Bioprocess MFG Associate (BPA)

Bioprocess MFG Associate (BPA) at Vector BioMed, Inc. Bioprocess MFG Associate (BPA) at Vector BioMed, Inc. in Washington Grove, Maryland Posted in 8 days ago.

Type:

full-time

Job Description:

About the Role Vector BioMed is building world-class capabilities to serve the rapidly expanding cell and gene therapy market. We are seeking a Bioprocess Associate to support the manufacture of high-quality lentiviral vectors for research, preclinical, and clinical applications. This role plays a key hands-on and mentoring function in a dynamic, GMP-compliant manufacturing environment. Key Responsibilities Bioprocess Manufacturing

• Execute and oversee lentiviral vector (LVV) production, including cell culture, purification, fill-finish, and formulation.
• Operate, monitor, and maintain bioreactors, filtration systems, chromatography systems, and related bioprocess equipment.
• Perform in-process testing, troubleshooting, and real-time issue resolution to ensure product quality and on-time execution. Process Improvement & Technology Transfer
• Analyze process data to identify trends, risks, and opportunities for improvement.
• Implement process optimizations to improve yield, purity, efficiency, and robustness.
• Support process scale-up and technology transfer activities. GMP Compliance & Documentation
• Perform all activities in compliance with cGxPs and regulatory guidelines.
• Accurately execute and finalize batch records, logbooks, and equipment documentation.
• Own and drive deviation investigations, CAPAs, change controls, and GMP document preparation and review. Training & Collaboration
• Mentor and train junior bioprocess associates in best practices, safety, and GMP behaviors.
• Contribute to procedure writing, training programs, and cross-functional improvement initiatives. Materials, Equipment & Inventory
• Support ordering, receipt, and inventory management of raw materials, reagents, and consumables.
• Take ownership of assigned equipment, including maintenance, calibration, validation, and documentation.
• Coordinate with Materials Handling and external vendors to ensure uninterrupted operations. Qualifications Required
• Bachelor's degree in science or engineering.
• Minimum 5 years of bioprocessing experience in biotech/pharma cGMP environments, with upstream and/or downstream manufacturing.
• Strong knowledge of GMP regulations, quality systems, and aseptic processing.
• Hands-on experience with bioprocess equipment (cell culture, chromatography, filtration, fill-finish).
• Demonstrates right-first-time mindset, problem-solving ability, attention to detail, and teamwork skills.
• Proficiency with Microsoft 365 (Word, Excel, PowerPoint, Teams, Point). Preferred
• Direct experience with mammalian production systems and viral vector is key; experience in plasmid production also desired.
• Experience with single-use systems and control systems.
• Willingness to cross-train across upstream and downstream operations.
• Strong communication, presentation, and organizational skills. Physical Requirements
• Ability to move up to 50 lbs.
• Ability to work in a GMP manufacturing and laboratory environment, including standing for extended periods and handling biological materials.
• Ability to qown qualify for Grade A/B areas (fill-finish).

What We Offer Competitive salary and comprehensive benefits package, including annual bonus. Opportunities for learning, growth, and career advancement. A collaborative, highly motivated team at the forefront of cell and gene therapy innovation. Use of on-site gym facility. Salary range $70k - $100k per year.