Matica Biotechnology, Inc. · 1 month ago
Analyst III, Quality Control
College Station, TX
Full-time
Hybrid
Mid Level
3+ years expMatica Biotechnology is at the forefront of biopharmaceutical research and development, providing rapid development and scale-up of cell and gene therapies. The Analyst III, Quality Control will be responsible for carrying out quality control assays, maintaining compliance with regulations, and collaborating with cross-functional teams to ensure high-quality production of therapies.
BiotechnologyHealth CareManufacturingMedicalPharmaceutical
Responsibilities
Carry out Quality Control Assays for Client specific processes with a high degree of accuracy and independence
Record test results, document processing steps on Quality Control Assays while adhering to good documentation practices (GDP)
Perform testing in conjunction with laboratory investigations and deviations
Participate in various special projects according to the needs of the department
Independently draft procedures and / or operating manuals
Participate in the qualification and calibration of laboratory instruments, as needed
Collaborate with cross-functional teams to resolve complex method development challenges
Train QC personnel as appropriate
Perform and maintain routine inventory
Interface with Analytical Development (AD) to transfer, train, and qualify analytical methods
Responsible for participation in internal audits, client audits and agency inspections of the site
Execute method qualification and validation, tech transfer, and verification testing autonomously
Support internal and external cGMP manufacture and supply of high-quality cell and gene therapy products including in-process testing, QC release and stability data analyses and method data trending, deviations, out of specification investigations, and Certificates of Analysis creation
Maintain current knowledge base of regulations, corporate policies, and industry best practices, trends, and standards to ensure Quality Control functions remain in compliance with applicable company requirements and global regulations
Proactively ensure lab is maintained (organized, clean, & properly supplied)
Observe and report any safety issues
Communicate with QC leadership and personnel any improvement ideas for processes
Ability to communicate effectively and work 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
Qualification
Required
BS/BA or greater in sciences, preferably in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related technical field
Or 7+ years related GMP experience in Biotechnology, Chemistry, Biochemistry, Microbiology, pharmaceutical, manufacturing or laboratory environment
3+ years related GMP experience in biotechnology, chemistry, biochemistry, microbiology, pharmaceutical, manufacturing or laboratory environment
Ability to interpret cGMPs and apply to non-routine situations
Demonstrated leadership, technical aptitude, and problem-solving skills
Must be flexible and able to manage and prioritize multiple tasks and assignments
Must have excellent verbal and written communication skills and comfortably and clearly articulate issues with peers and colleagues at all levels in the organization
Demonstrated capability in cross function team environment, working collaboratively with others in effective ways which attain goals while encouraging teamwork and synergies throughout the organization
Demonstrated capability in coaching and development of personnel
Capable of high through-put and high quality, Right the First-Time work
Ability to make informed and timely decisions independently
Highly motivated in the QC field with sustained performance and accomplishments
Ability and experience in turning around and remediating compliance challenges
Diplomacy, negotiation skills, written and oral communication, team building skills, independent work skills, strong work ethic, coaching, delegating skills
Preferred
Any of the following experience is desired: ddPCR, qPCR, Microscopy, ELISA, HPLC and Flow Cytometry
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
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