Maintenance Manager II

Calgon Carbon | A Kuraray Company is growing—and so can your career. Be part of a global leader in environmental solutions, where your work directly impacts the quality of air and water around the world. Position: Maintenance Manager II Location: Neville Island Plant – Pittsburgh, PA Excellent Benefits : Medical, dental, prescription & vision, HSA & retirement savings (401k) – Generous Company Match! Perks : Incentives/bonus plans, competitive pay, paid time off (vacation starting at 3 weeks), tuition reimbursement, wellness programs, fun events, learning & development opportunities. Hours of work: Full-time position with hours Monday-Friday 9:00-5:00 PM; outside hours as needed to accommodate peak activity The Maintenance Manager II will protect, maintain, and continuously improve the functions of plant assets to optimize asset life, on-stream factor, and total maintenance spend. The incumbent supports the overall NIP Profit Plan and performance objectives. The Maintenance Manager II plans, executes, and continuously monitors the Maintenance and Capital Plans, as well as leading establishment of programs for cost and productivity improvement. The Maintenance Manager II manages and supports up to 10-15 hourly workers in the maintenance SDWT and is responsible for portions of an annual budget of up to ~$1.5M plus turn around budgets and capital projects budget Duties and Responsibilities (not limited to) Lead and strongly advocate safety in all activities Lead by example, including execution of regular safety audits, safety contacts, near miss reports, safety meetings, incident investigation, etc. Incumbent is a member of the plant safety committee Develops, recommends, engineers and executes projects to expand plant production capacity, cost and quality Leads Facilities Engineering on large capital projects Lead or participate in special projects as assigned Projects may involve work outside the Neville Island Plant Continuously reviews and evaluates new technology, processes, methods, and equipment for possible use Communicates/ reports accomplishments, activities, issues/problems/risks, and status of projects in a monthly report Communicates major exceptions and issues on an on-going and immediate basis to the Neville Island Plant Manager Support NIP by ensuring safe and continuous production of finished product at established quality standards, within environmental permit requirements, and within financial constraints Plan, coordinate and execute facility Turnarounds that minimize cost of ownership while allowing the facility to continuously operate at or exceed, production, quality, and on-stream standards. This work must be executed within profit plan guidelines Maximizes quality, throughput, and yield standards by directing the maintenance teams, contractors, and maintenance functions Achieves continuous improvements by evaluating performance, taking corrective actions, and measuring progress Established key metrics to track performance in a balanced scorecard manner with emphasis on “leading indicators” Maximizes use of Total Productive Maintenance by identifying work, establishing schedules, training operators, and tracking performance Reliability center maintenance lead Provide technical guidance as needed Manages and supports the Maintenance SDWT to ensure optimum operation and function of plant facilities and equipment by focusing on true self-direction Provide clear direction and accountability Assesses and sources (in the most cost-effective manner) the technical and non-technical needs for maintenance personnel Manages and supports the Storeroom Associate to refine and preserve the plant stores and acquisition process so that it focuses on having the right parts in the right place at the right time Training for maintenance crew Vendor management for projects related Qualifications An associate’s degree (A.A.), or equivalent from two-year college or technical school is required (Mechanical, Electrical, or Chemical Engineering or comparable work experience) A bachelor's degree (B.A. or B.S.), or equivalent from four-year college or university is preferred 10 years of experience in maintenance and/or plant /facilities engineering SAP experience is preferred About Calgon Carbon At Calgon Carbon, we are scientific innovators with a proud legacy of over 80 years and more than 205 patents to our name. Since pioneering the first activated carbon products from bituminous coal in the 1940s, we’ve been at the forefront of developing cutting-edge technologies and solutions to meet the world’s evolving air and water purification needs. Today, our portfolio includes more than 700 direct market applications across a wide range of industries. Headquartered in Pittsburgh, Pennsylvania, Calgon Carbon employs approximately 1,685 professionals and operates 20 facilities worldwide dedicated to manufacturing, reactivation, innovation, and equipment fabrication. In Europe, we operate under the name Chemviron. In March 2018, Calgon Carbon became part of the Kuraray Group. Together, we offer complementary products and services, united by a shared commitment to delivering the highest quality and most innovative activated carbon solutions to customers around the globe. Calgon Carbon is an Equal Opportunity Employer, including disabled/veteran PIf6175681a09e-37344-41938500

EH&S Manager II

Calgon Carbon | A Kuraray Company currently has an opportunity where you can be a part of our growing team as we provide our customers with outstanding products that make the air we breathe and the water we use safe for generations to come . Position: EH&S Manager II Location: Big Sandy Plant – Catlettsburg, KY Excellent Benefits : Medical, dental, vision and retirement savings (401k) Hours of work: Mondays - Fridays, 9:00 AM - 5:00 PM, 40 Hrs / Wk The Site Environmental Health and Safety Manager II will provide leadership, vision, and direction in order to strengthen the site Environmental, Health and Safety culture at the Big Sandy manufacturing location. This individual will lead and develop a team of environmental, health and safety professionals and trainers to accomplish mission critical tasks. This role requires the creation of a strategic plan, that has prescribed key performance indicators that are monitored , audited, and focused on continuous improvement. This leader needs to prioritize and control significant plant level risks and work with all department leaders to sustain risk mitigation strategies. This individual will continuously define what good EHS looks like, communicate goals, and establish standards to meet expectations. Due to the number of EHS aspects and impacts associated with the Big Sandy Plant, the individual must be able to collaborate and communicate with regulatory agencies. With strategic guidance from both the central EHS function and local plant manager, this hands-on leadership position will: ensure local legislative compliance, develop and maintain ISO systems, develop an autonomous EHS culture, promote defined Health and Wellness programs, define EHS standard operating procedures, provide EHS training, develop risk identification and reduction awareness and methods, all achieved through participation and employee engagement. The Environmental Health and Safety Manager II proactively drives awareness, communicates best practices, and implements new programs related to EHS. This individual works to ensure safe behavior, machinery, and regulatory compliance for EHS at the site. They will lead continuous imp rovements of site EHS Man ag ement System. This role requires expertise in EH S regulat ions for air, waste, and water management, industrial hygiene, and safety regulations Duties and Responsibilities (not limited to) Lead a team for the filing of all internal, corporate, and required government reporting relating to regulatory compliance Maintains an EHS compliance calendar, audits compliance system routinely, and ensure compliance gaps are corrective Maintain site required ISO certifications where applicable Ensure compliance with site permits and plans (indirect discharge, SPCC, SWPPP, Air) Manage and ensure compliance with the waste management program (hazardous, non-hazardous, and universal) Develop and implement industrial hygiene programs to reduce exposure risk and prioritize hazard reduction philosophy Coach/mentor production managers and other plant leaders on EHS leadership Develop EHS direct reports to enhance expertise within the site Establish formal or informal mentorship programs that pair less experienced EHS staff with seasoned professionals or senior executives Develop behaviors, habits, processes and technologies that result in safety as a precondition Lead the development and Incorporate EHS tools into the daily operational activities (Shift meetings, production meetings, GEMBA walks). Help operations navigate complex regulations and company standards Develop and/or deliver budget plans with guidance from senior colleagues Establish both a short term and long term EHS strategy for the site in conjunction with guidance from the Plant Manager and CCC/ Chemviron Center of Excellence This EHS strategy shall be monitored as a KPI across the site and the incumbent will establish accountability channels to ensure that all levels of the organization delivers EHS results This individual shall also participate and lead cultural transformation across the site to achieve sustainable results Work closely with the Regional Center of Excellence leaders to verify quality of programs and processes via audit and self-assessment tools Develop a safety-first culture through leadership commitment and foster environment where workers feel secure reporting risks Promote continuous improvement using EHS data and inspection results to identify areas for continuous improvement Lead by example by conducting regular field observations firsthand, identify and resolve issues, and provide coaching Proactively drive awareness and communicates best practices related to Safety, Health and Environment, promoting an autonomous EHS culture Identify and champion impactful initiatives seeking continuous improvement in safety performance and environmental compliance Establish a site high consequence program to manage severe incidents with fatality (SIF) and ensure flawless execution of site life critical programs Lead high quality incident investigations, track corrective actions and monitor data for at-risk trends Qualifications Bachelor's degree (B.A. or B.S.), or equivalent from four-year college or university is required Master's degree (M.A.) or equivalent is preferred A professional environmental, safety or industrial hygiene certification is desired 10 years' experience in a manufacturing environment with a proven track record of success in reducing occupational injuries, working knowledge and expertise in Environmental regulations and maintaining compliance with pertinent regulation is required 10 years' experience of strong EHS background and experience in US EPA, OSHA, and KY state regulations and reporting is required 5-7 years e xperience of having the ability to identify change, communicate the need for change, and monitor integration for success is required 5-7 years of demonstrated abilities as an effective leader/trainer/coach is required 5-7 years of demonstrated abilities to communicate both horizontally and vertically is required About Calgon Carbon At Calgon Carbon, we are scientific innovators with a proud legacy of over 80 years and more than 205 patents to our name. Since pioneering the first activated carbon products from bituminous coal in the 1940s, we’ve been at the forefront of developing cutting-edge technologies and solutions to meet the world’s evolving air and water purification needs. Today, our portfolio includes more than 700 direct market applications across a wide range of industries. Headquartered in Pittsburgh, Pennsylvania, Calgon Carbon employs approximately 1,685 professionals and operates 20 facilities worldwide dedicated to manufacturing, reactivation, innovation, and equipment fabrication. In Europe, we operate under the name Chemviron . In March 2018, Calgon Carbon became part of the Kuraray Group. Together, we offer complementary products and services, united by a shared commitment to delivering the highest quality and most innovative activated carbon solutions to customers around the globe. Calgon Carbon is an Equal Opportunity Employer, including disabled/veteran PI956c051044bd-37344-41904259

Production Manager III

Calgon Carbon | A Kuraray Company is growing—and so can your career. Be part of a global leader in environmental solutions, where your work directly impacts the quality of air and water around the world. Position: Production Manager III Location: Columbus Plant – Columbus, OH Excellent Benefits : Medical, dental, prescription & vision, HSA & retirement savings (401k) – Generous Company Match! Perks : Incentives/bonus plans, competitive pay, dress for your day, hybrid schedules, paid time off (vacation starting at 3 weeks), tuition reimbursement, wellness programs, fun events, learning & development opportunities. Hours of work: Full-time position – standard hours are during the day shift plus on call 24/7 managed amongst the Production Management/Supervision team The Production Manager III will mentor and coach the Production Group leader I & Line Manager position, coach and reinforce expectations set in operator job descriptions, production operation sheets, and the overall safety of the operators. The incumbent will troubleshoot operational issues and provide technical support to the operations, review and approve production documentations and log sheets, certify operators and validate the training is adequate and complete, and motivate operators, as well as utilize process engineering skills to resolve problems and enhance plant efficiency. The Production Manager III will monitor equipment condition and housekeeping, then take action as necessary. Accountable for all planning, manufacturing and other support functions for the Columbus Plant to achieve safety, environmental, financial, production, and quality goals and responsible for a portion of $15 million operating budget and 35 employees. The Production Manager III will ensure that all operations at COL are carried out safely and efficiently to achieve maximum productivity, plus measure and collate all operational data (performance, maintenance and cost control). Duties and Responsibilities (not limited to) Review and approve production documents, administer OT as needed, and train employees as needed and required Maintain environmental compliance and facilitate activities with the environmental group Actively ensure processes & equipment is in compliance of permits through monitoring and coaching operators Serve as a model for working safely in the plant Conduct incident investigations on near misses, injuries, and accidents. Participate in Behavior Based Safety Observations Enforce safety policies and adherence to JSPs Maintain Environmental Compliance and facilitate activities with Environmental Agencies Manage Outside Agency Inspection Visits Review MOC for area of responsibility and ensure process/equipment changes are conducted in a safe and environmentally responsible manner Manage Cost Performance to Budget: materials, volume, spending. Manage Resource Requests (Material handling, Tools, housekeeping etc.) Monitor KPI's, Report on Performance, Act on Performance Issues. Identify work Process Improvement opportunities Administer company and plant policies maintaining effective labor relations Determine production line organization staffing needs, including overtime Review and approve Production Documentation (e.g., Log Sheets, Play Book) Review Production Plan and adjust product runs as needed Ensure resources are available for teams to produce on-time, quality product while they adhere to company and plant policies Lead teams in problem solving needs and motivate all teams to achieve plant goals/KPI's Determine production line organization staffing needs, including overtime Review and approve Production Documentation (e.g., Log, Monitor, and OP sheets, Yields, byproducts etc.) Review Production Plan and adjust product runs as needed Ensure that daily shift handover and area team meetings are held where issues are identified and root cause issues addressed Write and verify all the operators are trained and following all the Policies & Procedures Ensure supervisors, managers, and operators are maintaining training matrix, and up to date on SOP's Nurture the development of team employees including team leads Provide input to plant trainer to determine requirements of development for all employees to improve needed skills Qualifications A bachelor's degree or equivalent from a four-year college or university is required (Mechanical, Industrial, Chemical, or Process Engineering; equivalent education or work experience is also accepted) A master’s degree or equivalent is preferred 0-2 years of experience in a unionized manufacturing environment is required 3-5 years of supervisory experience is required 7-10 years of manufacturing experience is required About Calgon Carbon At Calgon Carbon, we are scientific innovators with a proud legacy of over 80 years and more than 205 patents to our name. Since pioneering the first activated carbon products from bituminous coal in the 1940s, we’ve been at the forefront of developing cutting-edge technologies and solutions to meet the world’s evolving air and water purification needs. Today, our portfolio includes more than 700 direct market applications across a wide range of industries. Headquartered in Pittsburgh, Pennsylvania, Calgon Carbon employs approximately 1,685 professionals and operates 20 facilities worldwide dedicated to manufacturing, reactivation, innovation, and equipment fabrication. In Europe, we operate under the name Chemviron. In March 2018, Calgon Carbon became part of the Kuraray Group. Together, we offer complementary products and services, united by a shared commitment to delivering the highest quality and most innovative activated carbon solutions to customers around the globe. Calgon Carbon is an Equal Opportunity Employer, including disabled/veteran PI0c7b347d4df2-37344-41480238

Certification Engineer II (Airworthiness)

Description: Position Summary: The Certification Engineer II is responsible for working as part of the certification team along with the internal program team, installers (TC/STC holders, MROs), suppliers, FAA, EASA and designees to research and to plan and execute large and small scale certification programs. Essential Duties and Responsibilities include the following, other duties may be assigned: Work as part of the certification team with FAA/EASA designees in developing certification basis and certification plans Liaison with OEMs, FAA/EASA, suppliers and internal customers to ensure timely project completion Maintain accurate and up-to-date certification records Manage Vendor testing and adherence to schedule to support final certification Develop tools, as necessary, to track deliverables, testing, compliance findings, to assure on-time completion of the project Reduce risks on programs by providing Risk Management reviews and surfacing issues real-time and providing risk assessment impact Responsible for the development of documentation required for obtaining approval from the aviation authorities (EASA / FAA). Interface with regulatory agencies (FAA/EASA/Other) for coordination and approvals Develop and execute certification programs with minimal supervision Coordination of certification-related tasks with other departments, such as program management, platform engineering, stress and testing Review and approve design changes in accordance with RECARO change management procedures, ensuring compliance with (E)TSO minimum performance standards. Follow internal company processes. Technical support of employees in the specialist departments in matters relating to certification. Support in the preparation of process instructions and compliance documents Participation in national as well as international technical conferences and collaboration in SAE working groups Train/mentor Certification engineering staff on Internal procedures and best practices Requirements: Education/Experience: A minimum of a Bachelors’ degree is required preferably in Aerospace / Mechanical / other engineering with at least 4 years’ relevant engineering experience or Master’s degree preferably in Aerospace / Mechanical / other engineering with at least 2 years’ experience in aircraft interior products. Aircraft Interior certification experience in TSO product testing is required. Knowledge on FAA and EASA requirements related to TSO/ETSO and aircraft interior certification. Knowledge of 14 CFR and CS Part 21, Part 25. Preparation of Certification plans, and Test plans related to certification in support of FAA and EASA requirements and compliance with airframe manufacturer requirements. Strong Project Management skills related to certification with the ability to establish track and maintain schedules from multiple suppliers or on multiple projects. Risk Management skills; ability to review current issues/program status and identify and manage project risks. Apply expertise in certification and testing in problem solving. Exceptional organizational skills, self-motivation, a sense of urgency and sensitivity to deadlines, and detail-oriented style are required. Ability to work within teams and lead projects, superior verbal and written communication skills is required. Have the ability to work with both domestic and international regulatory compliance offices and form good working relationships. Keep up-to-date with Industry guidance and develop new means of compliance, when applicable. PIe3548056ea8c-37344-41834914

Buyer (Plastics & Composites)

Description: Position Summary: Responsible for procurement of Plastic (thermoforming and injection mold) and Composite materials, components, supplies and/or services for the company in accordance with standard operating procedures, contractual requirements, financial and savings targets, and all regulatory requirements. Responsible for strategy execution, change management, source selection, contract negotiations, supplier management, and conflict resolution throughout the supply chain. Essential Duties and Responsibilities include the following, other duties may be assigned: Purchase Order Management Place and confirm purchase orders with approved suppliers for established material, parts, or services in accordance with contracts, master production schedule, independent spares/repair requirements, and established lead times. Ensure purchase orders are executed, goods received, and invoices paid in accordance with the approved terms and conditions. Master Data Management Maintain contracts and source rules within ERP system Manage lead time, part cost, setup cost, and mode of transportation Change Management Coordinate all engineering changes with the Engineering department, as assigned Perform analysis of inventory to include supplier WIP and transportation WIP Calculate cost impact due to engineering change to include cost of rework and scrap Manage effectivity date of change to minimize cost impact and maximize inventory consumption Ability to understand and read bills of material and Engineering drawings and RECARO standards Prepare all needed engineering data packages and facilitate submission to suppliers Manage supplier quote and negotiation process Manage PO revisions to support effectivity and master production schedule Resolve any documentation discrepancies Supplier Management Conduct monthly supplier management reviews to support business objectives & deliverables Manage supplier on time delivery and fill accuracy Manage all quality issues throughout the process to include first article, receiving inspection, discrepancies on the production line, and supplier corrective actions Management total cost of ownership to include part cost, transportation cost, cost of poor quality Maintain standard risk cube to include any mitigation plans Facilitate communication of forecasts with suppliers to ensure proper long range planning of capacity, manpower, and raw materials Manage any instances of supplier transition and present to sourcing board Ensure all RECARO owned tooling is properly tagged and logged into ERP system of record and maintain tool life, maintenance records and prepare annual tooling budget requirements Global Strategy Support RECARO global sourcing strategy Explore opportunities in low cost countries Support all exchange rate risk mitigation efforts Develop annual plan to accomplish cost targets Negotiation Ensure all required documentation is in place to include but not limited to: Non-Disclosure Agreement, Global Purchase Agreement, Quality Assurance Agreement, Supplier Questionnaire, Supplier Risk Assessment, Supplier Audit, Supplier Credit Report Lead negotiations of all terms and conditions of all agreements and contracts in the best interest of RECARO Ensure all negotiations are legal, ethical, and in accordance with company policies as well as any governing or regulatory agencies Supplier Selection Ensure supplier capabilities and core competencies are in line with the commodity family strategy and RECARO business objectives Conduct fair competition among qualified potential suppliers Evaluate supplier scorecard and audit results where applicable Present results to supplier selection board or sourcing board for approval Safety Follow all office safety policies Ensure compliance with all shop floor safety regulations when participating in activities within any production, logistics, warehousing, or staging areas. Compliance Ensure compliance with all RECARO policies, procedures, and work instructions Ensure compliance with any regulatory or governing body to include, but not limited to, AS9100, EN9100, ISO9001, ISO14001, FAA, EASA, Airbus, or Boeing Additional Any other duties as required by your supervisory staff. Requirements: Education/Experience: Bachelor’s degree in a related field plus 3 years of experience in procurement or 7 years of experience in procurement without a bachelor’s degree. Experience in thermoforming, injection mold, and/or composite procurement a plus. Engineered-to-order procurement is a plus Willing and able to travel throughout the United States and to other countries as required Computer Skills: Microsoft Word, Excel, PowerPoint, and Outlook required Familiarity with MRP systems/SAP experience preferred Familiarity with Teamcenter preferred PI0e9a4362749d-37344-41960444

Applications Engineer IV

Calgon Carbon | A Kuraray Company is growing—and so can your career. Be part of a global leader in environmental solutions, where your work directly impacts the quality of air and water around the world. Position: GAC Applications Engineer IV Location: US – Remote (West Coast) This is not an IT position Excellent Benefits : Medical, dental, prescription & vision, HSA & retirement savings (401k) – Generous Company Match! Perks : Incentives/bonus plans, competitive pay, dress for your day, hybrid schedules, paid time off (vacation starting at 3 weeks), tuition reimbursement, wellness programs, fun events, learning & development opportunities. Hours of work: Full-time position with hours Monday-Friday 9:00-5:00 PM Travel: Visits to customer/plant sites The Applications Engineer IV provides the primary technical support for the sale of carbon, equipment, and service in domestic or international markets. This role interfaces with Equipment Engineering, Research and Development, Equipment and Assembly, Product Management, and Sales to provide the technical justification for the use of activated carbon technology in customer applications. This position will assist in the technical development of emerging markets/applications as it pertains to their area of focus Duties and Responsibilities (not limited to) In coordination with Technical Director, Market Development and Sales Director, develop strategies and market-specific approaches to expand existing base business and develop new business opportunities through CCC technology adoption Regularly review and evaluate actual results, report/troubleshoot variances, adjust strategy as appropriate Provide support for the Business Unit on CCC global initiatives / cross-business segment groups Acts as technical support and back-up contact related to specific projects for Sales team Serves as liaison between Sales team and internal support teams including Product and Project Management and R&D Review bid specifications for clarity, accuracy, and acceptance Provide recommendations to improve technical quality of bid specifications and prevent undue risk to Calgon Carbon Serve as main Calgon Carbon contact to customer when Technical Sales Rep is unable to respond to customer Attend technical conferences and trade shows to gain technical knowledge and represent Calgon Carbon as a leader in the activated carbon market Prepare and present papers/posters at conferences, trade shows and virtual opportunities, e.g. webinars Develop and present technical presentations / trainings to engineering consultants, clients, regulators, legislators and other to influence selection of treatment solutions Represent CCC at Industry Groups and Governing Bodies, AWWA, etc. Use CCC and 3rd Party computer design programs to predict the performance of activated carbon in liquid and vapor applications Set-up and monitor pilot trials in the field to provide design information for future full scale systems Interpret data from lab and field trials for both pilot and full scale systems to provide technical design and operational recommendations Troubleshoot customer problems such as short filter run-times or unexpected contaminant breakthrough Provides application engineering support for a geographic region(s) or a set of Technical Sales Reps Provides consulting services for the customer as needed Authors pilot study reports as requested by customer Qualifications A bachelor's degree (B.A. or B.S.), or equivalent from four-year college or university is required (Chemical Engineering or related engineering/chemistry field) 3-5 years of experience in the use and troubleshooting of adsorption equipment at customer sites is required 5-7 years of experience in the application of carbon adsorption technology to address customer requirements in liquid and gas purification, including carbon modeling, equipment design and development, and equipment functionality Must be able to work under general supervision with a high degree of creativity and latitude Business/marketing experience is preferredWater treatment experience is preferred About Calgon Carbon At Calgon Carbon, we are scientific innovators with a proud legacy of over 80 years and more than 205 patents to our name. Since pioneering the first activated carbon products from bituminous coal in the 1940s, we’ve been at the forefront of developing cutting-edge technologies and solutions to meet the world’s evolving air and water purification needs. Today, our portfolio includes more than 700 direct market applications across a wide range of industries. Headquartered in Pittsburgh, Pennsylvania, Calgon Carbon employs approximately 1,685 professionals and operates 20 facilities worldwide dedicated to manufacturing, reactivation, innovation, and equipment fabrication. In Europe, we operate under the name Chemviron. In March 2018, Calgon Carbon became part of the Kuraray Group. Together, we offer complementary products and services, united by a shared commitment to delivering the highest quality and most innovative activated carbon solutions to customers around the globe. Calgon Carbon is an Equal Opportunity Employer, including disabled/veteran PI37957d67e016-37344-41971273

Histologist Registered - Laboratory

Description Summary: The Histologist Registered, assists with cuts, stains, and mounts specimens of human tissue to provide data on functioning of tissues and organs, causes and/or progress of disease, following established standards and practices. Responsibilities: Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders. Collects, processes, and stores surgical/cytological specimens Enters patient information, orders, and technical information into LIS; prints/organizes cassettes Prepares specimens/slides/blocks for referral Orders, maintains referral log, processes reports, and monitors pending Maintains grossing area, frozen section room, and autopsy suite including cleaning and stocking of supplies and preparation of solutions Performs technical procedures that result in the creation of microscopic slide preparation Within acceptable TAT guidelines, devises and directs performance of routine and special stains to provide appropriate slides for the microscopic evaluation of tissues, fluids, and other A/P specimens Operates microtomes, embedding stations, tissue processors, staining equipment, cover slippers and other AP equipment to provide quality slides for pathologist examinations Operates Immunostainer(s) to provide quality slides for diagnostics immunostains Performs manual stains, as needed, to provide quality slides for diagnostic immunostains Assists Pathologist’s / PA’s with frozen sections, fine needle aspirations, and autopsies Quality Control / Improvement: performs analysis and records QC according to policy and procedure following CLIA, CAP, and Joint Commission guidelines and standards Maintenance/Lab Management: performs established daily and periodic preventative maintenance with documentation; troubleshoots minor problems and initiates service calls as needed; orders and restocks supplies/reagents; reviews policy & procedure manual; dates reagents and discards expired reagents Continuing Education/Development: attends, reads, or listens by tape to material of 10-12 in-house educational programs yearly; trains new staff in practices Completes tasks or special projects within time frame as assigned, or as requested by Supervisors, Manager, or Director Accreditation: follows CAP, AABB, Compliance, CLIA, JCAHO, and OSHA standards and prepares/participates in all applicable inspections Follows established protocols for safety, infection control, security, compliance, and the use of hazardous materials. Job Requirements: Education/Skills High School Diploma or equivalent preferred. Completion of an accredited Histotechnology Program by CAHEA/NAACLS or military equivalent required. Successful completion of the core educational curriculum “Excellence at the Front End” required within one year of employment. Experience 2 years of experience in histopathology is required along with a High school Diploma. 1 year of experience in histopathology is required along with an Associate’s degree. Licenses, Registrations, or Certifications Certified Healthcare Access Associate through the National Association of Healthcare Access Management (NAHAM) preferred. Histotechnology certification by the American Society of Clinical Pathologists certification (ASCP) preferred. Work Schedule: 9AM - 6PM Work Type: Full Time

Medical Lab Technician II - Outpatient Lab

Description Summary: The Medical Laboratory Technician II performs complex clinical testing in assigned section/s such as general laboratory, Blood Bank, and Microbiology sections, with all duties necessary for accurate and timely results including quality control, performance improvement, proficiency testing, and preventative maintenance of equipment. Associates in this job recognize abnormal critical values and follow proper guidelines for notifying medical team members of results. Performs clerical, general, and phlebotomy duties related to daily operations in the laboratory. Provides/dispenses blood products as requested by medical staff. Responsibilities: Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders. Specimen Collection/Handling/Processing– obtains blood specimens via venipuncture and/or fingerstick, accurately identifies and labels appropriately; answers pneumatic tube system; follows procedures for processing and testing specimens, including operating various centrifuges; obtains other designated patient specimens as listed in procedure manuals. Result Reporting – recognizes errors or improbable results and takes appropriate action; reports critical values per Policy and Procedure; performs tests within established timeframe; performs laboratory testing, if designated, in the following sections: Hematology, Urinalysis, Coagulation, Chemistry, Special Chemistry, ER Stat Lab, and Microbiology; performs blood bank procedures, including crossmatching, ab id’s, and dispensing of blood products; operates laboratory automated analyzers according to established procedures. Performs, analyzes, and records QC according to Policy & Procedure following CLIA, CAP, AABB, and JCAHO guidelines; performs and records Performance Improvement indicators and reports results. Performs established daily and periodic preventative maintenance with documentation; troubleshoots minor problems and initiates service calls as needed; orders (or notifies assigned associate) and restocks supplies/reagents; reviews policy & procedure manual; dates reagents and discards expired reagents. Takes responsibility for seeking and achieving professional growth and continued education. Assists in training new associates and students in Laboratory practices. Follows CAP, AABB, Compliance, CLIA, JCAHO, and OSHA standards. Follows established protocols for safety, infection control, security, compliance, and the use of hazardous materials. Utilizes LIS and HIS computer systems appropriately to perform, charge, and report laboratory results. Completes annual competency assessment successfully and by assigned date. Job Requirements: Education/Skills Associate degree or higher in clinical laboratory science or medical laboratory technology from an accredited institution or equivalent laboratory training and experience meeting the requirements defined in the CLIA regulation 42CFR493.1489: Successfully completed an official U.S. military medical laboratory procedures training course of at least 50 weeks duration and currently hold the military enlisted occupational specialty of medical laboratory specialist (laboratory technician); OR 60 semester hours or equivalent from an accredited institution that, at a minimum, includes either 24 semester hours of medical laboratory technology courses, OR 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology, and 12 semester hours of chemistry, biology or medical laboratory technology in any combination; AND Laboratory training including either completion of a clinical laboratory training program approved or accredited by the ABHES, NAACLS, or other organization approved by HHS (note that this training may be included in the 60 semester hours listed above), or at least three months documented laboratory training in each specialty in which the individual performs high complexity testing. Experience No experience required for graduates of a clinical laboratory training program approved or accredited by NAACLS, or other organizations approved by HHS. OR Six Months of approved clinical laboratory experience, which must include a clinical rotation through the following sections of the laboratory: Blood Banking, Microbiology, Chemistry, and Hematology, Immunology, and Urinalysis/Body Fluids in the U.S. or with an accredited laboratory within the last 5 years. (This meets the AMT MLT eligibility requirement) AND less than 5 years of experience as a Medical Laboratory Technician (MLT). Licenses, Registrations, or Certifications MLT from ASCP, AMT, AAB, or HEW/HHS required. If certification with an expiration date is held, the certification must be maintained and kept current. Louisiana requires State Licensure. New Graduate that is Board Certified or eligible (must complete Board Certification within 1 year of hire, Louisiana excluded). Work Schedule: MULTIPLE SHIFTS AVAILABLE Work Type: Full Time

Clinical Pharmacist I - General Pharmacy

Description Summary: All pharmacists fill orders for drugs, monitor patient drug therapies and provide drug information. Pharmacists provide pharmacy services with compassion, excellence, and efficiency. Responsibilities: Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders. Operational Duties and Responsibilities Prepares and dispenses drug orders per physician request according to established policies, procedures, and protocols. Interprets drug orders (verbal and written) and transcribes/verifies into computerized patient medication record accurately. Maintains, accurate, complete patient drug record. Compounds and dispenses pharmaceuticals including non-sterile and sterile products, chemotherapy and parenteral nutrition products accurately. Issues controlled substances to patient care areas and maintains records as required by law and institutional policies. Provides services efficiently and in a timely fashion. Maintains current pharmacist license. Ensures applicable CE records and licensure are maintained in department files. Attends staff meetings. Completes all competency/skills assessment requirements. Supervises and directs pharmacy support personnel. Verifies the daily activities of pharmacy technicians Ambulatory care Pharmacist: Provides ambulatory pharmaceutical care services utilizing approved protocols and/or collaborative agreement with other providers, including managing patient drug therapy, anticoagulation management, providing patient education, and preparing and/or overseeing the preparation and dispensing of medications. Performs duties in the clinical areas assigned such as but not limited to anticoagulation clinics, intensive medical home, transition of care, Discharge Medication reconciliation, etc. Clinical Duties and Responsibilities Ensures safe, appropriate, cost-effective drug therapies for patients according to established policies, procedures, and protocols. Monitors drug therapy regimens for contraindications, drug-drug interactions, drug-food interactions, allergies and appropriateness of drug and dose. Assists with pharmacokinetics consult service and renal drug dosing per hospital protocol. Reads, extracts, and interprets information in patient medical records accurately. Detects and reports suspected adverse drug reactions accurately and in a timely manner. Sustains the hospital drug formulary, minimizing non-formulary procurements, utilizing therapeutic substitution protocols, and promoting rational drug therapy selection. Provides clinical consultation and clarification to practitioners as appropriate. Provides accurate, adequate, and timely drug information to the hospital’s professional staff. Provides drug education to patients and their families per institutional protocol. Participates in the quality improvement and medication use review activities of the department. Collects data, conducts monitors and inspections, and maintains logs, records and other documentation as assigned. Conducts designated interventions as defined in department Clinical Intervention activities (IV to PO, Renal Dosing, Pharmacokinetic dosing support, Anticoagulation). Baseline departmental standards for reporting interventions for clinical productivity as defined by departmental goals. Participates in antibiotic stewardship, opioid stewardship, and shortage management activities as assigned. Attends interdisciplinary rounds when assigned. Provides services efficiently and in a timely fashion. Occupational Hazards Potential for exposure to hazardous and toxic substances (including chemotherapeutic, cytotoxic drugs and cleaning solutions), sticks or cuts by needles and other sharp items. Risk 0 exposure category. Potential for musculoskeletal injuries if proper lifting and carrying techniques are not used. Potential exposure to biologic material when participating in direct patient care activities (e.g., patient education, code attendance). Job Requirements: Education/Skills Doctor of Pharmacy or BS Pharmacy degree required Experience Hospital experience preferred Licenses, Registrations, or Certifications Pharmacy state licensure required within 60 days of start date BLS or ACLS is required PALS (for pediatric practice) is required In accordance with the CHRISTUS Health License, Certification and Registration Verification Policy, all Associates are required to obtain the required certifications for their respective positions within the designated time frame. Work Schedule: 10PM - 8:30AM Work Type: Full Time

Hospital Pharmacy Technician

Description Summary: All pharmacy technicians work under the direction of Clinical Pharmacists to provide pharmacy services with compassion, excellence, and efficiency. Responsibilities: Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders. Must be 18 years or older. Operational Duties and Responsibilities Pharmacy Technicians perform ONLY non-judgmental technical duties under the direct supervision of a pharmacist. Prepares drug orders per physician request according to established policies, procedures, and protocols - Verifies computerized patient medication records accurately. Maintains, accurate, complete patient drug record. Compounds non-sterile pharmaceuticals. Provides services efficiently and in a timely fashion. Issues controlled substances to patient care areas and maintains records as required by law and institutional policies. Verifies the daily activities of the department are complete and recorded. Maintains competency required for current job title/position Maintains current technician license. Ensures applicable CE records and licensure are maintained in department files. Attends staff meetings. Completes all competency/skills assessment requirements. Specialty area - Serves as the technician in specialty areas such as the operating room or pharmacy work areas outside the central pharmacy. Ambulatory care - Provides ambulatory pharmaceutical care services as assigned such as but not limited to anticoagulation clinics, intensive medical home, transition of care, Discharge Medication reconciliation, etc. Retail - Performs outpatient distributive functions related to entering prescriptions orders, selecting the correct medications for new and refilled prescription orders, and coordinates delivery of medications for patient pick-up or delivery. Clinical Duties and Responsibilities Ensures safe, appropriate, cost-effective drug therapies for patients according to established policies, procedures, and protocols. Reads, extracts, and interprets information in patient medical records accurately. Detects and reports suspected adverse drug reactions accurately and in a timely manner. Coordinates pharmacist drug education to patients and their families per institutional protocol. Participates in the quality improvement and medication use review activities of the department. Collects data, conducts monitors and inspections, and maintains logs, records and other documentation as assigned. Provides services efficiently and in a timely fashion. Occupational Hazards Potential for exposure to hazardous and toxic substances (including chemotherapeutic, cytotoxic drugs and cleaning solutions), sticks or cuts by needles and other sharp items. Risk 0 exposure category. Potential for musculoskeletal injuries if proper lifting and carrying techniques are not used. Potential exposure to biologic material when participating in direct patient care activities (e.g., patient education, code attendance). Job Requirements: Education/Skills High School Diploma or equivalent preferred Experience Pharmacy experience preferred Licenses, Registrations, or Certifications Registered Pharmacy technician in the State of practice required Registered Pharmacy technician trainee accepted with the expectation of completion within two years Certified pharmacy technician preferred In accordance with the CHRISTUS Health License, Certification and Registration Verification Policy, all Associates are required to obtain the required certifications for their respective positions within the designated time frame. Work Schedule: MULTIPLE SHIFTS AVAILABLE Work Type: Per Diem As Needed

Supervisor Laboratory - General Lab

Description Summary: This Job meets the minimum CLIA qualifications of a Laboratory General Supervisor, and under the direction of the Laboratory Director and/or Laboratory Manager, coordinates and manages the day-to-day operations of their specific section(s) and shift(s). The Laboratory Supervisor serves in an administrative role with direct reports, and functions in an exempt pay status. In conjunction with the Laboratory Director and/or Laboratory Manager, this Job develops and implements new procedures, instrumentation, quality control, and reagent use. This Job is also responsible for the development and maintenance of policies and procedures that meet the standards of regulatory agencies and implement service quality improvements. The Laboratory Supervisor ensures all personnel are held accountable through ongoing personnel performance reviews and assists in the orientation and development of personnel competencies for their section(s). Responsibilities: Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders. Is responsible for providing day-to-day supervision of high, moderate, and waived complexity test performance by laboratory testing personnel. Must be accessible to address technical problems via on-site, telephone, or electronic consultation with testing personnel at any time that testing is performed in accordance with policies and procedures established by the laboratory Medical Director. Ensures compliance with all policies, procedures, and standards as promulgated by state and federal agencies, the hospital, and other regulatory entities such as CLIA, TJC, CAP, AABB, etc. Plans, organizes and coordinates the work activities of assigned section(s) and shift(s). Keeps accurate attendance records on all associates; maintains time and attendance records for the department. Assists the Director/Manager in maintaining the Laboratory budget to include monthly analysis and variance reporting on expense detail. Assists the Director/Manager in associate performance conversations that drive merit increases. Develops, implements, and maintains current procedural manuals of all tests performed in the section(s) assigned and updates and reviews manuals biennially or more often as necessary. Enforces all safety policies and procedures. Researches, evaluates and implements new and improved procedures, methodologies, instrumentation, and techniques as assigned by the Director/Manager, or Supervisor. Implements an appropriate section and/or shift-specific Quality Control Program and maintains all applicable Quality Control and Functional Verification records. Is responsible for monitoring test analyses and specimen examinations to ensure that acceptable levels of analytic performance are maintained. Reviews the work done by technologists/technicians working in the section(s) or shift(s) assigned to ensure a minimum of errors and corrective action in the interest of good patient care. Refers clinical problems to the laboratory director, manager, or supervisor as appropriate. Assures that all remedial actions are taken whenever test systems deviate from the laboratory's established performance specifications. Ensures that patient test results are not reported until all corrective actions have been taken and the test system is properly functioning. Operates, maintains, and troubleshoots all equipment in assigned section(s) to keep in good working order; makes minor repairs and adjustments when necessary; initiates and follows through with Biomedical Engineering/equipment manufacturer for safety checks and repairs; schedules preventive maintenance within the section with Biomedical Engineering, equipment manufacturer, or an outside contractor. Prepares and submits routine or special administrative and technical reports by due dates as required, requested, or delegated. Orders and maintains inventories for all necessary supplies and reagents in assigned section(s) to always have an adequate amount on hand. Trains new technologists and technicians in the assigned section(s) procedures and policies and provides subsequent training in all new or revised procedures and techniques for assigned shift(s) or provides remedial training as necessary. Responsible for maintaining orientation records on new associates. Assists the Director/Manager in designing, implementing, collecting, and analyzing data, and reporting all phases of a comprehensive performance improvement program that involves laboratory personnel in Performance Improvement activities. Prepares and conducts in-service education either formally or informally for assigned section(s) and shift(s). Provides input on personnel for hire, fire, transfer, interview, disciplinary probation, etc; counsels and documents technical deficiencies. Performs skills review and competency assessments and maintains appropriate documentation on all technical personnel as delegated by the Laboratory Manager/Director. Oversees and enforces expectations of personnel in assigned section(s). Participates in proficiency testing surveys; reviews and evaluates results and maintains copies of survey records in section(s). Coordinates and attends meetings as required to discuss changes and developments regarding policies, equipment, procedures, staffing, etc. Utilizes and has a thorough working knowledge of the Laboratory Information System and applications thereof. Demonstrates competence to perform assigned patient care responsibilities in a manner that meets the population-specific and developmental needs of patients served by the department. Appropriately adapt assigned patient assessment, treatment, and/or care methods to accommodate the unique physical, psychosocial, cultural, age-specific, and other developmental needs of each patient served. Processes patient specimens, including collection, handling, and distribution always cognizant of minimal pediatric specimen volumes (when required). Performs all routine and complicated laboratory procedures in the primary section which assigns age (Pedi) or sex-specific values. Provides notification and documentation of critical laboratory values obtained. Calculates, enters, and/or verifies results of laboratory procedures. Performs all duties in a manner that protects the confidentiality of patients and does not solicit or disclose any confidential information unless it is necessary for the performance of assigned job duties. Keeps abreast of Medical Technology, by reading Journals, texts, and technical bulletins; attends workshops and seminars; becomes active in local professional associations. Demonstrates adherence to the CORE values of CHRISTUS Health. Performs other duties as assigned. Job Requirements: Education/Skills • Bachelor's degree or equivalent education in chemical, physical, biological, clinical laboratory science, or medical technology from a regionally accredited college/university or equivalent years of experience required. Experience • 5 years of experience as a Medical Technologist, Clinical Laboratory Scientist, Medical Laboratory Scientist, or Medical Laboratory Technician required. • 5 years of full-time primary experience in the specific section of responsibility required. Licenses, Registrations, or Certifications • Certification for MT, MLS, CLS, or MLT from ASCP, AMT, AAB, or HEW/HHS required. Work Schedule: 5 Days - 8 Hours Work Type: Full Time

Outpatient Therapist (Medford, OR) - 5839

APPLY TODAY AND MAKE A DIFFERENCE IN THE MENTAL HEALTH FIELD! Relocation Assistance Available What We Offer Enjoy our many benefits and incentives including: Affordable Medical/Dental/Vision plansFlexible Spending AccountGenerous Paid Time OffWhole Health & Wellness Reimbursement ProgramSupervision toward Licensure Program (pending completion of introductory period)Professional development and training opportunities100% Vested Retirement Plan w/ up to 6% MatchHoliday Pay (9)Paid Personal Growth HoursPaid Time Off for Mental HealthCompany Paid Life InsuranceSpontaneous & Longevity BonusesLoan Forgiveness Program EligibilityEmployee Assistance Program (EAP) & Tobacco Cessation Program For more details about our benefits, visit our website ! About the Position We have an opportunity for Two (2) Outpatient Therapist's to provide On-Site clinical services at our Central Clinic in Medford, Oregon . The Outpatient Therapists make a meaningful impact within a collaborative, multidisciplinary network of medical providers, case managers, peer supports, and employment specialists. In this role, your clinical voice is valued and empowered as you deliver holistic, acuity-based behavioral health care through meaningful client assessments, tailored treatment plans, and active team synergy to drive positive, long-term patient outcomes for the Southern Oregon community. In addition, you will receive crisis de-escalation training, which requires performing various physical, hands-on maneuvers and techniques. Work Schedule: Monday through Friday, 8:00am to 5:00pm (Full Time, Day) What You’ll Make $76,800 - $90,000 per year DOE/Credentials. Additional 5% Language Differential offered for Bilingual or Multilingual candidates. Pay Scale Unlicensed: $76,800 - $84,000 per year Professional Oregon Mental Health License: $84,000 - $90,000 per year About the Program Our Outpatient Program provides assessment and evaluation, treatment plan development, and provides clinically indicated outpatient therapy, case management, skills training, and psychiatric (medication) services. The Psychiatric Services Team operates as a branch within the Outpatient Program, specializing in psychiatric, nursing, and medication services. Psychiatric services are provided both on-site and remotely through telemedicine. ColumbiaCare Services is a qualifying employer for the Public Service Loan Forgiveness (PSLF) Program. What You’ll Need Must be eligible for Qualified Mental Health Professional (QMHP) registration. Eligibility requires: Master's Degree in Psychology, Counseling, Social Work, or related fieldCurrent LCSW or LPC is Strongly Preferred Unlicensed therapists MUST be actively seeking or willing to obtain licensure. TWO (2) YEARS of post-graduate clinical experience in a mental health treatment setting is preferred If not already registered as a QMHP through the Mental Health & Addiction Certification Board of Oregon (MHACBO), we will assist you in registering within the first week of employment. Successful applicants must have the ability to pass a DHS criminal background check. Physical Requirements: This position requires the ability to frequently sit, talk, listen, and use hands and fingers. It may require the ability to occasionally walk, climb stairs and ladders, bend, stoop, squat/kneel, and perform other physical tasks as applicable; as well as lift, carry, push, and pull up to 20 pounds . Technology Requirement Employees are required to maintain access to a compatible smartphone capable of supporting the organization’s approved multi-factor authentication (MFA) application as a condition of employment. This requirement enables secure access to company systems. We recognize that expertise can arise from diverse experiences. If you're passionate about our mission but unsure about meeting all qualifications, we encourage you to apply. For any questions about eligibility or the application process, please contact our HR department. About Us ColumbiaCare Services is a non-profit, behavioral health and Veteran’s service agency offering a full spectrum of programming to help people get better. We are more than a company. We are a diverse team of individuals who are in the business of changing people's lives. We specialize in providing outpatient services, residential treatment programs, mental health housing, and other supports in beautiful and therapeutic service settings. We promote the whole health and wellbeing of the individuals and communities we serve. We value and honor the culture in our communities in all forms, including but not limited to race, gender, sexuality, ethnicity, nationality, spirituality, Veterans, people with disabilities, and members of the LGBTQ community. We welcome persons from historically underrepresented groups to apply. We seek applicants who can demonstrate experience working with individuals from different backgrounds and who will contribute to our mission, vision, and core values. We invite individuals from all walks of life to apply. We strive to deliver equitable employment best practices and opportunities for all, from recruitment, to interviewing and hiring, to our retention activities, promotions, and training and growth opportunities. We give priority to applicants who qualify under protected Veteran status and people with disabilities. Monday through Friday, 8:00am to 5:00pm (Full Time, Day) Compensation details: 76800-90000 Yearly Salary PI2bdd830bd2eb-37344-41720194