. Responsibilities include operating chromatography equipment, purifying antibodies and enzymes, filtration, buffer and media preparation, equipment setup and maintenance, batch documentation, inventory management, cleaning, calibration, and autoclave operation. The role also supports filling, media fills, SOP and batch record revisions, filter integrity testing, and independent manufacturing projects.
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!
Key Responsibilities:
- 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 onsite position. Days and hours of work are Monday through Friday 8:00 a.m. to 5:00 p.m. unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.
Compensation:
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.
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.
Avid Bioservices Tustin, California, USA Office
14191 Myford Rd, Tustin, California, United States, 92780 7020
Similar Jobs
Healthtech • Pharmaceutical
Performs downstream biopharmaceutical manufacturing in a GMP and aseptic cleanroom environment. Responsibilities include preparing equipment, materials, media, and buffers; operating chromatography skids; purifying antibodies and enzymes; managing filtration, filling, inventory, documentation, equipment maintenance, and batch records; and maintaining production areas. The role also supports process qualifications, filter integrity testing, autoclave operation, and assigned improvement projects.
Top Skills:
Affinity ChromatographyArs Frontier AutoclaveAseptic ProcessingBioprocess Chromatography SkidsCgmpCleanroom TechnologyGmpHydrophobic Interaction ChromatographyIon Exchange ChromatographySartocheck 3/4 Filter Integrity TesterSize Exclusion ChromatographySterile FiltrationTangential Flow FiltrationUltrafiltrationViral Filtration
Healthtech • Pharmaceutical
Executes downstream biologics manufacturing in a viral vector facility, including harvesting, clarification, TFF, chromatography, filtration, filling, buffer preparation, and analytical testing. Troubleshoots equipment and processes, maintains cleanrooms and inventory, completes GMP documentation, supports deviations and SOPs, and ensures regulatory compliance. Trains junior associates, communicates production issues, prepares resources, and contributes to continuous improvement while maintaining aseptic practices and product quality.
Top Skills:
Aseptic ProcessingCgmpChromatographyCleanroom OperationsConductivity TestingEmaFdaFilter Integrity TestingFiltrationGmpIsoOsmolality TestingPh TestingTangential Flow Filtration (Tff)Viral Vector ManufacturingVirus Purification
Healthtech • Pharmaceutical
Performs downstream biopharmaceutical manufacturing in a cGMP cleanroom environment. Responsibilities include preparing equipment, materials, media, and buffers; operating chromatography skids and columns; purifying antibodies and enzymes; managing filtration, aseptic processing, filling, cleaning, and autoclave operations; calibrating instruments; maintaining inventory; completing GMP documentation; and supporting batch records, SOPs, reports, and independent projects.
Top Skills:
Affinity ChromatographyArs Frontier AutoclaveBioprocess Chromatography SkidsCgmpGmpHydrophobic Interaction ChromatographyIon Exchange ChromatographySartocheck 3/4 Filter Integrity TesterSize Exclusion ChromatographySterile FiltrationTangential Flow FiltrationUltrafiltrationViral Filtration
What you need to know about the Los Angeles Tech Scene
Los Angeles is a global leader in entertainment, so it’s no surprise that many of the biggest players in streaming, digital media and game development call the city home. But the city boasts plenty of non-entertainment innovation as well, with tech companies spanning verticals like AI, fintech, e-commerce and biotech. With major universities like Caltech, UCLA, USC and the nearby UC Irvine, the city has a steady supply of top-flight tech and engineering talent — not counting the graduates flocking to Los Angeles from across the world to enjoy its beaches, culture and year-round temperate climate.
Key Facts About Los Angeles Tech
- Number of Tech Workers: 375,800; 5.5% of overall workforce (2024 CompTIA survey)
- Major Tech Employers: Snap, Netflix, SpaceX, Disney, Google
- Key Industries: Artificial intelligence, adtech, media, software, game development
- Funding Landscape: $11.6 billion in venture capital funding in 2024 (Pitchbook)
- Notable Investors: Strong Ventures, Fifth Wall, Upfront Ventures, Mucker Capital, Kittyhawk Ventures
- Research Centers and Universities: California Institute of Technology, UCLA, University of Southern California, UC Irvine, Pepperdine, California Institute for Immunology and Immunotherapy, Center for Quantum Science and Engineering
