Scientist II, Process Development - Upstream

Scientist II, Process Development - Upstream Matica Biotechnology, Inc. - 1.3 Bryan, TX Job Details 20 hours ago Qualifications Research design GMP Project management Bachelor's degree Experimental design Manufacturing company experience Statistical analysis tools Full Job Description 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!

Position Opportunity:

The Scientist II Upstream Process Development is involved in the development and optimization of processes to facilitate manufacturing and meet client requirements. The individual should display strong scientific knowledge and understanding of cell and virus culture, purification, and aseptic technique. This individual will reliably and consistently provide scientific and technical contributions in a team atmosphere working cross functionally with internal departments and external clients. This position is in the Bryan-College Station area. The expectation is to be on site five business days a week or as required. How you will make an impact: Independently execute experimental protocols and provide data analysis.

Authoring and revision of:

SOPs, batch records, data presentations, study design and protocols. Assist in experimental design and provide input with scientifically based reasoning. Operate and maintain a variety of lab equipment including but not limited to automated cell counters, bio-analyzers, microscopes, pumps, bioreactors, scales, tubing welders/sealers and pH/conductivity meters. Maintain lab cleaning procedures to ensure a state of control. Operate and maintain a variety of lab consumables and reagents. Assist in the technology transfer process to enable clinical manufacture, using novel processes, within the GMP environment. This may require direct involvement in clinical manufacturing as an SME. Provide feedback to leadership on the set up, execution and analysis of experimental protocols and technical reports. Provide input for improvements to department methods, documentation, procedures, and safety. Independently research and propose innovative solutions and ideas and share with the department. Able to lead onboarding and training of new team members and assist in the recruitment and interviewing of potential team members. Support Supervisor and leadership by assisting with task including but not limited to budget management (Infor), and scheduling. Maintain good communication across the team and to leadership. Perform other duties as required. As a future Matican you bring: Education Bachelor's degree minimum in a scientific discipline e.g., Biology, biochemistry, Virology, etc. Experience 4+ years in a Process Development role with cGMP experience, in the biotech industry. OR 2+ years in a Process Development role with cGMP experience, in the biotech industry with master's degree or Ph.D. Consideration will be given to relevancy and quality of the job experience. Hands-on experience with suspension cell culture, benchtop scale bioreactor and pilot scale (50L scale). Familiarity with Design of Experiments (DoE) and statistical analysis tools. (e.g. JMP, Minitab) Excellent technical writing, communication, and project management skills. Experience with scale-up and technology transfer to GMP manufacturing Skills Collaborative team player Attention to detail. Ability to wear appropriate PPE. Good verbal and written communication skills Integrity, discretion, and confidentiality Computer software skills, organization, record keeping and planning. Maintain clean room facilities Qualities & Attitude Strong work ethic with good written and oral communication. Ability to work collaboratively within a team and across departments. Proactive and self-motivated.

Competencies we look for:

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 We Value:

Matica's Values are at the forefront of everything we do, our culture, and the decisions we make. 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