Biopharma Manufacturing Associate I - GMP & Purification

Bora Biologics USA LLC; Rockville (MD); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive health coverage

Retirement savings plans

Paid time off

Professional development

Employee wellness programs

Employee Assistance Program

Job summary

Bora Biologics USA LLC is seeking a Manufacturing Associate I to support the Protein Purification area and manufacturing of biopharmaceutical material for multiple clinical programs. You will work in the GMP manufacturing suite to ensure materials meet specifications and regulatory requirements.

The role requires a high school diploma or higher with related biopharmaceutical experience or an associate/bachelor’s degree in a related field.

Qualifications

• Education & experience as listed in the Minimum Education section.
• Knowledge of protein purification techniques and GMP documentation.
• Ability to write and revise technical documents and maintain accurate records.

Responsibilities

• Participates in hands-on production in the manufacturing of commercial and clinical material in a GMP environment.
• Performs purification operations including filtration, chromatography, titrations, column packing, TFF and bulk fill.
• Maintains manufacturing area in a clean, neat, and orderly condition at all times.
• Adheres to SOPs and batch records under GMP regulations to document activities clearly and accurately.
• Follows safety policies when working with hazardous materials.

Skills

Protein purification techniques

Technical document writing

Team collaboration

Multi-tasking

Problem-solving

Equipment operation

Safety in GMP environment

Adaptability

Attention to detail

Education

High School Diploma or equivalent

Associate degree in related field (optional with 1 year experience)

Bachelor’s degree in related discipline (no experience)

Tools

SAP

Job description

Bora Biologics USA LLC is seeking a Manufacturing Associate I to support the Protein Purification area and manufacturing of biopharmaceutical material for multiple clinical programs. You will work in the GMP manufacturing suite to ensure materials meet specifications and regulatory requirements.

The role requires a high school diploma or higher with related biopharmaceutical experience or an associate/bachelor’s degree in a related field.