Matica Biotechnology, Inc. · 1 month ago
Scientist III, Process Development - Downstream
Bryan, TX
Full-time
Hybrid
Senior Level
6+ years expMatica Biotechnology, Inc. is at the forefront of biopharmaceutical research and development, specializing in cell and gene therapies. The Scientist III in Downstream Process Development will develop and optimize manufacturing processes, collaborate with project teams, and serve as a technical subject matter expert.
BiotechnologyHealth CareManufacturingMedicalPharmaceutical
Responsibilities
Identify, design, execute and analyze experimental protocols and present results to senior leadership, clients, and team members
Authoring and revision of: SOPs, batch records, data presentations, study design and protocols
Able to lead onboarding and training of new team members and assist in the recruitment and interviewing of potential team members
Serve as an SME for downstream process development AND/OR special equipment for PD
Operate and maintain a variety of lab equipment including but not limited to FPLC, TFF, 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
Lead in the technology transfer process to enable clinical manufacture, using novel processes, within the GMP environment. This may require direct involvement in clinical manufacture as an SME
To assess manufacturing processes supplied by client companies for suitability for GMP manufacture and identify any scale-up requirements/issues
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
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
Qualification
Required
Bachelor's degree minimum in a scientific discipline e.g., Biology, biochemistry, Virology, etc
6+ years in a Process Development role with cGMP experience, in the biotech industry
OR 4+ years in a Process Development role with cGMP experience, in the biotech industry with master's degree or Ph.D
Ability to Identify, design, execute and analyze experimental protocols
Ability to authorize and revise: SOPs, batch records, data presentations, study design and protocols
Ability to operate and maintain a variety of lab equipment including but not limited to FPLC, TFF, scales, tubing welders/sealers and pH/conductivity meters
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
Ability to maintain clean room facilities
Strong work ethic with good written and oral communication
Ability to work collaboratively within a team and across departments
Proactive and self-motivated
Company
Matica Biotechnology, Inc.
Matica Biotechnology, Inc.
51-200 employees
H1B Sponsorship
Matica Biotechnology, Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (2)
2023 (4)
2022 (1)
2021 (1)
Funding
Current Stage
Growth StageLeadership Team
Paul Kim
Chief Executive Officer
Recent News
Precedence Research
2025-11-27
2025-11-04
Company data provided by crunchbase