Manufacturing Associate IV - Lead

Matica Biotechnology is at the forefront of biopharmaceutical research and development. The Matica Bio team brings an average of 15 years of cell and viral vector manufacturing experience to the development and manufacture of advanced therapy products. At our purpose-built GMP facility in College Station, Texas, we provide rapid development and scale-up of cell and gene therapies, vaccines, and oncolytics meeting worldwide regulatory compliance.

The true value of a CDMO is determined by the quality of its people. Matica Bio consists of a dedicated team of experts. We’re a cell and gene therapy CDMO powered by people, and our people provide real benefits to the quality, safety and speed of the cell and gene therapy development pathway. Our inventive thinking and foresight help us strategize the best path to take therapies from the lab to the market.

Come join our dedicated team and make it happen with Matica Bio!

The Manufacturing Associate IV – Lead will execute the daily manufacturing schedule communicated by the Manufacturing Management, lead the manufacturing staff on the floor, and lead operations and act as the main point of contact within the cleanroom.

• Execute the daily manufacturing schedule communicated by the Manufacturing Management to include but not limited to cell expansion, bioreactor operations, and/or purification techniques (TFF and chromatography).
• Lead operations and act as the main point of contact within the cleanroom.
• Lead the manufacturing staff on the floor and make real‑time production decisions as required.
• Read and understand technical documentation and execute written instruction.
• Possess an advanced understanding and ability to put into practice cGMP principles.
• Possess advanced operational skills, troubleshooting skills, and advanced knowledge within an aseptic environment, biological safety cabinet to execute such processes as cell expansion, cell banking, filling, filtration, and column chromatography.
• Possess the ability to train junior‑level manufacturing associates.
• Plan, organize, and maintain material inventory for manufacturing processes and ensure all materials are kitted for upcoming cleanroom operations.
• Clearly communicate problems and observations with management from other departments.
• Ensure clean rooms are cleaned, organized, maintained, and audit‑ready at all times.
• Maintain an individual training plan and ensure your training profile remains up‑to‑date with training readiness at all times.

• AS/BS in Biotechnology, Biology, Chemistry, or equivalent
• Preferred area of study:
  Science‑related discipline
• High school diploma or equivalent may be considered

• 3–4 years of experience in manufacturing (minimum 4 years of experience without AS/BS)
• GMP setting preferred
• Previous upstream and/or downstream experience preferred

• Advanced knowledge of aseptic practices and clean‑room operations
• Advanced knowledge of the manufacturing process and ability to use the latest technologies
• Advanced knowledge of GMP, FDA, and EMA regulatory requirements applicable to biologics—including gene/viral therapy products focusing on upstream/downstream operations

• Proven logic and decision‑making abilities, critical thinking skills
• Computer software skills, organization, record‑keeping and planning skills, multiple projects and time management

• Leadership, diplomacy abilities
• Strong communication ability in both written and oral formats
• Strong desire and ability to work collaboratively as part of a team
• Possess independent work skills and a strong work ethic

Commitment to excellence, problem solving/decision making/analytical thinking, communication skills, teamwork/cooperation/supportiveness, flexibility/adaptability, initiative/taking ownership, focus on safety, ethical/trustworthiness, work ethic/reliability, thoroughness, customer service.

• Start with safety & quality
• Choose the path of openness, honesty, and integrity
• Nurture our differences to enable our collective success
• Learn continuously to ensure our value and relevance
• Commit to delivering life‑altering therapies

Mid‑Senior level

Full‑time

Research, Analyst, and Information Technology