Biomanufacturing Associate - Downstream

BioTalent; Tustin (CA); On-site; USD 30,000 - 47,000; Full time

Benefits offered by this job

Hourly pay

Bonus

Equity

Comprehensive benefits

Training provided

Cross-functional teamwork

Job summary

BioTalent in California is seeking a Biomanufacturing Associate, Downstream to support purification of biological products in a GMP environment. You will operate chromatography systems, perform TFF and sterile filtration, and help prepare buffers for production.

The role includes completing GMP batch records and supporting aseptic manufacturing in cleanrooms. Ideal candidates bring hands-on downstream experience (chromatography, filtration, purification) and a strong attention to quality.

Qualifications

• 4 months of experience in biopharmaceutical manufacturing.
• Experience in a GMP-regulated environment.
• Hands-on downstream processing, chromatography, filtration or related purification techniques.

Responsibilities

• Operate chromatography systems and purification equipment.
• Perform Tangential Flow Filtration (TFF) and sterile filtration processes.
• Prepare buffers and production materials.
• Complete GMP documentation and batch records.
• Support aseptic manufacturing in cleanroom environments.
• Maintain equipment and contribute to continuous manufacturing operations.

Job description

Now Hiring: Biomanufacturing Associate, Downstream

Are you passionate about biopharmaceutical manufacturing and ready to make an impact on patients' lives? Join a leading CDMO specializing in the development and manufacturing of biologics for clinical and commercial programs.

You'll be responsible for the purification of biological products while working with advanced downstream processing technologies in a cleanroom environment.

We're looking for candidates with:

4 months of experience (academic / professional) in biopharmaceutical or biotech manufacturing

Experience in a GMP-regulated environment

Hands-on experience (academic / professional) with downstream processing, chromatography, filtration, or related purification techniques

Strong attention to detail and commitment to quality

What you'll do:

Operate chromatography systems and purification equipment

Perform Tangential Flow Filtration (TFF) and sterile filtration processes

Prepare buffers and production materials

Complete GMP documentation and batch records

Support aseptic manufacturing in cleanroom environments

Maintain equipment and contribute to continuous manufacturing operations

• Hourly pay, bonus, equity, and comprehensive benefits.
• Training will be provided
• Work on impactful products in a regulated, high-quality environment
• Collaborate with cross-functional global teams
• Grow your career in a dynamic and innovative organization

Work Authorization:

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time