Quality Assurance Leader Job at Aramex

Quality Assurance Manager

The Quality Assurance Manager is responsible for supporting compliance, safety, ...

Location

United States , Lansing

Salary:

Not provided

Aramark

Expiration Date

Until further notice

Requirements

Bachelor's degree preferred in Business, Hospitality, Safety, Engineering, Operations, Environmental Management, or a related field
equivalent experience considered
3–5 years of experience in quality assurance, compliance, facilities administration, operations support, project coordination, or a related field preferred
Strong organizational and project management skills with the ability to manage multiple priorities simultaneously
Strong interpersonal and communication skills, with the ability to work effectively with both technical and non-technical stakeholders
Ability to interpret contracts, regulatory requirements, policies, and operational procedures
Experience preparing reports, maintaining records, and tracking compliance-related documentation
Demonstrated ability to identify issues, analyze data, and develop practical solutions
Working knowledge of preventive maintenance practices, facilities operations, or asset management systems preferred
Experience with CMMS, compliance tracking, or facilities management software preferred

Job Responsibility

Support property-wide compliance with Aramark standards and applicable federal, state, and local regulations
Coordinate and track required licenses, permits, inspections, certifications, and regulatory reporting obligations
Maintain documentation and records associated with compliance activities, including audit readiness and retention standards
Establish and support recurring internal audit processes and corrective action tracking
Remain current on applicable laws, regulations, and operational requirements impacting the business
Partner with department leaders to ensure Quality Assurance (“QA”) assessments, waste tracking, and related reporting are completed accurately in GMM and other required systems
Implement and maintain department-level Standard Operating Procedures (“SOPs”) through process review, documentation, and ongoing evaluation
Identify operational gaps, process inefficiencies, or non-conformance issues and help develop corrective action plans
Assist in developing reports, dashboards, and tracking tools that support operational performance and compliance visibility
Serve as MS3 Administrator and maintain the MS3 Master Scheduler and Facility Library systems in partnership with Performance Excellence and Project Management teams

Fulltime

Director, Quality Assurance

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

United States , Holly Springs

Salary:

181620.35 - 245721.65 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Bachelor's degree and 10 years of Quality/Manufacturing/Engineering experience OR Master's degree and 8 years of Quality/Manufacturing/Engineering experience OR Doctorate degree and 4 years of Quality/Manufacturing/Engineering experience
at least 4 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources
Bachelor's Degree in a Science field
15+ years of experience in Quality within the biopharmaceutical or regulated manufacturing industry
Previous experience in Quality oversight of Biologics drug substance operations
Strong knowledge of cGMPs and experience interacting with Regulators
Able to drive process improvement within area of responsibility
Able to successfully manage workload to timelines
Proven experience supporting regulatory inspections and site audits
Demonstrated leadership of cross-functional teams within a manufacturing site

Job Responsibility

Lead the quality team supporting drug substance manufacturing execution activities within our site's second FleX Batch manufacturing facility
Build and lead a high-performing quality organization responsible for supporting 24/7 manufacturing operations
Contribute to the development of the site Quality strategy leading teams accountable for all aspects of quality oversight of GMP systems and operations
Foster a culture of execution excellence, accountability, and continuous improvement
Provide Quality input and expertise to support project and operational design decisions
Lead operational readiness activities to implement quality systems, programs, business processes and procedures
Track progress and communicate status
Lead and participate in Quality Risk Assessments
Build organization according to hiring strategy that supports project milestones
Recruit, coach, develop, motivate, and retain staff

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
Retirement and Savings Plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives

Fulltime

Product Quality Leader

Join us as a Product Quality Leader at Ericsson’s US 5G Smart Factory (EFA) and ...

Location

United States , Lewisville

Salary:

Not provided

Ericsson

Expiration Date

Until further notice

Requirements

At least a Bachelor’s degree in engineering is required. Minimum of 5 years of quality engineering experience in a manufacturing setting
5+ years of experience leading or managing teams in quality or manufacturing engineering
Strong preference for experience with Surface Mount Technology and Automated Assembly processes
Solid working knowledge of quality management methods and tools, such as Six Sigma, APQP, SPC, FMEA, Control Plan, MSA, and ISO 9001
Excellent communication and presentation skills, with the ability to lead and present data analytics effectively to both technical and non-technical audiences
Demonstrated initiative, proactive approach, and strong critical thinking and problem-solving abilities, with a focus on results
Willingness to travel internationally up to 10%

Job Responsibility

Lead a cross-functional quality improvement team to execute and fulfill established quality plans, focusing on targets like yield, DPPM, inspection fault rate, CPK, customer claims, and repairs, ensuring product KPIs are met
Be responsible for driving quality assurance, the PQL provides reports to the Project Manager and stakeholders, offering technical recommendations and consequence analyses at each project milestone
Support the Project Manager with a quality perspective throughout each phase of NPI, TPI, GPI, and maintenance projects, contributing to producibility, reliability, and risk management
Leads the FRAG forum, continuously analyzing yield, claims, and repairs using necessary systems, tools, and Six Sigma methods, collaborating with engineers to resolve critical issues
Holds authority to independently perform tasks necessary to meet responsibilities, with delegated formal leadership from the Plant Quality Engineering Manager
Takes ownership of Quality Alerts and has access to all required information, systems, and tools to ensure product quality and carry out FRAG work. Manages risk decisions related to process exemptions when timing is crucial, ensuring competitive advantage

What we offer

Opportunity for an annual bonus
Choice of three medical plan options and a dental plan option
Company credits equal to the cost that Ericsson pays toward medical and dental premiums
Automatic 3% company contribution to 401(k) plan
Ericsson match $1 for every $1 on first 3% of eligible pay plus 50 cents on every $1 on next 2% of eligible pay
Basic life insurance and basic accidental death and dismemberment coverage
Short-term and long-term disability coverage
Option to participate in Ericsson’s Stock Purchase Plan
Minimum of 15 days of accrued vacation
Up to 3 personal days per year

Fulltime

Quality Assurance Engineer

The Professional, Quality Assurance Engineer (m/f/d) supports the delivery of hi...

Location

Germany , Leer

Salary:

Not provided

Forterro

Expiration Date

Until further notice

Requirements

Experience in software quality assurance or related testing roles
Understanding of test design, test execution and defect tracking
Ability to work independently within established QA frameworks
Clear communication skills with developers, product teams and other stakeholders
Ability to identify routine issues and recommend practical improvements
Education and experience in software testing, computer science or a related field

Job Responsibility

Designs and maintains test cases, test plans and test scenarios
Executes manual and automated tests across multiple platforms
Reviews requirements and supports the creation of accurate test scenarios
Tracks defects and issues and communicates them to development teams
Supports functional, regression, UI and integration testing activities
Describes QA practices, solutions and procedures to stakeholders
Escalates complex issues to senior team members
Checks testing processes and recommends improvements that enhance efficiency
Solves routine testing problems using prior experience and available guidance
Proposes solutions and enhancements for review by leaders

Fulltime

Executive Director, Research & Development Quality Assurance

Joining Moderna offers the unique opportunity to be part of a pioneering team th...

Location

United States , Cambridge; Bethesda

Salary:

224900.00 - 404600.00 USD / Year

Moderna

Expiration Date

Until further notice

Requirements

Bachelor's degree in a life science or related field
advanced degree preferred
15+ years of progressive experience in the biopharmaceutical industry with deep expertise in GCP, GLP, GCLP and GVP and the ability to provide expert guidance on complex quality issues occurring in clinical trials, regulatory submissions, laboratories and PV and clinical safety
10+ years' experience leading multifunctional quality organizations within the research and development sector, with proven excellence across all facets of quality management including experience developing and managing budgets and ensuring efficient allocation of resources to support both short-term initiatives and long-term organizational goals
Expertise to oversee comprehensive resource and staffing management, building high-performing teams and fostering a culture of continuous improvement and accountability
Experience in the development and execution of robust audit schedules, coordinating cross-functional efforts to ensure compliance with industry standards and regulatory requirements through proactive planning and collaboration
Demonstrated success in developing and executing global audit programs and hosting health authority inspections with a track record of positive outcomes
Extensive knowledge of FDA, EMA, MHRA, PMDA, ICH and EU PV regulations/guidelines, including ICH E2 and EU PV legislation
Extensive knowledge of FDA, EMA, MHRA, PMDA, ICH regulations, guidance and local legislation for clinical trials, including a ICH E6 (R3)
Proven ability to collaborate and influence in a fast-paced, matrixed environment

Job Responsibility

Provide enterprise governance and oversight of GCP, GVP, GLP, and GCLP compliance across Moderna's entire development portfolio
Define and execute a robust, forward-looking quality strategy in alignment with global regulatory requirements and Moderna's innovation agenda
Act as the primary Quality business partner to R&D functional leaders across Clinical, Non-Clinical, Research, and Pharmacovigilance areas
Embed risk-based quality management principles into study design, data generation, and vendor oversight practices
Serve as the Quality leader and Inspection Host during global regulatory inspections (FDA, EMA, MHRA), ensuring timely and effective resolution of findings
Drive modernization of vendor oversight and shared accountability models, elevating external partnership performance
Build and lead a high-performing, solutions-oriented R&D QA team, rooted in scientific credibility and operational excellence
Enhance Quality Culture across R&D by promoting real-time quality management, early issue detection, and continuous feedback loops
Establish and track quality metrics and leading indicators that drive meaningful risk mitigation and compliance
Own the end-to-end quality lifecycle for deviations, CAPAs, issue management, regulatory intelligence, and inspection readiness

What we offer

Best-in-class healthcare coverage, plus voluntary benefit programs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities to help you plan for the future
Location-specific perks and extras

Fulltime

Regional Quality Assurance Manager

Join Our Growing Team! Capital Vacations continues to expand across key markets,...

Location

United States , Kissimmee

Salary:

Not provided

Capital Vacations

Expiration Date

Until further notice

Requirements

5+ years of experience in the Timeshare industry required
3+ years in a QA leadership or multi-site management role preferred
Proven track record of reducing cancellations and improving compliance standards
Strong understanding of state and federal timeshare regulations
Advanced knowledge of contracts, funding processes, and sales compliance
Proficient in Microsoft Office Suite (Word, Excel, PowerPoint)
Ability to analyze performance data and identify actionable insights
Willingness to travel regularly within assigned region
Flexibility to work weekends and be available as needed

Job Responsibility

Provide strategic direction and oversight to on-site QA Managers and QA teams across multiple locations
Train, mentor, and develop QA leadership to ensure consistent performance and compliance standards
Conduct regular site visits, audits, and performance reviews
Establish accountability measures and corrective action plans where needed
Ensure adherence to all company policies, state regulations, and timeshare closing procedures
Protect the organization from misrepresentation and compliance violations
Investigate escalated client disputes and misrepresentation concerns
Partner with Legal and Executive Leadership when necessary
Collaborate with Regional Sales and Marketing Leaders to maintain acceptable cancellation rates and achieve company targets
Monitor performance metrics including net cancellation rate, closing percentages, and rescission trends

What we offer

Competitive Compensation Package with performance-based incentives
Leadership Growth & Career Advancement Opportunities
Comprehensive Benefits including medical, dental, vision, company-paid life insurance, and 401(k)
Travel Opportunities within assigned region
Supportive, high-performance culture focused on results and integrity
Medical Insurance
Dental Insurance
Vision Insurance
Discounted Resort Stays
Paid Time Off

Fulltime

Director, Quality Assurance

This role leads the Quality Assurance function for a medical device company spec...

Location

Canada , Mississauga

Salary:

150000.00 - 200000.00 CAD / Year

Profound Medical

Expiration Date

Until further notice

Requirements

A minimum of a bachelor’s degree in engineering (Mechanical, Electrical, Biomedical, Systems, or related field)
Quality Assurance certification (ASQ CQE, CQA, CMQ/OE) is an asset
10+ years of experience in Quality Assurance within the medical device industry
5+ years of leadership experience in a regulated manufacturing environment
Deep expertise in ISO 13485, ISO 14971, and medical device quality system practices
Strong engineering background with hands-on experience in: Design transfer
Process validation
Manufacturing quality controls
DMR/DHR management
Root cause analysis and problem-solving methodologies

Job Responsibility

Lead the development, implementation, maintenance, and continuous improvement of the regulatory compliant QMS
Serve as the Management Representative, reporting to senior management on QMS performance and improvement opportunities
Ensure effective document control, training, internal audits, CAPA, nonconformance management, supplier quality, and change control processes
Partner closely with R&D to ensure design controls are rigorously applied throughout the product lifecycle
Lead risk management activities (ISO 14971, DFMEA, PFMEA) and ensure risk files remain current and comprehensive
Ensure verification, validation, and usability engineering activities meet quality and safety requirements
Lead design transfer from R&D to manufacturing, ensuring readiness of processes, documentation, and controls
Conduct manufacturability assessments and collaborate with engineering to optimize product design for production efficiency and reliability
Oversee process validation (IQ/OQ/PQ) for manufacturing processes, test methods, and equipment
Ensure effective deployment and maintenance of the Device Master Record (DMR) and Device History Record (DHR)

What we offer

group RRSP
medical benefits paid by the employer

Fulltime

Sr Manager - IT, Change Management & Quality Assurance

The IT Senior Manager – Change Management & QA is responsible for leading the en...

Location

United States

Salary:

Not provided

Valvoline

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Computer Science, Information Systems, Engineering, or related field required
Master’s degree preferred
10+ years of experience in IT Quality Assurance, Testing, Change Management, or Release Management
5+ years leading global or enterprise-scale QA or change organizations
Experience supporting large ERP implementations (SAP ECC and/or S/4HANA) and complex integrations (EDI, middleware, APIs)
Demonstrated experience implementing structured change governance frameworks
ITIL Foundations certification required
Testing, QA, DevOps, or Agile certifications preferred (e.g., ISTQB, SAFe, DevOps)
Deep expertise in enterprise QA frameworks, test automation, and performance engineering
Strong understanding of ITIL-based change management and release governance

Job Responsibility

Define and own the global strategy for IT quality assurance, testing, performance validation, release governance, and IT change management
Establish enterprise standards, methodologies, KPIs, and governance models aligned with global delivery and transformation priorities
Ensure quality validation, release readiness, and structured change controls are embedded as formal gates in delivery and go-live decisions
Lead and develop a global, matrixed organization including QA Managers, Test Leads, Release Coordinators, and Change Analysts
Foster a culture of accountability, automation-first thinking, service discipline, and continuous improvement
Define career paths, skills development, and scalable operating models across regions and platforms
Oversee functional, integration, regression, and user acceptance testing leveraging OpenText ALM and UFT One
Lead enterprise tool strategy, including transition from Zephyr to OpenText toolsets and integration with JIRA and CI/CD pipelines
Establish automation standards and reusable frameworks to improve coverage and reduce cycle time
Govern enterprise performance and load testing strategies using OpenText LoadRunner and EDI load simulations

Fulltime

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Quality Assurance Leader

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