Bioprocess Research Associate - Downstream

Job Summary:

We are seeking a Bioprocess Research Associate - Downstream to support laboratory process development activities in a pharmaceutical, biotechnology, or life sciences environment. The ideal candidate will have hands-on laboratory experience and a strong background in downstream processing, supporting process development, optimization, and manufacturing operations.

Key Responsibilities:

• Execute laboratory experiments to support process development activities under the guidance of senior scientists.
• Perform downstream processing experiments, including centrifugation, filtration, and chromatography.
• Prepare buffers, media, and laboratory solutions following established procedures.
• Operate, clean, calibrate, and maintain laboratory equipment.
• Accurately document experimental procedures, observations, and results in laboratory notebooks and electronic systems.
• Analyze experimental data and prepare technical reports and presentations.
• Follow all laboratory safety, GMP, and quality procedures.
• Collaborate with cross-functional teams to support process development and technology transfer activities.

Required Qualifications:

• Bachelor's degree in Life Sciences, Biotechnology, Biochemistry, Chemical Engineering, Biomedical Engineering, or a related scientific discipline.
• Hands-on laboratory experience in the pharmaceutical, biotechnology, or life sciences industry (academic or industry).
• Required experience with downstream processing techniques, including centrifugation, filtration, and chromatography.
• Experience preparing laboratory buffers and solutions.
• Strong analytical, organizational, and problem-solving skills.
• Excellent written and verbal communication skills.
• Ability to work independently and collaboratively in a fast-paced laboratory environment.
• Ability to lift up to 20 lbs.

Preferred Qualifications:

• Experience with viral vectors, biologics, cell and gene therapy, vaccines, or protein purification.
• Familiarity with GMP/GLP laboratory practices and documentation.
• Experience supporting process development, scale-up, or manufacturing operations.