Quality control microbiology supervisor full time jobs

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we're making better health outcomes easier to achieve. Hims & Hers is a public company, traded on the NYSE under the ticker symbol “HIMS.” To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company's outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit *********************************** About the Role: We are seeking an experienced Quality Control Manager to join our Quality Unit at our large-scale compounding pharmacy located in New Albany, OH. The Quality Control Manager will play a critical leadership role in driving continuous improvement initiatives that ensure the highest quality products for our patients and customers. Reporting to the Director of Quality, this role will oversee quality control operations, lead in-process and final product inspections, and ensure compliance with USP standards, cGMP practices, internal SOPs, and applicable regulatory requirements. You Will: Lead and perform in-process and post-production quality checks, including product inspection, testing, and disposition at various stages of the compounding process. Manage day-to-day activities on the production floor to ensure product and raw material compliance. Compile, analyze, and present trending data and quality reports to QA management. Oversee investigations related to non-conformances, deviations, and customer complaints, and drive root cause analysis and corrective actions. Manage the product retain program and ensure timely and compliant inspections. Collaborate with production and pharmacy teams to implement quality improvement initiatives. Maintain oversight of critical equipment verifications (e.g., pH meters, balances) and calibrations. Review and approve compound records, Certificates of Analysis (COAs), and raw material documentation to ensure quality standards are met. Draft, revise, and implement SOPs, protocols, and related documentation in alignment with USP standards and regulatory requirements. Ensure ongoing compliance with USP guidelines for sterile and non-sterile compounding and applicable cGMP practices. Support internal audits and external third-party inspections. Manage relationships with contract laboratories for external product testing. Train and mentor pharmacy and production staff on quality standards, processes, and procedures. Have a Pharmacy Technician license or be willing to obtain one within your first six months of employment (we cover costs and will help you obtain your trainee hours). You Have: Strong experience with Environmental monitoring. Must have experience working in a sterile floor environment. 3+ years of experience in quality control or quality assurance, ideally in a non-sterile compounding or pharmaceutical manufacturing environment. Strong working knowledge of USP and applicable cGMP standards and making sure protocols are being followed. Experience in a regulated environment (FDA 21 CFR 210/211 experience a plus). Proven leadership skills with the ability to coach and develop quality and production personnel. Exceptional interpersonal, verbal, and written communication skills. Strong proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook); MRP system experience preferred. Ability to manage multiple priorities, work independently, and maintain high attention to detail. Strong technical writing skills for SOPs, protocols, and reports. Familiarity with quality metrics, root cause analysis, and statistical quality control methods. Proven ability to build and maintain strong cross-functional partnerships, paired with clear, effective communication across all levels of the organization. Bachelor's degree in Chemistry, Biology, Pharmacy, Quality Management, Engineering, or related discipline (preferred). Nice to Have: Experience working in a 503A or 503B compounding facility. Prior management of environmental monitoring or contamination control programs. Experience supporting facility expansions, FDA inspections, or operational scale-up projects. Our Benefits (there are more but here are some highlights): Competitive salary & equity compensation for full-time roles Unlimited PTO, company holidays, and quarterly mental health days Comprehensive health benefits including medical, dental & vision, and parental leave Employee Stock Purchase Program (ESPP) 401k benefits with employer matching contribution Offsite team retreats Conditions of Employment: This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required. This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR). Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve-hour shift. Must be able to lift up to 50lbs. Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs. We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply-even if you're not sure if your background or experience is a perfect match. Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address. To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.

Job Description Decima International is a professional services company, providing project management and controls services to clients in the United States and the Middle East. Our mission is to become the premier professional services provider across all industry sectors we are engaged in. To accomplish this, Decima International's founders established a simple yet powerful formula: Approach each client engagement as a partnership, create an environment that attracts the most talented professionals and allows them to flourish, and regulate growth to maintain excellence in our service standards. If you are interested in a long and rewarding career working with high-profile clients on some of the most challenging projects in the world, then Decima is where you belong. At Decima, you will be able to explore incredible growth and professional development opportunities. We are looking for a driven and capable Senior Quality Construction Manager to support us with the development of multiple data center projects for one of the top technology clients in the world. This is a client-facing role that requires strong interpersonal, communication, and organizational skills, the ability to self-direct, client representation, and an emphasis on strong project management fundamentals. Must be able to manage multiple projects concurrently and across multiple regions. A strong background in data center development, design, engineering, controls, and operations requirements is a big plus. You will play an integral role in ensuring the implementation and management of the Quality Management System (QMS) in addition to the coordination, performance, and completion of all construction inspection and testing services of a project. The Senior Quality Construction Manager is accountable for the guarantee of the work performed as well as meeting the project's contractual requirements set forth by the client. We are looking to bring in dedicated individuals with a passion for innovation and talent for multitasking in a fast-paced environment. We will help you grow, pursue, and fulfill what inspires you so we can make big impacts on the world, together. RESPONSIBILITIES Develop a sound knowledge of the project scope and requirements. Ensure compliance with stringent contract and owner quality requirements. Prepare comprehensive, project-specific QC plans. Review and verify material submittals for A/E and Client review. Verify that delivered materials comply with approved submittals. Provide and review submittals, RFI logs, maintenance logs, and other project-related materials in a timely manner. Review and update QC punch lists and coordinate punch list completion with GC and subcontractors. Verify the implementation and operation of the quality assurance and control systems by planning and conducting internal quality audits and inspection of activities on-site. Ensure implementation and continuous improvement in overall Quality Systems. Ensure that all contractual / company and local authority requirements for Quality, Health, Safety, & Environment (HSE) requirements are complied with. Review, update, and verify the distribution of the Quality Management Procedure, Quality Manual, and related procedures for Infrastructure, MEP, Civil, and other subcontractors, and divisions by the GC. Verify that GC implements adequate training/awareness of company personnel for quality systems. Ensure that all non-conformance issues are promptly investigated, corrective and preventive actions are proposed/implemented, and are quickly closed out. Ensure that the contractual quality requirements of a project are fully communicated to all key personnel, so that their roles in fulfilling these requirements are fully understood. Ensure that all GC and subcontractors' quality systems and plans are acceptable to the company as applicable to the "Project Contract". Ensure that Subcontractors'/Suppliers' quality systems are implemented and effective. Ensure that the calibration of all inspection, measurement, and test equipment is conducted according to the defined schedule. Conduct reviews of the approved suppliers and subcontractors' list. Liaise with the General Contractor, Client, and Project Management team to ensure that all potential and actual quality issues are fully resolved. Establish a strong relationship with the GC and Client and communicate with both technical and management-level personnel. Prepare PowerPoint decks and present to management on progress, findings, and recommendations. Review project plans, requirements, and specifications. Perform other related duties as required and assigned. QUALIFICATIONS Required Qualifications: 20+ years of construction quality management experience. Bachelor's degree in Civil, Mechanical, Electrical Engineering, or a related field. Experience with managing field engineering, inspection, and NDE related to all QA/QC functions. Ability to develop and manage non-conformance, deficiencies, and reporting programs, including root cause analysis. Experience in developing and monitoring project QA/QC budgets. Ability to ensure correct codes, standards, job specifications, project procedures, and federal and provincial regulations are properly identified, correctly specified in detail, and met or exceeded. Must have the ability to work within strict deadlines and under pressure while maintaining a professional demeanor. Experience working as a QA/QC Manager for large Commercial, Industrial, or Mission-Critical Facilities construction projects. An excellent understanding of construction Quality Management Systems (QMS). Experience developing various types of reports, targeting different audiences. Experience in client-facing positions. Demonstrated ability to understand technical and complicated construction programs and the ability to communicate progress to both technical and management-level personnel. Strong communication skills, including the ability to communicate with any audience clearly and accurately. Proficient in Microsoft Office programs. Preferred Qualifications: Project Management Professional (PMP) certification. Certified Construction Manager (CCM) certification. Strong background in data center development and construction. POSITION DETAILS: Primary Location (On-site): Conesville, Ohio Position: Senior Quality Construction Manager Position Classification: Salary-based full-time hours Current US work permit required. This position does not offer sponsorship for employment (e.g., H-1B visa sponsorship or transfer not offered) PRODUCTIVITY TOOLS: Microsoft Office Microsoft 365 Decima International is an Equal Opportunity Employer who is committed to the safety and wellbeing of all. All qualified applicants will receive consideration for employment without regard to race, religion, creed, color, national origin, ancestry, sex (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, medical condition, marital or domestic partner status, sexual orientation, gender, gender identity, gender expression and transgender status, mental disability or physical disability, genetic information, military or veteran status, citizenship, low-income status or any other status or characteristic protected by applicable law. At Decima International, we offer a competitive salary package, including paid time off and performance-based bonuses. We also provide excellent medical, vision and dental insurance for our employees.

**SIGNING BONUS AVAILABLE FOR A LIMITED TIME! APPLY TODAY!** State Bank, a growing Community Bank, has an opportunity for a self-motivated and leadership-minded individual to join and lead our team of Quality Control Analysts. We are seeking a Full Time Quality Control Manager. This position is responsible for leading our Quality Control Analysts Group in order to establish advanced quality controls and to implement continuous improvement standards and procedures for State Bank. A B.S. or B.A. or equivalent preferred, or experience in lieu of degree; Mortgage Lending, HMDA and Quality Control training or practical experience. Experience in mortgage and commercial lending or related positions required. Consumer, SBA, and Retail banking deposit experience preferred. State Bank offers an extensive benefits package including paid vacation and PTO, medical/dental/vision insurance, company-paid life and AD&D insurance, a company-matched 401(k) retirement plan, company-provided short and long-term disability, quarterly incentive payouts, a community volunteer program, and growth opportunities. Apply today and see why State Bank is a great place to work! Equal Opportunity Employer

**Department:** Laboratory Administration **Weekly Hours:** 40 **Status:** Full time **Shift:** Days (United States of America) As the Manager, Specialty Lab, you will plan, organize, lead, develop and coordinate your assigned technical specialty. This includes the responsibility for system-wide standard policies, procedures, and equipment. You will maintain a cost-effective and efficient lab department to ensure high levels of client satisfaction and service. You will work with medical directors and staff to develop, implement, and maintain quality standards and improve performance. The above summary is intended to describe the general nature and level of work performed in this role. It should not be considered exhaustive. REQUIREMENTS + Must have a bachelor's degree in chemical, physical, biological, or clinical laboratory science + Requires a minimum of five (5) years clinical laboratory experience + Must be certified by the American Society of Clinical Pathologists (ASCP) PREFERRED REQUIREMENTS + 3-5 years management experience **ProMedica** is a mission-driven, not-for-profit health care organization headquartered in Toledo, Ohio. It serves communities across nine states and provides a range of services, including acute and ambulatory care, a dental plan, and academic business lines. ProMedica owns and operates 10 hospitals and has an affiliated interest in one additional hospital. The organization employs over 1,300 health care providers through ProMedica Physicians and has more than 2,300 physicians and advanced practice providers with privileges. Committed to its mission of improving health and well-being, ProMedica has received national recognition for its clinical excellence and its initiatives to address social determinants of health. For more information about ProMedica, please visit promedica.org/aboutus (****************************************************** . **Benefits:** We provide flexible benefits that include compensation and programs to help you take care of your family, your finances and your personal well-being. It's what makes us one of the best places to work, and helps our employees live and work to their fullest potential. Qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, religion, sex/gender (including pregnancy), sexual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category. In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with ProMedica, please contact **************************** Equal Opportunity Employer/Drug-Free Workplace

Job Title: Quality Control Manager - Welding Industry Full-Time | Flexible 1st Shift Hours Salary: $80,000 - $90,000 (Based on Experience) Full Benefits Package Included About Us:We are a leading steel fabrication company based in Cleveland, Ohio, with a strong reputation in the bridge construction and welding industry. Our team is committed to excellence in fabrication quality, safety, and compliance, and we are looking for an experienced Quality Control Manager to ensure our operations meet the highest industry standards. Position Overview:As a Quality Control Manager, you will oversee all aspects of welding quality control and compliance. You will ensure that welds and fabrication processes meet or exceed industry codes, maintain QA documentation, and lead internal and external audit processes. This is a hands-on leadership role ideal for someone with deep experience in welding and inspection, and a strong working knowledge of industry standards such as AWS, AISC, ISO, and NDT protocols. Key Responsibilities: Oversee and implement all quality control procedures for welding and fabrication processes. Ensure compliance with AISC Bridge Code, ISO 9001, and other applicable standards. Maintain and organize QA/QC documentation for inspections, audits, and certifications. Schedule and track internal audits and third-party inspections. Work closely with production and engineering to resolve welding and quality issues. Review and approve Welding Procedure Specifications (WPS) and Procedure Qualification Records (PQR). Supervise Non-Destructive Testing (NDT) processes and evaluate results. Lead root cause analysis and implement corrective actions. Train and mentor welders and quality team members on best practices and code compliance. Act as primary contact for quality matters during client audits and regulatory inspections. Requirements: 5+ years of experience in Welding Quality Control, preferably in structural steel or bridge fabrication. Must have a strong understanding of welding processes (SMAW, FCAW, GMAW, GTAW) and fabrication standards. Certification or familiarity with: Certified Welding Inspector (CWI) Non-Destructive Testing (NDT) methods AISC Bridge Code ISO 9001 Quality Systems Strong communication and documentation skills. Familiarity with QA software or digital inspection tools is a plus. Excellent organizational and problem-solving abilities. What We Offer: Competitive Salary: $80,000-$90,000 based on experience. Flexible 1st Shift Schedule (M-F). Comprehensive Benefits Package: Medical, Dental, Vision 401(k) with Company Match Paid Vacation & Holidays Ongoing Training and Certification Reimbursement A supportive, team-oriented environment focused on safety, quality, and growth. Keywords:Welding Quality Control, CWI, AWS D1.1, AISC Certified Fabricator, Welding Inspector, ISO 9001, NDT Level II, Bridge Welding Code, Structural Steel, Weld Audit, WPS, PQR, SMAW, FCAW, GMAW, Welding Supervisor, QA/QC, Fabrication Quality, Welding Certification, Quality Assurance Manager, Cleveland Welding Jobs, Manufacturing QA, Steel Fabrication, Welding Code Compliance, Welding Process Control. If you feel you have the above qualifications, please apply for immediate consideration.All qualified applicants will receive consideration for employment without regard to race, color, religion, ethnicity, national origin, sex, gender identity, sexual orientation, disability status, protected veteran status or any other protected status under the law.EverStaff is an equal opportunity employer (M/F/D/V/SO/GI)

Department: Laboratory Administration Weekly Hours: 40 Status: Full time Shift: Days (United States of America) As the Manager, Specialty Lab, you will plan, organize, lead, develop and coordinate your assigned technical specialty. This includes the responsibility for system-wide standard policies, procedures, and equipment. You will maintain a cost-effective and efficient lab department to ensure high levels of client satisfaction and service. You will work with medical directors and staff to develop, implement, and maintain quality standards and improve performance. The above summary is intended to describe the general nature and level of work performed in this role. It should not be considered exhaustive. REQUIREMENTS * Must have a bachelor's degree in chemical, physical, biological, or clinical laboratory science * Requires a minimum of five (5) years clinical laboratory experience * Must be certified by the American Society of Clinical Pathologists (ASCP) PREFERRED REQUIREMENTS * 3-5 years management experience ProMedica is a mission-driven, not-for-profit health care organization headquartered in Toledo, Ohio. It serves communities across nine states and provides a range of services, including acute and ambulatory care, a dental plan, and academic business lines. ProMedica owns and operates 10 hospitals and has an affiliated interest in one additional hospital. The organization employs over 1,300 health care providers through ProMedica Physicians and has more than 2,300 physicians and advanced practice providers with privileges. Committed to its mission of improving health and well-being, ProMedica has received national recognition for its clinical excellence and its initiatives to address social determinants of health. For more information about ProMedica, please visit promedica.org/aboutus. Benefits: We provide flexible benefits that include compensation and programs to help you take care of your family, your finances and your personal well-being. It's what makes us one of the best places to work, and helps our employees live and work to their fullest potential. Qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, religion, sex/gender (including pregnancy), sexual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category. In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with ProMedica, please contact ************************ Equal Opportunity Employer/Drug-Free Workplace

Job Location: Paninesville, Ohio Job type: Full-time Type of role: On-site Work Schedule: DuPont Schedule (12-hour rotating shift) About Lubrizol The Lubrizol Corporation, a Berkshire Hathaway company, is a specialty chemical company whose science delivers sustainable solutions to advance mobility, improve wellbeing and enhance modern life. Founded in 1928, Lubrizol owns and operates more than 100 manufacturing facilities, sales, and technical offices around the world and has about 8,000 employees. For more information, visit ***************** We value diversity in professional backgrounds and life experiences. By enabling a consistent, unbiased, and transparent recruitment process, Lubrizol seeks to create a positive experience for candidates so we can get to know them at their best. We recognize unique work and life situations and offer flexibility, ensuring our employees feel engaged and fulfilled in every aspect of life. Join Our Thriving Team at Lubrizol as a Quality Control Lab Analyst Unleash Your Potential. At Lubrizol we're transforming the specialty chemicals market and looking for exceptional talent to join us on this journey. If you are ready to join an international company with talent around the world, and want to make a real impact, we want you on our team. What You'll Do: Performs all QC Lab activities, including but not limited to: all Standard Work Process (SWP), Management Systems, and analytical responsibilities. What We're Looking For: * Provide internal and external customers with the highest level of customer service in responsiveness while performing QC activities. * Interface with all corporate, commercial, supply chain, customer experience, and lab / operations personnel. * Communicate between departments when reporting results and execute SWP / SOP in an exemplary manner. * Perform all test methods without supervision within precision and accuracy standards. * Prepare all solutions needed for testing. * Perform testing on raw material, in-process, finished good, and miscellaneous samples. * Document all data in corresponding laboratory notebook, SAP, LIMS as business needs dictate. * Dispose of all chemicals safely * Perform required testing pertaining to customer complaints, discrepancies, & laboratory investigations. * Report results to operations, in a timely manner. * Review and approve laboratory results as needed. * Assist in the performance of qualifications and validations of instruments, test methods, and basic PMs. * Troubleshoot/self-evaluate OOS results. * Assist in writing SWP, SOPs, methods, protocols, and reports. * Perform daily laboratory maintenance. * Oversee the training of new employee's basic laboratory skills and functions. * Perform simple problem solving and participate in improving daily work Skills That Make a Difference: * Associate degree in chemistry or a related technical field or 5 years' experience in an industrial manufacturing laboratory. * Experience with one of the following analytical techniques: * physical property testing * wet chemistry * advance instrumental analytical techniques. * Highly self-motivated individual, focused on providing high quality laboratory data in an efficient manner, while exhibiting excellent workplace skills. * Solid background in Microsoft Office and computer-based instrument control systems for analytical equipment. * Excellent verbal and written communication skills. * Advanced problem-solving skills and the ability to make competent, independent, decisions in a timely manner to ensure excellent progress on assigned tasks. * Ability to effectively manage multiple and or changing priorities with minimal to no supervision. * Must possess the ability to interact effectively and professionally with internal customers, external customers, vendors, and various stakeholders. Considered a Plus: * Bachelor's degree in chemistry with 1-5 years relevant experience. * Industrial chemical manufacturing laboratory experience is preferred with 1-5 years' experience. * Analytical experience with advanced instrumental techniques like GC, LC, ICP, and NMR. * Analytical experience with wet chemistry and physical property testing. * Experience with LIMS and SAP QM modules. * Experience with proper usage and administration of Lab notebooks / elog notebooks. * Experience with root cause problem solving techniques and tools. * Experience with Statistical Quality Control methodologies. * Experience working in ISO9001/14001 environments. * Experience with internal auditing a plus. Perks and Rewards That Inspire: * Competitive salary with performance-based bonus plans * 401K Match plus Age Weighted Defined Contribution * Competitive medical, dental & vision offerings * Health Savings Account * Paid Holidays, Vacation, Parental Leave * Flexible work environment Learn more at benefits.lubrizol.com! Ready for your next career step? Apply today and let's shape the future together! It's an exciting time to be part of Lubrizol. Lubrizol is not staying put. We are continually learning and evolving. Our passion delivers our success - not only for Lubrizol but for those who count on us every day: our employees, customers, and communities. As a diverse, global team, we work together to solve some of the world's most pressing challenges. We impact everyday lives through science only Lubrizol can deliver, and we never stop pushing to do it better. One of the founding principles of The Lubrizol Corporation more than 90 years ago was treating every employee with dignity and respect. That same commitment is only stronger today. More than that, we are committed to providing an environment where every employee can be the best they can be, no matter their race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic. #LI-CS1

Looking for a new Lab Leadership job? My name is Leah and I'm a healthcare recruiter, I'm here to help! I have an awesome Microbiology Supervisor role available near Walbridge, Ohio! Details - Full-time and permanent - Shift: Days - Opportunities for growth - Full, comprehensive benefits package (PTO, health insurance, life insurance, 401k, etc) Requirements - College degree - ASCP cert - Prior experience, including leadership + microbiology Click apply or email your resume to leah@ka-recruiting.com/call or text 617-746-2751! You can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min. REF#LM3179

The Sanitation Technician will be responsible for all aspects of externally sanitizing all production equipment and the cleanliness for the entire plant. Schedule: 2nd Shift (4:00PM - 3:30AM) ESSENTIAL DUTIES AND RESPONSIBILITIES: Knowledge of all cleaning agents and applications, external, internal, cleaners, and sanitizers. Properly document and follow all procedures set forth in the frequency guide and standards. Ability to properly clean all production and packaging equipment as specified. Ability to properly measure and follow proper mixing procedures. Ability to evaluate equipment sanitation to food and safety standards. Ability to accurately interpret written instructions, handles complex and difficult jobs efficiently Responsible for compliance of company rules and regulations of food and safety standards. Other duties assigned by supervisor LANGUAGE SKILLS: Ability to read reports and other documents, analyzes, and interprets common information. Ability to effectively present information to management as required. PHYSICAL DEMANDS: While performing the duties of this job, the employee is regularly required to walk, stand or sit for long periods of time. The employee frequently is required to use hands and fingers, to handle, or feel equipment for the purpose of sanitation. Run heavy equipment. Must be able to lift up to 50 pounds. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Field positions will be exposed to various unfamiliar conditions where Personal Protective Equipment (PPE) must be worn and which may include, but are not limited to manufacturing and warehouse plants, and other locations as directed by supervisor. The noise level in the work environment is usually moderate, but increases significantly in warehouse and manufacturing plants. MINIMUM 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. High School Diploma or GED or equivalent work experience required. Prior experience in the carbonated soft drink industry a plus. Understands and can follow all OSHA/GMP/HACCP required training. Must be 18 years or older Favorable background and drug screen. Ability and willingness to work a flexible Full Time schedule that may include weekends and holidays. Must be able to provide own transportation to various locations in organizational service areas, as required by duties. Shasta Beverages, Inc. provides equal employment opportunities to all applicants for employment without regard to race, color, religion, sex, national origin, age, disability, gender, genetics, gender identity, disabled veterans or sexual orientation.

Job DescriptionJob Title: Logistics Quality Control (QC) Specialist Department: Logistics Reports To: Logistics Manager / Quality Manager Type: Full-Time The Logistics Quality Control (QC) Specialist is responsible for ensuring all packaged cannabis products meet internal quality standards and Ohio regulatory requirements before being released to the vault as finished goods and prior to outbound distribution. This role serves as a critical control point between Packaging, Inventory, and Logistics, verifying product accuracy, compliance, and documentation integrity. The ideal candidate is highly detail-oriented, self-motivated, and capable of working independently in a fast-paced, regulated environment. Key ResponsibilitiesFinished Goods & Lot Quality Control ● Perform detailed QC inspections on all packaged lots received from the Packaging Department prior to vault intake. ● Verify lot integrity, SKU accuracy, unit counts, weights, packaging configuration, heat/tamper seal and labeling compliance. ● Ensure all required regulatory information is present and accurate, including: License numbers Batch/lot numbers Harvest and packaging dates Net weight Required warning statements ● Confirm packaging meets internal quality standards and is free of defects, damage, or contamination. ● Accurately document QC approvals, rejections, and findings per SOP requirements. Order Quality Control & Fulfillment Verification ● Conduct final QC checks on all outbound orders prior to shipment or delivery. ● Verify each order is 100% accurate, including: Correct SKUs and product types Correct lot numbers Correct quantities and unit configurations Matching manifest and sales order documentation ● Ensure orders comply with Ohio cannabis transportation and distribution regulations. ● Identify, escalate, and document discrepancies before orders leave the facility. Compliance & Documentation ● Maintain accurate and complete QC records in accordance with Ohio Division of Cannabis Control (DCC) regulations. ● Ensure inventory movements and lot releases are accurately reflected in the state seed-to-sale tracking system. ● Adhere strictly to GMP, SOPs, and internal quality policies. ● Support audits and inspections by providing documentation and traceability records when requested. Cross-Functional Communication ● Communicate QC findings clearly and professionally with Packaging, Inventory, Logistics, and Management teams. ● Escalate quality or compliance risks immediately and participate in root cause analysis as needed. Support continuous improvement initiatives by identifying trends or recurring issues. Required Qualifications ● Previous experience in quality control, logistics, inventory, or regulated manufacturing preferred. ● Strong attention to detail with the ability to spot discrepancies quickly and accurately. ● Ability to work independently with minimal supervision. ● Strong organizational and documentation skills. ● Comfortable working in a highly regulated environment with strict compliance standards. ● Ability to stand, walk, and handle packaged products throughout the shift. Preferred Qualifications ● Experience in the cannabis industry, particularly in packaging, inventory, logistics, or QC. ● Familiarity with Ohio cannabis regulations and seed-to-sale tracking systems. ● GMP or quality systems experience. ● Experience performing lot and order audits in a warehouse or distribution environment. Core Competencies ● Exceptional attention to detail ● Independent decision-making ● Regulatory compliance mindset ● Clear written and verbal communication ● Integrity and accountability Powered by JazzHR n1JebPyvvy

Job Details Kettering Health Hamilton | Hamilton | Full-Time | First Shift Responsibilities & Requirements Accountable for the development and ongoing management of Hamilton Infection Control Program. The CIC Specialist is responsible for: ongoing employee education regarding infection control; performance of surveillance activities; implementation of prevention and control measures in response to a suspected or known bioterrorism-related outbreak; and specific audits that promote high quality care to all patients and reduces the risk of infection for employees and patients. Available to all departments, the Specialist serves as a resource for infection control questions and issues. The CIC specialist is accountable for his/her own professional development and practice within the scope of care defined by law. Utilizing organizational resources, the CIC specialist acts as a patient advocate for the delivery of safe care, which includes the delegation of care and participation in performance and practice improvement activities. The delivery of nursing care at Hamilton reflects the philosophies, mission, vision and values of the organization and nursing department. Performs infection control surveillance activities, and specific audits that promote high quality care to all patients and reduce the risk of infection for employees and patients. Job Responsibilities Demonstrates solid skill in medical record review, abstraction of data, NHSN and other entity surveillance definitions and reporting. Demonstrates solid skill in reviewing lab data, isolation needs, and tagging and flagging charts for infection prevention, assessing unit compliance with infection prevention (cleaning, isolation, hand washing, etc.). Communications clearly, verbally, and in writing, to a variety of internal and external groups or individuals. Presents material in a clear manner when educating staff during orientation, or in committees. Leads infection prevention teams using LEAN and PDSA methods. Participates in survey readiness and surveys as needed. Attends at least two infection prevention meetings per year and keeps up working knowledge of infection prevention control evidenced based information. Job Requirements Bachelor's Degree in Nursing (state of Ohio) or related healthcare field Active Ohio Registered Nursing Licensure or Laboratory Science, Epidemiology or other clinical area required Certification in Infection Control (CIC) obtained within 3 years of hire Minimum 1 year of clinical experience Preferred Qualifications Over 2 years of Infection Prevention and Control experience preferred. Master's degree in Nursing or related healthcare field preferred Overview Kettering Health is a not-for-profit system of 13 medical centers and more than 120 outpatient facilities serving southwest Ohio. We are committed to transforming the health care experience with high-quality care for every stage of life. Our service-oriented mission is in action every day, whether it's by providing care in our facilities, training the next generation of health care professionals, or serving others through international outreach.

This is a remote part-time position only available to US residents of Ohio and Texas We are primarily looking to staff part time, Mon-Fri 8am-6pm EST/8am-5pm CDT This role is not eligible for anyone currently employed full time elsewhere Job Overview: This is a remote, part-time, entry-level position. We are looking for a Part Time Production QC Associate to help ensure the deliverability of our product. Production QC Associates primarily test our content by sending SMS messages across various providers and carriers and log the results, while making changes as necessary. You will be provided with a company laptop and set of three cell phones to use for testing. If you are a computer savvy person with a keen eye for detail, who's self-motivated and a quick learner, we are interested in hearing from you! Compensation: $10-12/hour Hours: Part time, 12-28 hours/week Mon-Fri (8am-6pm EST/8am-5pm CDT). Flexible hours to fit your schedule! Specific Duties, Activities, and Responsibilities: Test for the reliable delivery of SMS Text messages through extensive review of QC test results across multiple cellular carriers. Adjust, retest, and document changes made to SMS campaigns. Map specific pre-determined responses to frequent messages Assist with miscellaneous data audits as needed Skills/Qualifications: Computer capability - Microsoft Office (Word/Outlook/Excel) College level English language grammatical skills. Strong organizational skills - attention to detail, and exceptional verbal/ written skills Problem-Solving - ability to interpret data, draw conclusions, and spot trends. Work Ethic - Self-motivated and able to work independently or with a team Cell Phone Reception - It is a requirement that you have adequate cell phone reception with the following cellular carriers: AT&T, T-Mobile, and Verizon Wireless What is Drips? Drips is an AI driven conversational SMS marketing platform; the first Conversational Texting company of its kind, founding a new category and leading the way for some of the biggest brands in the world to improve engagement rates and outcomes for their prospects and customers. Operating completely remote, Drips helps clients increase lead conversions by communicating with their customers in the same way that people communicate with each other. Using conversational SMS, calls, email, and direct mail campaigns, Drips automates conversation in a way that works, and works well. Drips enables brands to connect with consumers through an AI-powered conversational outreach strategy that includes human-like two-way texting, scheduled calling, and voicemail messages. Backed by a proprietary natural language processing model, our platform has handled over half a billion humanized conversations to date, enabling us to deliver automation at a scale that no other competitor in the messaging industry has been able to match. That's why we're the platform of choice for some of the world's most recognizable brands. Drips' focus on empowering brands to capture intent and drive meaningful conversations has sparked rapid growth since the company was founded in 2016. And we are looking to accelerate the next era of growth and expansion of our team. Check us out! ************************** ****************************************** *************************************** **************************************

Job Description Job Title: Quality Control Specialist Friday, Saturday & Sunday 7:00am - 7:30pm We are seeking a detail-oriented and reliable Quality Control Specialist to join our team on a full- time basis. This role is essential in ensuring that products meet our quality standards and comply with regulatory requirements. Key Responsibilities: Perform routine quality inspections on incoming materials, in-process production, and finished goods Document inspection results and report any deviations or non-conformances Assist with sample collection and testing according to established protocols Maintain accurate and organized quality records Communicate effectively with production and QA teams to resolve quality issues Support continuous improvement initiatives and compliance with GMP standards Qualifications: Food Science, Microbiology, or working towards this type of degree preferred Previous experience in quality control or manufacturing environment is a plus Strong attention to detail and ability to follow procedures Basic computer skills (Excel, data entry), Google Drive Ability to work independently and manage time effectively Familiarity with GMP and quality standards preferred

System One is seeking a NDE Quality Oversight professional for a long-term contract to hire, full time opportunity, onsite in Orville, Ohio. The ideal candidate will have a strong background in nuclear quality assurance, NDE, and fabrication operations, with a deep understanding of NQA-1 and ASME standards. This role will focus on ensuring quality through oversight, auditing, and compliance within a nuclear fabrication environment. Responsibilities: + Provide quality assurance oversight of NDE (Non-Destructive Testing) and fabrication operations. + Ensure compliance with NQA-1, ASME, and other nuclear quality standards. + Conduct audits to maintain quality program integrity. + Review and approve procedures, ensuring alignment with applicable standards. + Generate and review final quality packages for completeness and accuracy. + Collaborate with teams to identify and resolve quality issues. Qualifications: + Required Experience: + Hands-on expertise in nuclear quality programs, including NQA-1 and ASME standards. + Proficiency in NDE techniques and fabrication processes. + Experience in auditing, procedure review, and final package generation. + Must be local to Orrville, OH or willing to commute (no per diem provided). + Strong communication and organizational skills. System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #161-Managed Staffing Charlotte System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

If you want an exciting job with one of the largest off-price retail stores in the nation, join the Burlington Stores, Inc. as a **Shortage Control Lead** ! As a Shortage Control Lead you will be responsible for mitigating theft and fraud in high shortage areas of the store while promoting a safe and secure store environment. You will engage with our customers and associates in a manner consistent with our company core values by providing a strong and energetic greeting with eye contact and a smile. The Shortage Control Lead will be a valuable partner to store and field leadership by assisting in the training and development of the Shortage Control Associates, identifying and reporting theft incidents, and driving shortage education and awareness to all associates. Your confidence, positive attitude, command presence, and expertise in store shortage reduction programs will positively influence behaviors and reduce theft and fraud. **Responsibilities:** + Provide an effective deterrent to dishonest behaviors throughout the store by demonstrating a command presence through role modeling impression of control, following dress code in the company issued vest and earpiece, demonstrating a positive demeanor, strong posture, and an energetic greeting + Maintain a safe and secure store for our customers and associates with a strong attention to detail, ability to multi-task, strong communication, and aligned partnership with store leadership + Enthusiastically engage with every customer and associate in areas of the store with highest risk for shortage. These interactions are positive, respectful, and promote a strong impression of control and best in class customer service + Display a strong working knowledge of top shortage areas and support programs designed to identify and reduce theft + Gather and document indicators of external theft and share with store and field leaders. Network with local law enforcement as directed and support evidence gathering to address large scale or organized retail crime or repeat theft incidents + Support store manager by providing internal controls and operational oversight including conducting associate package/bag, monitoring point of sale transactions, conducting store audits, and promoting Asset Protection programs + Provide leadership with onboarding and ongoing support of associate training in shortage reduction programs and processes + Assist store leadership in the preparation and execution of the semi-annual inventory process and developing action plans to reduce shortage + Role-model behaviors that demonstrate that safety is a top priority + Is highly disciplined in managing stressful situations and address unsafe practices at every opportunity Candidates must be able to work a flexible schedule; including nights, weekends, and holidays as required. **If you...** ... are excited to deliver great values to customers every day; ... take a sense of pride and ownership in helping drive positive results for a team; ... are committed to treating colleagues and customers with respect; ... believe in the power of diversity and inclusion; ... want to participate in initiatives that positively impact the world around you; **Come join our team. You're going to like it here!** You will enjoy a competitive wage, flexible hours, and an associate discount. Burlington's benefits package includes medical, dental, and vision coverage including life and disability insurance. Full Time associates may also be eligible for up to 12 days of paid time off annually, up to 8 paid holidays, paid sick time in accordance with applicable law, and a 401(k) plan. We are a rapidly growing brand, and provide a variety of training and development opportunities so our associates can grow with us. Our store teams work hard and have fun together! Burlington associates make a difference in the lives of customers, colleagues, and the communities where we live and work every day. Burlington Stores, Inc. is an equal opportunity employer committed to workplace diversity. **Base Pay:** **$14.00 per hour** **-** **$14.00 per hour** **Location** 01138 - Hilliard **Posting Number** P1-1075633-4 **Address** 1760 Hilliard Rome Rd **Zip Code** 43026 **Position Type** Regular Full-Time **Career Site Category** Store Associate **Position Category** Retail Store **Base Pay** $14.00 - $14.00 per hour

Job Description: Quality Control & Receiving Associate The Quality Control & Receiving Associate is responsible for inspecting, verifying, and documenting incoming materials and finished goods to ensure compliance with company and customer specifications. This role plays a critical part in maintaining product quality, verifying supplier shipments, and supporting overall production efficiency in a secondary packaging manufacturing environment. What you'll do as a Quality Control & Receiving associate Receiving: Verify incoming shipments against purchase orders, packing slips, and invoices for accuracy in quantity, product type, and condition. Inspect raw materials, components, and packaging supplies for defects, damage, or non-conformance. Properly label and document received goods in the company's inventory system. Coordinate with purchasing and suppliers to resolve discrepancies, shortages, or damaged goods. Ensure materials are stored in compliance with safety, quality, and organizational standards. Quality Control: Perform in-process and final inspections of packaged products to verify compliance with quality standards and customer requirements. Check incoming materials (up to and including containers, labels, inserts, part numbers, etc.) for proper specifications, accuracy, and condition. Document inspection results, deviations, and corrective actions in accordance with company procedures. Work closely with production and purchasing teams to identify, communicate, and resolve quality issues in real time. Support corrective and preventive action processes (CAPA) for recurring or significant quality concerns. Assist with product testing, measurement, and verification using appropriate tools and equipment. General: Maintain accurate and organized records for audits, certifications, and traceability requirements. Follow all company safety, housekeeping, and compliance policies. Participate in training programs to stay current on quality and regulatory requirements. Support continuous improvement initiatives to enhance efficiency, quality, and customer satisfaction. What we're looking for Education & Experience: High school diploma or equivalent required; associate degree or technical certification in quality, manufacturing, or logistics preferred. Prior experience in quality control, receiving, or inventory management in a manufacturing environment (packaging experience a plus). Skills & Competencies: Strong attention to detail with the ability to identify defects and inconsistencies. Understanding of quality management systems and inspection tools, including calipers, Ability to read and interpret packing slips, purchase orders, and product specifications. Strong organizational skills with accurate record-keeping. Proficiency with Microsoft Office and ERP/inventory management systems preferred. Effective communication and problem-solving skills. Ability to work independently and collaboratively in a fast-paced production environment. Tool Reading Competencies Ability to read and interpret blueprints, and GD&T symbols Skilled in using calipers, micrometers, height gauges, and bore gauges Familiar with thread gauges, protractors, and alignment tools Accurate in documenting and reporting measurement results Physical Requirements: Ability to lift up to at least 50 lbs. Standing, walking, and moving materials throughout the shift. Manual dexterity and visual acuity to perform inspections. Job Type: Full-time

About Our Team At Tolco Corporation, we are the trigger sprayer experts. With a foundation of over 64 years of selling best-in-class cleaning tools, our major product categories focus on dispensing, including trigger sprayers, pumps, bottles and closures. We attribute our success to our dedicated team who strive to provide quality customer service and take pride in providing fast and efficient shipping. We often collaborate across teams to get the job done; however, we don't take ourselves too seriously. It is important for us to have fun too! About You The ideal candidate is a detail-oriented problem-solver with a strong commitment to quality. A proactive mindset, technical aptitude, and strong communication skills are essential to thrive in this role. If you take pride in ensuring products meet high standards and enjoy working in a structured, process-driven environment, we encourage you to apply. Job Summary The Quality Control Analyst ensures that all inbound and returned products meet Tolco's quality standards through systematic inspection, documentation, and testing. This role involves evaluating product performance, chemical resistance, output, and compliance with specifications, while also inspecting goods produced or assembled by Tolco as directed by the manager. This position reports to the Quality Control Manager. Job Responsibilities Perform timely inspections of inbound goods against Tolco's product specifications Select samples from the warehouse/receiving area and transport them (using non-motorized handcart) to the inspection station Conduct functional tests to verify proper operation, chemical resistance, output and performance Use testing equipment to measure product compliance Evaluate customer-returned products as directed by the QC Manager to determine root causes of defects or failures Inspect internally produced or assembled goods before outbound shipment to ensure compliance with quality standards Record test results and document inspection findings Maintain organized and up-to-date quality records in the Quality Control Master Specification Worksheet Requirements Education & Experience: Associates Degree in Quality Assurance Mgmt preferred, and/or minimum of 3+ years experience in quality control, inspection, or manufacturing Certifications: Quality Control/Inspection (i.e. CQT or CQI) preferred but not required Technical Skills: Basic computer skills, including proficiency in Microsoft 365, Google Suite and an ERP Physical Requirements: Ability to lift/move items up to 50 lbs and stand for extended periods of time Soft Skills: Detail-oriented, analytical, and able to follow standardized procedures Benefits and Other Important Information This is a full-time, on-site position 8am-5pm, Monday-Friday. Tolco offers a comprehensive benefits package, including medical, dental, vision, voluntary life insurance, 401k disbursements, paid vacation, and more. More About Tolco Tolco Corporation is a leading manufacturer of cleaning tools used in the Janitorial, Beauty & Barber, Animal Health, and Auto Detailing markets. Our major product categories focus on dispensing, which include trigger sprayers, pumps, bottles, and containers. Additionally, we offer over 1000 products, and carry items in the restroom care, floor & window cleaning, utility, and safety categories. Tolco is a third-generation family business operating out of Toledo, OH since 1961.

Summary/Objective The Quality Control Associate is responsible for the day-to-day functionality of inspecting picked orders for accuracy. Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Department Duties - Review picked orders for accuracy and that all stated requirements for the order are met. - Receive, identify, mark and place materials sent to the warehouse according to established procedures. - Prepare various merchandise for delivery; prepare packages for shipping according to established procedures. - Communicate with various personnel, departments, product managers and others to provide and receive information, resolve questions and issues, and coordinate activities. - Maintain work time records per company policy. - Operate a computer to process reports and forms and maintain an inventory of warehouse materials as required. - Assist team to help ensure the facility is maintained in a safe, clean and orderly condition. Competencies - Good organization skills and basic warehouse understanding of picking, shipping, receiving, issuing materials, proper and orderly storage, optimum space utilization and/or stock inventory procedures. - Ability to clearly read/listen and understand work instructions. - Ability to work well in time-sensitive situations. - Basic knowledge of Microsoft Excel - Team-oriented operating style with effective interpersonal skills that allow successful interactions with individuals of a variety of work styles, personalities, and career levels. Requirements Work Environment Warehouse Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. - Ability to move and handle merchandise weighing 1 ounce - 50 pounds - Ability to stand, bend and stoop for an extended period of time Education and Experience Preferred: - At least one (1) year of prior job-related experience in a Quality Control environment - High School diploma or equivalent education Position Type/Expected Hours of Work - Monday through Friday, 40 hours per week with possible overtime Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the associate for this job. Duties, responsibilities and activities may change at any time with or without notice. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the company. EEO Statement Wild Republic is an Equal Opportunity Employer. Applicants for employment, recruitment, hiring, training, transfer, promotion, pay, benefits, lay-off, demotion or termination of employment will be made without consideration of race, color, religion, sex, sexual orientation or preference, gender identity, national origin, age, disability, military status, ancestry, veteran status, or any other protected classification under applicable federal, state or local law.

Full-time Description This position is responsible for ensuring the Bank maintains a sound loan portfolio ensuring compliance with all state and federal laws and regulations and Civista Bank lending policies and procedures. The Analyst will review a variety of new and modified commercial loan types in this role - C&I, CRE, SBA, Participations, Swap, and others. Additionally, the Analyst will review documentation for accuracy, completeness, and compliance in both pre-close and post-close while promoting and maintaining a positive internal and external customer relationship. Key Accountabilities and Expectations: To maintain regular contact and proper escalation with the Commercial Quality Control Supervisor regarding the status of loans in process, audit requests. Reviews complex commercial loan documentation and related supplements to support business partners, ensuring accuracy and adherence with Bank loan policy and guide. Determines document options and presents options to lenders/documentation specialists as applicable. Embraces change and continuous improvement concept, constantly looking to improve both efficiency and effectiveness of the Quality Control team and their processes. Responds to all requests for information and assistance in a prompt, efficient and friendly manner by relaying information as requested, and follows up on all situations that cannot be handled immediately. Resolves complaints in a reasonable timeframe. Maintain a good working knowledge of all Bank policies and procedures and identify deviations from policy, escalating as appropriate to the Commercial Quality Control Supervisor. Develop deep relationships with business partners, including Lenders, Credit Analysts, and Administrative Assistants to ensure optimal efficiency and effectiveness regarding services provided. To provide accurate, efficient, courteous, prompt, and professional telephone service to all customers and potential customers. To research, respond to customer inquiries and resolve customer complaints/issues in a timely and effective manner. To ensure loan documents and files are complete, accurate and in accordance with Bank loan policy. To track all outstanding loan documents/collateral items to ensure Bank's lien position is obtained. To assist with additional loan operation roles, as requested or necessary. Requirements Qualifications, Knowledge and Skills: 3-5 years of related loan processing experience and/or training; or the equivalent combination of education and experience. Work related experience should consist of Audit, Legal, Compliance, Financial Analysis, Credit Review, or similar fields. Educational experience, through in-house training sessions, formal school or financial industry related curriculum, should be business or financial industry related. Bachelor's degree in accounting, business, finance, or equivalent experience. A significant level of trust and diplomacy is required, in addition to normal courtesy and tact. Work involves extensive personal contact with others and is usually of a sensitive nature. Outside contact becomes important and fostering sound relationships with other entities (customers, vendors, etc.) becomes necessary. Solid working knowledge of banking industry practices relative to bank loan operations with respect to loan products, services, and terminology. Knowledge of commercial, construction, real estate and consumer loan products and processing. Knowledge of related state and federal lending and compliance laws and regulations, and other Bank lending policies. Highly accurate data entry skills and strong level of skill working with a variety of PC and internet applications, including spreadsheets (creating formulas) and the ability to navigate key industry specific Internet sites. Strong multi-tasking, time management, thoroughness, and accuracy skills required. Solid communication and organizational skills with focus on teamwork and cooperation. A high level of confidentiality is required. Ability to work under deadlines with frequent interruption. Physical Requirements: Work involves eye strain due to the constant use of computer screens, reading of reports, and sitting the majority of the day. Work involves being able to concentrate on the matter at hand, under sometimes distracting work conditions. Work involves lifting and moving loan files of up to 20 pounds. EOE - Race/Sex/Disability/Veteran This Position Description is not a complete statement of all duties and responsibilities comprising this position.Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this position at any time.