Job Opportunities

Title: Project Manager II at CDOR in Denver CO

Company: Colorado Department of Revenue (CDOR) https://www.colorado.gov/revenue

Location: 1375 Sherman, Denver CO

SALARY: $6,262.00 – $9,492.00 Monthly ($75,144.00 – $113,904.00 Annually)

Job Application Opening Date: 01/17/17

Job Application Closing Date: 01/30/17 05:00 PM US-MT

Job Type: Full Time

Note: This Posting Will Remain Open Until The Position Is Filled; Candidates Are Encouraged to Apply Early.

DESCRIPTION OF JOB:

• As part of a team, this position will oversee projects under the agency standardize project management plan, including overall project coordination, scheduling, planning, and monitoring for all phases of assigned projects.
• Additional duties include:
  • Formulating work plans, tracking project progress, and identifying scheduling problems;
  • Overseeing and coordinating the development, design, and implementation of new business processes and technology solutions designed to meet the needs of the Department of Revenue and its customers;
  • Overseeing the development of requirements and Statements of Work (SOWs) for approved departmental projects;
  • Monitoring implementation progress of approved departmental initiatives for adherence to strategic and tactical plans;
  • Providing recommendations to the Director of the Project Management Office and Project Steering Committees regarding business process improvements, and proposed projects to meet strategic objectives and business goals;
  • Coordinating with assigned Business Analyst on all analysis activities to ensure that user requirements are accurately defined and documented, costs and benefits are properly analyzed.
  • Manage projects from initiation through implementation, including new program enhancements and modifications.
• Collaborates with Quality Assurance team to conduct testing.
• At times, the individual that is selected for this position will be required to manage multi-million dollar, multi-year projects.

MINIMUM QUALIFICATIONS:

• Bachelor’s degree from an accredited college or university in Business Administration, Business Management, Computer Science, Project Management, or a closely related field (at the discretion of the hiring agency).
• Four (4) years of full-time professional project management experience which included professional high-level experience in one or more of the following:
• Administering, planning, organizing, executing and overseeing projects.
• Must be familiar with Microsoft Project software for managing project schedules.

NECESSARY SPECIAL MINIMUM REQUIREMENT:

• A Project Management Professional (PMP) certification issued by PMI or comparable entity (At the discretion of the hiring agency).
• If you do not currently have a certification, you will need to obtain your certification within one (1) year of hire date

PREFERRED QUALIFICATIONS AND COMPETENCIES

• The preferred candidate will possess the following:
• BS/BA in one of the following fields: Business Administration, Business Management or Computer Science
• Eight (8) years of professional full-time project management experience which included professional high-level experience in one or more of the following: administering, planning, organizing, executing and overseeing projects
• A Project Management Professional (PMP) certification issued by Project Management Institute
• Must be able to provide direction to a project team including assignments of individual responsibilities, tasks and technical functions
• Manage relationships with vendors and contracts, project sponsors, team members and stakeholders
• Prepare and present project deliverables including project management, risk management, budget and quality management, and communication plans, schedules, status report plans and quality management
• Exceptional oral and written skills
• Successful in planning and managing multiple medium-to-large projects of significant magnitude in terms of complexity, cost, time-constraints, internal and external staffing to completion

CDOR REQUIRED SKILLS & COMPETENCIES:

Competencies required for all DOR positions include good communications skills (both oral and written), interpersonal skills, the ability to follow written and oral instructions, the ability to multi-task, the ability to work with confidential information, the ability to work in high-stress environments, and the demonstrated ability to assist customers in an effective, efficient, and elegant manner.

For more information and to apply

see job description web page 

Company: Cuattro, LLC

Location: 3760 Rocky Mountain Avenue, Loveland CO

Job Title: Software Test Engineer

Department: Quality Assurance

Supervisor: Director of Quality Assurance

Position Summary

• Test Engineer to assist in testing Windows WPF applications.
• Work closely with Quality Assurance and Development team members in the testing of Cuattro/Heska software applications, with a focus on the development of automated tests to improve test coverage and system reliability.

Responsibilities

• Responsible for the execution of software testing prior to release.
• Lead the effort to automate testing in the following areas
  • Create and implement functional tests for back-end services
  • Unit tests
  • User Interface Testing
  • Other application test areas as needed

Necessary Education/Experience/Training

• Two-year technical degree with focus on Software or Test
• Experience writing Unit Tests and using Mock Objects
• Experienced in C#. Must be willing to follow best practices and coding standards.

Desired Experience/Certification/Training

• Technical Writing experience
• Familiarity with Microsoft Team Foundation Server and Microsoft Test Manager
• Fundamentals of Software Testing (FOST)
• ISTQB Certified Tester, Foundation Level (CTFL) or ASQ Certified Software Quality Engineer
• Familiarity with acceptance test frameworks such as FitNesse and SpecFlow
  Additional
• Motivated self-starter with the ability to maintain focus on the task at hand.
• Work with team leads to ensure objectives are accomplished
• Good communication over email and instant messaging (skype)

Training expected upon hire

• Cuattro Quality System documentation (Quality manual, Design controls, etc.)
• Good Manufacturing Practices (US FDA Quality System Regulations)
• HIPAA Training

For more information and to apply contact

Note: Please include job position in all contacts

Matthew Taylor, Director, Quality Assurance / Regulatory

Cuattro, LLC, 3760 Rocky Mountain Avenue, Loveland, CO 80538

Phone: 970-775-2247

email: mtaylor@cuattro.com

Company: Yampa Valley Medical Center (YVMC)

Location: Steamboat Springs CO

Title: Quality & Patient Safety Manager

Application Web page:

Purpose

• Responsible for the operational functions of the Quality and Patient Safety Department.
• Coordinates and supports the facility’s quality and safety programs.
• Collaborates with Medical Staff, Nursing Staff and Department Directors, and with Process Improvement, Infection Prevention, Risk Management, Clinical Documentation Improvement and Information Services to drive quality and safety initiatives and achieve optimal quality outcomes.
• Coordinates compliance with regulatory and accreditation standards and programs.

Responsibilities:

• Leads and manages the quality and safety programs at Yampa Valley Medical Center, aligning the programs with the strategic plan of the hospital, regulatory requirements and programs, government requirements and programs, and accreditation efforts. Educates and supports the Medical, Nursing and administrative staffs of the hospital in achieving aligned quality, safety and regulatory outcomes.
• Oversees and is responsible for the activities of the Performance Excellence Committee (PEC), supporting the Committee’s Chair and its member departments/functions in fulfilling their responsibilities to the Committee. Supports the PEC Chair in preparing for reports to the Medical Executive Committee and the Quality and Safety Committee of the Board.
• Coordinates and oversees the Patient Safety and Quality Team/Committee and its activities. Coordinates other assigned quality and patient safety committees. Represents Quality and Safety Management at organizational meetings, including departmental meetings, and meetings of the Medical Executive Committee and the Quality and Safety Committee of the Board.
• Serves as a content expert for designing and providing formal and informal education for the Medical and Nursing Staffs, clinical leaders and others, related to healthcare quality, government quality programs and patient safety.
• Oversees the Quality and Patient Safety Analyst/Peer Review Coordinator to assure key quality and safety performance indicator reports are abstracted, prepared, analyzed and submitted, including oversight of external regulatory data reporting and internal reporting to support YVMC’s quality and safety objectives. Also oversees the Analyst/Coordinator position to ensure that Peer Review quality and reporting functions are supported. Assures the development of quality and safety outcomes dashboards that are focused to the needs of YVMC, with revisions as necessary to support regulatory reporting.
• Advises and collaborates with Medical and Nursing Staffs to create department-specific integrated quality, safety and operational dashboards. Assists the Chief Medical Officer in selecting quality and safety outcomes to support clinician/provider quality and safety alignment.
• Collaborates with the Manager of Process Improvement (PI) to facilitate the application and implementation of PI activities to quality and safety projects, when indicated, to optimize outcomes.
• Collaborates with the Risk Manager on patient safety issues to optimize patient safety outcomes at YVMC.
• Serves on the Infection Prevention (IP) Committee and collaborates with the IP team to evaluate and risk-assess for infections at YVMC. Participates in IP education and activities.
• Applies analytics to identify and target various populations to drive quality improvement and measurable outcomes.
• Responsible for establishing and ensuring compliance with departmental budget.
• Perform other duties as assigned. Must be HIPAA compliant.

Qualifications:

• Education: Nursing degree (BSN) preferred. Bachelor’s degree in business or organizational development or related field strongly desired.
• Work Experience: Minimum three years quality and safety management, risk management and regulatory standards experience. Peer review experience preferred. Supervisory experience required.
• Licenses/Certifications: RN Required . CPHQ preferred; required within 18 months of hire. Six-Sigma Greenbelt (or Lean equivalent) required within 12 months of hire; black belt within 24 months of hire preferred.
• Knowledge, Skills, Abilities: Advanced knowledge of reportable quality and safety outcomes, and principles of performance measurement and reporting, quality improvement, standards and practices related to quality of care, hospital safety programs, outcomes data management/measurement and hospital reimbursement required. Working knowledge of regulatory standards required. Strong computer skills (MS Office and web-based application) are necessary. Excellent communication and interpersonal skills, and ability to function as an educator, required. Ability to function effectively as a mediator and resolve conflict necessary.
• Working Environment: Works in a temperature controlled environment with natural and artificial lighting.
• Essential Physical Requirements: Able to perform repetitive standing, sitting, stooping, walking, and reaching. Performs minimal lifting of 15 lbs, carrying 15 lbs, and reaching over head 10 lbs.

For more information and to apply vist YVMC job “Quality & Patient Safety Manager” web page

All YMVC Job web page

Company: Yampa Valley Medical Center (YVMC)

Location: Steamboat Springs CO

Title: Coordinator – Peer Review and Quality

Application Web page:

Purpose

• Facilitates the gathering and review of key quality indicators for the purpose of ensuring strong quality outcomes and accountability to support the facility’s strategic plan and regulatory requirements.
• Supports Medical Staff quality programs, including medical staff peer review, data gathering, reporting and review for Ongoing Professional Practice Evaluation (OPPE) and Focused Professional Practice Evaluation (FPPE), as well as medical staff issues related to occurrence reports.
• Duties include concurrent and retrospective chart review; and providing clinical intervention and education to staff and physicians regarding the outcomes of all of the above.
• Supports an effective medical staff professional practice evaluation process that supports medical staff reappointment, advancement, and clinical quality.

Responsibilities:

• Utilizing organizational and industry standard tools, will abstract, enter and report on required key data elements necessary for coordination of provider review and the collection of national quality indicators data. Maintains knowledge of Evidence-based, CMS and TJC clinical metrics (i.e. Core Measures, AHRQ Quality and Safety Indicators, Hospital Acquired Conditions).
• Reviews daily census to assist with early identification of patients who meet indicators of triggers for peer review or meet quality and safety measure criteria to ensure metric compliance concurrently. Functions as a resource to provide clinical intervention, education and follow up to providers and appropriate department leaders regarding the peer review process.
• Queries multiple databases for clinical, administrative, and peer review data. Conducts (RN) screening of cases in the data in a timely and objective manner in order to determine level of peer review needed. Communicates with HIM, Risk Management and Compliance to prepare medical records appropriately during the peer review process. Works collaboratively with the Chief Medical Officer, Medical Staff Medical Director, and Chair of Peer Review as needed to screen and approve cases for reciprocal or external review. Initiates sending of and receiving of all reviews and alerts providers of reports when received. Communicates committee dispositions to providers in a timely manner and according to policy. Works collaboratively with the Quality and Patient Safety Teams, appropriate clinical departments and teams to develop and implement plans for improvement as needed.
• Assists the Quality Manager in the coordination of key quality and safety indicators throughout the YVMC system. The quality and safety measures can include, but are not limited to, the core measures created by CMS and The Joint Commission, measures to support the IPPS and OPPS programs of CMS, AHRQ safety and quality measures, Hospital Engagement/Hospital Improvement and Innovation Network measures, and quality measures created to support the strategic plan of YVMC. Coordination includes manual abstraction of measures, data collection and analysis, and interaction with key stakeholders that impact these measures.
• Applies statistical principles to calculate appropriate summary measures and provides quarterly summary reports on Quality and provider review for administration and clinical leadership. Identifies and incorporates comparative benchmark practices into reporting. Coordinates with the facilitators of other quality committees (Trauma, Infection, Robotics etc.) to receive quality of care reports, assist with interpretation of data and presents that information routinely at appropriate meetings and committees as appropriate.
• Performs routine and intensive medical record audits. Coordinates data for professional practice evaluation including abstracting, filing, and maintaining professional practice evaluation (PPE) log and tier three reviews. Assists the Chief Medical Officer, Chief of Staff, Department Chairs, and appropriate committees to identify process deficit trends and/or practice patterns.
• Utilizes professional critical thinking skills and knowledge of clinical care guidelines and national priorities for care review. Accurately and completely documents and reports results of case review (clinical care as well as system or process issues) in a timely manner, compiles case summary, and refers to appropriate parties for follow up. Tracks cases to ensure timely resolution and follow up as appropriate.
• Facilitates the Multi-disciplinary Professional Practice Evaluation Committee (PPEC, including preparing agenda, case review materials, minutes etc.). Participates in case discussions as appropriate for cases presented for committee review. Ensures appropriate communication and resolution of issues with all parties involved based on committee recommendation/ action. Maintains database of PPE activities. Ensures all appropriate documentation is copied to the corresponding quality file within Medical Staff Services.
• Ensures compliance with applicable regulatory guidelines and requirements, State and Federal statutes, and Medical Staff Bylaws, Rules, and Policies. Must be HIPAA compliant. Utilizes superior discretion and ability to maintain the confidentiality of highly sensitive PPE information. Uses appropriate safeguards to prevent inappropriate use or disclosure of confidential case review information.
• Actively participates in departmental performance improvement and survey readiness activities.
• Performs other duties as assigned.

Qualifications:

• Education: Bachelor of Science in Nursing or health related field preferred.
• Work Experience: 2 years of Quality Assurance/Performance Improvement experience highly desired with 5 years previous experience in acute care clinical setting necessary. Professional Practice Evaluation (Peer review) experience required.??Proficiency with electronic medical record systems required. Experience in project development, project management and strong analytical skills, including data entry, manipulation, management, and data analysis preferred.
• Licenses/Certifications: CO Licensed Registered Nurse required. Certified Professional in Healthcare Quality preferred
• Knowledge, Skills, Abilities: Proficient in Windows-based operating software (Microsoft Office) and systems.
• Knowledge of patient quality, safety and satisfaction performance measures and indicators, data definitions and sources and relevant national databases and benchmarks; knowledge of healthcare quality, safety and satisfaction data design, collection, aggregation and summarization; and knowledge of performance improvement models, methods and systems strongly preferred. Excellent written and oral communication and presentation skills required. Must promote and demonstrate a logical, systematic and non-judgmental approach to case review with the ability to formulate concise and relevant summaries with competing factors. Solution driven with the ability to address difficult situations with tact and diplomacy
• Ability to work under minimal supervision, ability to adapt quickly to changes within the work environment.
• Ability to work with providers of all levels to coach and provide feedback on performance. Must be a team player and have proven success applying a collaborative and professional approach and ability to work in conjunction with physicians, clinical managers/directors, colleagues and customers in a supportive way to communicate sensitive information and troubleshoot issues.
• Working Environment: Works in a temperature controlled environment with natural and artificial lighting.
• Essential Physical Requirements Able to perform repetitive standing, sitting, stooping, walking, and reaching. Performs minimal lifting of 15 lbs, carrying 15 lbs, and reaching over head 10 lbs.

For more information and to apply vist YVMC job “Coordinator – Peer Review &
Quality” web page

All YMVC Job web page

Company: Platinum Registration

Location: 2401 South Downing Street, Denver, CO 80210

Title: Subcontract Auditors

Platinum Registration is looking for subcontract auditors who have completed ISO 9001:2015 training and

• is able to become certified to either IRCA or Global Exemplar Quality Auditor.
• This is not a full time position and there is no guarantee for number of days per month.
• Some travel may be required
• We are looking for local auditors to perform 3rd party audits in the Front Range area.

For more information and to apply
Melody Sands, Staff Auditor, Platinum Registration,

• 2401 South Downing Street, Denver, CO 80210
• Office: 303-639-9001
• Direct: 720.280.7632
• email: melody@platinumregistration.com
• web site: www.platinumregistration.com

Company: Cavendish Scott Inc.

Location: 984 S Vine St., Denver, CO

Summary : Associate/Contract ISO Auditors

Details:

• Cavendish Scott is interested in establishing good relationships with professional, reliable and trustworthy professional auditors.
• We need help to cope with fluctuations that occasionally occur in our business and can sometimes provide more consistent assignments.
• Ideally you would be a current auditing contractor, with an established workload of audits and are wishing to supplement that.
• Ideally your focus would be on auditing so that you have a clear development goal, and would not be consulting in ISO implementation or at least not significantly.
• We consider this to present a potential conflict although its not insurmountable.
• You should like travel because that is one of our most difficult situations that we have to address.
• You should probably have an IRCA or EG auditor card – or an equivalent independent way of demonstrating your competency and professionalism.
• Personality and loyalty are paramount.
• You have to operate as part of a team and fit in with our established processes and methods.

Application:

• To apply please briefly email us and tell us why you are right for the position.
  Some of the technical requirements for the job are important but personality and overall ability are probably better things to convince us of.
• Let’s keep it to 10 email lines (about 300 words).
• No resumes, no application forms. We’ll see where it goes from there.

email: Info@cavendishscott.com

For more information and to apply see Cavendish Scott, Inc job page

Company: Cavendish Scott Inc.

Location: 984 S Vine St., Denver, CO

Summary : Entry Level ISO Auditor

Details:

• Cavendish Scott is looking for additional resources in the form of an entry level ISO auditor.
• We see this as an entry position, with plenty of support provided and firstly focusing on auditing and then developing into training and consulting if desired and as opportunities arise and competency is established.
• Ideally you will have some experience of ISO 9001 (maybe similar standards such as FDA).
• You may have been involved in the implementation of ISO 9001 (or similar) or been responsible for its upkeep and maintenance.
• You may have conducted internal audits and been responsible for interfacing with the certification body.
• Perhaps you have even performed audits for a certification body.
• Ideally, you would have had some managerial experience (oversight of the QMS may be enough but other formal experience might be equally useful).
• You should be familiar with most/all typical organization processes and be comfortable talking with management about ISO and relevant topics.
• You must be confident and comfortable presenting in order to be able to fill the role of auditor.
• You will be an effective writer possibly having written procedures, instructions and management reports.
• Personality is critical to us.
• You will be easy going, dynamic, self-motivated, self-starter, hard working, and capable of standing alone.
• You also cannot be afraid of new standards, situations or challenges.
• You will be given support but you have to be able to act professionally and come up with solutions on your own.
• We need someone who is available to travel.
• Even likes travel.
• The job minimally would require 14-16 trips a year of 2-3 days on average.
• But plan on being able to cope with an average of two trips a month of 3+ days (this is not what we currently do but you never know).
• We will provide training and support to develop the right candidate to a fully qualified ISO professional (it’s not just 9001 but AS9100, 13485, R2, 27001, 45001, 18001, 17025 to mention but a few).
• We are not particularly looking for a contractor or part time person to fill this position – but try us.
• The job is great! You will learn all about/get exposure to a variety of organizations, management systems, standards and so many other things you get exposed to.
• You get to meet some really cool people and work from home.
• Conversely you are expected to work the hours you need to in order to satisfy your customers (they tend to work normal hours) and then work more to make sure you answer emails, stay responsive and do what needs to be done to be successful.
• This is NOT a 9-5 job and sometimes deadlines will mean
• you have to put extra hours in.
• Historically there has been plenty of free time to develop your skills, help develop training material, work on marketing and presentations, etc.
• You manage yourself and the compensation package is probably more than is generally available.
• Benefits include health, 401k, disability.
• All work expenses are paid. All equipment (phone, computer, etc.) are provided.

Application:

• To apply please briefly email us and tell us why you are right for the position.
  Some of the technical requirements for the job are important but personality and overall ability are probably better things to convince us of.
• Let’s keep it to 10 email lines (about 300 words).
• No resumes, no application forms. We’ll see where it goes from there.
• email: Info@cavendishscott.com

For more information and to apply see Cavendish Scott, Inc job page

Company: Denver Health

• Title: Lean Facilitator
• Facility: 601 Broadway, Denver CO
• Area of Interest: LEAN/Process Improvement
• Shift Type: Day
• Requisition ID: 44362
• Employment Type: Full-Time
• Salary Range: $66,146.383 to $99,219.57
• Experience Required: 3 – 5 Years
• Education Required: Bachelors Degree

Job Summary

•  Under general supervision, functions as a facilitator for organizational Lean and Getting it Right redesign implementation.
• Primary function is facilitation of organizational or cross-departmental Rapid Improvement Events (RIEs) as directed by Senior Lean Specialist, through the Lean implementation infrastructure.
• Coordinates planning, RIE, and follow-up activities for assigned redesign implementation.
• Trains, coaches and facilitates improvement efforts of redesign teams using the principles of Lean, line management and staff throughout the organization.
• Works in partnership with assigned Value Streams, Executive Sponsors, business units, project engineers, and RIE teams to develop Lean strategies and ensure adherence to Denver Health Lean Systems Improvement Department standard work and principles of Lean thinking.

Minimum Qualification

• Education:
  • Bachelor’s degree in Health Care Administration, Business, Industrial Engineering or other related field.
  • Combination of experience, education and training will be considered.
• Experience:
  • Typically, two years experience driving Lean initiatives with proven results.
  • Healthcare management with team leadership experience, preferred.
• Knowledge, Skills & Abilities:
  • Knowledge of Toyota Lean Production System tools and implementation is preferred.
  • Able to drive change up and down the organization and through cross functional teams.
  • Able to document and measure results.
  • Able to influence and motivate others.
  • Able to use Microsoft Office tools.
  • Able to be an effective team builder and problem solving abilities.
  • Strong leadership, facilitation, interpersonal, team building, project management, written/verbal communication, conflict resolution skills, basic statistical analysis and data management skills.
• Certificate/License/Registration: None

For more information and to apply visit Denver Health job id 44362 web page 

Company: Denver Health

• Title: Lean Coordinator
• Facility: 601 Broadway, Denver CO
• Area of Interest: LEAN/Process Improvement
• Shift Type: Day
• Requisition ID: 44376
• Employment Type: Full-Time
• Salary Range: $59,059.27 to $88,588.898
• Experience Required: 3 – 5 Years
• Education Required: Bachelors Degree

Job Summary

• Under general supervision, coordinates activities for Lean Systems Improvement Coordinates aspects of planning, event, and follow-up activities.
• Facilitates small groups and meetings.
• Documents improvement events and related activities.
• Provides basic project management/activity tracking support for all LSI work products as appropriate.

Minimum Qualification

• Education:
  • Bachelor’s degree in Health Care Administration, Business, Industrial Engineering or other related field.
  • Combination of experience, education and training will be considered. .
• Experience:
  • Typically 3 years of experience in process improvement or project management
  • Healthcare related experience with team leadership experience, preferred.
• Knowledge, Skills & Abilities:
  • Facilitation experience preferred.
  • Strong facilitation skills preferred.
  • Coaching experience preferred.
  • Coaching skills preferred.
  • Knowledge of Lean Toyota Production System implementation and approach is preferred.
  • Knowledge of Lean tools preferred.
  • Basic statistical analysis and data management skills preferred.
  • Effective team building skills.
  • Able to document and measure results.
  • Strong project management skills preferred.
  • Able to use Microsoft Office software including PowerPoint.
  • Strong written/verbal communication.
  • Strong troubleshooting/Problem-solving skills.
  • Able to influence and motivate others.
  • Strong interpersonal skills.
  • Strong Conflict management/mediation skills.
• Certificate/License/Registration: None

For more information and to apply viist Denver Health job id 44376 web page

Company: Medtronic

Location: 5744 Central Ave #100, Boulder, CO 80301

Title: Senior Supplier Quality Engineer opportunity

MINIMUM:

• Bachelor’s degree in EE and 7+ yr design, manufacturing, or quality engineering required
• Experience in supplier Quality management
• Experience as member of product development team.

PREFERRED:

• Green or Black Belt Six Sigma Certification and CRE/CQE.
• Experience in Quality/reliability engineering practice in regulated environment (FDA 21 CRF, ISO 13485, etc).

For more information and to apply

Contact Margaret Zachman via email margaret.zachman@medtronic.com with subject “Sr Supplier Quality Engineer”