Testing Technologist I

Creative Testing Solutions•San Marcos, TX

19h•Onsite

About The Position

Under direct supervision at the Plasma Testing Laboratory, the Testing Technologist I performs high complexity testing of laboratory samples assigned to the department in a fast-paced laboratory. This role involves operating and maintaining complex testing equipment, documenting and reporting test results in compliance with departmental procedures while meeting established production demands. The technologist performs all assigned tasks with a high degree of quality and proficiency, providing appropriate documentation following CLIA, FDA, EMA, etc. regulatory requirements in a GMP environment. The position receives specific direction from a supervisor and performs work under the general direction of a technical supervisor. Creative Testing Solutions is a leading nonprofit blood and plasma donor testing laboratory organization with worldwide impact, with over 900 team members testing blood and plasma donation samples for all infectious disease markers and screening tests required by the Food and Drug Administration and other applicable regulatory bodies. They also have a specialty lab department that performs eye, tissue and organ donor testing, and additional centralized testing as needed. Their Phoenix-based research and development department supports research through sample provision and innovative testing.

Requirements

Bachelor’s or higher degree in Biology or Chemistry required, or science related degree where education and training meet CFR 493.1489.
CLIA requirements for High Complexity Testing required.
California testing requirements where required by law or SOP.
Appropriate state licensure and/or certificate, where applicable, required.
Must possess High Complexity Testing competencies required by Standard Operating Procedures (SOPs), CLIA, and other applicable regulatory and accrediting bodies required.
Must have knowledge of dilutions, ratios, and other basic laboratory math.
Strong organization skills and legible handwriting are essential.
Must speak, read, and write English.
Must have the ability to apply rational thinking and understanding to carry out detailed written and/or oral instructions, and the capacity to identify and troubleshoot problems within regulatory guidelines and standard operating procedures.

Nice To Haves

Certification as a Medical Technologist (MT)/Medical Laboratory Scientist (MLS), Clinical Laboratory Scientist (CLS) or Medical Laboratory Technician (MLT), Clinical Laboratory Technician (CLT) or equivalent preferred.

Responsibilities

Accurately and consistently performs assigned laboratory test procedures as outlined in established standard operating procedures.
Uses proper techniques for sample handling and processing to ensure the validity of test results.
Conserves laboratory resources by using equipment and supplies as needed to accomplish job results.
Ensures training qualifications for independent testing are current and accurate.
Learns complex concepts, technical specifications, and written procedures utilizing a combination of self-paced and hands-on training techniques.
Adheres to the laboratory's quality control policies: processes controls at defined intervals; evaluates control results; takes appropriate actions to resolve failures, and accurately documents all quality control activities.
Performs instrument calibrations and maintenance according to established schedules and procedures; verifies successful completion prior to testing.
Accurately identifies problems that may adversely affect test performance or reporting of test results.
Maintains technical knowledge of complex automated testing equipment to resolve instrument and analytical errors or testing inconsistencies.
Reviews test result data for accuracy and compliance to standard operating procedures and regulatory standards prior to release.
Recognizes invalid test results, takes appropriate corrective action, and documents all findings.
Follows cGMP regulations and laboratory policies on material handling; make sure reagents/test kits have received dates, expiration dates, and if applicable opened dates.
Inspects, takes inventory, and stores reagents and supplies when needed.
Verifies material expiration dates and takes appropriate actions to limit waste.
Follows GMP for documentation using ALCOA; ensures that regulations pertaining to records, reports, and data integrity policies are met.
Documents all errors and corrective actions taken when test systems deviate from the laboratory's established performance specifications.
Works as a member of a team responsible for completing the Plasma Testing Laboratory daily workload.
Works efficiently to consistently complete heavy workloads while maintaining all quality and safety standards.
Disinfects work areas and empty biohazardous waste.
Follows CLIA, FDA, EMA, and safety guidelines as described in their respective guidelines.
Maintains donor confidence and protects the company by keeping information confidential.
Performs all other duties, at the discretion of management, as assigned.
Works periodic over-time, holidays, or weekends as needed.