Job Description Summary Under general supervision, this position is responsible for applying standard procedures to ensure test results, including the quality of cGMP laboratory testing processes, are met for final approval and release to laboratory customers. Applies quality methodologies to ensure required outcomes. Job Description PRIMARY DUTIES AND RESPONSIBILITIES Duties and responsibilities regularly performed by and assigned to Quality Specialist levels I, II, and III: Reviews and approves quality control and verifications for the routine testing of biological samples. Ensures thorough test batch review and verifies that all source data meets quality attributes and cGMP regulation conformance prior to result reporting. Approves final test results for release to laboratory customers. Maintains accurate records and documentation as required by established procedures and good documentation practice regulations. Ensures donor, patient, and employee confidentiality. Supports the archival record organization and classification maintenance process. Ensures standard operating procedures (SOPs) are properly followed. Partners with personnel from various departments. Resolves routine problems by following SOPs and escalates as appropriate. Analyzes environmental monitoring. Assists with problem investigations and ensures any temperature and/or humidity issues are addressed. May review equipment re-qualifications and release instrumentation back into the production environment. May review and approve general laboratory equipment calibrations and verifications and ensure acceptance criteria are met. May review and approve critical testing reagents for use in production. Assists with lot changes as directed. May pack and ship supplies and/or specimens. Participates in performance improvement teams and training programs, as required. Assures quality customer service to all customers. Performs all assigned duties in compliance with internal SOPs and external regulations. Brings compliance issues to the attention of management. Maintains good attendance and punctuality per the absence policy. Performs all other duties, at the discretion of management, as assigned. Additional duties and responsibilities regularly performed by and assigned to Quality Specialist levels II and III: Maintains test batches and results in the laboratory information system. Completes constructive investigations and resolves batch review discrepancies. Serves as a resource for moderate complexity corrections and/or clarifications. Provides mentorship, guidance, and training to newer staff. Assists with internal and external audits. May coordinate data collection and evaluation of un-assayed control lots for release. Additional duties and responsibilities regularly performed by and assigned to Quality Specialist level IIIs: Performs responsibilities with minimal instruction for day-to-day operations. Provides advanced cross-departmental and/or cross-site support. Analyzes testing and QC data to identify and/or investigate trends. Resolves a wide range of complex quality and production problems to ensure test results meet all quality attributes prior to release. Assists with workflow coordination. Assists with establishing quality standards for new work practices as required. Assists with investigating and completing CAPA associated deviations. Maintains working knowledge of assay processes performed at the laboratory. May coordinate laboratory proficiency and blind sample challenges. REQUIRED QUALIFICATIONS Education: Bachelor’s degree required. Appropriate state licensure and/or certificate, where applicable, required. Experience: Quality Specialist II: A minimum of 2 years of professional experience working in a cGMP regulated environment required. Quality Specialist III: A minimum of 4 years of professional experience working in a cGMP regulated environment, To Include: previous training experience and comprehensive understanding of laboratory production processes required. PREFERRED QUALIFICATIONS Bachelor’s in biology, chemistry, or other science related degree preferred. Previous experience with adult training concepts and their applications. Trainer Certification preferred. SKILLS AND ABILITIES Must possess the skills and abilities to successfully perform all assigned duties and responsibilities. Must possess strong critical thinking and problem-solving skills. Must be able to maintain confidentiality. Must have proficient computer skills. Must be knowledgeable in computer operation in a Windows environment and able to follow company procedures to resolve issues. Ability to work in a team environment and participate as an active team member. Must be able to understand, follow, and give precise written and verbal instructions, and perform all activities safely. Must be able to read and comprehend written procedures and instructions. PHYSICAL & TRAVEL REQUIREMENTS Lab work environment: Exposure to biological fluids with potential exposure to infectious organisms. Exposure to extreme cold ( ≤ -20⁰C), miscellaneous production chemicals, moving machinery and production equipment. Exposure to high levels of noise on the production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Specific vision abilities required by this job include close vision, distance, color, peripheral vision, depth perception and the ability to adjust focus. Travel: < 5% 5+ hours per shift: Sitting, standing, handling, finger dexterity, pinching 3- 5 hours per shift: Lifting to 40 pounds Up to 3 hours per shift: Walking, climbing, bending, squatting, reaching above shoulders, reaching waist to shoulder, reaching knee to waist, reaching floor to knee, grasping items, carrying/move items up to 40 pounds INTERNAL ADVANCEMENT STATEMENT In order to be considered for advancement to the next Quality Specialist level, employees must possess the required qualifications, skills, and abilities as stated in the job description AND regularly demonstrate the qualities and behaviors commensurate with our CTS mission, vision, and values. The above statements are intended to describe the general nature and level of work performed by people assigned to this job. They are not intended to be an exhaustive list of responsibilities, duties, and skills required of personnel so classified. The job description reflects the general details considered necessary to describe the principal functions of the job identified and shall not necessarily be construed as a detailed description of all the work requirements that may be inherent in the job. Creative Testing Solutions is an Equal Opportunity Employer. Additional Job Details: Shift 1 Sunday to Wednesday 7:00 AM to 3:30 PM Creative Testing Solutions is an equal opportunity employer. EEO/Minorities/Females/Disabled/Veterans Our organization is an equal employment/affirmative action employer. If you need accommodation for any part of the employment process because of a medical condition or disability, please send an e-mail to [email protected] to let us know the nature of your request. A representative will respond to accommodation requests within five business days. Please note that this email is for medical/disability accommodations only and any other inquiries will not receive a response. Please see the below information about applicant rights and our commitment to compliance: Know Your Rights: Workplace Discrimination is Illegal Pay Transparency Nondiscrimination Provision E-Verify Participation Right to Work All candidates who receive a conditional written offer of employment will be required to undergo a pre-employment drug test in accordance with the Company's established guidelines. Creative Testing Solutions is a leading nonprofit blood and plasma donor testing laboratory organization with worldwide impact. Over 900 team members test 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. We have a specialty lab department that performs eye, tissue and organ donor testing, and additional centralized testing as needed. Our Phoenix-based research and development department supports research through sample provision and innovative testing. CTS partners with over 100 healthcare entities and operates seven facilities in Charlotte, North Carolina; Dallas, Texas; Memphis, Tennessee; Phoenix, Arizona; St. Louis, Missouri; San Marcos, Texas; and Tampa, Florida. CTS is a 501(c)(3) organization governed by a board of 13 directors.

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