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qa specialist iii

CTMC

<div><div>About CTMC
CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, and located in the renowned Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, ETC, and TCR-T. Our expert team collaborates closely with MD Anderson&rsquo;s research and clinical faculty, bringing impactful cell therapies to cancer patients.
In our first year alone, we have filed four INDs, each ahead of schedule, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience, an ambitious biomanufacturing organization that has raised $2 billion in two years, enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results.
Our state-of-the-art, 60,000 sq. ft. facility in the Texas Medical Center is staffed by an integrated team of 94+ industry veterans and scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our mission.
At CTMC, we value our employees and offer a variety of development opportunities within our novel corporate structure. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission. 
Responsibilities (The responsibilities listed are specified as but not limited to):<ul><li>
Perform line-clearance/ change-over activities.</li><li>
Disposition/ Hold/ Rejection of raw materials, starting material and in-house prepared materials.</li><li>
Generate and reconcile in-process and Drug Product labels.</li><li>
Review and approve executed documents related to manufacturing operations, QC and other departments.</li><li>
Initiate deviations, CAPAs and Change Controls associated with Quality Operations practices.</li><li>
Create procedures and practices within Quality Operations to implement quality standards.</li><li>
Partner with other departments to implement and optimize batch records and procedures.</li><li>
Other duties as required.</li></ul>
Qualifications/Skills<ul><li>
Bachelor&rsquo;s degree in a scientific field.</li><li>
3+ yrs experience in a related field, preferably QA or equivalent combination of education and experience.</li><li>
Understanding of Cell and Gene Therapies.</li><li>
Understanding of cGMPs, GLPs and GXPs.</li><li>
Knowledge of local and global regulations.</li><li>
Verbal and written communication skills.</li><li>
Interpersonal and customer service skills.</li><li>
Organizational skills and attention to detail.</li><li>
Time management skills with a proven ability to meet deadlines.</li><li>
Analytical and problem-solving skills.</li><li>
Proficient with Microsoft Office Suite or related software.</li></ul>
Working Conditions, Equipment, Physical Demands
The incumbent in this position works in an office environment. The incumbent in this position will use the following equipment and shall have the following physical demands:
Equipment- Computer, printer, fax, and telephone.
Physical Demands- Prolonged periods of sitting at a desk and working on a computer and must be able to lift up to 15 pounds at times. In addition, ability to sterile-gown and perform activities in the manufacturing suite as well as raw material area when applicable. 
The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act.
The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.</div></div>

QA Specialist III

EFOR

<div>
 
 
 About the Role
 
 
 
 Our consulting firm is placing a driven and detail-oriented QA Specialist II with one of our leading biopharmaceutical clients in Houston, TX. In this role, you will be an integral part of ensuring that manufacturing processes meet the highest quality and regulatory standards. You'll work alongside manufacturing, QC, materials management, and other support functions to uphold cGMP compliance and contribute to the success of a cutting-edge cell and gene therapy product portfolio.
 
 
 
 
 
 If you thrive in a fast-paced biopharmaceutical environment and are passionate about quality, this is the opportunity for you.
 
 
 
 
 
 
 What You'll Do
 
 
 <ul>
 <li>
 Oversee regulatory compliance by confirming that all operations align with ISO/GMP quality system requirements and applicable regulatory guidance.
 </li>
 <li>
 Monitor CAPA and deviation programs, ensuring corrective and preventive actions, as well as minor deviations, are properly tracked and closed.
 </li>
 <li>
 Conduct QA floor walkthroughs to proactively identify compliance gaps and partner with manufacturing and support teams to implement timely resolutions.
 </li>
 <li>
 Provide QA presence during critical manufacturing activities, including in-process monitoring and real-time event management.
 </li>
 <li>
 Review and approve GMP documentation, including Master Batch Records (MBRs) and executed records from QC, manufacturing, and materials management teams to support lot disposition.
 </li>
 <li>
 Perform buffer/media review and release activities as operationally required.
 </li>
 <li>
 Facilitate investigations by applying structured problem-solving methodologies, and assist in driving corrective actions and change controls through to completion.
 </li>
 <li>
 Track and maintain quality records, ensuring data integrity and documentation standards are upheld at all times.
 </li>
 <li>
 Champion a safety-first mindset within the QA Operations team and across manufacturing functional areas.
 </li>
 </ul>
 
 
 
 
 
 What You Bring
 
 
 <ul>
 <li>
 Bachelor's degree in Life Sciences, Engineering, or a related discipline
 </li>
 <li>
 3-5 years of GMP experience in the biologics or pharmaceutical industry
 </li>
 <li>
 Working knowledge of equipment/facilities qualifications in GMP and GDP environments
 </li>
 <li>
 Familiarity with US and EU regulatory frameworks for biopharmaceutical manufacturing
 </li>
 <li>
 Hands-on experience in a biopharmaceutical manufacturing setting
 </li>
 <li>
 Background in equipment, facilities, and/or utilities validation activities
 </li>
 <li>
 Strong foundation in Good Documentation Practices
 </li>
 </ul>
 
 
 
 
 
 Why This Opportunity?
 
 
 
 This placement is with a world-class organization at the forefront of cell and gene therapy manufacturing. You'll be joining a collaborative quality team where your contributions make a direct impact on patient outcomes while gaining invaluable experience in a highly specialized and growing therapeutic area.
 
 
 
 
 
 Interested? Apply today and a member of our team will be in touch to discuss next steps.
 
 
 
 
 
 
 We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability status, veteran status, or any other characteristic protected by law.
 
 
 
 
</div>

Quality Assurance Specialist - Quality Operations

T.D. Williamson

<div>
 
 At TDW we put people first - that means working everyday to ensure the pipelines that run through our communities are operating safely and reliably. What sets us apart is our expertise, experience and commitment.
 
 
 
 
 Each day we dedicate ourselves to treating each other, our customers and our community with care and respect.
 
 
 
 
 Overview
 
 
 
 The Quality Specialist is responsible for ensuring that products and processes meet established quality standards and regulatory requirements. This role supports quality, operations, manufacturing and engineering teams by performing inspections, audits, and documentation reviews to maintain quality compliance. This role also supports engineers and others with testing, failure analysis and data reporting for quality assurance and continuous improvement.
 
 
 
 Key Responsibilities
 
 
 
 
 Primary duties may include, but are not limited to
 
 :
 
 
 <ul>
 <li>
 Perform routine inspections and audits of materials, components, and finished products.
 </li>
 <li>
 Document inspection results and maintain accurate quality records.
 </li>
 <li>
 Assist in identifying and reporting non-conformances.
 </li>
 <li>
 Support calibration and maintenance of QA tools and equipment.
 </li>
 <li>
 Conduct failure analysis (preliminary RCA) to identify primary and direct causes of failure.
 </li>
 <li>
 Collaborate with production and engineering teams to resolve quality issues.
 </li>
 <li>
 Performs other duties as assigned
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 Technical Degree or equivalent experience and 1+ years of experience in a quality assurance or inspection role preferred.
 
 
 </li>
 </ul>
 
 Knowledge, Skills, And Abilities
 
 
 
 <ul>
 <li>
 Understanding of quality principles and inspection techniques.
 </li>
 <li>
 Familiarity with ISO 9001 or similar quality standards.
 </li>
 <li>
 Basic Failure Analysis/ Technical Problem Solving
 </li>
 <li>
 Strong attention to detail and documentation accuracy.
 </li>
 <li>
 Proficiency with Microsoft Office and basic QA software tools.
 </li>
 <li>
 Effective communication and teamwork skills.
 </li>
 </ul>
</div>

Quality Assurance Specialist I

Huyett

<div>Digital Marketing Specialist - Revenue Operations Specialist 
Compensation: Starting pay of $58,000 to $73,000 annually + three performance bonuses a year! 
Location: SOUTH HOUSTON (This is NOT a remote position.)
YOU MUST HAVE HUBSPOT EXPERIENCE TO QUALIFY FOR THIS ROLE
Huyett is a leading B2B master distributor and manufacturer, serving OEMs, distributors, and manufacturers that rely on speed, accuracy, and reliability to keep their operations running. As our digital and sales channels continue to scale, the ability to connect marketing activity directly to revenue outcomes is critical.
The Digital Marketing Specialist &ndash; Revenue Ops Specialist plays a key role in that connection. This position is responsible for leveraging HubSpot as a revenue engine, supporting account‑based marketing (ABM), managing lead and pipeline operations, and ensuring high‑quality data flows across Marketing, Sales Operations, Outside Sales, and E‑Commerce.
This is a hands‑on, systems‑oriented role for someone early in their RevOps career who enjoys building processes, working in HubSpot daily, and enabling sales teams with better data, visibility, and follow‑up. The work directly impacts how Huyett identifies, engages, and converts high‑value accounts&mdash;improving customer acquisition, pipeline efficiency, and long‑term customer lifetime value.
What You&rsquo;ll Do
HubSpot &amp; Revenue Operations<ul><li>
Configure and maintain HubSpot lifecycle stages, lead statuses, deal stages, pipelines, and custom properties aligned to Huyett&rsquo;s revenue process</li><li>
Build, test, and optimize workflows for lead capture, scoring, enrichment, routing, and follow‑up</li><li>
Support marketing‑to‑sales handoff by maintaining SLAs, routing logic, and task/queue automation</li><li>
Document processes and ensure consistent system usage across teams</li></ul>
Account‑Based Marketing (ABM) Support<ul><li>
Build and maintain target account and contact lists based on ICPs, firmographics, and buying roles</li><li>
Support multi‑touch ABM programs (email nurtures, sales follow‑up, reporting) within HubSpot</li><li>
Track account engagement and progression through the funnel to identify sales‑ready opportunities</li></ul>
Data Enrichment &amp; Prospecting<ul><li>
Use ZoomInfo (or similar tools) to prospect and enrich company and contact data</li><li>
Maintain data quality standards including completeness, normalization, and duplicate management</li><li>
Ensure enriched data supports accurate segmentation, routing, and reporting</li></ul>
Campaign &amp; Email Operations<ul><li>
Build and QA email campaigns, landing pages, forms, lists, and CTAs in HubSpot</li><li>
Apply segmentation strategies to deliver relevant messaging to prospects and customers</li><li>
Support designers and content creators by coordinating assets and final campaign setup</li></ul>
Reporting &amp; Funnel Visibility
Create and maintain dashboards and reports covering:
Lead volume and conversion (MQL<ul><li><ul><li> SQL)</li><li>
Pipeline health and opportunity progression</li><li>
ABM engagement and campaign performance</li></ul></li><li>
Deliver regular insights to Marketing, Sales Ops, and leadership to support decision‑making</li></ul>
Cross‑Functional Collaboration<ul><li>
Work closely with Sales Operations, Outside Sales, Marketing, and E‑Commerce teams</li><li>
Support training and adoption of HubSpot processes and reporting</li><li>
Act as a bridge between systems and teams to reduce friction and improve execution</li></ul>
What We&rsquo;re Looking For
Required Qualifications<ul><li>
1&ndash;3 years of hands‑on experience using HubSpot (Marketing Hub required; Sales or Ops Hub a plus)</li><li>
Experience building workflows, lists, properties, and reports in HubSpot</li><li>
Understanding of lead management, pipeline concepts, and marketing automation</li><li>
Strong attention to detail and comfort working with data and systems</li><li>
Ability to follow defined processes while identifying opportunities for improvement</li></ul>
Preferred Qualifications<ul><li>
Experience with ZoomInfo or other data enrichment/prospecting tools</li><li>
Exposure to B2B marketing, ABM, or sales enablement workflows</li><li>
HubSpot certifications (Marketing Software, Sales Software, RevOps)</li><li>
Intermediate Excel or Google Sheets skills</li></ul>
Why This Role Matters at Huyett<ul><li>
Directly supports revenue growth by improving lead quality and sales follow‑up</li><li>
Enables account‑based strategies critical to B2B manufacturing and distribution</li><li>
Improves visibility across the customer journey, from first touch to repeat purchase</li><li>
Establishes Revenue Operations as a scalable competency for the company&rsquo;s next phase of growth</li></ul>
What Success Looks Like<ul><li>
Clean, reliable HubSpot data supporting confident sales outreach</li><li>
Faster, more consistent lead follow‑up from Marketing to Sales</li><li>
Improved conversion rates and clearer pipeline visibility</li><li>
Strong adoption of HubSpot processes across teams</li></ul>
Work Environment: This is a manufacturing plant environment. Exposure to high temperatures, moving machinery, moving equipment, heights and confined spaces.
EEOE: Huyett is an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, disability, or genetic information.
To Learn More About Huyett:<ul><li>
See www.huyett.com to learn about the company&rsquo;s products, services and commercial offerings.</li></ul></div>

Digital Marketing Specialist

Established Virtual Mailbox Provider

Head of Operations (Multi-Site Logistics &amp; Compliance) Company: US Global Mail Location: Houston, TXAbout the Role US Global Mail operates a distributed network of secure mail processing and warehouse facilities across the U.S. We are looking for a Head of Operations to take full ownership of performance across all locations. This is not a maintenance role. You will be responsible for driving measurable improvements in productivity, accuracy, compliance, and cost structure across a multi-site operation. You will work directly with the COO to standardize operations, enforce SOPs, and build a high-performance operational culture.What You&rsquo;ll Own 1. Operational Performance &amp; Productivity<ul><li>Increase throughput per employee across all facilities</li><li>Identify inefficiencies and reduce unnecessary headcount without impacting service quality</li><li>Implement KPIs, dashboards, and accountability systems across locations</li></ul>2. SOP Enforcement &amp; Process Discipline<ul><li>Ensure all locations strictly follow documented SOPs</li><li>Audit operations regularly and close gaps quickly</li><li>Standardize workflows across all warehouses</li></ul>3. Error Reduction &amp; Quality Control<ul><li>Reduce mail handling and processing errors across all facilities</li><li>Build QA processes and implement root-cause analysis systems</li><li>Track and improve accuracy metrics continuously</li></ul>4. Compliance &amp; Mail Handling Standards<ul><li>Ensure strict adherence to USPS Form 1583 requirements and internal compliance processes</li><li>Maintain audit-ready operations at all times</li></ul>5. Facility &amp; Physical Security Oversight<ul><li>Own physical security standards across all locations (access control, surveillance, handling protocols)</li><li>Ensure facilities align with customer expectations and compliance commitments</li></ul>6. Channel Partner &amp; Vendor Operations<ul><li>Improve performance and accountability of partner-operated locations</li><li>Strengthen relationships while enforcing operational standards</li></ul>7. SOC 2 &amp; Operational Compliance (Strong Plus)<ul><li>Lead or support SOC 2 implementation from an operational and warehouse perspective</li><li>Ensure processes, controls, and documentation meet compliance standards</li></ul>What Success Looks Like (First 6&ndash;9 Months)<ul><li>Measurable increase in productivity per location</li><li>Reduction in error rates and customer-impacting issues</li><li>Clear KPI reporting across all facilities</li><li>SOP adherence across 100% of locations</li><li>Improved partner performance and accountability</li><li>Audit-ready compliance posture</li></ul>Who You Are 8&ndash;15+ years in operations leadership, ideally in logistics, warehousing, or fulfillment<ul><li>Proven experience managing multi-site operations</li><li>Strong track record of improving productivity and reducing costs</li><li>Deep experience implementing and enforcing SOPs</li><li>Highly analytical and data-driven (you manage by metrics, not intuition)</li><li>Comfortable holding teams accountable and making tough calls</li><li>Experience with compliance-heavy environments (mail, financial services, healthcare, etc.) is a strong plus</li><li>Experience with SOC 2 or similar frameworks is highly preferred</li></ul>Why This Role Matters This role is critical to the next stage of growth at US Global Mail. You will directly impact scalability, profitability, and customer experience across the business.Compensation<ul><li>Competitive salary + performance-based bonus</li><li>Opportunity to shape and scale a national operation</li></ul>How to Apply Include a brief note describing:<ul><li>A specific example where you improved productivity across multiple locations</li><li>A time you reduced operational errors or implemented a QA system</li></ul>Pay: $70,000.00 - $100,000.00 per yearBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Application Question(s):<ul><li>Can you cite a specific example where you improved productivity across multiple locations?</li><li>Can you cite an example where you reduced operational errors or implemented a QA system?</li></ul>Work Location: In person

Head of Operations

US Bolt Manufacturing

We have a Direct Hire opportunity in Houston, TX!This is a Full-Time opportunity as QA Inspector. This position is with a well-known/well established Organization &amp; they are looking to grow their team. Duties:Performs inspections, tests and calibrations.Job Responsibilities:Other duties may be assigned.Prepare and maintains quality assurance documentation required by the Company and documentation required by the Laboratory.Qualifications:To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to perform these operations using units of American money and weight measurement.Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence.Education and/or Experience:High school diploma and three (3) years experience in quality assurance at least two (2) of which are related to fastener testing and inspection and the preparation and maintenance of associated documentation or GED or four (4) years experience in quality assurance at least two (2) of which are related to fastener testing and inspection. Training in ISO (000 and ISO Guide 25 requirements.Excellent Compensation and Benefit Package Available.EOE.Job Type: Full-timePay: $20.00 - $21.00 per hourBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Education:<ul><li>High school or equivalent (Required)</li></ul>Experience:<ul><li>Manufacturing: 1 year (Preferred)</li><li>QA Inspector: 2 years (Required)</li><li>Fastener testing and inspection: 1 year (Required)</li></ul>Work Location: In person

Quality Assurance Inspector

HCA Houston Healthcare

<div><h5 class="jobSectionHeader">Introduction</h5>
Do you have the PRN career opportunities as a(an) Cardiac Cath Lab Tech PRN you want with your current employer? We have an exciting opportunity for you to join HCA Houston Healthcare Northwest which is part of the nation's leading provider of healthcare services, HCA Healthcare.<h5 class="jobSectionHeader">
Benefits</h5>
HCA Houston Healthcare Northwest, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:<ul><li>
Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as telemedicine services and free AirMed medical transportation. 
</li><li>
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more. 
</li><li>
Fertility and family building benefits through Progyny 
</li><li>
Free counseling services and resources for emotional, physical and financial wellbeing 
</li><li>
Family support, including adoption assistance, child and elder care resources and consumer discounts</li><li>
401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service)</li><li>
Employee Stock Purchase Plan 
</li><li>
Retirement readiness and rollover services and preferred banking partnerships 
</li><li>
Education assistance (tuition, student loan, certification support, dependent scholarships) 
</li><li>
Colleague recognition program 
</li><li>
Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence)</li></ul> 
Learn more about Employee Benefits
Note: Eligibility for benefits may vary by location. 
Our teams are a committed, caring group of colleagues. Do you want to work as a(an) Cardiac Cath Lab Tech PRN where your passion for creating positive patient interactions is valued? If you are dedicated to caring for the well-being of others, this could be your next opportunity. We want your knowledge and expertise!<h5 class="jobSectionHeader">
Job Summary and Qualifications</h5>
The Cardiac Cath Lab Technician safely performs a variety of technical procedures, utilizing specialized angiographic equipment for diagnosis of cardiovascular and/or peripheral vascular disease entities; as well as for therapeutic intervention to treat disease processes.
 We are an amazing team that works hard to support each other and we are seeking a phenomenal addition like you who feels patient care is as meaningful as we do. We want you to apply now!
What You Will Do In This Role:<ul><li>Operates Specialized Equipment /Radiation Safety: Operates specialized radiographic and invasive procedure equipment</li><li>Understands needs and identifies needed supplies appropiately for invasive procedures. Ensures supplies available for procedures.</li><li>Employs radiation protection devices and techniques as required.</li><li>Independently assists physician as scrub person and operates fluoroscopic/specialized equipment safely.</li><li>Understands and practices sterile technique</li><li>Orients new employees as related to special procedure technologist duties</li><li>Participates in departmental performance improvement activities</li><li>Fulfills assigned on call obligations.</li></ul> 
What Qualifications You Will Need:<ul><li>Completion of an accredited and approved Radiology Technologist or Cardiovascular Technologist program.</li></ul><ul><li>Current Registered Radiographer (ARRT) or Cardiovascular Technologist (RCIS) certification is required; Registered Cardiovascular Interventional Specialist (RCIS) credential preferred over ARRT.
</li></ul><ul><li>American Red Cross or American Heart Association (BLS OR BCLS, and ALS OR ACLS) Course Completion and Certification.</li></ul>
HCA Houston Healthcare Northwest is a 415+ bed acute care hospital that has been serving the north Houston communities for more than 40 years, providing a wide range of medical services including cardiology, maternity care, Level III NICU, pediatrics, bariatrics and neurology. We comprehensively serve our community by employing expert physicians, specialists, nurses and support staff who work together as a unified team to offer a range of diagnostic treatment and support services. From our 24-hour emergency department with Level II Trauma capabilities, to women&rsquo;s services, to cardiology, we are dedicated to improving the health of our community by delivering exceptional, personalized healthcare. We are members of HCA Houston Healthcare, the most comprehensive family of hospitals in the region and part of the leading provider of healthcare in the country, HCA Healthcare. Together we are stronger, smarter and more accessible in providing the patient-centered care you need close to home.
HCA Healthcare has been recognized as one of the World&rsquo;s Most Ethical Companies&reg; by the Ethisphere Institute more than ten times. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses. 
 
&quot;Bricks and mortar do not make a hospital. People do.&quot;- Dr. Thomas Frist, Sr. 
HCA Healthcare Co-Founder
If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Cardiac Cath Lab Tech PRN opening. We review all applications. Qualified candidates will be contacted for interviews. Unlock the possibilities and apply today!
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status</div>

Cardiac Cath Lab Tech PRN

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