Sr. Manufacturing Associate, Downstream
About this role
Your Role:
Key Responsibilities:
- Support in prioritizing manufacturing schedule requirements and responsible for executing the daily manufacturing schedule within a fast-paced manufacturing operation with primary activities of virus purification techniques virus purification techniques virus purification techniques virus purification techniques including but not limited to Harvest, Clarification, Purification Techniques (TFF and Chromatography), Various Filtration Techniques, and Product Filling.
- Troubleshoot equipment and processes in partnership with Manufacturing Science and Technology department.
- Conduct analytical tests such as osmolality, pH and conductivity in addition to filter integrity testing.
- Clearly communicate problems and observations with management from manufacturing and other departments.
- Possess the ability to train junior level manufacturing associates.
- Ensure the timely setup of equipment and materials for each production run.
- Plan and prepare all necessary resources for various processes and activities.
- Assist in other production areas as needed.
- Demonstrate exceptional aseptic techniques with precise, deliberate movements.
- Ensure cleanrooms are cleaned, organized, maintained and audit ready at all times. Maintain department inventory and ensure all materials are kitted for upcoming cleanroom operations.
- Plan, organize and maintain material inventory for manufacturing processes.
- Comply with Good Manufacturing Practices (GMP) documentation standards.
- Demonstrate initiative to revise and initiate Batch Production Records, Standard Operation Procedures, study protocols, and reports.
- Attend meetings, participate in continuous improvement projects. Demonstrate strong technical writing abilities (Deviation initiations, Sops, Logbooks, Working Instructions, Forms creation, etc.).
- Prepare media and buffer solutions critical for production processes.
- Adhere to cGMPs (and/or ISO standards) is always required during the manufacture of Bulk Drug products, Final Drug substances and research products. Own the quality of what they deliver and is responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions.
- BS in Biotechnology, Biology, Chemistry, or equivalent preferred. Preferred area of study: biochemistry or biology.
- 2+ years of experience in GMP manufacturing of biologics, previous experience in downstream process is essential.
- Proven logic and decision-making abilities, critical thinking skills. Aseptic practices and clean room operations:
- Advanced knowledge of GMP, FDA and EMA regulatory requirements applicable to Biologics including Gene/Viral therapy products focusing on Downstream Operations.
- Advanced knowledge of the manufacturing process and possesses the understanding of or ability to use the latest technologies.
The compensation range for this role is $23.46 - $29.32 hourly annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
- 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?