quality assurance 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)
TuBXaWOaue</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)
 
 
 Powered by JazzHR
 
 
 TuBXaWOaue
</div>

PwC Middle East

<div>
 
 Line of Service
 
 
 
 Internal Firm Services
 
 
 
 Industry/Sector
 
 
 
 Technology
 
 
 
 Specialism
 
 
 
 IFS - Internal Firm Services - Other
 
 
 
 Management Level
 
 
 
 Senior Associate
 
 
 
 Job Description &amp; Summary
 
 
 
 At PwC, our people in data management focus on organising and maintaining data to enable accuracy and accessibility for effective decision-making. These individuals handle data governance, quality control, and data integration to support business operations.
 
 
 In data quality assurance at PwC, you will be responsible for the accuracy and reliability of data through testing and validation processes. You will play a crucial role in maintaining data integrity and identifying areas for improvement in data management systems.
 
 
 Focused on relationships, you are building meaningful client connections, and learning how to manage and inspire others. Navigating increasingly complex situations, you are growing your personal brand, deepening technical expertise and awareness of your strengths. You are expected to anticipate the needs of your teams and clients, and to deliver quality. Embracing increased ambiguity, you are comfortable when the path forward isn&rsquo;t clear, you ask questions, and you use these moments as opportunities to grow.
 
 
 
 Skills
 
 
 
 Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to:
 
 
 <ul>
 <li>
 Respond effectively to the diverse perspectives, needs, and feelings of others.
 </li>
 <li>
 Use a broad range of tools, methodologies and techniques to generate new ideas and solve problems.
 </li>
 <li>
 Use critical thinking to break down complex concepts.
 </li>
 <li>
 Understand the broader objectives of your project or role and how your work fits into the overall strategy.
 </li>
 <li>
 Develop a deeper understanding of the business context and how it is changing.
 </li>
 <li>
 Use reflection to develop self awareness, enhance strengths and address development areas.
 </li>
 <li>
 Interpret data to inform insights and recommendations.
 </li>
 <li>
 Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements.
 
 
 </li>
 </ul>
 
 Minimum Years Experience Required
 
 
 
 <ul>
 <li>
 Add here AND change text color to black or remove bullet and section title if not applicable
 
 
 </li>
 </ul>
 
 Additional Application Instructions
 
 
 
 <ul>
 <li>
 Add here AND change text color to black or remove bullet and section title if not applicable
 
 
 </li>
 </ul>
 
 Education
 
 
 (if blank, degree and/or field of study not specified)
 
 
 
 Degrees/Field of Study required:Degrees/Field of Study preferred:
 
 
 
 Certifications
 
 
 (if blank, certifications not specified)
 
 
 
 
 Required Skills
 
 
 
 
 Optional Skills
 
 
 
 Accepting Feedback, Accepting Feedback, Active Listening, Analytical Thinking, Communication, Creativity, Database Administration, Database Management System (DBMS), Database Performance Management, Database Quality Assurance, Database Troubleshooting, Data Error Checking, Data Integrity, Data Management, Data Management Plan (DMP), Data Management Platform (DMP), Data Profiling, Data Quality, Data Quality Assessment, Data Quality Assurance Testing, Data Quality Automation, Data Quality Improvement Plans (DQIP), Data Science Troubleshooting, Data Warehousing Quality Assurance, Embracing Change {+ 15 more}
 
 
 
 Desired Languages
 
 
 (If blank, desired languages not specified)
 
 
 
 
 Travel Requirements
 
 
 
 Not Specified
 
 
 
 Available for Work Visa Sponsorship?
 
 
 
 No
 
 
 
 Government Clearance Required?
 
 
 
 Yes
 
 
 
 Job Posting End Date
 
</div>

ETIC, Quality Assurance - Senior Associate

KSHM

Job Title: Operations Associate &ndash; Quality &amp; Inventory Location: Gurugram, Sec 56 Mode: Onsite, Full-Time Experience: 1&ndash;3 Years (or as per requirement)About the Brand: Kshm is committed to delivering high-quality products while ensuring operational excellence. We focus on precision, efficiency, and reliability across all stages of production and distribution.Role Overview: We are looking for a responsible and proactive Operations Associate to manage quality assurance of materials and optimize inventory. The ideal candidate will ensure materials meet quality standards, maintain accurate inventory records, and support smooth operational workflows. A personal vehicle is required for transporting materials and site visits.Key Responsibilities:<ul><li>Conduct quality checks of incoming materials and ensure compliance with company standards.</li><li>Identify defects, inconsistencies, or deviations and report them promptly.</li><li>Maintain accurate inventory records and optimize stock levels to minimize wastage and overstocking.</li><li>Coordinate with suppliers, production teams, and logistics to ensure timely material availability.</li><li>Support operational workflows by transporting materials as needed using personal vehicle.</li><li>Ensure safe handling, storage, and documentation of all materials.</li><li>Report issues or process gaps to management and suggest improvements.</li></ul>Requirements:<ul><li>1&ndash;3 years of experience in operations, inventory management, or quality assurance.</li><li>Strong attention to detail and analytical skills.</li><li>Responsible, proactive, and able to work independently.</li><li>Must have a personal vehicle for material transportation.</li><li>Good organizational and communication skills.</li><li>Knowledge of inventory management tools/software is a plus.</li></ul>Why Join Us:<ul><li>Work in a structured environment focused on operational excellence.</li><li>Opportunity to take ownership and contribute directly to quality and efficiency.</li><li>Exposure to supply chain, inventory optimization, and quality assurance processes.</li></ul>Job Type: Full-timePay: &#8377;20,000.00 - &#8377;30,000.00 per monthWork Location: In person

Operation Associate

VIrtesys LLP

We are a US-based facility services company seeking a Quality Assurance Associate to review photos and documentation from sign maintenance projects. This is a night shift, on-site role in Karachi.This is an On-site job. Office timing Monday to Friday 06:00 pm to 03:00 am (an hour ahead during daylight saving October to March).Responsibilities:<ul><li>Review and verify job photos for quality and compliance</li><li>Check paperwork accuracy for sign maintenance and service orders</li><li>Communicate with internal teams to ensure documentation standards are met</li></ul>Requirements:<ul><li>Experience working with an international company is a must</li><li>Strong attention to detail and communication skills</li><li>Familiarity with QA processes and digital photo/file handling</li><li>Must be fluent in English</li></ul>Immediate availability preferred!Night Shift: 6pm to 3amLocation: PECHSHow to Apply:WhatsApp: 0301-3528439Email: hiring@virtesys.pkApply now if you're detail-oriented and have prior international work experience.Job Type: Full-timeApplication Question(s):<ul><li>Are you willing to work in night shift (6pm to 3am) ?</li><li>Have you worked for an international client? For how long?</li><li>Do you have experience as project coordinator </li></ul>Experience:<ul><li>project coordinator: 1 year (Preferred)</li></ul>Language:<ul><li>English (Preferred)</li></ul>Work Location: In person

Project Coordinator (Sign maintenance/Documentation Review and Photo QA)

United Biosource Corporation

<div>As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation.
Embark on a rewarding career journey with UBC! Grow your career while making a meaningful impact on the world around you. UBC fosters a culture built on our Core Values being: Collaborative, Conscientious, Curious, Consultative, and Compassionate. We believe in an inclusive workplace that fosters creativity.
If you are seeking a career that will challenge, inspire, and reward you, join us at UBC! 
Job Posting Title: Quality Compliance Associate 
Brief Description:
The Quality Compliance Associate provides core compliance functions and project support for the Quality Compliance department including SOP document preparation and updates, training file maintenance, and compliance audits. Audit support includes, but is not limited to, audit scheduling, logistics, and document preparation and support. The Quality Compliance Associate provides additional assistance with special projects including CAPA document management, compliance-related continuous improvement projects and training document creation/updates within the Learning Management System (LMS). This position may also provide administrative support to the Quality Compliance department as appropriate. 
Specific job duties:<ul><li>
Ensure SOPs and corresponding test assessments are created and updated within a timely manner according to internal policies and procedures. Ensure appropriate formatting of SOP documents.</li><li>
Support and management of the Quality Management Systems (QMS) to include:<ul><li>
Problem Notification Forms (PNFs)</li><li>
Corrective/Preventive Actions (CAPAs)</li><li>
Compliance Audits (Client/Vendor/Internal)</li><li>
Document Management (SOPs/PSPs/WIs/Job Aids)</li></ul></li><li>
Support SOP review and approval process as deemed appropriate</li><li>
Provide Regulatory/Client Audit Support<ul><li>
Assist with audit scheduling and audit calendar maintenance</li><li>
Assist with meeting coordination/logistics<ul><li>
CDA Requests</li><li>
Auditor Code of Conduct</li><li>
Setting up internal trackers and portals</li><li>
Setting up and providing secure Box access for auditor(s) when required</li></ul></li><li>
Assist with Quality Compliance documentation review prior to and during audit.</li><li>
Ensure audit reports and responses are stored as per UBC record retention procedures.</li></ul></li><li>
Provide assistance with Problem Notification Form (PNF) and CAPA data entry and administrative review when required.</li><li>
Provide administrative support (i.e., agenda, minutes, metrics) for the Quality Assurance department.</li><li>
Support the maintenance and archival of all QA records.</li><li>
Assist in department-related special projects.</li><li>
Assist with Learning Management System document management where needed.</li><li>
Other duties as assigned.</li></ul> 
Supervisory Responsibility:
N/A
Desired Skills and Qualifications:<ul><li>
Bachelor&rsquo;s degree or equivalent work experience.</li><li>
1 &ndash; 2 years of relevant experience preferably within a regulated pharmaceutical and/or medical device industry.</li><li>
Proficient PC knowledge required including Microsoft Office Suite and Internet, SharePoint.</li><li>
Excellent written and oral communication skills essential for professional phone and email interactions.</li><li>
Good interpersonal skills.</li><li>
Continual attention to detail in composing, typing and proofing materials, establishing priorities and meeting deadlines.</li><li>
Ability to work independently.</li><li>
Strong organizational and time management skills.</li><li>
Ability to interact and work within a team environment.</li><li>
Ability to keep sensitive information confidential.</li><li>
Preferred experience working within the bounds of Standard Operating Procedures/policies.</li><li>
Preferred experience providing project support.</li></ul> 
At UBC, employee growth and well-being are always at the forefront. We offer an extensive range of benefits to ensure that you have everything you need to thrive personally and professionally.
Here are some of the exciting perks UBC offers:<ul><li>
Remote opportunities</li><li>
Competitive salaries</li><li>
Growth opportunities for promotion</li><li>
401K with company match*</li><li>
Tuition reimbursement</li><li>
Flexible work environment</li><li>
Discretionary PTO (Paid Time Off) OR 20 days (about 3 weeks) of PTO</li><li>
Paid Holidays</li><li>
Employee assistance programs</li><li>
Medical, Dental, and vision coverage</li><li>
HSA/FSA</li><li>
Telemedicine (Virtual doctor appointments)</li><li>
Wellness program</li><li>
Adoption assistance</li><li>
Short term disability</li><li>
Long term disability</li><li>
Life insurance</li><li>
Discount programs</li></ul> 
UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state, or local protected class. We are committed to a diverse, equitable and inclusive culture that fosters respect for each other, our clients, and our patients. 
#LI-REMOTE
#LI-HB1</div>

Quality Compliance Associate

BDO in India

<div>
 
 
 About Company:
 
 
 
 
 
 
 BDO India LLP is the India member firm of BDO International. BDO India offers strategic, operational, accounting, tax &amp; regulatory advisory and assistance for both domestic and international organizations across a range of industries. We are led by more than 250 Partners &amp; Directors with a team of over 9000 professionals operating across 12 cities &ndash; Ahmedabad, Bengaluru, Chandigarh, Chennai, Coimbatore, Hyderabad, Goa, Kochi, Kolkata, Mumbai, New Delhi &ndash; Gurugram and Pune. We take pride in our service portfolio on the backing of a rich blend of experience and expertise, bringing to fore a work culture that is both client-centric and knowledge driven. Our focus on delivering exceptional client service is backed by a partner driven approach to offer tailor-made solutions ensuring quality excellence &amp; time efficiencies.
 
 
 
 
 
 
 Responsibilities
 
 
 <ul>
 <li>
 Strong article ship experience of 0 to 1 year in Assurance Services or in a similar environment (Assurance and Accounting firms)
 </li>
 <li>
 Execution of client engagements - Ensuring quality delivery as per client requirements.
 </li>
 <li>
 Understanding business &amp; industry issues / trends.
 </li>
 <li>
 Ensuring timely delivery of working papers as per the defined methodology
 </li>
 <li>
 Ensuring compliance with engagement plans, internal quality &amp; risk management procedures.
 </li>
 <li>
 Be willing to travel within India or abroad
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 
 
 
 <ul>
 <li>
 CA Qualified (May 25)
 </li>
 <li>
 Strong communication and interpersonal skills
 </li>
 </ul>
 
 
</div>

Associate - Bangalore - Assurance

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