Associate Director, Toxicologist - Stamford, CT - KatalystHLS.com

Associate Director, Toxicologist - Stamford, CT Katalyst HealthCares & Life Sciences KatalystHLS.com ------------------------------------------------------- Primary Responsibilities: To oversee the conduct of general toxicity and drug safety studies in accordance with current scientific and applicable regulatory standards (ICH, FDA) and GLPs and will monitor safety studies related to drug registration. The incumbent will be specialized in general safety evaluation including carcinogenicity evaluation and may have experience in one or more of the following areas genetic toxicology, safety pharmacology, reproductive toxicology. #toxicology #pharmacology #drugsafety #KatalystHLS

https://www.indeed.com/job/associate-director-toxicologist-7927c790cceec664

Legal Specialist - Stamford, CT KatalystHLS.com

Legal Specialist - Stamford, CT KatalystHLS.com Katalyst HealthCares & Life Sciences -------------------------------------- Primary Responsibilities: Assist attorneys with all phases of litigation and government investigations. Assist with discovery and e-discovery, including but not limited to document collection and document productions. Assist with categorizing documents by subject matter, prepare a chronology of facts and create collection and production charts. #paralegals #attorneys #paralegal #patent #patentlaw #KatalystHLS #contractjobs

https://www.indeed.com/job/legal-specialist-25a0e60dc620324e

Manufacturing Engineer - Gainesville, FL - KatalystHLS.com

Job Description: Strong knowledge and very good experience in EUMDR activity\'s. Deep understanding of and experience in EU MDR preparedness Create a framework and strategy for key Medical Affairs and Medical Safety aspects to be compliant with EU MDR Excellent knowledge in International Medical Quality and Regulatory Standards e.g. IEC, FDA, CFR, MDD, UL, CE, CSA, BIS etc.

https://www.indeed.com/job/manufacturing-engineer-58505f7fc8f615f7

Technical Services Engineer - South Plainfield, NJ 07080 - KatalystHLS.com

Overview: Responsible for process development, scale-up and performing process optimization/validation studies for existing products, new product development and product transfers.

https://www.indeed.com/job/technical-services-engineer-d0d5761a0113b116

Manufacturing Engineer - Gainesville, FL - KatalystHLS.com

Job Description: Strong knowledge and very good experience in EUMDR activity\'s. Deep understanding of and experience in EU MDR preparedness Create a framework and strategy for key Medical Affairs and Medical Safety aspects to be compliant with EU MDR.

https://www.indeed.com/job/manufacturing-engineer-58505f7fc8f615f7

Regulatory Affairs Professional III - Wilmington, DE - KatalystHLS.com

Regulatory Affairs Specialist supports changes to commercial in vitro diagnostic reagents and consumables at Siemens Healthineers\' or prepare and submit product related regulatory submissions to international Regulatory Affairs team members.

https://www.indeed.com/job/regulatory-affairs-professional-iii-24da8a86e8e9826c

Regulatory Affairs Professional III - Wilmington, DE - Katalyst.com

Description: Regulatory Affairs Specialist supports changes to commercial in vitro diagnostic reagents and consumables at Siemens Healthineers\' or prepare and submit product related regulatory submissions to international Regulatory Affairs team members.

https://www.indeed.com/job/regulatory-affairs-professional-iii-24da8a86e8e9826c

Clinical SAS Programmer - Cambridge, MA - KatalystHLS.com

Clinical SAS Programmer - Cambridge, MA - KatalystHLS.com Looking for quality candidate to support the SAS stats programming for clinical & non-clinical projects/studies, including developing, testing, maintaining, validating, and documenting SAS programs to meet the project\'s needs.

https://www.indeed.com/job/clinical-sas-programmer-782837259d9920d1

Biostatistician - Beverly Hills, CA - KatalystHLS.com

Biostatistician - Beverly Hills, CA - KatalystHLS.com Work closely with team to ensure deliverables in accordance with ICH-GCP, define relevant Standard Operating Procedures (SOPs) and/or client-specific requirements. Develop, revise and maintain SOPs and provide training on new and revised SOPs as needed. Drive CAPA/remediation as needed for biostatistics activities. Develop and implement training programs for appropriate departmental teams.

https://www.indeed.com/job/biostatistician-a0d69fb39b943489

October 29, 2019 - World Psoriasis Day

October 29, 2019 - World Psoriasis Day Katalyst HealthCares & Life Sciences World Health Organization #WorldPsoriasisDay2019 aims at: Raise awareness; Spread information; Improve access to treatment; Give the psoriasis community a voice #Psoriasis #KatalystHLS #WHO KatalystHLS.com

http://katalysthls.com/

Business Development Manager, Staffing - South Plainfield, NJ 07080 - KatalystHLS.com

Business Development Manager, Staffing - South Plainfield, NJ 07080 - KatalystHLS.com Business Development Manager sells the staffing process/services of Katalyst HLS by obtaining, securing, and sustaining business with professionals within the Pharma/Biotech/Medical Device/CRO industries. Katalyst HLS is specialized in the connecting top employers with the best talent around. Our focus areas include: #ClinicalResearch #ClinicalDataManager #Biostatistician #ClinicalSAS #DrugSafety #Pharmacovigilance #MedicalWriter #RegulatoryAffairs #Manufacturing #QualityAssurance @QualityEngineer #Validations #ValidationEngineer #Staffing #BusinessDevelopmentManager #VMS #MSP

https://www.indeed.com/job/business-development-manager-staffing-dc7e7571df4d69ac

Clinical Data Manager - Boston, MA - KatalystHLS.com

Clinical Data Manager - Boston, MA. KatalystHLS.com Serve as an active member of Study Teams. Work with other functions to manage timelines and ensure that clinical data management deadlines are met. Liaise with third-party vendors such as CROs and central laboratories in support of timelines and data-related deliverables. Work with database builders to develop EDC databases, edit checks and reports. May define database and edit check specifications to support the protocol and analyses

https://www.indeed.com/job/clinical-data-manager-2ea0bf8b5dadc561

Biostatistician - Beverly Hills, CA - Indeed.com

Biostatistician - Beverly Hills, CA - Indeed.com Overview: Our Medical Device client in CA is looking for a Biostatistician who can be on site 40 hours a week to help with their clinical studies. They are a Medical Device client, but the consultant can come from Pharma as Device experience is a plus not a must. The candidate must be a go getter, willing to learn, takes direction and is adaptable to a fast-paced environment. The manager is open to an individual who has 2-7 years\' experience (more is OK, but she said she has struggled in the past with these people as they are not as adaptable to follow the company processes).Roles & Responsibilities: Work closely with team to ensure deliverables in accordance with ICH-GCP, define relevant Standard Operating Procedures (SOPs) and/or client-specific requirements. Develop, revise and maintain SOPs and provide tr

https://www.indeed.com/job/biostatistician-a0d69fb39b943489

Senior Statistical Programmer - Deerfield, IL - Indeed.com

Senior Statistical Programmer - Deerfield, IL - Indeed.com Roles and Responsibilities: Develop programs that convert raw SAS datasets into standard format and improve existing programs by creating standard programs and macros. Collaborate with manager and other programmers through participation in formal and ad-hoc meetings. Prepare documentation on all production programming and validation activities; utilize best industry business practices and data standards for clinical data submissions to the FDA and other global regulatory agencies. Assist manager through contributions to continuous improvement by developing standard programs and macros that follow CDISC guidelines required for regulatory submissions. Independently program CDSIC SDTM, ADaM datasets. Map raw data to SDTM (Study data table model) in compliance with CDISC data model standards and create specifications for programming. Create ADaM Specifications & datasets from SDTM datasets per CDISC analysis data model standards an

https://www.indeed.com/job/senior-statistical-programmer-b426b445abad4e8f

Labeling Resource - Salt Lake City, UT

Skills and Experience Required: Medical device experience (senior level, class II preferred) Labeling expertise, including IFU EU MDR and MDD knowledge Design change experience Global Regulatory assessments Excellent written and oral communication IVD experience Remediation experience preferred.

https://www.indeed.com/job/labeling-resource-e0e637825a38328e

Regulatory Affairs Specialist III - Swiftwater, PA - KatalystHLS.com

Primary Duties: program/project management - need to be able to multitask, organized preparing for inspections of drugs in global clinical trials managing CAPAs/audits process integration managing vendors contract to perm can be at Lexington site instead of Cambridge site experience in Track Wise a plus GCP, systems/metrics experience (not GXP - this is an R&D role) Key areas of accountability and budget responsibility, if applicable. Under the direction of the Head of Internal & Supplier Audits, this position is responsible for supporting the overall execution of the overall Internal Suppler & Audit (ISA) strategy and ensure adherence to R&D QA & Compliance (QA&C) Operational objectives.

https://www.indeed.com/job/regulatory-affairs-specialist-iii-09bfc38f993bd3f1

Quality Assurance & Compliance Manager - Cambridge, MA - KatalystHLS.com

Primary Duties: program/project management - need to be able to multitask, organized preparing for inspections of drugs in global clinical trials managing CAPAs/audits process integration managing vendors contract to perm can be at Lexington site instead of Cambridge site experience in Track Wise a plus GCP, systems/metrics experience (not GXP - this is an R&D role)

https://www.indeed.com/job/quality-assurance-compliance-manager-76029a8119b0c765

Senior Clinical Data Manager - New York, NY

The Clinical Data Manager will be responsible for all data management responsibilities for a sponsor-initiated cancer study. This person will be developing CRF\'s, supporting data entry and collecting Adverse events in real time. Train users on EDC functionality. Understand, update and optimize existing queries/reports. Analyze data to find potential issues/inconsistencies/areas, etc.

https://www.indeed.com/job/senior-clinical-data-manager-446b51280676f12d

Quality Engineer - Greenville, SC - KatalystHLS.com

Develop and initiate standards and methods for inspection, testing and evaluation. Devise sampling procedures and design and develop forms and instructions for recording, evaluating and reporting quality and reliability data. Implement process controls and develop quality assurance plans and procedures Develop and implement methods and procedures for disposition of discrepant material and devise methods to assess cost and responsibility.

https://www.indeed.com/job/quality-engineer-65a4d0582175d86d

Senior Clinical Data Manager - New York, NY - KatalystHLS.com

The Clinical Data Manager will be responsible for all data management responsibilities for a sponsor-initiated cancer study. This person will be developing CRF\'s, supporting data entry and collecting Adverse events in real time. Train users on EDC functionality. Understand, update and optimize existing queries/reports. Analyze data to find potential issues/inconsistencies/areas, etc. Assist in design of queries using SQL to check for missing or inconsistent eCRF data.

https://www.indeed.com/job/senior-clinical-data-manager-446b51280676f12d

Senoir Validation Consultant - Gloucester, MA - KatalystHLS.com

Absolutely need to have experience providing Quality oversight of laboratory systems and instrumentation. Contract manufacturing (CMOs) and/or contract labs (CTLs) They have a lot of work coming in, new equipment and vendors they are bringing in where this person will be providing quality oversight. Not writing of documents but overseeing all their contents. Rolling out new system design life cycles

https://www.indeed.com/job/senior-validation-consultant-d1c3b5d5714b05d3

Clinical SAS Programmer - Princeton, NJ - KatalystHLS.com

Programs statistical analyses (via SDTM, analysis datasets, tables, figures, listings, etc.) using an appropriate statistical analysis system. Serves as a key member of the project team by attending team meetings and working with biostatisticians, data managers and project managers. Performs quality review of analysis dataset and TFL programs developed by other programmers and biostatisticians.

https://www.indeed.com/job/clinical-sas-programmer-8ab51e01517fb46f

Clinical Data Manager - Boston, MA - Katalyst HLS.com

Serve as the client DM team member on the client study team and as the sponsor DM representative on the client-CRO study team. Provide direct oversight to the CRO during study start-up, maintenance, and lock ensuring the protocol is being followed. Review of external vendor data including biomarker data. Review of Medidata Rave eDC generated data.

https://www.indeed.com/job/clinical-data-manager-e57beb6bba855ac9

Senior Statistical Programmer - Boston, MA - Katalyst HLS.com

To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.

https://www.indeed.com/job/senior-statistical-programmer-313e2bda74a60f56

Quality Engineer - Berkeley, CA - Katalyst HLS.com

The Operations / Quality Engineer is responsible for supporting existing product lines to ensure safety, compliance and product availability. In addition, provide engineering support to manufacturing for transition of new products and scale-up for production.

https://www.indeed.com/job/quality-engineer-22bb4aaf17837dcb

Regulatory Consultant - East Hanover, NJ - Katalyst HLS.com

Regulatory consultant works under minimal supervision to support the development of digital and other innovative technologies, as stand alone or in combination with Client products. This role supports Global Program Regulatory Directors (GPRDs) and Digital Development teams in operationally implementing the global regulatory strategy for the development of Client technologies and approaches to clinical development, applying expertise in drug development and medical device regulations.

https://www.indeed.com/job/regulatory-consultant-60cf979ee9614683

Regulatory Submission Publisher - Princeton, NJ -KatalystHLS.com

Roles and Responsibilities: Responsible for both Submission and Document Level Publishing. Responsible for the creation, assembly, and publishing of global electronic submissions, including MAAs/NDAs, INDs, CTAs, Annual Reports, Periodic Safety Reports, Supplements, Amendments, Variations, Renewals, etc. Knowledge of health authority procedures/guidance\'s regarding electronic submissions required. May interface with project managers, regulatory product managers, and or content authors to discuss submission preparation.

https://www.indeed.com/job/regulatory-submission-publisher-53c207c5aebebbf3

Principal SAS Programmer - Rumford, RI - katalysthls.com

Roles and Responsibilities: Convert study design and specifications into programs to support clinical trials. Validate SAS programs written by others. Assists Management in maintaining SOPs and work instructions relevant to SAS programming. Follow regulatory requirements and guidelines for the development, usage, and maintenance of programs to support regulatory submissions.

https://www.indeed.com/job/principal-sas-programmer-b7c53af9174fe76f

Computer System Validation Lead - San Diego, CA

Computer System Validation Lead - San Diego, CA

https://www.indeed.com/job/computer-system-validation-lead-dfe5039f442c70fc

Statistical Programmer - Rogers, AR - KatalystHLS.com

Apply SAS programming and analytical skills using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS Design, develop, evaluate, validate and modify computer programs using SAS to analyze clinical data Produce and deliver standard datasets, program edit checks, quality tables, figures and listings in a timely and high quality fashion Create and validate CDISC standard datasets Provide input in the design and development of clinical trial protocols, case report forms and clinical databases Work closely with clinical operations, data management and statisticians to generate statistical output - tables/listing/figures Liaise with vendors as needed to facilitate electronic data transfers and statistical programming

https://www.indeed.com/job/statistical-programmer-290c4c44a1be59f7

Clinical Data Manager - Bozeman, MT -KatalystHLS.com

Manage data from database design through delivery to Biostatistics for analysis. Interpret the study protocol and develops detailed specifications that include the event schedule and layout of new eCRF pages and builds forms in database system. Maintain data collection definitions and documents data entry guidelines to ensure consistency of data. Set up data review plans, develops data edit check routines, reviews data for missing and incongruent data and utilizes the query management system to facilitate data resolution and clean-up, Monitor the progress of study data, assesses for analysis milestones and releases data to Biostatistician for analysis.

https://www.indeed.com/job/clinical-data-manager-51b42f2a31aac0c8

Validation Engineer II - Somerville, NJ - KatalystHLS.com

Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to product and process quality, writes qualification protocols for operating systems and records related test results; prepares final reports that identify the results of protocol testing and the conditions of release.

https://www.indeed.com/job/validation-engineer-ii-a569aadb114bafe5

Clinical Data Specialist - Boston, MA - KatalystHLS.com

Independently ensure all study data is validated in accordance with regional and federal clinical study guidelines. Oversee database design, testing, and optimization. Create and implement clinical trial methods for collecting and analyzing site- and patient-specific clinical trial data.

https://www.indeed.com/job/clinical-data-specialist-1f1eb1b4b7744585

Senior Clinical Data Manager/Client: Allergan - Madison, NJ - KatalystHLS.com

The Senior Manager, Clinical Data Management is responsible for leading internal and outsourced Clinical Data Management activities in support of Clinical Research studies, managing the definition of Case Report Form (CRF) requirements, creation of the Data Management Plan, coordination of Centralized Data Review activities (a key component of Risk Based Monitoring), and is accountable for data integrity, quality, and consistency at Database Lock.

https://www.indeed.com/job/senior-clinical-data-managerclient-allergan-e9676f4f7063437c

Clinical Data Manager - Bozeman, MT - KatalystHLS.com

Manage data from database design through delivery to Biostatistics for analysis. Interpret the study protocol and develops detailed specifications that include the event schedule and layout of new eCRF pages and builds forms in database system.

https://www.indeed.com/viewjob?t=clinical+data+manager&jk=51b42f2a31aac0c8&_ga=2.38037987.1326352972.1562606511-1429968906.1557248850

Manufacturing Quality Engineer - Costa Mesa, CA -KatalystHLS.com

Update the purchasing spec with compliance to the requirement from Central Remediation Team Coordinate with TPE team to complete the DFM review / alignment with external suppliers Initiate EC relevant to the change of the purchase parts

https://www.indeed.com/viewjob?t=manufacturing+quality+engineer&jk=38b209149910970e&_ga=2.75378002.1326352972.1562606511-1429968906.1557248850

Lead Regulatory Publisher - Atlanta, GA -KatalystHLS.com

Produce regulatory publishing submissions (e.g., INDs, NDAs, NDSs, MAAs, annual reports, routine submissions, Clinical Study Reports) in accordance with US and global requirements, using electronic publishing tools, and an EDMS system. Perform independent publishing QC on published output, complete appropriate checklists and/or provide assessments for the activities around the quality of report-level publishing and submission readiness of source documents for submission-level publishing.

https://www.indeed.com/viewjob?t=lead+regulatory+publisher&jk=6b3e4123e8334bea&_ga=2.80677975.1326352972.1562606511-1429968906.1557248850

Project / Program manager - Gaithersburg, MD - KatalystHLS.com

The Project Manager (PM) consultant will support 2 to 3 projects depending on the stage and complexity level of the program. Project assignments will include pipeline, life cycle management, technology and/or continuous improvement initiatives. In this role the PM will work with limited direction and will effectively prioritize and manage their workload to meet Team goals.

https://www.indeed.com/viewjob?t=project+program+manager&jk=ce5eb3ceb6535bb9&_ga=2.74984914.1326352972.1562606511-1429968906.1557248850

Documentation Coordinator/ Client: Allergan - Pleasanton, CA - KatalystHLS.com

The primary responsibility of this position is assisting with processing documentation in a controlled document management system and assigning training to personnel to meet regulatory, quality and company requirements in a medical device design and manufacturing environment.

https://www.indeed.com/viewjob?t=documentation+coordinator+client+allergan&jk=bdcf7640aec52cb1&_ga=2.120867912.1326352972.1562606511-1429968906.1557248850

Drug Safety Specialist - Westbrook, ME - KatalystHLS.com

Conduct the assessment of all serious individual adverse event case reports stemming from pre-clinical studies, post-marketed and literature sources. Performs quality control of key data fields, and makes updates in the safety database per process conventions Executes case assessment (review events, determine expectedness, review/update drug and medical term coding, determine causality) Creates clear, medically concise case narrative procured from relevant information in form of various source documents Drafts pharmacovigilance company comment Determines follow-up actions and generates letters/queries as appropriate

https://www.indeed.com/viewjob?t=drug+safety+specialist&jk=e0a8f642e0d79a81&_ga=2.45614436.1326352972.1562606511-1429968906.1557248850

Quality Engineer - Cleveland, MS -Katalyst HLS.com

Gather project requirement and understand the scope of each project. Able to lead risk management activities including creation/update of Risk Management Plan, Hazard Analysis, Design FMEA, Product User Risk Analysis, Risk Benefit Analysis and Risk Management Report Support Internal/external Audit. Able to record Audit observations, and closure of the same. Understand and perform the product complaint analysis, Customer Quality procedures Supports Quality, Manufacture, Service, and Marketing departments on product Quality issues. Perform statistical analysis using statistical software like Minitab

https://www.indeed.com/viewjob?t=quality+engineer&jk=74aa1e2077a89887&_ga=2.113011140.1326352972.1562606511-1429968906.1557248850

Senior Engineer (Client: Allergan) - Somerville, NJ -KatalystHLS.com

Consultants will provide hands-on expertise to revise and document the Quality Management System, Clinical, Post-Market Surveillance, and Supplier Management processes as necessary for compliance with the European Union Medical Device Regulations (EU MDR). In addition, medical device technical files will be reviewed to ensure use of prohibited hazardous substances are in accordance with the limits set forth in the General Product Safety Requirements (Annex I), and records will be created as necessary to fulfill the requirements of the various Annexes.

https://www.indeed.com/viewjob?t=senior+engineer+client+allergan&jk=374d5d6ec7c8584c&_ga=2.50801001.1326352972.1562606511-1429968906.1557248850

Statistical Programmer - Albuquerque, NM - KatalystHLS.com

Apply SAS programming and analytical skills using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS Design, develop, evaluate, validate and modify computer programs using SAS to analyze clinical data Produce and deliver standard datasets, program edit checks, quality tables, figures and listings in a timely and high quality fashion Create and validate CDISC standard datasets

https://www.indeed.com/viewjob?t=statistical+programmer&jk=3fc990aaed8ac1fa&_ga=2.50670697.1326352972.1562606511-1429968906.1557248850

Clinical SAS Programmer - Rockville, MD - KatalystHLS.com

Clinical SAS Programmer - Rockville, MD - KatalystHLS.com Develop SAS macro libraries to standardize routine analysis or implement new methods. Manage the Clinical SAS Programming Team, maintain standards for Clinical SAS programming activities, and guide/coach the Clinical SAS Programmers.

https://www.indeed.com/viewjob?t=clinical+sas+programmer&jk=25e313def12bcf9d&_ga=2.105719235.1326352972.1562606511-1429968906.1557248850

Clinical SAS Programmer - Albuquerque, NM - Katalyst HLS

Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes\' SDTM Implementation Guide, project standards, and the study protocol Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets Review and QC submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate Provide CDISC training and serve as a subject matter support to project staff

https://www.indeed.com/viewjob?t=clinical+sas+programmer&jk=91e2055a4d36b31e&_ga=2.37506144.1326352972.1562606511-1429968906.1557248850

Clinical SAS Programmer - Albuquerque, NM - Indeed.com

Clinical SAS Programmer - Albuquerque, NM

https://www.indeed.com/viewjob?t=clinical+sas+programmer&jk=91e2055a4d36b31e&_ga=2.11815668.1326352972.1562606511-1429968906.1557248850

Regulatory Affairs Coordinator-Boston, MA - KatalystHLS.com

Demonstrated ability to coordinate complex projects. Strong oral and written communication and presentation skills Solid working knowledge of the US Regulations and European medical device directives Good analytical and problem-solving skills. Demonstrate in-depth understanding of advanced technical/scientific principles related to MDR IVD reagent chemistry, laboratory automation, and software components of MDR / IVD medical devices.

https://www1.jobdiva.com/portal/?a=irjdnw4aqkb0a5bhkjucv8p00hyqhk05031z6ahtakm0pgjg8f34dc29wtyqerjr&compid=0&jobid=12937328

Validation Expert - Winston-Salem, NC - KatalystHLS.com

Author and review process validation protocols and reports. Support execution of validation activities at the shop floor. Reviews Master Batch Records and associated change controls. Maintain all activities and projects under own responsibility in an inspection ready status. Provides technical expertise (and may facilitate) pre-validation risk assessments using risk management tools.

https://www.indeed.com/viewjob?t=validation+expert&jk=63798748bf39c2e2&_ga=2.47009255.1326352972.1562606511-1429968906.1557248850

Validation Engineer - Houston, TX - KatalystHLS.com

Role Summary/Purpose Internal the Quality Engineer demonstrates leadership in communicating, developing, and executing program schedules, process developments, and analysis in various organizational settings regarding internal and external business goals.

https://www.indeed.com/viewjob?t=validation+engineer&jk=47ab02ea6dea93a5&_ga=2.12994039.1326352972.1562606511-1429968906.1557248850

QA COMPLAINT SPECIALIST - Austin, TX - KatalystHLS.com

They will be responsible for answering inbound calls and collecting all pertinent information for the complaints. They essentially are responsible for asking the Who, What, When, Where, and How can we assist questions. They are the front-lines of the business, so they must have excellent customer service skills, be able to type without looking at the key board with a low error rate.

https://www.indeed.com/viewjob?t=qa+complaint+specialist&jk=799a5181abb5988c&_ga=2.154170872.1335194151.1562012451-1429968906.1557248850