sterile processing tech

Medical City Healthcare

<div><h5 class="jobSectionHeader">Introduction</h5>
Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring for patients with purpose and integrity. We care like family! Jump-start your career as a(an) Sterile Processing Tech PRN Seasonal Contract today with Medical City Plano.<h5 class="jobSectionHeader">
Benefits</h5>
Medical City Plano 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 free 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>
Free counseling services and resources for emotional, physical and financial wellbeing 
</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 with 10% off HCA Healthcare stock 
</li><li>
Family support through fertility and family building benefits with Progyny and adoption assistance. 
</li><li>
Referral services for child, elder and pet care, home and auto repair, event planning and more 
</li><li>
Consumer discounts through Abenity and Consumer Discounts 
</li><li>
Retirement readiness, rollover assistance 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><li>
Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.</li></ul> 
Learn more about Employee Benefits
Note: Eligibility for benefits may vary by location. 
Come join our team as a(an) Sterile Processing Tech PRN Seasonal Contract. We care for our community! Just last year, HCA Healthcare and our colleagues donated $13.8 million dollars to charitable organizations. Apply Today!<h5 class="jobSectionHeader">
Job Summary and Qualifications</h5>
As a Sterile Processing Technician, you'll play a critical role in delivering safe, high-quality surgical care by making sure every instrument is thoroughly cleaned, sterilized, and ready when needed. Your focus on safety and attention to detail helps protect patients and empowers a team that&rsquo;s committed to the care and improvement of human life &ndash; one surgery at a time.
Your responsibilities will include:
<ul><li>Cleaning, disinfecting, sterilizing, and organizing surgical instruments and supplies following safety standards</li><li>
Monitoring sterilization cycles, documenting results, and resolving issues promptly to deliver on our commitment to safe, high-quality care</li><li>
Preparing and organizing instrument trays and surgical rooms based on the daily schedule and procedural needs</li><li>
Safely handling and disposing of biohazardous materials while keeping the work area clean and organized</li><li>
Working closely with nurses and surgeons to anticipate needs and support smooth, efficient surgeries</li></ul><h6 class="jobSectionHeader">
What qualifications you will need:</h6>
Medical City Plano opened in 1975 and provides Plano and Collin County with advanced health care. Medical City Plano is a 600+ bed acute care hospital. We have more than 2,000 employees and over 1,400 physicians on staff. Our main campus in Plano has a cancer treatment center and cardiovascular programs. We have The Bariatric Surgery Institute, a Wound Care Center and inpatient rehabilitation. We also offer complete women's and children's services. This includes a high-risk antepartum unit and a Level 3 neonatal intensive-care unit. We were the first hospital in Dallas, Collin or Denton counties to be named a Comprehensive Stroke Center by the Texas Department of State Health Services. Medical City Plano was the first Level I Trauma Center in Collin County and The Burn &amp; Reconstructive Center of Texas was the first burn center in Collin County. As a part of the Medical City network of hospitals and specialists, patients are ensured access to leading medical experts and advanced healthcare innovations. 
&quot;The great hospitals will always put the patient and the patient's family first, and the really great institutions will provide care with warmth, compassion, and dignity for the individual.&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 Sterile Processing Tech PRN Seasonal Contract opening. We promptly review all applications. Highly 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>

Sterile Processing Tech PRN Seasonal Contract

Dr Aravinds IVF Fertility centre

Contact : 6381490061 Location: Tirupur, Coimbatore, Erode Job Description: An Operation Theatre Technician, also known as a Surgical Technologist or Scrub Tech, plays a crucial role in the operating room team by assisting surgeons, nurses, and other surgical personnel during surgical procedures. They are responsible for ensuring the operating theatre is prepared with the necessary equipment, instruments, and supplies, and they help maintain a sterile environment to minimize the risk of infections. 1.Preparation and Setup2.Assistance During Surgery 3.Maintaining Sterile Environment4.Post-Operative Duties5.Documentation and Communication Document accurate records of surgical procedures, instrument counts, and patient care.Communicate effectively with other healthcare team members, including surgeons, nurses, and anesthesiologists.Job Types: Full-time, PermanentPay: ₹12,000.00 - ₹18,000.00 per monthBenefits:<ul><li>Provident Fund</li></ul>Work Location: In person

Operation Theatre Technician

Dr Aravinds IVF private limited Hospital

Job Description:An Operation Theatre Technician, also known as a Surgical Technologist or Scrub Tech, plays a crucial role in the operating room team by assisting surgeons, nurses, and other surgical personnel during surgical procedures. They are responsible for ensuring the operating theatre is prepared with the necessary equipment, instruments, and supplies, and they help maintain a sterile environment to minimize the risk of infections.1.Preparation and Setup2.Assistance During Surgery3.Maintaining Sterile Environment4.Post-Operative Duties5.Documentation and CommunicationDocument accurate records of surgical procedures, instrument counts, and patient care.Communicate effectively with other healthcare team members, including surgeons, nurses, and anesthesiologists.Phn Np: 9360427505Job Type: Full-timePay: ₹20,000.00 - ₹30,000.00 per monthBenefits:<ul><li>Health insurance</li><li>Provident Fund</li></ul>Work Location: In person

CoxHealth

<div>Facility:
CoxHealth South: 3801 S National Ave, Springfield, Missouri, United States of America, 65807&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;
Department:
1064 Sterile Processing South
Scheduled Weekly Hours:
40
Hours:
Work Shift:
Evening Shift (United States of America)
CoxHealth is a leading healthcare system serving 25 counties across southwest Missouri and northern Arkansas. The organization includes six hospitals, 5 ERs, and over 80 clinics. CoxHealth has earned the following honors for workplace excellence:
<ul><li>Named one of Modern Healthcare&rsquo;s Best Places to work five times.
</li><li>Named one of America&rsquo;s Greatest Workplaces by Newsweek .
</li><li>Recognized as a Greatest Workplace for Women in both 2023 and 2024.
</li><li>Listed as one of the Greatest Workplaces for Diversity in 2024.
</li><li>Acknowledged by Forbes as one of the Best Employers for New Grads.
</li><li>Ranked among the Best Employers by State for Missouri.
</li><li>Healthcare Innovation's Top Companies to Work for in Healthcare in 2025.
</li></ul>Benefits
<ul><li>Medical, Vision, Dental, Retirement Plan with employer match, and many more!</li> 
<li>
</li></ul>Job Description:
Under the direction of the Sterile Processing Department (SPD) Manager the Sterile Processing Shift Supervisor monitors daily operations in the SPD department, ensuring that technicians are trained in and abide by all departmental policies and procedures. Monitors productivity and quality of product of individual employees and of an assigned shift. Assists SPD Manager with budget monitoring. Participates with SPD Manager in planning for future needs and project implementation related to personnel, program development, instrumentation, equipment, interdepartmental relationships and department goals. Assesses and troubleshoots safety, instrument and equipment issues. Establishes and maintains professional rapport with medical, nursing and other staff. Assumes responsibilities for department as a whole in the absence of the SPD Manager.
<div>Education:
<ul><li>Preferred: Graduate from a School of Surgical Technology
</li></ul>Experience:
<ul><li>Required: 9 months experience in SPD or Surgery
</li><li>Preferred: 2 Years&rsquo; experience in SPD or Surgery
</li></ul>Skills:
<ul><li>Excellent communication skills, verbal and written
</li><li>Detailed knowledge of department policies and procedures and outside regulatory requirements
</li><li>Knowledge of computer systems including basic computer knowledge, MS Office, databases, and inventory management systems
</li><li>Ability to operate complex machinery including washers, ultrasonic cleaners, and sterilizers
</li><li>Demonstrated ability to competently perform multiple, complex tasks
</li><li>Knowledge of medical terminology
</li><li>Knowledge instrumentation
</li><li>Ability to multitask
</li></ul>Licensure/Certification/Registration:
<ul><li>Required: CRCST or CBSPD; CHL and CIS must be obtained within 1 year of hire</li></ul></div></div>

Sterile Processing Supervisor Cert

Sushen Medicamentos

ORGANIZATIONAL DETAILSCompany: Sushen Medicamentos Pvt. Ltd. Department: Projects &amp; Maintenance - Sterile Manufacturing Location: Ahmedabad, Gujarat Reports To: Maintenance and Projects Head Position Type: Full-Time, Permanent Experience Level: 4-5 Years (Mandatory: EU GMP Approved Plant Experience)ABOUT SUSHEN MEDICAMENTOSSushen Medicamentos Pvt. Ltd. is a globally recognized pharmaceutical services company specializing in:<ul><li>Pharmaceutical Project Management Services (PMS): Complete turnkey solutions for manufacturing infrastructure including sterile facilities</li><li>Contract Development and Manufacturing Organization (CDMO): Specialized manufacturing services across multiple dosage forms</li></ul>Operating under stringent regulatory standards including cGMP, WHO-GMP, USFDA, and EMA compliance, Sushen maintains world-class pharmaceutical manufacturing capabilities with particular expertise in sterile product manufacturing.POSITION SUMMARYThe IV Fluid Projects &amp; Maintenance Engineer will be responsible for dual functions: executing engineering projects for IV fluid manufacturing facility setup/expansion and ensuring optimal maintenance of sterile manufacturing equipment and critical utilities. This role demands specialized expertise in aseptic processing, sterile manufacturing environments, and stringent EU GMP compliance for injectable products.The position requires hands-on experience with IV fluid/sterile injectable manufacturing equipment, cleanroom systems, and critical utility management in EU GMP approved pharmaceutical facilities. The engineer will play a crucial role in both maintaining existing operations and implementing new projects for capacity expansion or technology upgrades.KEY RESPONSIBILITIESA. PROJECT EXECUTION Sterile Facility Projects<ul><li>Execute engineering projects for IV fluid manufacturing facility setup, expansion, and modernization including:</li><li>Cleanroom construction and upgrades (Grade A, B, C, D areas)</li><li>Installation of sterile manufacturing equipment</li><li>Utility systems installation and upgrades</li><li>Process equipment integration and commissioning</li><li>Automation and control system implementation</li><li>Prepare detailed project plans with timelines, milestones, and resource requirements</li><li>Coordinate with cross-functional teams (Production, QA, Regulatory, EHS) for project execution</li><li>Manage equipment procurement process including vendor selection and technical evaluation</li><li>Oversee installation, commissioning, and qualification activities (IQ/OQ/PQ)</li><li>Ensure projects comply with EU GMP requirements for sterile manufacturing facilities</li></ul>Equipment Installation &amp; QualificationLead installation of IV fluid manufacturing equipment:<ul><li>Ampoule/vial washing and depyrogenation systems</li><li>Filling and sealing machines (ampoules, vials, IV bags, IV Bottles)</li><li>Autoclave/sterilization equipment</li><li>Inspection systems (visual and automated)</li><li>Labeling and packaging lines</li><li>Material handling systems for sterile areas</li></ul><ul><li>Execute Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT)</li><li>Develop and execute qualification protocols (IQ/OQ/PQ) as per EU GMP requirements</li><li>Coordinate validation activities with Quality Assurance team</li><li>Prepare comprehensive project documentation and as-built drawings</li></ul>Utilities &amp; Critical Systems Projects<ul><li>Implement critical utility systems:</li><li>Water for Injection (WFI) generation and distribution systems</li><li>Clean Steam generation and distribution</li><li>HVAC systems for cleanrooms with HEPA filtration</li><li>Compressed air systems (instrument air, breathing air)</li><li>Nitrogen and other utility gases</li><li>Pure steam generators</li><li>Clean-in-Place (CIP) and Sterilize-in-Place (SIP) systems</li><li>Manage DQ (Design Qualification) for utility systems</li><li>Ensure compliance with pharmacopeial requirements (USP, EP) for utilities</li></ul>B. MAINTENANCE OPERATIONS (50-60% of Role)Sterile Manufacturing Equipment Maintenance<ul><li>Execute preventive and corrective maintenance on IV fluid manufacturing equipment:</li><li>Washing Equipment: Ampoule/vial washing machines, tunnel washers</li><li>Depyrogenation Equipment: Dry heat sterilizers, depyrogenation tunnels</li><li>Filling Systems: Aseptic filling machines, blow-fill-seal (BFS) systems, form-fill-seal machines</li><li>Sealing Equipment: Ampoule sealing, vial capping machines</li><li>Sterilization Equipment: Autoclaves (steam sterilizers), dry heat ovens, pure steam generators</li><li>Inspection Systems: Manual/semi-automatic/automatic inspection machines, leak testing equipment</li><li>Labeling &amp; Packaging: Labelers, cartoning machines, case packers</li><li>Material Transfer Systems: Pass-through chambers, LAF units, material airlocks</li><li>Maintain Grade A/B Isolators and Restricted Access Barrier Systems (RABS) if applicable</li><li>Troubleshoot complex equipment breakdowns with minimal production impact</li><li>Coordinate with equipment OEMs for specialized technical support</li><li>Maintain equipment logbooks and history cards as per GMP requirements</li></ul>Critical Utilities Maintenance<ul><li>Ensure 24/7 availability of critical utilities supporting sterile manufacturing:</li><li>WFI Systems: Generation (distillation/RO+EDI), storage, and hot/cold loop distribution</li><li>Clean Steam Systems: Generation and distribution for sterilization</li><li>HVAC Systems: AHUs, HEPA filters, differential pressure control, temperature and humidity management</li><li>Compressed Air: Oil-free compressors, dryers, filtration systems</li><li>CIP/SIP Systems: Automated cleaning and sterilization systems</li><li>Environmental Monitoring Systems: Particle counters, microbial monitoring, pressure differential monitors</li><li>Monitor critical utility parameters and maintain within specified limits</li><li>Execute preventive maintenance schedules for all utility systems</li><li>Manage emergency response for utility failures</li></ul>Electrical/Mechanical Systems ManagementFor Electrical -<ul><li>Maintain electrical systems in classified cleanroom areas with explosion-proof/safe area requirements</li><li>Troubleshoot PLC-based control systems for sterile manufacturing equipment</li><li>Manage automation systems including recipe management, batch control, and data logging</li><li>Maintain UPS systems ensuring uninterrupted power to critical equipment</li><li>Handle electrical qualification and calibration of instruments</li><li>Ensure proper functioning of cleanroom monitoring systems (particle counters, pressure differential monitors)</li><li>Maintain electrical interlocks and safety systems in aseptic areas</li></ul>For Mechanical -<ul><li>Maintain mechanical systems of filling machines, sealers, and washing equipment</li><li>Manage steam systems, condensate recovery, and steam traps</li><li>Maintain pumps, valves, and piping systems for WFI and clean steam</li><li>Handle alignment, balancing of high-speed filling and sealing equipment</li><li>Manage compressed air systems and gas distribution networks</li><li>Maintain material handling systems and cleanroom pass-throughs</li></ul>EU GMP Compliance &amp; Documentation<ul><li>Execute all maintenance and project activities in strict compliance with EU GMP Annex 1 (Sterile Medicinal Products)</li><li>Maintain comprehensive GMP documentation:</li><li>Preventive maintenance schedules and execution records</li><li>Calibration certificates and schedules</li><li>Equipment qualification documentation (IQ/OQ/PQ)</li><li>Change control for equipment modifications</li><li>Deviation and CAPA records</li><li>Project documentation and validation reports</li><li>SOPs for equipment operation and maintenance</li><li>Equipment cleaning and sterilization records</li><li>Support regulatory audits (EMA, USFDA, MHRA, WHO) with technical documentation</li><li>Ensure maintenance activities maintain cleanroom integrity and sterility assurance</li><li>Follow gowning protocols and aseptic behavior in Grade A/B areas</li><li>Participate in environmental monitoring and contamination control programs</li></ul>C. TECHNICAL SUPPORT &amp; CONTINUOUS IMPROVEMENTProcess Support<ul><li>Provide technical support during production operations for equipment-related issues</li><li>Participate in batch investigations and failure analysis</li><li>Support new product introductions and process validations</li><li>Assist in media fills and aseptic process simulations</li><li>Contribute to risk assessments (FMEA, HACCP) for sterile processes</li></ul>Improvement Initiatives<ul><li>Identify opportunities for equipment reliability enhancement</li><li>Participate in root cause analysis for equipment failures and contamination events</li><li>Implement predictive maintenance strategies (vibration analysis, thermography, oil analysis)</li><li>Support technology upgrades and automation projects</li><li>Contribute to energy efficiency and sustainability initiatives</li></ul>Vendor &amp; Spare Parts Management<ul><li>Coordinate with equipment vendors and service providers</li><li>Manage spare parts inventory for critical sterile manufacturing equipment</li><li>Evaluate and qualify vendors for maintenance services</li><li>Support annual maintenance contracts (AMCs) and service agreements</li></ul>D. SAFETY &amp; COMPLIANCE<ul><li>Ensure compliance with electrical/mechanical safety standards in cleanroom environments</li><li>Follow lockout-tagout (LOTO) procedures for equipment isolation</li><li>Maintain EHS compliance including chemical safety, steam safety, and confined space entry</li><li>Participate in safety training and incident investigations</li><li>Ensure proper handling of hazardous materials (cleaning agents, sanitizers)</li><li>Maintain housekeeping and 5S standards in maintenance areas</li></ul>REQUIRED QUALIFICATIONSEducation<ul><li>Bachelor's degree in Electrical Engineering OR Bachelor's degree in Mechanical Engineering (B.E./B.Tech)</li></ul>Experience<ul><li>Total Experience: 4-5 years in projects and/or maintenance engineering roles</li><li>Mandatory Requirement: Minimum 3 years of hands-on experience in EU GMP approved pharmaceutical manufacturing plants</li><li>Sterile Products Experience: Proven experience with IV fluids, large volume parenterals (LVP), small volume parenterals (SVP), or injectable manufacturing</li><li>Project Experience: Demonstrated experience in equipment installation, commissioning, or facility projects (preferred)</li></ul>Technical SkillsSterile Manufacturing Expertise:<ul><li>Hands-on experience with aseptic filling equipment (ampoules, vials, IV bags, IV Bottles , BFS systems)</li><li>Knowledge of sterilization processes (moist heat, dry heat, filtration)</li><li>Understanding of depyrogenation principles and equipment</li><li>Familiarity with cleanroom design, HVAC systems, and environmental control</li><li>Experience with WFI and clean steam systems</li><li>Knowledge of CIP/SIP systems and validation</li></ul>Core Technical Competencies:<ul><li>Equipment installation, commissioning, and qualification</li><li>Troubleshooting complex sterile manufacturing equipment</li><li>Reading and interpreting P&amp;IDs, electrical schematics, and mechanical drawings</li><li>Project planning and execution</li><li>Preventive and predictive maintenance methodologies</li></ul>GMP &amp; Regulatory Knowledge<ul><li>Mandatory: Thorough understanding of EU GMP requirements, particularly Annex 1 (Manufacture of Sterile Medicinal Products)</li><li>Knowledge of equipment qualification and process validation principles</li><li>Understanding of cleanroom classifications (ISO 14644, EU GMP Grade A/B/C/D)</li><li>Familiarity with pharmacopeial requirements (USP, EP) for sterile products</li><li>Change control, deviation management, and CAPA systems</li><li>Documentation practices for GMP compliance</li><li>Understanding of contamination control strategies</li></ul>PREFERRED QUALIFICATIONS<ul><li>Experience with multiple sterile dosage forms (ampoules, vials, pre-filled syringes, IV bags)</li><li>Exposure to Blow-Fill-Seal (BFS) or Restricted Access Barrier Systems (RABS) technology</li><li>Knowledge of isolator technology for aseptic processing</li><li>Experience with regulatory inspections (EMA, USFDA, MHRA)</li><li>Familiarity with CMMS systems (SAP PM, Maximo)</li><li>Training in Lean Manufacturing, Six Sigma, or TPM</li><li>Understanding of pharmaceutical water systems (Purified Water, WFI, Clean Steam)</li><li>Experience with lyophilization (freeze-drying) equipment</li><li>Knowledge of Building Management Systems (BMS) and Building Automation Systems (BAS)</li><li>Project management certification (PMP/Prince2) - advantage</li></ul>CORE COMPETENCIESTechnical Competencies<ul><li>Sterile manufacturing equipment expertise</li><li>Project planning and execution</li><li>Equipment troubleshooting and problem-solving</li><li>Qualification and validation protocol development</li><li>Technical documentation and GMP record-keeping</li><li>Vendor and contractor management</li><li>Critical utilities management</li></ul>Quality &amp; Compliance<ul><li>EU GMP Annex 1 compliance mindset</li><li>Aseptic technique understanding</li><li>Contamination control awareness</li><li>Risk-based thinking</li><li>Regulatory compliance orientation</li><li>Documentation rigor and attention to detail</li></ul>Professional Competencies<ul><li>Project management skills</li><li>Analytical and problem-solving abilities</li><li>Multi-tasking and prioritization</li><li>Cross-functional collaboration</li><li>Communication skills (verbal and written)</li><li>Leadership and ownership</li><li>Adaptability and learning agility</li><li>Safety consciousness</li></ul>Job Types: Full-time, PermanentPay: ₹40,000.00 - ₹70,000.00 per monthWork Location: In person

IV Fluid Projects & Maintenance Engineer

SCA Health

<div>Overview:
<div>
At SCA Health, we believe health care is about people &ndash; the patients we serve, the physicians we support and the teammates who push us forward. Behind every successful facility, procedure or innovation is a team of 15,000+ professionals working together, learning from each other and living out the mission, vision and values that define our organization.</div><div></div><div> 
As part of Optum, SCA Health is redefining specialty care by developing more accessible, patient-centered practice solutions for a network of more than 370 ambulatory surgical centers, over 400 specialty physician practice clinics and numerous labs and surgical hospitals. Our work spans a broad spectrum of services, all designed to support physicians, health systems and employers in delivering efficient, value-based care to patients without compromising quality or autonomy.</div><div> 
</div><div>What sets SCA Health apart isn&rsquo;t just what we do, it&rsquo;s how we do it. Each decision we make is rooted in seven core values:</div><div></div><ul><li> 
Clinical quality</li><li>
Integrity</li><li>
Service excellence</li><li>
Teamwork</li><li>
Accountability</li><li>
Continuous improvement</li><li>
Inclusion</li></ul><div></div><div> 
Our values aren&rsquo;t empty words &ndash; they inform our attitudes, actions and culture. At SCA Health, your work directly impacts patients, physicians and communities. Here, you&rsquo;ll find opportunities to build your career alongside a team that values your expertise, invests in your success, and shares a common mission to care for patients, serve physicians and improve health care in America. 
</div><div></div><div>At SCA Health, we offer a comprehensive benefits package to support your health, well-being, and financial future. Our offerings include medical, dental, and vision coverage, 401k plan with company match, paid time off, life and disability insurance, and more. Please visit, https://careers.sca.health/why-sca, to learn more about our benefits.</div><div></div><div> 
Your ideas should inspire change. If you join our team, they will.</div>
Accountabilities / Responsibilities:
<div>
We are actively hiring for an Instrument Technologist.</div><ul><li>
Promote the mission, vision, and values of SCA.</li><li>
Demonstrate safe operation of equipment and machinery and follows procedures for reporting and correcting an unsafe situation.</li><li>
Speak up with safety concerns.</li><li>
Adhere to standard precautions including the use of personal protective equipment.</li><li>
Follow established protocols for cleaning, decontaminating, preparing and packaging, disinfecting or sterilizing, and storing medical and surgical supplies and equipment.</li><li>
Distribute medical and surgical supplies from sterile processing areas to other areas within the facility or health care organization as needed.</li><li>
Protect the patient&rsquo;s rights, dignity, and privacy.</li><li>
Adhere to standard precautions including the use of personal protective equipment.</li><li>
Follow safety procedures and manufacturer&rsquo;s instructions when handling cleaning solutions, supplies and equipment.</li><li>
Monitor, interpret, and document results of physical, chemical and biological indicators for all types of sterilizers used in the sterile processing areas.</li><li>
Inventory, receive, and restock materials used for supporting sterile processing services.</li><li>
Comply with organizational policies, regulatory and accreditation standards, and professional guidelines.</li><li>
Provide hand-off report to other teammates that are accurate, concise and pertinent.</li><li>
Document accurately, timely, completely, and legibly.</li><li>
Demonstrate effective communication and collaboration skills with members of the team and other stakeholders.</li><li>
Serve as a member of a multidisciplinary team in planning patient care.</li><li>
Participate in quality review and performance improvement projects.</li><li>
Participate in the performance appraisal process.</li><li>
Use problem-solving and conflict resolution skills to foster effective work relationships.</li><li>
Maintain required competencies.</li><li>
Pursue professional growth.</li><li>
Act as a patient advocate and maintain privacy and confidentiality of individuals and health information.</li><li>
Comply with all SCA and facility policies and procedures, regulatory and accreditation standards and professional guidelines when providing patient care.</li><li>
Actively participate in team meetings, trainings, and daily safety huddles.</li><li>
Demonstrate fiscal responsibility.</li><li>
Perform all other duties as assigned.</li></ul>
Qualifications:
<div>
Education, Experience, and Licensure:</div><ul><li>
High school graduate or equivalent.</li><li>
Understanding of sterilization and high-level disinfection technologies including industry standardized principles and practice in sterilization and disinfection required.</li><li>
Prior experience in instrument processing preferred.</li><li>
Prior experience as a surgical technologist/procedure technologist preferred.</li><li>
Successful completion of BCLS Course within 90 days of employment or documentation of current BCLS certification.</li><li>
Certification in instrument processing is preferred.</li></ul>
Min: USD $22.00/Hr. Max: USD $31.00/Hr.</div>

Instrument Tech, Part-Time - Duluth Surgical Suites

Wrangler Instruments

Job SummaryWe are seeking a Clean Room Supervisor to oversee clean room operations involved in the cleaning, disinfection, inspection, packaging, and labelling of surgical instruments. The ideal candidate will have prior experience in a medical environment, preferably Operation Theatre (OT), CSSD, hospital sterile services, or medical device manufacturing, with strong knowledge of cleanliness protocols and infection control standards.The role requires hands-on supervision to ensure strict adherence to clean room SOPs, quality standards, and regulatory requirements.Key ResponsibilitiesClean Room Operations &amp; Supervision<ul><li>Supervise daily activities in the clean room to ensure cleanliness, hygiene, and compliance with approved protocols.</li><li>Ensure proper implementation of clean room procedures, gowning practices, and controlled environment discipline.</li><li>Monitor environmental cleanliness and coordinate corrective actions when required.</li></ul>Cleaning &amp; Disinfection Control<ul><li>Oversee cleaning and disinfection of surgical instruments according to approved SOPs.</li><li>Ensure correct use of cleaning agents, disinfectants, and validated processes.</li><li>Verify instruments are free from contamination, residues, and defects before packaging.</li></ul>Inspection, Packaging &amp; Labeling<ul><li>Supervise clean packaging and labeling activities to ensure accuracy, traceability, and compliance.</li><li>Ensure instruments are handled, packed, and labeled in a contamination-free environment.</li><li>Coordinate with Quality Control for inspections and documentation.</li></ul>Quality &amp; Compliance<ul><li>Ensure compliance with ISO 13485, CE, FDA, and internal quality standards.</li><li>Maintain proper records related to cleaning, disinfection, inspection, and packaging.</li><li>Support internal audits, external audits, and regulatory inspections.</li></ul>Team Management &amp; Training<ul><li>Supervise clean room staff and ensure tasks are performed efficiently and correctly.</li><li>Train staff on clean room behavior, hygiene, infection control, and SOP compliance.</li><li>Enforce discipline, safety, and cleanliness standards at all times.</li></ul>Coordination &amp; Reporting<ul><li>Coordinate with QC, Production, and Management to ensure smooth workflow.</li><li>Report non-conformities, deviations, or risks related to cleanliness or quality.</li><li>Assist in continuous improvement of clean room processes.</li></ul>Required Qualifications &amp; Experience<ul><li>Minimum 1-2 years of relevant experience in a clean room, OT, CSSD, sterile processing, or medical device manufacturing environment.</li><li>Medical-related background preferred (OT Technician, CSSD staff, hospital sterile services, or similar).</li><li>Strong understanding of cleanliness protocols, infection control, and sterile handling.</li><li>Familiarity with clean room SOPs and quality standards.</li><li>Basic documentation and reporting skills.</li></ul>Preferred Skills &amp; Attributes<ul><li>Attention to detail and strong sense of responsibility.</li><li>Ability to supervise staff and enforce protocols.</li><li>Good communication and coordination skills.</li><li>Understanding of surgical instruments is a plus.</li><li>Physically fit to work in a controlled clean room environment.</li></ul>What We Offer<ul><li>Opportunity to work with a globally compliant medical device manufacturer</li><li>Professional growth in a regulated quality environment</li><li>Competitive salary based on experience</li><li>Stable and long-term career opportunity</li></ul>Job Type: Full-timePay: Rs50,000.00 - Rs60,000.00 per monthWork Location: In person

Pharmaceutical Packaging Supervisor / Clean Room Supervisor

Search 8100+ Sterile processing tech jobs near you this January. New roles added regularly across leading industries. Apply today.

8100 sterile processing tech jobs NEAR_ME

Sterile Processing Tech PRN Seasonal Contract

Operation Theatre Technician

Operation Theatre Technician

Sterile Processing Supervisor Cert

IV Fluid Projects & Maintenance Engineer

Instrument Tech, Part-Time - Duluth Surgical Suites

Pharmaceutical Packaging Supervisor / Clean Room Supervisor