Analyst III, Quality Control

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.

We’re a 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 lab to market.

This role is looking for a highly motivated QC professional with strong technical expertise and hands‑on experience in analytical methods for cell and gene therapy. The focus will be on flow cytometry, serving as a key contributor to assay qualification/validation and data analysis. As a level 3 team member, you will assist the QC team and operate independently in the day‑to‑day activities of the QC lab.

• Carry out Quality Control assays for client‑specific processes with a high degree of accuracy and independence.
• Record test results and document processing steps on QA assays while adhering to good documentation practices (GDP).
• Perform testing in conjunction with laboratory investigations and deviations.
• Participate in special projects as needed.
• Draft procedures and operating manuals independently.
• Participate in the qualification and calibration of laboratory instruments.
• Collaborate with cross‑functional teams to resolve complex method development challenges.
• Train QC personnel as appropriate.
• Maintain routine inventory.
• Interface with Analytical Development (AD) to transfer, train, and qualify analytical methods.
• Participate in internal audits, client audits, and agency inspections.
• Execute method qualification and validation, tech transfer, and verification testing autonomously.
• Support cGMP manufacture and supply of high‑quality cell and gene therapy products, including in‑process testing, QC release and stability data analyses, method data trending, deviations, out‑of‑spec investigations, and certificates of analysis.
• Maintain current knowledge of regulations, corporate policies, and industry best practices to ensure QC functions remain compliant.
• Ensure the lab is maintained (organized, clean, properly supplied).
• Observe and report any safety issues.
• Communicate improvement ideas for processes to leadership and personnel.
• Communicate effectively in a fast‑paced team environment.
• Maintain a high level of integrity and professionalism when interacting with co‑workers and clients.
• Other duties as assigned by Quality Control Management.

Education

• BS/BA or greater in sciences, preferably in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related technical field.
• Or 7+ years of related GMP experience in biotechnology, chemistry, biochemistry, microbiology, pharmaceutical or manufacturing laboratory environment.

Experience

• 3+ years of related GMP experience in biotechnology, chemistry, biochemistry, microbiology, pharmaceutical, manufacturing or laboratory environment.

Skills

• Ability to interpret cGMPs and apply them to non‑routine situations.
• Demonstrated leadership, technical aptitude, and problem‑solving skills.
• Flexibility to manage and prioritize multiple tasks.
• Excellent verbal and written communication skills and ability to articulate issues clearly.
• Capability to work in a cross‑functional team environment, encouraging cooperation and synergy.
• Capability in coaching and development of personnel.
• Desirable experience in ddPCR, qPCR, microscopy, ELISA, HPLC, and Flow Cytometry.
• Capacity for high throughput and high quality, right‑the‑first‑time work.
• Ability to make informed and timely independent decisions.

Qualities & Attitude

• Highly motivated in the QC field with sustained performance and accomplishments.
• Diplomacy, negotiation, and communication skills, team‑building, independent work, strong work ethic, coaching, delegating, and strong, reliable work ethic.

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

• 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

Quality Assurance