quality manager

Thermo Fisher Scientific

<div>Work Schedule
First Shift (Days)
Environmental Conditions
Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
As part of the Thermo Fisher Scientific team, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world&rsquo;s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
How will you make an impact?
The Quality Manager receives assignments in the form of site and functional objectives and determines how to deploy people, time, and resources to meet schedules, quality standards, and business goals. This role provides leadership and guidance to the Quality Control and Quality Assurance organizations within established company policies, recommends improvements to policies and procedures, and ensures effective execution of QC laboratory operations and QA systems. The Quality Manager is accountable for short- to mid-term (1&ndash;2 year) performance, compliance, and continuous improvement results for the quality function, with primary emphasis on QC laboratory excellence while maintaining robust QA systems and compliance.
What will you do?<ul><li>
Translate site and quality function objectives into actionable plans, priorities, and resource allocations to meet operational schedules and quality goals.</li><li>
Provide leadership and direction to the Quality Control team, managing through QC Supervisors as applicable, and ensuring alignment with site priorities.</li><li>
Ensure timely, compliant execution of QC testing, batch record review, and disposition of finished goods.</li><li>
Monitor quality performance metrics, identify trends, and take corrective actions to improve quality, efficiency, and reliability.</li><li>
Guide and support supervisors and individual contributors within established company policies, procedures, and quality systems.</li><li>
Recommend updates to QC and QA policies, procedures, and workflows and establish local procedures that impact the immediate organization.</li><li>
Manage the QA function to create a culture of quality awareness, teamwork, and compliance across the organization.</li><li>
Engage in daily oversight and guidance of nonconforming material investigations, complaint records, corrective and preventive actions, and change controls to drive timely and scientifically sound closure.</li><li>
Provide guidance and direction to stakeholders to ensure ISO 9001 compliance and Quality Management System adherence.</li><li>
Collaborate across functions and sites, leveraging quality and manufacturing expertise to troubleshoot problems, interpret data and determine next steps based on risk-based approach.</li><li>
Manage accuracy, completeness, and timeliness of Quality records.</li><li>
Lead external regulatory inspections and customer audits</li><li>
Oversee internal audits program.</li><li>
Develop quality talent through coaching, feedback, and performance management, with accountability for near-term capability needs, succession planning, and meeting personal career goals while achieving organization goals.</li><li>
Design, plan, and lead Practical Process Improvements (PPI) initiatives focusing on scientific practices, knowledge, best practice, standard work, or quality initiatives.</li></ul>
REQUIREMENTS
Education and Experience<ul><li>
Advanced degree plus 6 years of experience, or Bachelor's degree plus 8 years of experience in regulated pharmaceutical/biotech/medical device industry</li><li>
Preferred Fields of Study: Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, Biotechnology, Engineering, Microbiology, or related scientific field</li></ul><ul><li>
5+ years of people management experience leading QC laboratory teams</li><li>
Strong understanding of analytical testing methods and laboratory operations</li><li>
Knowledge of cGMP regulations, quality systems, and regulatory requirements preferred</li><li>
Demonstrated success implementing and improving quality systems and processes</li><li>
Experience with laboratory information management systems (LIMS) and data integrity requirements</li><li>
Experience leading conversations with customers and auditors and supporting regulatory inspections</li></ul>
Knowledge, Skills, Abilities<ul><li>
Proven understanding of Quality Control Laboratory operating principles and Quality Assurance procedures, processes, and guidelines</li><li>
Leadership experience developing and mentoring staff with ability to affect performance and development of individuals across the Quality department</li><li>
Ability to drive functional, technical, and operational excellence</li><li>
Ability to think strategically with the ability to direct the resolution of technical problems using innovative approaches</li><li>
Project management and organizational skills</li><li>
Clear written and verbal communication skills with ability to analyze data, summarize results, present data, and address feedback</li><li>
Practical application experience in continuous improvement methodologies to improve processes, strengthen quality, and drive efficiency</li><li>
Highly skilled in Quality tools e.g. FMEA, Risk Analysis, Root Cause Analysis</li></ul>
Compensation and Benefits
The salary range estimated for this position based in New Jersey is $112,500.00&ndash;$155,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:<ul><li>
A choice of national medical and dental plans, and a national vision plan, including health incentive programs</li><li>
Employee assistance and family support programs, including commuter benefits and tuition reimbursement</li><li>
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy</li><li>
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan</li><li>
Employees&rsquo; Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount</li></ul>
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards</div>

Quality Manager

Hitachi Energy

<div>Location:
Ramadan City , El-Sharkia, Egypt
Job ID:
R0088769
Date Posted:
2025-05-15
Company Name:
HITACHI ENERGY TRANSFORMERS S.A.E
Profession (Job Category):
Quality Management
Job Schedule:
Full time
Remote:
No
Job Description:
The opportunity
We are seeking a motivated and enthusiastic Quality Manager to join our team. In this role you will oversee the implementation of quality strategies, standards, and practices within the Factory to ensure compliance with customer and regulatory requirements. Adapt global quality methodologies to local conditions and drive continuous improvement initiatives. Lead quality processes and audits while fostering cross-functional collaboration to enhance product and service quality.
How you&rsquo;ll make an impact
<ul><li>Overseeing adherence to HSE regulations in all quality activities.
</li><li>Executing BU, GPG, Product Line and HUB quality strategies.
</li><li>Defining and implementing the factory Quality Improvement Plan (QIP).
</li><li>Leading and coordinating all Quality Management System, Quality Assurance, and Quality Control and Testing processes and activities in the factory.
</li><li>Ensuring resources and training for quality management system management, quality assurance and control are in place.
</li><li>Capturing and analyzing customer feedback and internal quality issues.
</li><li>Promoting awareness of compliance obligations throughout the factory.
</li><li>Monitoring and analyzing quality management system performance data.
</li><li>Coordinating internal and external quality audits.
</li><li>Leading factory strategic quality improvement initiatives and risk assessments.
</li><li>Initiating and driving corrective actions for quality issues.
</li><li>Identifying and implementing continuous improvement initiatives.
</li><li>Communicating quality performance insights to stakeholders.
</li><li>Collaborating with cross-functional teams on quality improvements and objectives.
</li><li>You will be responsible for ensuring compliance with applicable external and internal regulations, procedures, and guidelines.
</li><li>Living Hitachi Energy&rsquo;s core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business.
</li></ul>Your background
<ul><li>Bachelor&rsquo;s or master&rsquo;s degree in an Engineering.
</li><li>Minimum of 5 years of experience in quality management, with at least 2 years in a leadership role within a
</li><li>manufacturing environment.
</li><li>Strong understanding of quality management systems, regulatory standards, and compliance requirements, with the ability to navigate complex regulatory environments.
</li><li>Proven experience in leading cross-functional teams and driving continuous improvement initiatives using Lean Six Sigma methodologies.
</li><li>Excellent data analysis and problem-solving skills, with the ability to use data-driven insights to inform decision-making and strategic planning.
</li><li>Exceptional communication and interpersonal skills to effectively influence stakeholders at all levels and foster a culture of quality excellence across the organization.
</li><li>Proficiency in both spoken &amp; written English is required.
</li></ul>Accessibility and reasonable accommodation
Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a general inquiry form on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process. 
 
This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response. 
 
Use of Al and automated tools in recruitment
As part of our recruitment process, Hitachi Energy uses digital and automated tools, including Al-supported solutions, to assist with activities such as application screening, job matching, and interview scheduling. These tools are designed to support our recruiters and do not replace human decision-making. Candidate data is processed in accordance with applicable data protection and employment laws as well as Hitachi's Global Data Privacy Notice.
 
 
Background Screening and Security Checks
As part of the hiring process, Hitachi Energy conducts pre-employment background checks that may include verification of employment history, education, criminal records, and other relevant information, in accordance with applicable laws.
For certain roles&mdash;particularly those involving access to sensitive information, financial responsibilities, client data, regulated environments, or security-sensitive functions&mdash;additional or more comprehensive background or security screenings may be required. These may include, but are not limited to, enhanced criminal history checks, credit history reviews (where legally permissible), sanctions screening, or other due diligence measures aligned with the responsibilities of the position.
The scope and depth of any background or security review will be determined based on the nature of the role and business necessity, and will always be conducted in compliance with applicable federal, state, and local laws. Candidates will be notified and, where required, asked to provide consent prior to the initiation of any such checks.</div>

Precoat Metals

<div>Company Description 
 Since 1961, Precoat Metals (www.precoat.com) has been setting the standards in the coil coatings industry worldwide. We are committed to this level of quality in both our product line and customer service, and focus our resources on investigating and implementing new coil coating technologies, developing unique coatings, ink and film systems, and designing multifaceted prints while reducing the cycle time to market. We are able to achieve this &quot;culture of excellence&quot; thru the hard work and talent of the people on our team. 
Job Description 
Are you focused on process quality, continuous improvement, claims management, and training to ensure operations meet or exceed external and internal quality requirements? If you answered yes, then our Regional Quality Manager is the career opportunity for you. Together with the Regional General Manager, Vice President &ndash; Manufacturing and Vice President &ndash; Quality &amp; Technical Service you'll develop and execute actionable plan and priorities.
As the selected RQM, you will ensure that the region is:<ul><li>
Adhering to quality control plan, with specific parameters developed pursuant to customer demands</li><li>
Driving compliance with process quality assurance protocols</li><li>
Evaluating &amp; implementing corrective actions</li><li>
Ensuring new technology is successfully implemented &amp; embraced</li><li>
Identifying opportunities to assist customers &amp; provide value-added services</li><li>
Partnering with corporate resource to ensure ISO procedures are being implemented &amp; followed</li></ul>
Additionally, you will be<ul><li>
Actively participating in trials for region; ensuring &quot;critical-to-quality&quot; factors are addressed prior to run</li><li>
Ensuring corrective action effectiveness &amp; assisting plants with identifying quality improvement initiatives</li><li>
Developing &amp; training plant quality team &amp; technical service staff; ensuring standard work is in place for each position; identifying competency gaps &amp; providing training or resources to correct</li><li>
Directing technical service reps - ensuring claims are handled in timely manner, appropriate corrective actions are implemented, and reps are partnering with plants to resolve problems</li><li>
Evaluating &amp; implementing best practices across region</li><li>
Identifying opportunities for kaizen events and leading and/or overseeing effective implementation</li><li>
Identifying systemic problems in region, specifying projects related to those areas and following up to measure progress</li><li>
Reviewing claims set to be denied to ensure research is completed accurately</li></ul> 

Qualifications 
What education, skills &amp; experience will you need to take the regions quality to the next level? 
 
Bachelor&rsquo;s Degree in Metallurgy and/or Material Sciences. 
Master&rsquo;s in Metallurgy and/or Material Sciences Degree preferred. 
7-10 years progressive quality management experience in a coil coating setting and/or an equivalent combination of education and experience. 
Blackbelt strongly preferred &ndash; will be required within 24 months of assuming the position. 
Professional demeanor. 
Communicates well with all levels of management. 
Ability to quickly learn new tasks. 
Must be flexible and able to balance priorities. 
Strong oral and written communication skills, strong interpersonal/negotiation skills. 
Good organizational skills. 
Must be willing to work in a plant environment, 
Must be able to travel up to 50% with limited notice. 
Apply Today 
Additional Information 
We are an Equal Opportunity Employer.
Precoat Metals is a Drug Free Workplace<div></div>
We are an Equal Opportunity Employer.
Precoat Metals is a Drug Free Workplace</div>

Regional Quality Manager

Parsons

<div>In a world of possibilities, pursue one with endless opportunities. Imagine Next! 

At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what&rsquo;s possible. 
Job Description:
Parsons is looking for an amazingly talented Project Quality Manager to join our team!
What You'll Be Doing<ul><li>
Lead the development and implementation of the Project Quality Management Plan (PQMP).</li><li>
Establish and manage quality objectives, procedures, processes, and performance indicators across the project lifecycle.</li><li>
Provide direction and support to QA/QC teams, engineers, inspectors, consultants, and contractors to ensure project quality requirements are met.</li><li>
Ensure quality requirements are integrated into design, procurement, construction, testing, commissioning, and handover activities.</li><li>
Review and monitor contractor and consultant Quality Management Plans (QMPs), Inspection and Test Plans (ITPs), and related quality procedures.</li><li>
Conduct quality audits, assessments, and compliance reviews, and follow up on corrective and preventive actions.</li><li>
Oversee construction quality activities for airport terminals, airside infrastructure, roads, utilities, MEP, ICT, and specialist airport systems.</li><li>
Manage Non-Conformance Reports (NCRs), site observations, audit findings, and quality improvement actions, ensuring timely closure.</li><li>
Support design quality reviews, technical assurance, constructability assessments, and compliance with codes, standards, and client requirements.</li><li>
Support testing, commissioning, and operational readiness by reviewing procedures, test results, and completion documentation.</li><li>
Coordinate with client representatives, airport authorities, consultants, contractors, and suppliers on all quality-related matters.</li><li>
Prepare quality dashboards, reports, and performance updates for senior management and recommend improvements.</li></ul>
What Required Skills You'll Bring<ul><li>
Bachelor&rsquo;s degree in engineering, construction management, quality management, or a related discipline.</li><li>
Minimum 15 years of experience in quality management, QA/QC, or construction quality assurance.</li><li>
Proven experience on major airport, aviation, transportation, or large-scale infrastructure projects.</li><li>
Strong experience managing quality systems across complex, multidisciplinary projects, including EPC/PMC/Delivery Partner environments.</li><li>
Solid knowledge of quality management systems and international standards, especially ISO 9001ISO 9001.</li><li>
Experience in inspection processes, ITP development and review, NCR management, root cause analysis, audits, and testing/commissioning.</li><li>
Strong leadership, communication, analytical, and stakeholder management skills.</li></ul>
WHAT DESIRED SKILLS YOU'LL BRING<ul><li>
Certified Quality Manager (CQM), Certified Quality Auditor (CQA), CQI, or equivalent.</li><li>
Professional Engineer (PE), Chartered Engineer (CEng), or equivalent registration.</li><li>
Experience on international airport mega-projects.</li><li>
Knowledge of ICAO, FAA, IATA, and aviation infrastructure quality requirements.</li><li>
Experience with FIDIC or similar international contract frameworks.</li><li>
Experience with Design-Build, EPC, PMC, or Delivery Partner models.</li><li>
Experience implementing digital quality management systems and managing quality across multiple contractors and packages.</li></ul>
Parsons equally employs representation at all job levels no matter the race, color, religion, sex (including pregnancy), national origin, age, disability or genetic information.
We truly invest and care about our employee&rsquo;s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest&mdash;APPLY TODAY!<div>
Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/.</div></div>
 <div><div><div>COMPETITIVE BENEFIT OFFERINGS</div></div><div><div><div> 
Financial Wellness</div><div> 
We care about your financial wellbeing. Parsons offers competitive pay and retirement plans to help you build wealth for the future while giving you the flexibility to diversify your investments.</div></div><div><div>
Work Life Harmony</div><div> 
Balance in life is important and time away from the office is imperative to allow you to refresh and focus your attention on the things that matter to you. Parsons supports your time away by providing paid time off and paid flexible holidays.</div></div><div><div>
Career Development</div><div> 
We are committed to fostering the personal and professional growth of our employees. Develop and advance yourself though our comprehensive training, educational and mentorship programs.</div></div><div><div> 
Veteran Support</div><div> 
We provide Industry leading benefits to support veterans and active-duty members to provide security for you and your family by offering robust leave and benefits; including paid active-duty military leave and paid time off when transitioning back to civilian life.</div></div><div><div>
Mind &amp; Body</div><div> 
At Parsons we inspire healthier habits, heathier minds, and a healthier you through our wellness program. Participate in our weekly Meditation Mondays and Wellness Wednesdays. Wellness, at Parsons, is more than just your annual checkup.</div></div><div><div>
Health</div><div> 
Health is not a one size fits all. At Parsons, we offer a robust Employee Assistance Program as well as comprehensive medical, dental and vision plans through large, national carriers with the choice of regional PPO, HDHP, or HMO networks.</div></div></div></div>

Project Quality Manager

Delta International PK

Project Quality Manager.Who is motivated to work at Reko Diq project site.Bachelor Degree from Civil EngineeringMore than 15 years of experience required.Completed 2 projects as QC managerAdvance EnglishOverseas project experience.Salary will be discussed with candidate.Work Location: In person

Sarah Cannon Research Institute

<div>It&rsquo;s More Than a Career, It&rsquo;s a Mission. 
 
Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
Our Mission 
 
People who live with cancer &ndash; those who work to prevent it, fight it, and survive it &ndash; are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.
<div><div>Job Description
</div></div><div><div><div><div><div><div><div><div><div>Our Research Quality Manager is responsible for implementing the quality assurance program, managing and performing consult/support visits at investigative sites, assisting with onsite external audits and inspections, and providing routine quality support for assigned investigative sites.
This is a fully remote position in the US; relocation assistance and visa sponsorship are not available.
Duties include but are not limited to:
<ul><li>Develops and maintains effective relationships with investigative sites and other SCRI departments and colleagues
</li><li>Monitors and modifies policies and procedures
</li><li>Utilizes quality tools that assess the quality indicators of study operations
</li><li>Monitors quality indicators for all sites using Risk-Based approach and within framework of QBD &ndash; Quality by Design - and prioritizes quality indicators depending on severity/urgency
</li><li>Identifies areas of deficiency in quality and reports those deficiencies to SC Directors and other appropriate colleagues
</li><li>Assists the business in development and modification of process documents
</li><li>Assists with preparation and hosting of external audits
</li><li>Assists research staff in maintaining regulatory compliance
</li><li>Performs process / focused audits (as needed) of research sites utilizing research audit tools to ensure quality and reports audit findings to the appropriate leadership.
</li><li>Ensures timely and appropriate follow-up in areas of deficiency.
</li><li>Communicates observations and deficiencies to the Site Director / Manager and study PI, as appropriate.
</li><li>Assists sites with Root Cause analysis and responses to external audits and CAPAs.
</li><li>Maintains records of audits and reports.
</li><li>Communicates with monitors and auditors of clinical trials, as needed.
</li><li>Educates staff in quality improvement methods and industry trends
</li><li>Other duties as assigned
</li></ul>Qualifications needed
<ul><li>Bachelor&rsquo;s Degree required, Master&rsquo;s Degree preferred
</li><li>Minimum 3 years&rsquo; work experience in Quality Assurance, Quality Management, or Quality Auditing preferably in a clinical research, healthcare or life sciences field
</li><li>Expertise in GCP, FDA and other applicable regulations in a risk-based environment
</li></ul></div></div></div></div></div></div></div></div></div>About Sarah Cannon Research Institute 
 
Sarah Cannon Research Institute (SCRI) is one of the world&rsquo;s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI&rsquo;s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.
 
 
We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That&rsquo;s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves.
 
 
As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.
McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson&rsquo;s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
 
 
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application. 
 
McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.
McKesson job postings are posted on our career site: careers.mckesson.com .
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</div>

Research Clinical Quality Manager - Remote US

looking for motivated QC Manager to work at Reko Diq project site.Bachelor Degree from Civil EngineeringMore than 15 years of experience required.Completed 2 projects as QC managerAdvance EnglishOverseas project experience.Core Responsibilities&middot; Quality Planning: Develop, implement, and maintain project-specific Quality Assurance and Quality Control (QA/QC) plans.&middot; Inspections and Testing: Execute the three-phase inspection process (preparatory, initial, and follow-up) for materials, soil compaction, concrete testing, and structural integrity.&middot; Compliance Management: Ensure all workmanship meets international engineering standards and contractual obligations.&middot; Documentation and Reporting: Track submittals, write technical reports, and maintain verified documentation for all quality records, test reports, and corrective actions.&middot; Stakeholder Coordination: Liaise with clients, architects, and external third-party testing agencies. Oversee subcontractor compliance and address non-conformances.&middot; Site Audits: Conduct regular site safety and quality visits, enforcing the continual improvement of quality systems.Key Qualifications&middot; Education: B.Sc. or B.E. in Civil Engineering (or a related construction/engineering degree).&middot; Experience: 7+ years of dedicated site-based QA/QC experience, with a proven track record in management or supervisory roles.&middot; Certifications: Certifications in Quality Control or Quality Management Systems (e.g., ISO 9001 compliance) are highly preferred.&middot; Technical Knowledge: Strong command of industry regulations and international codes (ASTM, ACI, BS, etc.).&middot; Soft Skills: Exceptional leadership, clear documentation skills, and conflict resolution capabilities.Work Location: In person

Project Quality Manager - QC

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Research Clinical Quality Manager - Remote US

Project Quality Manager - QC