Bioprocess MFG Associate (BPA)

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, SharePoint).

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.