quality associate

Hyde Park Developments

<div>The Quality Associate Manager at Hyde Park Developments will be responsible for ensuring that all construction projects meet the company's quality standards and comply with regulatory requirements. This role requires a focus on maintaining high-quality standards throughout all phases of construction, from initial planning through project completion.
Key Responsibilities:<ul>
<li><ul>
<li>Distribute relevant QA/QC documentation to site Contractors.</li>
<li>Assesses the implementation of the Quality Plan and Quality Control Plans on site.</li>
<li>Supervises the Quality Control functions/ packages activities of the project construction
</li><li>Managing the collection and organizing Quality Records.</li>
<li>Supports and participate to all the internal/external audits.</li>
<li>Coordinate and support the preparation of the Final Handover documentation activities to ensure smooth handover</li>
</ul></li><li><ul><li>Ensure all quality control documentations are compiled and competed for as-built hand over through the Contractor&rsquo;s QC turnover engineer.</li>
<li>Control all nonconformance reports and undertake remedial action.</li>
<li>Coordinate and chair a QA/QC site weekly meeting with the project&rsquo;s Contractors QC personnel.</li>
</ul></li>
</ul>Requirements<ul>
<li>
Bachelor&rsquo;s degree in Civil Engineering, Construction Management, or a related field.</li>
<li>7 - 10 years of experience in quality assurance and quality management within the construction or real estate development industry.
</li><li>Strong understanding of quality assurance principles, methodologies, and regulatory requirements.</li>
<li>Excellent analytical skills and attention to detail.</li>
<li>Demonstrated ability to manage multiple projects while maintaining quality standards.</li>
<li>Strong communication and interpersonal skills to effectively collaborate with various stakeholders.</li>
<li>Familiarity with quality management software and tools is a plus.</li></ul></div>

Quality Associate Managers

Snoonu

<div>
 
 🚀 Welcome to Your Next Adventure!
 
 
 
 We are looking for a
 
 Content Quality Associate
 
 who will enhance the quality of our selection content. This role is critical in ensuring that our offerings are well-structured, relevant and optimized in Arabic &amp; English, to meet customer needs and drive engagement.
 
 
 
 🛠 What You&rsquo;ll Get Your Hands On
 
 
 
 <ul>
 <li>
 Browse our app and website for content opportunities and improvements
 </li>
 <li>
 Work on content quality initiatives and tasks for existing and new selection.
 </li>
 <li>
 Identify systematic and operational problems then contribute to their resolution.
 </li>
 <li>
 Check the quality of selection received internally and externally through different moderation and quality tools.
 </li>
 <li>
 Collaborate with cross-functional teams to implement catalogue-related improvements efficiently.
 </li>
 <li>
 Provide regular feedback and actionable insights to improve catalogue quality.
 
 
 </li>
 </ul>
 
 🧙&zwj;&male;️ The Magic You Bring
 
 
 
 <ul>
 <li>
 Native Arabic language required.
 </li>
 <li>
 Bachelor&rsquo;s degree in Translation, Linguistics, Marketing or equivalent experience.
 </li>
 <li>
 2-5 years of experience in content moderation, translation, or e-commerce.
 </li>
 <li>
 Demonstrated experience in using analytics tools and content management platforms.
 </li>
 <li>
 Familiarity with marketplace dynamics and product discovery flows.
 </li>
 <li>
 Ability to work on a custom schedule with flexible weekend days off.
 </li>
 <li>
 Excellent written and verbal communication skills.
 </li>
 <li>
 effectively in a fast-paced, dynamic environment.
 </li>
 <li>
 Proactive problem-solving skills with a focus on process improvements.
 </li>
 <li>
 Deep understanding of product categorization and customer behavior.
 </li>
 <li>
 Attention to detail and ability to think strategically.
 
 
 </li>
 </ul>
 
 ✨ Bonus Points If You Have
 
 
 
 <ul>
 <li>
 Fluency in local dialect is a plus.
 
 
 </li>
 </ul>
 
 Inside Snoonu&rsquo;s Universe
 
 
 
 Snoonu is Qatar&rsquo;s homegrown Super App, reinventing daily life with blazing-fast delivery, ride-hailing, and shopping - all in one place. Powered by tech, driven by a global team, and obsessed with making life easier.
 
 
 
 The Dream We&rsquo;re Chasing
 
 
 
 To be the first Qatari Super App that propels the region and its community through innovation and technology. We envision a global expansion where what we do surpasses norms and limitations every time.
 
 
 
 The Quest We&rsquo;re On
 
 
 
 To radically transform how people live by leveraging technology to connect them with endless possibilities.
 
 
 
 Our Everyday Superpowers
 
 
 
 
 👥 Be Customer Obsessed:
 
 &ldquo;Focus on the customer and all else will follow.&rdquo;
 
 
 
 💪 Act with Integrity:
 
 &ldquo;We are honest, ethical, and trustworthy in everything we do.&rdquo;
 
 
 
 🧪 Be Curious and Creative:
 
 &ldquo;We constantly innovate and create solutions to bring a lasting positive impact.&rdquo;
 
 
 🏅
 
 Lead by Example and Take Ownership:
 
 &ldquo;Be the change you want to see and take ownership.&rdquo;
 
 
 
 🚀 Work Smart and Deliver Results:
 
 &ldquo;You can do more by doing less, better, and faster.&rdquo;
 
 
 
 👨&zwj;💼 It's All About People:
 
 &ldquo;Be a team player; together we are stronger.&rdquo;
 
 
 
 Perks &amp; Worklife Magic At Snoonu
 
 
 
 
 🌐 Remote &amp; Global Vibes &ndash;
 
 Collaborate with a worldwide crew.
 
 
 
 🧠 Brain Boosters &ndash;
 
 Learning budgets, access to courses, and tools for your growth.
 
 
 
 🚒 Builder&rsquo;s Playground &ndash;
 
 Own your tasks, own your path! We&rsquo;re big on autonomy.
 
 
 
 📦 Shared Success &ndash;
 
 We offer equity because we build this together.
 
 
 
 🌺 Flexible Time Off &ndash;
 
 We take recharging seriously. Generous leave and wellness policies.
 
 
 
 🛠️ Agile Everything &ndash;
 
 Scrum isn&rsquo;t a buzzword here. It&rsquo;s how we roll, from product to ops.
 
 
 
 Beyond the Code: Giving Back Matters
 
 
 
 We don&rsquo;t just build an app. We&rsquo;re committed to doing business sustainably and giving back to the community that fuels us. From eco-conscious practices to CSR projects, we&rsquo;re always finding ways to do better&mdash;and we invite you to be a part of that mission.
 
 
 
 Diversity Isn&rsquo;t Just a Buzzword
 
 
 
 At Snoonu, fairness and inclusion are the foundation of everything we do. We&rsquo;re proud to be an equal opportunity workplace that welcomes people from every walk of life. Be bold. Be you. Thrive here.
 
 
 
 Let&rsquo;s Build the Future Together
 
 
 
 Apply now to join a tech team where your code sparks change, your voice is heard, and your growth is guaranteed. Let&rsquo;s make some tech magic together.
 
 
 Stay in the loop&mdash;connect with us on LinkedIn!
</div>

Content Quality Associate

Eli Lilly

<div>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
Job Description<ul><li>
Ensure that all deviation occurred are properly reported, investigated, and closed in accordance with standard procedure. Must ensure that the corresponding plan of corrective and preventive actions, involving relevant areas, is established and completed on time.</li><li>
Inspect and release batches of finished products for sale.</li><li>
Manage product complaints as a Responsible Complaint Person.</li><li>
Support Monitoring tests of cold chain passive containers which are used for the shipment of Refrigerated products.</li><li>
Report immediately suspected theft, tampering or other situations that could jeopardize the product quality.</li><li>
Ensure that local customization is performed following the guidelines established by the quality area and according to global policies and standard operating procedures that apply locally.</li><li>
Monitor compliance with the external party.</li><li>
Ensure that the process of Change Control follows as indicated in the standard procedure for local operation and any proposed change (internal or external) that could potentially affect product quality.</li><li>
Prepare all quality documentation relating to GMP/GDP operations.</li><li>
Assist on training programs to external customers.</li></ul>
Qualifications/Requirements<ul><li>
A bachelor's degree in Faculty of Pharmacy from T&uuml;rkiye</li><li>
Minimum 2 years of experience in the area of quality assurance applied to the pharmaceutical industry</li><li>
Fluent in English (conversational, writing and reading)</li><li>
Knowledge and mastery of basic computing tools (Microsoft office).</li><li>
Good interpersonal relations</li><li>
Ability to train working groups</li><li>
Good analytical skills and attention to details</li></ul>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLilly</div>

Product Quality Associate

Minerva Research Solutions

<div>
 
 JOB DESCRIPTION:
 
 
 
 Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
 
 
 Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.
 
 
 We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.
 
 
 Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.
 
 
 
 Responsibilities:
 
 
 
 <ul>
 <li>
 Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness
 </li>
 <li>
 Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations
 </li>
 <li>
 Perform quality control checks; identify and track source documentation errors and non-conformances with requirements
 </li>
 <li>
 Provide ongoing compliance support including but not limited to:
 </li>
 <li>
 Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans
 </li>
 <li>
 Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs)
 </li>
 <li>
 Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities
 </li>
 <li>
 Assist in preparing for all Sponsor and FDA audits
 </li>
 <li>
 Assist in conducting internal audits to review key processes
 </li>
 <li>
 Provide appropriate support to assigned cross-functional workgroups
 </li>
 <li>
 Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement
 </li>
 <li>
 Query resolution and data entry and questionnaire preparation regarding the respective studies
 </li>
 <li>
 Other related Quality Assurance projects as assigned
 </li>
 <li>
 The QA Associate will report to the Quality Assurance Lead
 
 
 </li>
 </ul>
 
 Knowledge, Education, and Experience:
 
 
 
 <ul>
 <li>
 Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc) with a keen interest in Clinical Research are strongly encouraged to apply
 </li>
 <li>
 In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials
 </li>
 <li>
 Knowledge of IRB requirements
 </li>
 <li>
 1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred.
 </li>
 <li>
 Experience including external clinical/regulatory and document auditing will be a plus
 
 
 </li>
 </ul>
 
 Skills and Abilities:
 
 
 
 <ul>
 <li>
 Good communication skills (interpersonal, written, verbal)
 </li>
 <li>
 Strong attention to detail and good time management skills
 </li>
 <li>
 Flexible attitude concerning work assignments
 </li>
 <li>
 Ability to manage multiple and varied tasks in a fast-moving environment
 </li>
 <li>
 Ability to interact professionally at all levels within the organization
 </li>
 <li>
 Knowledge of the HIPAA Privacy Act and its application to clinical research
 
 
 </li>
 </ul>
 
 Benefits:
 
 
 
 <ul>
 <li>
 Competitive salary and performance-based bonuses
 </li>
 <li>
 Medical health insurance coverage
 </li>
 <li>
 Employees Old-age benefits coverage
 </li>
 <li>
 Flexible work hours and remote work options
 </li>
 <li>
 Professional learning and development support
 </li>
 <li>
 Generous vacation and paid time off
 </li>
 <li>
 Employee assistance programs for mental health
 </li>
 <li>
 Company-sponsored events and team-building activities
 </li>
 <li>
 Diverse, professional, and inclusive work environment
 </li>
 <li>
 Opportunities for career growth
 </li>
 <li>
 Cutting-edge technology and tools
 </li>
 <li>
 Family-friendly policies, including parental leave
 </li>
 <li>
 Commuter benefits or transportation assistance
 </li>
 <li>
 Social responsibility and community involvement programs
 
 
 </li>
 </ul>
 
 Openings:
 
 
 
 04 positions
 
 
 Full-time
 
 
 On-site job
 
 
 
 Work Schedule Timings:
 
 
 
 Monday to Friday
 
 
 Evening Shift (07 PM to 03 AM)
 
 
 (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
 
 
 Powered by JazzHR
 
 
 RlJhA3EJD3
</div>

Clinical Trials Quality Assurance Associate (Night)

<div>JOB DESCRIPTION: 
 
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements. 
 
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. 
 
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.
Responsibilities:<ul><li>
Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness.</li><li>
Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations.</li><li>
Perform quality control checks; identify and track source documentation errors and non-conformances with requirements.</li><li>
Provide ongoing compliance support including but not limited to:</li><li>
Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans.</li><li>
Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs).</li><li>
Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities.</li><li>
Assist in preparing for all Sponsor and FDA audits.</li><li>
Assist in conducting internal audits to review key processes.</li><li>
Provide appropriate support to assigned cross-functional workgroups.</li><li>
Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement.</li><li>
Query resolution and data entry and questionnaire preparation regarding the respective studies.</li><li>
Other related Quality Assurance projects as assigned.</li><li>
The QA Associate will report to the Quality Assurance Lead</li></ul>
Knowledge, Education, and Experience:<ul><li>
Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc) with a keen interest in Clinical Research are strongly encouraged to apply.</li><li>
In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials.</li><li>
Knowledge of IRB requirements.</li><li>
1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred..</li><li>
Experience including external clinical/regulatory and document auditing will be a plus</li></ul>
Skills and Abilities:<ul><li>
Good communication skills (interpersonal, written, verbal)</li><li>
Strong attention to detail and good time management skills</li><li>
Flexible attitude concerning work assignments</li><li>
Ability to manage multiple and varied tasks in a fast-moving environment</li><li>
Ability to interact professionally at all levels within the organization.</li><li>
Knowledge of the HIPAA Privacy Act and its application to clinical research.</li></ul>
Benefits:<ul><li>
Competitive salary and performance-based bonuses.</li><li>
Medical health insurance coverage.</li><li>
Employees Old-age benefits coverage.</li><li>
Flexible work hours and remote work options.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional, and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul>
Openings:
04 positions 
Full-time 
On-site job 
 
Work Schedule Timings: 
Monday to Friday 
Evening Shift (07 PM to 03 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
RlJhA3EJD3</div>

Fortrea

<div>The Vendor Manager Associate plays a key role in our Vendor Quality and Qualification team in supporting the qualification of third-party clinical vendors. This position will be responsible for supporting the process in the qualification and requalification of third-party vendors, who provide services/ products that directly support clinical trials. 
 
Responsibilities:<ul><li>
Supports the vendor qualification process for Fortrea clinical vendors, including the assessment of capabilities under the direction of the Manager-level or higher in Vendor Quality and Qualification</li><li>
Coordinates the qualification process with SMEs for QA, Clinical Sourcing, functional area SMEs, etc, maintaining effective tracking of the process and completion in a timely manner</li><li>
Includes issuance, collection and review of vendor qualification documents i.e. CDA, DDF and RFI and ensuring proper follow up on vendor qualification requests</li><li>
Partner with QA department in vendor qualification audits</li><li>
Creation/ maintenance of Qualified Supplier List (QSL). Ensures the QSL is maintained and provides clear information on the available approved vendors</li><li>
Ensure the maintenance of accurate and complete vendor files, ensuring documentation is available for QA, Clinical Sourcing, compliance and clinical audits</li><li>
CAPA/ audit support</li><li>
Participates in and supports other CVS initiatives as required</li></ul> 
Requirements:<ul><li>
Bachelor&rsquo;s degree in Life Sciences</li><li>
3+ years of experience in the life sciences industry e.g. CRO, pharma, biotech and experience in the job discipline (vendor qualification/ vendor management/ QA) is preferred</li><li>
Experience in clinical research, understanding of clinical research, and comprehensive knowledge of clinical trial services and vendors</li><li>
Experience working independently with minimal supervision and in a team environment under time and resource pressures</li><li>
Excellent interpersonal, oral and written communication skills when dealing with both external and internal customers with an ability to prioritize and meet deadlines</li><li>
Good presentation skills</li><li>
Proficient with MS Office programs</li><li>
Proactive self-starter</li><li>
Multi-tasker</li><li>
Creative problem solver (to improve processes, create new approaches)</li><li>
Excellent Project Management skills to ensure proper proactive planning and follow up</li><li>
Well Organized</li><li>
Team player</li><li>
Enthusiastic agent of change</li></ul>
Learn more about our EEO &amp; Accommodations request here.</div>

Vendor Manager Associate (On contract)

CALO

<div>About Calo
Launched in Bahrain in November of 2019, Calo is on a mission to make healthy easy. We&rsquo;re a team of dedicated people driving this mission by providing better, faster, and cheaper ways to access food through technology. 
Role overview
We are looking for a dedicated Quality Specialist who will support with checking the quality of all incoming and outgoing material and products as well as the production procedures. You will be a firm advocate of quality in our business.
The ideal candidate possesses a trained eye for detail and is reliable and committed. General knowledge and comprehension of quality standards are essential to ensure that our products are made of flawless materials. That way, our customers will enjoy high-quality services so that we can achieve long-term success. 
Main Responsibilities<ul><li>
Maintain records of quality reports, statistical reviews and relevant documentation</li><li>
Formulate procedures to inspect and report quality issues</li><li>
Monitor all operations that affect quality</li><li>
Implementing preventative measures to prevent health hazards</li><li>
Ensuring checklists are met on a regular basis</li><li>
Conduct multiple audits on floor and for suppliers</li><li>
Collaborate with other departments to deal with quality and safety issues</li><li>
Implement root cause analysis with suppliers</li><li>
Inspect procedures of the entire production cycle to ensure they are efficient and comply with quality standards</li><li>
Implementation of Food Quality strategy, goals, and objectives</li><li>
Implement, and maintain food safety goals, objectives, policies, and procedures such as HACCP, sanitation, temperature logs, cleaning list, etc</li><li>
Assure the reliability and consistency of production by checking processes and final output</li><li>
Ensure all legal standards are met</li><li>
Identifies quality defects and food safety issues and other problems, particularly when problems recur in multiple products; recommends solutions to these issues</li><li>
Train the team on food safety and implement policies and procedures that will improve day-to-day operations</li><li>
Ensure work environments are adequate and safe</li><li>
Project a positive image of the organization to employees, customers, industry, and community</li><li>
Ensuring products are designed with adherence to legal and safety standards</li></ul> 
Ideal Candidate
Qualifications<ul><li>
A fresh graduate with a Bachelor's degree in Biotechnology/Pharmacology/Biological Sciences or any other relevant degree.</li><li>
General knowledge of methodologies of quality standard</li><li>
Must be based in Saudi Arabia</li></ul>
Knowledge and competency<ul><li>
Excellent written &amp; communications skills in English</li><li>
Great attention to detail with a results-driven approach</li><li>
Fast learner, reliable and Trustworthy</li><li>
Able to promote a food safety culture</li><li>
Excellent analytical, decision-making, and problem-solving skills</li><li>
Pleasant personality and able to lead with empathy and patience</li></ul>
El1ik0GIr2</div>

Quality Specialist

Search 10000+ Quality associate jobs near you this January. New roles added regularly across leading industries. Apply today.

10000 quality associate jobs NEAR_ME

Quality Associate Managers

Content Quality Associate

Product Quality Associate

Clinical Trials Quality Assurance Associate (Night)

Clinical Trials Quality Assurance Associate (Night)

Vendor Manager Associate (On contract)

Quality Specialist