Preschool Quality Assurance Specialist (3253)
West Palm Beach, FL jobs
Lutheran Services Florida (LSF) envisions a world where children are safe, families are strong, and communities are vibrant.
LSF is seeking a talented Preschool Quality Assurance Specialist who wants to make an impact in the lives of others.
The schedule for this position is Monday - Friday, 7:30am - 5:30pm.
Purpose and Impact:
The Preschool Quality Assurance Specialist seeks to perform the duties required to monitor activities conducted at Head Start/Early Head Start sites to meet compliance mandates defined by the Head Start Performance Standards. Participates in the HS/EHS Quality Assurance efforts.
Essential Functions:
Monitor quality and compliance at assigned sites, such as: education files, licensing requirements, referral systems for families and children, provision of social services, and ERSEA systems.
Assesses curriculum implementation throughout the agency on an ongoing basis.
Provides CLASS observations for all teaching staff on a rotating basis.
Serve as a resource to the staff at assigned sites in the areas of mental health, nutrition, education, social services, etc.
As needed, assist in the provision of parent training to parents of enrolled children in areas such as community resources, ERSEA, and child development.
Meet monthly with site managers/liaisons to keep them abreast of new developments in the Head Start Program on state regional and national levels or program changes concerning Head Start/Early Head Start.
Generate and analyze reports as requested and use this information to implement strategies as needed to contribute to continuous quality improvements.
Submit monthly to the Director of Continuous Quality Improvement via the QA Manager compliance reports detailing on-site observations and action taken.
Prepare monthly narrative report outlining activities, concerns and recommendations.
Work with staff to ensure the development and maintenance of an effective, informative, supportive, and inviting environment for staff, children, parents, and community volunteers.
Work as part of the Head Start leadership team in long- and short-term planning for Head Start.
Assist in the creation of procedures, documents, and other systems to maintain compliance with Head Start Performance Standards.
Assist the QA Manager and Director of Continuous Quality Improvement in managing the maintenance of accurate program data.
Participate in strategic planning for all quality assurance initiatives.
Maintains strict confidentiality with respect to HS/EHS children, families and staff in accordance with LSF and HS/EHS policies and procedures.
Attends training and workshops as directed.
Attends all required staff and parent meetings, as well as Committee meetings, as directed.
Performs other related duties as assigned.
Other Functions:
Note: The duties above are illustrative and not exhaustive. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position. Depending on assigned area of responsibility, incumbents in the position may perform some or all of the activities described above.
Physical Requirements:
Prolonged periods of sitting at a desk and working on a computer.
Ability to use hands and fingers to operate a computer keyboard, mouse, and other office equipment.
Occasionally required to stand, walk, reach with hands and arms, and lift or move up to 15 pounds.
Visual acuity to read printed materials and a computer screen.
Verbal and auditory ability to communicate effectively with staff, partners, and stakeholders.
Reasonable accommodation may be made for otherwise qualified persons with disabilities.
Education:
Requires a bachelor's degree in Social Work, Social Services, Early Childhood Education OR Early Childhood Development; OR Business Administration with relevant experience related to Head Start Operations.
Experience:
Requires two years of experience working in a social services or education management or specialist position.
Bilingual preferred: English/Spanish or English and other languages present in the local area.
Also required: Successful completion of a Level II background screening, local criminal record check and drug screening prior to hiring.
Knowledge, Skills and Abilities:
Knowledge of Head Start philosophy, goals and regulations.
Knowledge and experience with Head Start specific software packages.
Math skills needed to calculate figures and amounts such as discounts, percentages and overtime.
Computer skills to produce and interpret graphs, charts, spreadsheets and other mathematical reports.
Ability to define problems, collect data, establish facts, and draw valid conclusions; make recommendations and develop implementation strategies.
Ability to communicate effectively verbally and in writing.
Ability to write reports and business correspondence.
Ability to interpret agency, federal and state laws pertaining to the program.
Exceptional organization skills and attention to detail are required and the candidate must be able to meet designated deadlines.
Other:
Must demonstrate sensitivity to our service population's cultural and socioeconomic characteristics and needs.
Principal Accountabilities:
Team player with co-workers and central service office staff.
Cost effective program operations.
Adherence to agency policies, procedures and performance standards.
Effective customer service and group leadership.
Why work for LSF?
LSF offers 60 programs across the state of Florida serving a wide range of populations in need. Mission Driven staff members become part of the LSF community while transforming the lives of those in need. Our staff additionally find growth opportunities as they explore areas of interest within the organization.
Amazing benefits package including:
Medical, Dental and Vision
Telehealth (24/7 online access to Doctors)
Employee Assistance Program (EAP)
Employer paid life insurance (1X salary)
13 paid holidays + 1 floating holiday
Generous PTO policy (starting at 16 working days a year)
Note: Head Start employees paid time off and holiday schedule may differ
403(b) Retirement plan with 3% discretionary employer match OR 3% student loan repayment reimbursement
Tuition reimbursement
LSF is proud to be an equal opportunity employer.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Compliance QA Manager - Systems
Alameda, CA jobs
The Compliance QA Manager - Systems is responsible for the oversight, support, and administration of client's Quality Management Systems (QMS) to ensure these are effective and efficient, and maintained to support GxP functions. Supports end users and QA requirements, account management, and evaluates changes for implementation and continuous improvement initiatives.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
As QA Core, supports QA Partner:
· Analyze user enhancement requests to deliver solutions focused on establishing and improving business processes that improve efficiency, address process gaps, and enable automation and growth of the organization.
· Gather and document user and functional requirements
· Participate in the authoring and execution of implementation plans, development of solutions and manage project/change timelines
· Perform User Acceptance testing (UAT), Performance Qualification (PQ) and Validation testing, if applicable
Day to day business system administration:
· Manage system access and permissions
· Perform change management activities
· Design solutions and manage configuration
· Liaise with users to resolve issues
· Create reports based on defined requirements
· Maintain system documentation
· Create and run reports; track follow-up actions to ensure data quality and compliance
· Reviews and approves validation deliverables (URS, FS, IQ/OQ/PQ, etc.)
· Identifies, mitigates, escalates, and resolves issues and risks
· Authors and review CSV, DI policies, procedures, lifecycle documents
· Help generate metrics to support business goals
· Maintain end-user support information
· Manage updates to business guidance and user reference documentation
· Continuously look for ways to improve monitoring, user issues and deliver better value to the customer
· Support activities related to internal and external audits/inspections
· Support activities related to Computer System Validation and Data Integrity program.
· Oversee and maintain the Integration tool with the Leaning Management System, ComplianceWire, if applicable
SUPERVISORY RESPONSIBILITIES:
· None
EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:
Education/Experience:
· Bachelor's degree in science or related field and a minimum of 7 years of related experience; or,
· Equivalent combination of education and experience.
Experience/The Ideal for Successful Entry into Job:
· At least 5 years of experience working on validated applications in a pharmaceutical or regulated environment.
· Experience and knowledge of the quality and regulatory business processes.
· Direct hands-on experience implementing GxP computerized systems and maintaining validated state.
· Strong process improvement skills and orientation.
· Must have proven business and technology skills with success providing customer- oriented technology solutions environment.
· Proven strong communication skills interacting with user and technical communities.
· Ability to communicate ideas in both technical and user-friendly language.
· Collaborative working approach.
Knowledge/Skills:
· General knowledge of System Administration with the Veeva Platform (Quality QMS, Quality QDocs)
· Working knowledge/experience with Other Regulated Applications, such as Learning Management Systems and Quality Management Systems.
· General knowledge of database and computer networking
· Working knowledge/experience with SaaS systems
WORKING CONDITIONS:
Environment: primarily working indoors, performing office work.
Desired Skills and Experience
Roth Staffing is looking for a Compliance QA Manager
All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.
Associate Director Quality Assurance
Indianapolis, IN jobs
Looking for a Pharmaceutical leadership role where you can shape quality operations, build strong teams, and influence the direction of a fast-growing organization? This opportunity is ideal for someone who thrives in
startup or scale-up environments
and enjoys creating structure, elevating standards, and driving continuous improvement.
Pay: $140k-$160k
Schedule: 1st shift
Type of Job: Direct Hire
Location: 100% On-site (Indianapolis area)
At this time, Astrix cannot transfer nor sponsor a work Visa for this position.
Relocation assistance is not available for this position.
Associate Director, Quality & Compliance: Daily Tasks: What you will do:
Responsible for the oversight of the QA teams responsible for supporting all production/processing areas.
Leads investigations of product complaints and manufacturing discrepancies for manufactured products and ensures completion of appropriate documentation.
Responsible for QA review and approval of Investigations, CAPAs, SOPs, Change Controls, and protocols/reports.
Contributes in Regulatory/FDA inspections and audits by providing information or obtaining information required by the auditors.
Performs review of root-cause analysis and ensures completeness, accuracy and compliance of all documentation.
Develops and observes appropriate KPI's for batch documentation review and support of timely batch release.
Accountable for the QA department planning, talent development, and budget administration.
Associate Director, Quality & Compliance Qualifications/Requirements:
Bachelor's Degree is required
6+ Years of progressive QA/QC experience
3+ years in a managerial role in a pharmaceutical or regulated industry
We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
Adobe Quality Assurance
Saint Louis, MO jobs
CDP Tester (Adobe Experience Platform / Customer Data Platform)
100% Remote
Long Term Contract through Dec 2026
**Unable to Provide Sponsorship or Do C2C**
We are seeking a CDP Tester to support a large-scale Adobe Experience Platform (AEP) implementation for a major healthcare client. This role focuses on validating data ingestion, audience logic, and end-to-end functionality within the Customer Data Platform (CDP). Candidates with experience working in Adobe AEP, CDPs, or complex data validation environments will be highly successful in this role.
This position is ideal for QA professionals or junior developers who enjoy testing, validating datasets, and ensuring accurate audience creation for real-time personalization and healthcare outreach campaigns.
Key Responsibilities
Test and validate customer data ingestion pipelines and transformations within Adobe CDP/AEP.
Review and understand audience definitions, rules, and segmentation logic.
Verify that audiences are built correctly based on business requirements and healthcare use cases (e.g., identifying care gaps for targeted outreach).
Use qTest or similar QA tools to document, execute, and track test cases.
Partner closely with Senior Developers and a Team Lead to ensure accurate deployment and performance of CDP updates.
Validate data sets involving Medicare/Medicaid member information, ensuring accuracy and compliance.
Collaborate with cross-functional teams, including data engineering (Snowflake), product owners, and architects.
Support testing of new audience builds used in SMS/email outreach campaigns.
Participate in meetings aligned with project deliverables and sprint requirements.
Serve as a key owner of data accuracy within the CDP environment.
Required Skills & Experience
Experience testing within a Customer Data Platform (Adobe AEP preferred).
Understanding of audience segmentation and data-driven customer journeys.
Strong experience with QA methodologies and tools (qTest highly preferred).
Ability to read and validate business logic, datasets, and transformations.
Familiarity with healthcare data, ideally Medicare or Medicaid.
Strong analytical skills with high attention to detail.
Ability to work onshore in the U.S. and collaborate in CT/ET time zones.
Nice-to-Have Skills
Exposure to Adobe Experience Platform (AEP), XDM schemas, or CDP audience building.
Experience with Snowflake or similar data environments.
Background in healthcare analytics or care-gap data.
Light scripting or SQL knowledge to support data validation.
What Makes This Role Exciting
Work directly on a major enterprise CDP initiative with long-term funding (through 2026).
Support critical healthcare outreach programs that improve patient outcomes.
Collaborate with a highly skilled team including senior CDP developers, architects, and data engineers.
BENEFITS OF WORKING WITH BROOKSOURCE:
Direct communication with the hiring manager, which allows us to move candidates through the interview process faster.
Dedication to keep an open line of communication and provide full transparency.
We are an equal opportunity employer and value diversity at our company. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Director of Quality and Population Health
Kokomo, IN jobs
Job Title: Director of Quality and Population Health
Client: Healthcare Provider Client
Length: 6-month Contract-to-Hire
Under direction of the Chief Medical Officer and in close partnership with executives, site leaders, and others, the Director of Quality and Population Health (the Director) provides the leadership necessary to assure that the client stays in compliance with HRSA, UDS reporting, Joint Commission accreditation, payer quality programs, and internal clinical standards.
Creates and sustains a high-quality, safe, clinical care enterprise,
Sustains upper quarter performance of the clinical quality measures to which they are held accountable (Uniform Data System (UDS) Clinical Quality Measures, Health Resources and Services Administration (HRSA), Healthcare Effectiveness Data and Information Set (HEDIS) payer quality programs and internal clinical standards, as examples),
Maximizes the client's performance in value-based payment relationships
Positions the client to progressively improve its impact on the Social Determinants/Drivers of Health which influence the outcomes of clients.
The Director demonstrates behaviors consistent with professional standards of practice, care, and the mission, values, and goals of the client.
Essential Duties and Responsibilities
Devises and implements the Quality Improvement Plan in accordance with the client's Mission and goals, state and federal laws and regulations, Health Resources and Services Administration (HRSA) compliance, Joint Commission and other accreditation standards.
Facilitates and leads the Quality Improvement/Quality Assurance (QI/QA) committee.
Administers the Quality Program: structure, committee cadence, and dashboards
Defines quality goals, targets and expected workflows for clinics.
Leadership and direction of members of the Quality Department using Lean, PDSA or Six Sigma tools
Owns corrective action plans after audits, site visits, or adverse events
Oversee the client's QI/QA programs and policies.
Builds and supports development of standardized clinical workflows for chronic disease management, preventive care access and care coordination to assure a reliably high level of efficient clinical care across the entire JPCHC enterprise.
Partners with nursing, providers, and site managers to close care gaps
Standardizes rooming, immunization, lab follow-up, and referral workflows.
Monitors documentation accuracy and supports provider feedback loops
Maintains HRSA FTCA compliance, QA/QI program documentation, and audit readiness
Manages incident reporting, root-cause analyses, and follow-up
Works with compliance to reduce sentinel event risk and standardize practices
Tracks infection control, med-safety, and safety culture metrics
Assists in designing training for quality workflows, documentation standards, and PDSA (Plan-Do-Study-Act)
Coaches site leaders on operationalizing quality initiatives
Ensures protocols meet federal, state and accreditation standards
Identifies and advises organizational leadership on staffing needs to achieve the position's goals.
Identifies and helps to eliminate unbeneficial variations in clinical practice.
Directs processes to establish a culture of event detection, reporting, analysis, resolution, improvement, and learning.
Is a student of continuous improvement and high reliability concepts and works to strengthen organizational capacity and impact with these skills.
Participates and assists with committees, meetings, and team projects related to HRSA policy, Patient Centered Medical Home (PCMH), clinical protocols, and other relevant processes.
Supporting Grant Management: Provides input on and assumes appropriate levels of responsibility for compliance and achievement of grant expectations related to this scope of work.
Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education and Experience
Masters level public health, nursing, or pharmacy training. (i.e. MPH, MSN, DNP, PharmD).
Certified Professional in Healthcare Quality (CPHQ)
preferred
.
Minimum of five (5) years' experience as a supervisor and leader in an ambulatory care setting; primary care
preferred.
Experience and familiarity with Federally Qualified Health Center model of care.
Experience within and knowledge of the Patient-Centered Medical Home initiative
preferred
Knowledge of concepts of disease management, population health management.
Skilled in healthcare population-level data analysis.
Knowledge of pay-for-performance and value-based payment programs. Demonstrated success with leading their achievement
preferred
.
Experience with project management, Six Sigma, lean, or other improvement methodology. Formal certification in lean or six-sigma
preferred
.
Possessing personal attributes of being highly organized, attending to detail, strong follow-up skills, taking initiative, persuasive, and mission-focused with well-developed oral and written communication skills.
Demonstrates sound judgment, decision-making and problem-solving skills.
Exhibits professionalism and confidentiality with all aspects of information in accordance with practice, State and Federal regulations.
Proficient computer skills including with Microsoft Office and electronic health records.
Ability to travel up to 50% of the time to regional practice locations
Salesforce Test Lead
Pennington, NJ jobs
Seeking Salesforce Test Lead
As a Salesforce Test Lead you will act as a validation and quality assurance expert and review the functionality of existing systems. You will conduct requirement analysis, define test strategy & design and lead execution to guarantee superior outcomes. You will have the opportunity to collaborate with some of the best talent in the industry to create innovative high quality and defect-free solutions to meet our clients' business needs. You will be part of a learning culture, where teamwork and collaboration are encouraged, excellence is rewarded, and diversity is respected and valued.
Required Qualifications:
Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.
At least 7+ years of Information Technology experience
Candidates authorized to work for any employer in the United States without employer-based visa sponsorship are welcome to apply. Unable to provide immigration sponsorship for this role at this time.
Candidate must be located within commuting distance of Pennington, NJ or be willing to relocate one of these areas. This position may require travel in the US and Canada.
Experience in Software Development and Software Development life cycles (Waterfall/Agile)
Preferred Experience:
4+ years of relevant experience in Salesforce Testing and Automation.
Have knowledge and relevant experience in Sales Cloud, Service Cloud, Marketing Cloud and Experience Cloud.
Experience in Sales Cloud, Service Cloud, Marketing Cloud and Experience Cloud.
Experience in Automation - Selenium, Provar, Copado CRT etc.
Experience with Writing Testing Strategies, Test Plan and Hands-on Test Execution (as required)
Participate in test planning and preparation, represent QA team in scrum calls.
Prepare Test Plan for the project.
Prepare and share the Effort Estimation for manual as well as automation.
Perform System Testing, System Integration Testing, End to End Testing and Automation.
Record test evidence - sufficient to demonstrate test coverage.
Raise defects and take ownership until resolution.
Work with business users to refine test approach, as required.
Defining the Automation standards and best practices to be followed.
Conducting Feasibility analysis for Test cases to be automated.
Maintaining Traceability between requirements and automation scripts.
Guiding the Team in creating automation scripts.
Review test cases, test scripts, execution, and test results.
Produce Test Completion Report.
Undertake defects prevention activities.
Interface with customers for issue resolution and review knowledge management activities.
Escalating risks/issues to Program Manager/Product Owner.
Strong analytical, problem solving and Presentation Skills with strong Interpersonal and organization skills.
Experience with version control systems (e.g., Git) and continuous integration/continuous deployment (CI/CD) pipelines.
Good hands-on experience in other tools like Selenium, Copado CRT, JIRA, Azure DevOps.
Associate Director of Quality Assurance
Phoenix, AZ jobs
Full Time | On-Site | Salary: $100,000-$125,000
About the Company
A fast-growing pharmaceutical manufacturer is seeking an Associate Director of Quality Assurance to oversee quality systems and regulatory compliance across its sterile production operations. The company specializes in producing high-quality pharmaceutical products for healthcare organizations nationwide and maintains a strong focus on cGMP standards, process reliability, and continuous improvement.
Position Summary
The Associate Director of Quality Assurance will provide both strategic and hands-on leadership for the QA function, ensuring all products, processes, and documentation meet applicable regulatory requirements. This role supports day-to-day oversight of manufacturing and laboratory activities, leads QA personnel, and drives the maturity of the company's quality systems. Candidates with experience in sterile or aseptic manufacturing environments are strongly preferred.
Key Responsibilities
Lead QA operations across multiple production and laboratory areas, ensuring consistent alignment with internal quality standards and federal regulations.
Manage batch record review, product disposition, deviation investigations, and CAPA processes.
Ensure ongoing compliance with FDA 21 CFR regulations, cGMP requirements, and applicable industry standards such as ISO 9001.
Conduct internal audits and support external inspections from regulatory agencies and customer auditors.
Collaborate with cross-functional teams (Manufacturing, QC, Validation, Engineering) to resolve quality issues and maintain a compliant production environment.
Oversee training programs related to cGMP, aseptic practices, and quality procedures.
Review and approve SOPs, validation protocols, and other controlled documents.
Provide leadership for cleanroom oversight, environmental monitoring programs, and process validation activities.
Participate in risk assessments and support root-cause investigations for quality-related events.
Mentor and develop QA staff to support team growth and performance.
Qualifications
Required:
Bachelor's degree in Chemistry, Microbiology, Pharmacy, or a related scientific field.
7+ years of quality experience in pharmaceutical manufacturing or another FDA-regulated environment.
Strong knowledge of cGMP, quality systems, and regulatory expectations.
Demonstrated success leading QA teams or managing key quality functions.
Exceptional communication, documentation, and problem-solving skills.
Preferred:
Experience in sterile/aseptic operations or parenteral manufacturing.
Advanced degree (MS, PharmD, MBA, or similar).
Familiarity with QMS software, electronic batch records, LIMS, or related systems.
Prior involvement in regulatory inspections or customer audits.
Work Environment
This is a fully on-site role requiring routine interaction with production, laboratory, and cleanroom areas. Occasional flexibility may be needed during audits, investigations, or time-sensitive production activities. Some travel between company locations may be required.
Compensation & Benefits
Salary range: $100,000-$125,000, depending on experience.
Annual performance bonus eligibility.
Medical, dental, and vision coverage.
401(k) with employer match.
Paid time off and company-observed holidays.
Ongoing training and professional development opportunities.
Quality Management Specialist II
Princeton, NJ jobs
Duration: 12 months
The Quality Management Specialist II tasks include:
CW shadows 3 ongoing studies and supports 7 ongoing studies (planning to reporting stage) to provide Quality oversight, to recommend best practices. Communicates and collaborates with the stakeholders (CM and FAs) partnering for cross-functional team support and attendance of project and study level meetings.
With the assistance of Senior GCP Level 1 members, consults on major and critical quality issues, potential Serious Breaches, significant noncompliance, data integrity issues and protocol deviations, escalates to Senior Management, and performs periodic resolution checks for assigned studies.
Supports risk assessments and risk-based approaches for the annual GQM Audit Plan, identifies the number of site audits and vendor audits based on risk-criteria with input from study teams. Provides study and site related information and documentation to the audit team, GCP Level 2 in preparation for audits.
Participates in the risk assessment of preferred and active vendors utilizing risk assessment tools to prepare the annual GQM Vendor Audit Plan.
Involved in CAPA review of Quality Issues, Audits, Inspections, eTMF audit responses.
Participates and contributes to weekly, monthly, and quarterly GQM GCP meetings.
Attends QA:QA and Quality Council meetings with CRO accompanied by a Senior Member from the GCP In-Line Quality (Level 1)
Participates in the review and harmonization process of controlled documents such as protocols/ICF, CSRs, amendments, procedural documents & templates.
Receives GCP training of ICH Guidelines E6 R3 and Modules from 21CFR and reads GCP Material. Team Members in training participate in weekly team support meetings.
Involved in the Portfolio-wide proactive Inspection Readiness support (Sponsor, Site, CRO) - conducts Do & Don't training, participates in interview preparations/debriefs, assesses Inspection Readiness Visits and Pre-Inspection Visits outcomes.
Reviews and assesses Pharmacovigilance System Master File (PSMF) and performs PV related activities as assigned.
Qualifications:
Bachelors Degree; preferably some Pharmaceutical background and GCP ICH E6 knowledge.
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: Vicky
Email: **********************************
Internal Id: 25-54443
ETL PYTHON TEST LEAD
Austin, TX jobs
Seeking a ETL Python Test Lead.
As an ETL SDET Test Lead, you will act as a validation and quality assurance expert and review the functionality of existing systems. You will conduct requirement analysis, define test strategy & design and lead execution to guarantee superior outcomes. You will also be required to design an optimal test environment to simulate real-time scenarios. You will have the opportunity to collaborate with some of the best talent in the industry to create innovative high quality and defect-free solutions to meet our clients' business needs. You will be part of a learning culture, where teamwork and collaboration are encouraged, excellence is rewarded, and diversity is respected and valued.
Required Qualifications:
Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.
At least 7+ years of Information Technology experience.
Candidates authorized to work for any employer in the United States without employer-based visa sponsorship are welcome to apply. Unable to provide immigration sponsorship for this role at this time
Work location is Fort Mill, SC/ Austin, TX. This position may require travel.
At least 5 years of working experience in QA Testing
Experience with Lean / Agile development methodologies.
Preferred Qualifications
At least 4 years of experience in test strategy and test Design
At least 4 years of experience in test execution analysis & reporting.
Expertise in estimating story points for the agile testing projects
Strong expertise in automation using Selenium w/ Java
Strong in DB validations using SQL
Good understanding of AWS cloud platforms
Good in setting up testing pipeline using Jenkins/ TeamCity
Should have strong co-ordination, communication & reporting, analytical skills
Should have Strong leadership skills
Ability to work in team in diverse/ multiple stakeholder environment
Communication and Analytical skills
Experience and desire to work in a Global delivery environment
Experience for API testing using Postman/RestAssured would be a plus
At least 4 years of experience in using any programming language like Java/Python
Thorough understanding of test automation, UI/Backend test automation concepts
Good Analytical and problem-solving skills.
Ability to work independently and take ownership.
Abilities in Test Strategizing, planning and co-ordination.
Ability to contribute towards in depth technical content required on test automation proposals.
Translate user requirements and application features into testing requirements.
Ability to work in team environment and client interfacing skills.
At least 4 years of experience on Automation Testing (SIT and UAT), test execution analysis & reporting
Test Lead Wi-Fi
Philadelphia, PA jobs
We are seeking a hands-on Lead to manage and drive all activities for their Test House at Philly. This role involves overseeing end-to-end testing operations, ensuring high-quality performance testing of devices on Wi-Fi, Fiber, DOCSIS, WAN, and LAN environments. The ideal candidate will have strong leadership skills, multitasking ability, and a proven track record of getting things done.
Key Responsibilities:
Lead and manage all activities in the Test House, ensuring smooth operations.
Drive Wi-Fi performance testing.
Oversee testing across Fiber, DOCSIS, WAN, and LAN technologies.
Collaborate with stakeholders, lead project calls, and prepare PowerPoint presentations for status updates.
Work closely with another tester in the facility to coordinate tasks and priorities.
Perform manual testing with some automation; ensure hands-on involvement in test execution.
Reproduce and troubleshoot issues in a fully equipped Test House environment.
Ensure timely delivery of test results and maintain high-quality standards.
Required Skills & Experience:
Strong QA background.
Solid understanding of Wi-Fi technologies and performance testing.
Ability to multi-task, manage priorities, and deliver results under tight timelines.
Excellent communication skills for driving calls and preparing presentations.
Hands-on experience in manual testing; exposure to automation is desirable.
Problem-solving mindset with the ability to reproduce and resolve complex issues.
Quality Project Manager
Horsham, PA jobs
This position will lead and participate in projects for the integration of new products into systems that impact the US Pharm Local Operating Company (LOC) and Deliver organizations. Open to candidates located in Horsham PA or Titusville NJ.
Responsibilities:
Key responsibilities include, but are not limited to:
Projects (100%)
Provide project leadership and support related to quality systems for US Pharm CQ and US Deliver initiatives.
Complete GMP documentation to ensure compliance.
Track completion of project deliverables.
Coordinate and collaborate with project team members.
Propose process improvements.
Provide routine project updates.
Perform additional tasks as needed to support project deliverables.
Others:
Execute compliance activities on behalf of team leadership, including but not limited to the creation and revision of regional and local procedures and/or work instructions.
Escalate appropriate issues to management.
Make quality decisions based on assessments of compliance risks, balanced with overall business needs.
Drive strategic initiatives for both CQ and distribution centers.
Ensure strategies are implemented and closed out in a compliant and timely manner.
Experience:
Minimum of 3 years' experience in the Medical Device, Pharmaceutical, or Consumer Products industry.
Experience working in a highly regulated industry.
Proven experience leading projects and influencing team members to achieve results without direct supervision.
Strong written and verbal communication skills, with the ability to take initiative independently as well as collaborate as part of a team.
Demonstrated problem-solving, decision-making, data analysis, inductive reasoning, critical thinking, and root cause analysis skills.
Excellent communication and presentation skills.
Strong change management, collaboration, and influencing skills to effectively partner across functions.
Ability to work under tight timelines and maintain customer focus.
Must be able to manage and provide leadership across multiple sites.
Advanced proficiency in PowerPoint and Microsoft Excel, including VLOOKUPs and pivot tables.
Demonstrated flexibility to handle complexity and multiple initiatives.
Proven ability to successfully partner and collaborate with business partners outside of Quality.
Experience interpreting compliance requirements and regulations.
Preferred Skills and Experience:
Project Management certifications.
Understanding of FDA 21 CFR Part 210, 211, ISO 9001 and/or ISO 13485.
Understanding of Installation Qualification, Operational Qualification, Process Qualification (IQ, OQ, PQ), and associated report writing.
Familiarity with Comet.
Skills:
Project Management
Biomedical Industry
Pharmaceutical Regulatory Compliance
Education:
Bachelor's/University degree.
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: Azhar
Email: ****************************
Internal Id: 25-53768
RxClaim Test Lead
Richardson, TX jobs
Role : RxClaim Test Lead
Fulltime role
seeking a Technical Test Lead,
As an Automation Test Lead/ SDET, you will act as a validation and quality assurance expert and review the functionality of existing systems. You will conduct requirement analysis, define test strategy & design and lead execution to guarantee superior outcomes. You will have the opportunity to collaborate with some of the best talent in the industry to create innovative high quality and defect-free solutions to meet our clients' business needs. You will be part of a learning culture, where teamwork and collaboration are encouraged, excellence is rewarded, and diversity is respected and valued
Required Qualifications:
Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.
4+ years of Information Technology experience
Candidate must be located within commuting distance of Richardson, TX or be willing to relocate to the area. This position may require travel in the US.
Good knowledge on Healthcare, Pharmacy benefit management (PBM) domains.
Preferred Qualifications:
3 years of experience in test execution & reporting, testing lifecycle processes and test tools like Rally, HP ALM, JIRA etc.
Experience and desire to work in a Global delivery environment.
Should have experience in Agile and DevOps methodology.
Excellent Client Interfacing skills
Good Analytical and problem-solving skills
4 years of experience in Pharmacy and RxClaim systems (RxClaim Adjudication, eligibility etc.)
3+ years of hands-on experience on AS400/Mainframes (Cobol, JCL and DB2)
4 years of experience in RxClaim in creating Test Strategy, Test Plan, Test scenarios and Test cases
Experience with Testing strategies and Test Execution
Knowledge and experience with full SDLC lifecycle
Understanding of one or more Estimation methodologies, Knowledge of Quality processes.
Along with competitive pay, as a full-time Infosys employee you are also eligible for the following benefits:
SAP SD Test Lead
Richardson, TX jobs
Seeking an SAP SD Functional Test Lead.
As a SAP SD Functional Test Lead, you will act as a validation and quality assurance expert and review the functionality of existing systems. You will conduct requirement analysis, define test strategy & design and lead execution to guarantee superior outcomes. You will have the opportunity to collaborate with some of the best talent in the industry to create innovative high quality and defect-free solutions to meet our clients' business needs. You will be part of a learning culture, where teamwork and collaboration are encouraged, excellence is rewarded, and diversity is respected and valued.
Required Qualifications
Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.
7+ years of Information Technology experience
Candidates authorized to work for any employer in the United States without employer-based visa sponsorship are welcome to apply. Unable to provide immigration sponsorship for this role at this time
Candidate must be located within commuting distance of Chicago, IL/ Hartford, CT/ Phoenix, AZ/ Raleigh, NC/ Indianapolis, IN/ Richardson, TX or be willing to relocate to the area. This position may require travel in the US and Canada
Strong understanding of testing processes and testing life cycle
Preferred Experience:
Must have played the role of SAP SD Functional Test Lead for implementation, rollout, and upgrading projects. Experience in managing S4 HANA testing is preferred.
Should have good knowledge of any SAP SD functional module - Order to Cash, Order Management, Shipping, Billing Management - E2E Business Processes
Should have played the role of onsite lead coordinator for onsite-offshore global delivery model
Proven experience of test planning, recommending test approaches and test strategies, conducting Impact Assessments, identifying, and managing Testing risks
Good knowledge of SAP Testing w.r.t integration, regression testing and test automation associated with SAP S4 HANA
Should be able to manage customer stake holders as well as internal stake holders across the testing life cycle.
Should be able to drive defect triage calls across various cycles.
Able to send the daily, weekly, monthly status report associated with testing to expected stakeholders. Should have experience in preparing, monitoring, testing metrics.
Identify tools and technologies to be implemented, aligning with that already used across the broader testing function and in-line with the skill set of the team
In-depth knowledge of current industry-wide testing techniques, tools, and methodologies
Excellent verbal and written communication skills
Need to closely work SI Partner, IT, Business, 3rd Party Vendors & offshore Team for the successful completion of the Testing as per defined Timeline
Need to have a good knowledge in SAP Test Automation Tools like TOSCA / Worksoft
Manual QA
Indianapolis, IN jobs
Responsibilities
Strong skills in test planning and traceability for compliance and audit purposes.
Lead with curiosity to further requirements discussions and uncover test scenarios.
Review requirements and specifications to ensure testability.
Ability to identify critical business workflows and ensure they remain intact after changes.
Develop and maintain manual test cases based on functional requirements and acceptance criteria.
Execute manual tests and document results.
Log and track defects using appropriate tools.
Perform regression testing after bug fixes and new feature deployments.
Collaborate with developers, product owners, and other stakeholders to clarify requirements.
Participate in test planning and estimation.
Ensure quality standards are met before release.
Provide clear and detailed defect reports and communicate effectively with the team.
Contribute to continuous improvement of Agile and QA processes.
Required Skills
Strong understanding of software testing methodologies (functional, regression, smoke).
Ability to create, execute, and maintain test cases and test plans.
Familiarity with bug tracking tools (Azure DevOps, Jira).
Strong knowledge of SDLC and Agile methodologies.
Strong analytical and problem-solving skills.
Excellent written and verbal communication for reporting defects and collaborating with teams.
Ability to ask 'Why' and 'What If' questions to enhance discussion and discovery.
Attention to detail and ability to identify edge cases.
Hands on experience with API testing (using tools like Postman is a plus).
Hands on experience with SQL and database queries.
Experience with large-scale regression suites.
Ability to prioritize test cases for high-risk areas.
Knowledge of impact analysis for upgrades and migrations.
Ability to coach others and create a testing mindset.
Ability to work in a team environment.
Ability to self-organize and prioritize tasks within multiple teams.
Preferred Skills
Knowledge of version control systems (e.g., Git).
Understanding of server architecture (Windows).
Familiarity with cloud platforms (Azure).
Ability to validate configuration changes and deployment impacts.
Awareness of test automation frameworks (Selenium, Cypress, Playwright) - even if not hands-on yet.
Ability to learn and adapt to automation tools and scripting.
Strong analytical thinking for identifying automation opportunities.
Education
Bachelor's degree in Computer Science, Information Technology, or related field.
Equivalent experience in QA/testing may be considered in lieu of formal education.
Certifications (Preferred but not mandatory)
ISTQB Foundation Level (preferred)
Any Agile or Scrum certification (e.g., Certified Scrum Tester).
Experience
4+ years of experience
Specialist 2, Quality Assurance
Lititz, PA jobs
The Quality Specialist II will be accountable to support Product Review reports and to support investigations pertaining to observations or trends discovered during data collection. The Quality Specialist II will also be accountable for supporting Laboratory Information Management System (LIMS) Master Data changes needed by the Quality Control Laboratory.
Responsibilities:
Communicate to Quality Management the observations or trends discovered during the data collection and review of the Product Reviews. Maintain metrics and support management reviews and other presentations.
Performs other duties, as assigned.
Excellent analytical, prioritization, multi-tasking, communication, and strong leadership skills and the ability to work independently without supervision is required
Ability to work effectively on cross functional teams is required.
Experience:
Support Product Review completion per scheduled timeline and store in document management system.
Fulfill LIMS Master Data requests.
Review Master Data submissions for accuracy and provide feedback as necessary
Skills:
Excel, LIMS, Word
Medium, must be able filter and sort spreadsheets
ASQ Certification welcome
Education:
Bachelors
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: Azhar
Email: ****************************
Internal Id: 25-54038
Specialist, QA Validation
Sanford, NC jobs
Pay $76-$81 per hour
On-site Role
1 year extendable contract
Medical, Dental, Vision, 401k
The Specialist, QA Validation will be primarily responsible for the implementation, execution and assessment of quality systems, procedures, and records to support compliant GMP operations. This position works closely with Validation, Engineering, Manufacturing, Quality Control, Facilities, and Automation.
Responsibilities and Accountabilities:
• Provide hands on QA support and oversight to internal staff and suppliers/contractors to ensure compliance with local and global quality standards, regulatory requirements, and industry guidance.
• Provide QA review and approval for commissioning/qualification/validation documents.
• Provide QA review and approval of qualification and validation deviations and discrepancies and support investigation and corrective actions.
• Author, review and approved controlled documents for the Quality organization including SOPs, specifications, protocols, and reports.
Qualifications:
• B.S. degree in Biological/Physical/Chemical sciences, engineering, or equivalent focus of study and 3-5+ years of experience or M.S. degree and 1-3+ years of experience in a QA function in a biologics manufacturing facility
• Experience with qualification/validation of process equipment, analytical instruments, clean utilities, automation, sterile filling, and clean facilities.
• Strong understanding of FDA, EMA, local regulations and guidelines, ICH guidelines, and industry best practices.
• Successful history working in a fast-paced team environment, meeting deadlines, and prioritization of work from multiple projects
• Strong analytical and communication skills as well as sound judgment, with the ability to work effectively with others
• Excellent problem-solving skills and experience with root cause investigations and CAPA determination
• Off hours coverage and flexibility may be required
Project Manager 2 - Quality Engineering
Wilson, NC jobs
Duration: 12 months
Skills Required
Role will be 100% onsite in Wilson, NC
There will be 2 interviews; 1 video conference, and 1 will be onsite
Bachelors degree is required
This role is considered a Quality Management Platform Analyst
Will assist with a plan, a template with utilizing software platform for method transfers and qualifications
Must have Method Transfer knowledge/experience
Must have Programming exp
Required to have Kneat experience
Work within the team to help develop the system
Knowledge of method verification or method transfers
Basic SQL exp, NOT coding
Must have communication skills
Must be self-driven
CGMP exp
Should have 8-10 years of exp
MUST be able to show the candidate has used Kneat to generate protocols!
Description:
Quality Management Platform Analyst, located in Wilson, NC.
We need a forward-thinking, data analyst, to evaluate, road map and construct an area within our workspace in Kneat to house our method verification and transfer execution worksheets protocols and reports
Key Responsibilities:
• Train on and establish an account in Kneat,
• Evaluate how to optimally apply the system,
• Construct the needed infrastructure in our workspace and roadmap the execution
Qualifications Education:
BS Experience
• Incumbent must be proficient with Word, Excel, Power Point, have the soft skills needed to nurture change, as well as, the acuity to use software nuanced to operate in a regulated environment.
- Generally Requires 8-10 Years Work Experience
- Kneat experience required
Preferred:
A Major in Bio-Medical Engineering, Chemistry or Biology Other: Available to work full-time (40 hrs./week) with reliable transportation to and from work
Must be available to work Monday through Friday 8AM to 5PM Must be able to work in the US and must not require sponsorship for employment visa status now or in the future (e.g., FI, H1-B status)
Top Three Skills: Experience using Kneat, MS word and in writing method validation or transfer protocols
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions is an Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: I.Prudvi kumar
Email: *******************************
Internal Id: 25- 54461
Sterility Assurance Scientist
Concord, NC jobs
Title: Sterility Assurance Scientist
Duration: 6 Month Contract (potential of extension)
Responsibilities:
The Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's
sterility assurance programs and provides technical guidance and expertise in environmental monitoring,
contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization
strategies, including disinfectant efficacy. The principal role is a position that develops and implements a
technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The
principal role is also expected to serve as a mentor within the TSMS team and engage in upstream and external
to site activities related to sterility assurance contamination control strategies are established.
Key Objectives/Deliverables
• (Associate/Senior) Ensure and provide oversight and technical guidance for sterility assurance programs
at the manufacturing floor level.
• Lead or provide technical oversight for Provide technical support for activities related to sterility
assurance programs including but not limited to:
• Airflow Pattern Testing
• Environmental Monitoring Performance Qualifications
• Aseptic Process Simulations
• Cleaning, Sanitization, and Disinfection
• Gowning within GMP Classified Areas
• Aseptic Processing Techniques
• Contamination Control
• Assist in the development and implementation of processes and facility monitoring to ensure effective
contamination control strategies are established.
• (Senior) Lead or assist in the development and implementation of processes and facility monitoring to
ensure effective contamination control strategies are established.
• (Senior) Lead/assist with support and/or provide technical expertise for developing the site's
contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy
strategies.
• (Senior) Lead/assist with support and/or provide technical expertise for the facility's cleanroom
gowning and aseptic technique strategy/program.
• (Principal) Knowledge in pharmaceutical Microbiology, related to microbiological media,
microbiological enumeration techniques, and microorganism isolation and identification.
• (Principal) Lead/provide technical oversight for one or both the Environmental Monitoring (EM) or
Aseptic Process Simulation (APS) program:
• (EM) Authoring EM Performance Qualifications (EM PQ) and overseeing the execution.
• (EM) Evaluating EM data and authoring EM Trend Reports.
• (EM) Assist with identifying facility environmental isolates and how to create and maintain
environmental isolated cultures.
• (APS) Authoring APS protocols and overseeing the execution.
• (APS) Evaluating the APS data, including personnel qualifications, and authoring APS reports.
• (APS) Assist with tracking and tending APS to ensure all regulatory requirements and Global
Quality Standards are met for each manufacturing line/process.
• Apply sterility assurance risk management to evaluate manufacturing processes and associated controls
with respect to potential introduction of microbial, endotoxin, and particulate contamination.
• Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities
for continuous improvements.• Lead or provide technical support for root cause investigations associated with sterility assurance
programs.
• Participate and/or provide technical sterility assurance support during internal and external audits.
• Create, execute, review, and/or approve technical documents and change controls related to sterility
assurance programs.
• Work within cross-functional teams to implement TS/MS objective and deliver on business and quality
objectives.
Basic Qualifications:
• Bachelor's or master's degree in microbiology, Biology, Biochemistry, Biochemical Engineering,
Chemical Engineering, or other related scientific discipline.
• Demonstrated understanding and relevant experience of scientific principles required for manufacturing
parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance,
validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing.
• (Senior) 2+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or
related dept).
• (Principal) 5+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or
related dept).
Additional Skills/Preferences:
• Possess strong interpersonal skills to work cross-functionally within a team.
• Possess strong self-management and organizational skills.
• Possess strong oral and written communication skills for communicating to colleagues, management,
and other departments.
• Experience with data analysis and trending.
• Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing
warehouse, or laboratory areas.
• Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities.
Additional Information:
• Role is Monday through Friday based and will be phased from a project support role to a routine support
role as the development facility and processes progress. Must be flexible in providing support to
accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hours and / or
off-hour work may be required.
• Tasks may require repetitive motion and standing or walking for long periods of time.
• Travel may be required during the project phase for training and implementation of sterility assurance
programs.
This is intended to provide a general overview of the job requirements at the time it was
prepared.
The job requirements of any position may change over time and may include additional responsibilities not
specifically described in the . For GMP purposes, the job description should be updated for
significant changes. As always, you should consult with your supervisor regarding your actual job
responsibilities and any related duties that may be required for the position.
Quality Engineer
Lewisville, TX jobs
Job Title: Quality Engineer
Duration: 6 Months
Type: Contract to Hire
Additional Notes
is 100% onsite, Monday-Friday, 8 AM to 5 PM, with no overtime required.
The role is temp-to-hire, and a Bachelor's degree is required for conversion.
Occasional travel to Mexico may be required (1-2 trips per year) to support the Video EMS site; all travel, lodging, and transportation will be arranged and paid by Motorola. Breakfast and lunch provided; dinner reimbursed.
Work environment may include office, EMS factory, or distribution center; safety equipment will be provided as needed.
Approximately 2 weeks of training will be provided before independent work is expected.
Interview process includes:
• 1 virtual Google Meet interview
• 2 onsite interviews (30 minutes each) with the hiring manager and team members
The role sits within the Quality department and collaborates closely with supply chain, manufacturing, and regulatory teams.
Top priorities in the first 90-120 days: improving video quality, reducing cycle time, and resolving customer cases.
Required foundational skills include basic quality tools (5 Why, Fishbone, Histogram).
Six Sigma Green Belt is highly preferred.
Candidates should be proficient with Google Suite, Minitab, and SAP.
Required Skills & Experience
Bachelor's Degree in technical/science field, Master is a plus
Minimum 5 years' experience in Supplier/ Supply Chain quality roles, experience with
Distribution Centers and Product Manufacturing processes is welcomed.
Solid technical knowledge, (products, systems, complex integrated solutions).
In depth understanding of quality standards and quality improvement methods.
Experience in Lean and Six Sigma methodologies as certified Belt is an advantage.
Problem-solving mindset as well as an attitude to follow through on plans.
Good communication and negotiation skills.
Experience in wing in cross-cultural environment
What You Will Be Doing
Roles and Responsibilities
Serve as the liaison for suppliers and manage the supply chain for both Distribution Centre as well as Motorola Manufacturing sites.
Monitor Suppliers performance to assess ability to meet quality and delivery requirements.
Increase quality reliability, use engineering skills to regulate product transition requirements.
Take part in local Quality Audits and Regulatory Compliance audits.
Local Maintenance of the Suppliers Quality Ranking System.
Meet with suppliers to discuss performance metrics, to provide performance feedback and
manage process controls, establishing schedules for reviewing supplier and quality performance.
Report and maintain accurate quality records, certifications, and database screens.
Prioritize critical cases addressing Customer complains associated with the products delivered to them.
Support quality improvement processes/projects at internal or external sites
Quality Engineer
Houston, TX jobs
We are seeking an experienced QE Developer with strong automation expertise and a technical background suited for a fast-paced environment. This role will focus on designing, developing, and maintaining automated test frameworks and validations for the GasQuest application. The ideal candidate will have hands-on experience with Java-based automation, CI/CD execution pipelines, and modern QA tooling, along with the ability to work both independently and in cross-functional teams.
Responsibilities
Develop, maintain, and enhance automated test scripts using Java and Playwright.
Implement hybrid test automation frameworks leveraging Page Object Model (POM) principles.
Integrate automation scripts with CI/CD pipelines to support continuous testing and deployment.
Conduct API testing and validation using Rest Assured and related test utilities.
Execute automated test suites across containerized environments using Docker and Selenium Grid.
Validate database operations leveraging MySQL JDBC for test data verification and backend checks.
Monitor execution dashboards, analyze failures, and deliver actionable defect reporting through Extent Reports and CircleCI.
Collaborate with developers, QA analysts, and product teams to align automation efforts with release cycles and business expectations.
Participate in code reviews, source control workflows, and best practices using GitHub.
Assist in on-call support rotations and after-hours deployment testing when required.
Required Technical Skills
Proficiency in automation testing using Playwright Java API.
Strong Java programming experience for script development.
Hands-on experience with:
Extent Reports (HTML-based reporting)
Maven (build and dependency management)
TestNG (execution framework)
Experience with CI/CD execution pipelines, especially CircleCI, Docker, and Selenium Grid.
Familiarity with debugging tools, Chrome DevTools, and repository workflows (branching, PRs, merging).
Additional Preferred Skills
SQL experience (Aurora and/or Redshift).
Basic AWS familiarity (S3 navigation, Lambda log review, CLI usage).
API testing with Postman.
JSON data format understanding.
PowerBI, Excel, and PowerShell or Git Bash for scripting.
Experience using Snag-It or similar screenshot/documentation tools.
Knowledge of Oil & Gas industry applications is a plus.