Manufacturing Technician II/III - Upstream/Downstream (M-F, 7am-3:30pm)

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.

Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.

• •Execute routine and non-routine production activities according to the manufacturing schedule.
• •Follow cGMP requirements, SOPs, batch records, and solution preparation records.
• •Use the Enterprise Resource Planning (ERP) system to execute transactions accurately and in real-time.
• •Demonstrate and apply aseptic processing techniques.
• •Operate in production areas such as, but not limited to, Pre-culture, USP, DSP, buffer preparation, and Fill Finish.
• •Perform troubleshooting activities within established procedures.
• •Participate in shift handoffs and communicate critical production information.
• •Support off-shift, overtime, and holiday production activities as required.

• •Identify and communicate opportunities for process, procedural, and operational improvements.
• •Participate in continuous improvement initiatives and problem-solving activities.

• •Complete manufacturing documentation accurately and in real time following GDP principles.
• •Review batch records, solution records, logbooks, and forms for completeness and accuracy.
• •Maintain training compliance and ensure

• •Perform routine equipment cleaning and standardization activities.
• •Support product changeovers and manufacturing readiness activities.
• •Assist with equipment, process qualification, and validation efforts.
• •Conduct facility walkthroughs and maintain manufacturing areas in an inspection-ready state.
• •Coordinate equipment and facility issues with Senior and Lead Technicians.

• •Maintain an individual development plan and continuously build technical expertise.
• •Complete annual self-assessments and actively participate in performance development discussions.
• •Demonstrate open-mindedness and self-awareness in receiving and acting upon feedback.

• •Excellent written, verbal, and interpersonal communication skills with ability to effectively communicate across departments.
• •Ability to effectively apply technical expertise and experience to achieve assigned objectives.
• •Working knowledge of and adherence to SOPs, Good Documentation Practices (GDP), and applicable regulatory requirements.
• •Commitment to maintaining compliance with company internal and regulatory (EMA, FDA) policies, processes and procedures.
• •Exceptional attention to detail, strong organizational skills, and a structured, process-driven approach to work.
• •Ability to prioritize tasks and manage multiple

While performing the duties of this job, the employee is required to meet the following physical demands:

• •Regularly sit for long periods of time.

• •Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms
• •Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl

• •Frequently lift and/or move up to 40 pounds

• •Frequently utilize close vision and the ability to adjust focus

• •Frequent