quality assurance

HRC Recruitment

<p><b>QA Pharmacist &ndash; Quality Assurance &amp; Medication Safety</b></p><p><b>Job Summary</b></p><p>We are seeking a detail-oriented and clinically driven <b>QA Pharmacist</b> to ensure medication safety, regulatory compliance, and quality assurance across all prescribing and medication-related processes within our organization. This role focuses on chart audits, medication reviews, adherence to clinical guidelines, and continuous quality improvement initiatives to support high-quality, compliant in-home patient care.</p><p>The ideal candidate will have strong clinical judgment, regulatory knowledge, and a passion for improving medication management standards.</p><p><b>Key Responsibilities :</b></p><ul><li>Review and audit medication orders, prescriptions, and treatment plans for accuracy, safety, and clinical appropriateness.</li><li>Identify potential drug interactions, contraindications, therapeutic duplications, and dosing errors.</li><li>Ensure adherence to evidence-based clinical guidelines and best practices in medication management.</li><li>Provide medication-related clinical recommendations and support to healthcare providers as needed.</li><li>Collaborate with interdisciplinary teams to promote safe and effective pharmacotherapy.</li></ul><p><b>Chart Audits &amp; Regulatory Compliance</b></p><ul><li>Conduct regular chart audits focused on medication documentation, prescribing standards, and compliance requirements.</li><li>Ensure compliance with federal and state regulations, including Centers for Medicare &amp; Medicaid Services (CMS), Medicare, Medicaid, and Health Insurance Portability and Accountability Act (HIPAA).</li><li>Monitor adherence to payer policies and quality standards.</li><li>Identify compliance gaps and recommend corrective action plans.</li><li>Support internal and external audit readiness activities.</li></ul><p><b>Quality Improvement &amp; Process Development</b></p><ul><li>Participate in continuous quality improvement initiatives related to medication safety and prescribing practices.</li><li>Develop and implement audit tools, tracking mechanisms, and reporting metrics.</li><li>Assist in creating and updating medication management policies and procedures.</li><li>Provide education and training to staff on medication safety and regulatory standards.</li></ul><p><b>Qualifications</b></p><ul><li>Doctor of Pharmacy (PharmD) required.</li><li>2+ years of clinical, quality assurance, or medication safety experience preferred.</li><li>Strong knowledge of CMS, Medicare, Medicaid, and HIPAA regulations.</li><li>Experience with chart audits and regulatory compliance in home health or value-based care settings preferred.</li><li>Excellent analytical, documentation, and communication skills.</li><li>Ability to work independently and collaboratively in a fast-paced healthcare environment.</li></ul><p>Preferred Skills</p><ul><li>Experience in home health, managed care, or population health.</li><li>Familiarity with electronic health record (EHR) systems.</li><li>Knowledge of quality metrics and performance improvement methodologies.</li></ul><p>Job Type: Full-time</p><p>Pay: Rs50,000.00 - Rs60,000.00 per month</p><p>Work Location: In person</p>

Quality Assurance

Crystal Corporation L.L.C.

<p>We are hiring a <b>Quality Assurance Officer</b> to establish, implement, and maintain a <b>company-wide Quality Management System (QMS)</b> in compliance with <b>ISO 9001 requirements</b>.<br/>This role is responsible for ensuring <b>system-level quality assurance</b> across <b>Production, Warehouse, Logistics, Purchasing, Sales, and Accounts</b>, ensuring all processes comply with documented procedures, ISO standards, and internal controls.</p><p>The focus of this position is <b>process compliance, system discipline, internal audits, and continuous improvement</b>, rather than product inspection alone.</p><p><b>Key Responsibilities</b></p><p><b>Quality Management System (ISO 9001 &ndash; Full System Scope):</b></p><ul><li>Design, implement, and maintain a <b>company-wide QMS</b> aligned with ISO 9001 requirements.</li><li>Ensure all departments (<b>Production, Warehouse, Logistics, Purchasing, Sales, and Accounts</b>) operate according to approved <b>SOPs, ISO clauses, and regulatory requirements</b>.</li><li>Act as the <b>ISO system owner</b>, ensuring compliance, readiness, and continual improvement.</li></ul><p><b>Documentation &amp; Control:</b></p><ul><li>Develop, review, and control <b>SOPs, work instructions, forms, and records</b> for all departments.</li><li>Ensure document control, version management, and record retention as per ISO standards.</li><li>Enforce documentation discipline and traceability across functions.</li></ul><p><b>Internal Audits &amp; Compliance:</b></p><ul><li>Plan and conduct <b>internal audits</b> covering all departments (operational, logistical, commercial, and financial processes).</li><li>Identify <b>non-conformities (NCRs)</b>, issue audit findings, and ensure timely <b>Corrective and Preventive Actions (CAPA)</b>.</li><li>Verify effectiveness of corrective actions and report audit outcomes to management.</li></ul><p><b>Process &amp; Operational Controls:</b></p><ul><li>Establish <b>process controls and compliance checks</b> for:</li><li>Production &amp; in-process quality</li><li>Warehouse operations (incoming inspection, storage, segregation, batch/lot traceability, inventory control)</li><li>Logistics &amp; dispatch processes</li><li>Purchasing &amp; supplier evaluation</li><li>Sales order processing and customer requirements compliance</li><li>Accounts-related process controls (documentation flow, approvals, records accuracy)</li><li>Ensure adherence to defined acceptance/rejection criteria and control points.</li></ul><p><b>Monitoring, Reporting &amp; Improvement:</b></p><ul><li>Track and analyze quality KPIs (process compliance, audit findings, defects, scrap, customer complaints, system gaps).</li><li>Prepare periodic <b>management reports</b> highlighting risks, trends, and improvement opportunities.</li><li>Lead <b>root cause analysis</b> (5 Why, Fishbone, Pareto) and drive cross-functional corrective actions.</li></ul><p><b>Training &amp; Awareness:</b></p><ul><li>Train employees across departments on <b>ISO requirements, SOP compliance, documentation, and quality responsibilities</b>.</li><li>Promote a culture of process discipline, accountability, and continuous improvement.</li></ul><p><b>Requirements:</b></p><ul><li>Hands-on experience in <b>Quality Assurance / Quality Management Systems</b> within a manufacturing or industrial environment.</li><li>Strong practical knowledge of <b>ISO 9001 implementation and internal auditing</b> across multiple departments.</li><li>Experience in <b>system-level QA</b> (not limited to product or inspection-based QC).</li><li>Excellent documentation skills (SOPs, forms, records, audit reports).</li><li>Strong analytical and problem-solving skills.</li><li>Proficient in <b>Excel and reporting tools</b>; ERP experience (e.g., Odoo) is an advantage.</li><li>Organized, firm, and detail-oriented personality with strong follow-up skills.</li><li>Strong communication and coordination ability across departments.</li><li>Fluent in <b>English</b> (written and spoken).</li></ul><p>Job Type: Full-time</p>

Accenture

<div><b>Project Role : </b>Quality Assurance Practitioner<br>
<b>Project Role Description : </b>Provide general support to quality assurance (QA) directors, conduct in-depth quality assurance reviews, assist on recovery teams and with root cause analysis.
<br>
<b>Must have skills : </b>Angular<br>
<b>Good to have skills : </b>NA<br>
Minimum <b>2</b> year(s) of experience is required<br>
<b>Educational Qualification : </b>15 years full time education<br>
<br>
Summary:
<br>
As a Quality Assurance Practitioner, you will provide essential support to quality assurance directors, ensuring that quality standards are met across various projects. Your typical day will involve conducting thorough quality assurance reviews, collaborating with recovery teams, and engaging in root cause analysis to identify areas for improvement. You will play a vital role in maintaining high-quality standards and enhancing overall project performance through your contributions and insights.<br>
<br>
Roles &amp; Responsibilities:
<br>
<ul><li>Expected to perform independently and become an SME.</li><li>Required active participation/contribution in team discussions.</li><li>Contribute in providing solutions to work related problems.</li><li>Assist in developing and implementing quality assurance processes and methodologies.</li><li>Collaborate with cross-functional teams to ensure alignment on quality objectives.</li></ul>
<br>
Professional &amp; Technical Skills:
<br>
<ul><li>Must To Have Skills: Proficiency in Angular.</li><li>Strong understanding of web application development and testing methodologies.</li><li>Experience with automated testing tools and frameworks.</li><li>Familiarity with performance testing and quality metrics.</li><li>Ability to analyze and interpret data to drive quality improvements.</li></ul>
<br>
Additional Information:
<br>
<ul><li>The candidate should have minimum 2 years of experience in Angular.</li><li>This position is based at our Bengaluru office.</li><li>A 15 years full time education is required.</li></ul></div>
<br>
15 years full time education

Quality Assurance Practitioner

Michigan Farm Bureau

<div>OBJECTIVE:
<div><b>
Quality Assurance Analyst Objective</b></div><div>
To be responsible for the quality, technical feasibility, and reliability of software and systems that are utilized by internal and external customers. To provide quality assurance expertise and direction on the functionality and usability of software and systems. To work closely with business analysts, software developers, and customers to understand business requirements. To design, develop, test, execute, and maintain test strategies, plans, and cases. To understand and execute automated testing scripts. To execute defect management, providing feedback, reporting defects, and projecting timelines for completion.</div>
RESPONSIBILITIES:
<div><b>
Quality Assurance Analyst Reponsibilities</b></div><div>
Participate in requirements gathering sessions, providing analysis and direction on testability from an assurance perspective, ensuring feasibility and quality releases. Review and comprehend requirements, specifications, and technical design documents.</div><div></div><div><br>
Provide estimates, prioritize, plan, and coordinate testing activities. Communicate priority, plan, and risks to management, stakeholders, and project team members.</div><div></div><div><br>
Design, create, and execute test strategies, plans, and cases. Analyze software and system components, to identify discrepancies, defects, risks, and improvement areas. Comprehend and execute automated test scripts.</div>
QUALIFICATIONS:
<div><b>
Quality Assurance Analyst Qualifications</b></div><div><b>
Required</b></div><div>
Bachelor's degree in business technology, computer science, software engineering, or business administration required, or equivalent experience may be considered.</div><div></div><div><br>
Strong information technology skills, understanding of software development lifecycle and quality assurance principals required.</div><div></div><div><br>
Ability to develop and execute manual and automated testing strategies, testing plans, and test cases required.</div><div></div><div><br>
Ability to communicate verbally and in written form in a clear and concise manner through various formats required.</div><div></div><div><br>
Willingness to participate in software quality assurance and insurance training classes required.</div><div></div><div><b><br>
Preferred</b></div><div>
Coursework in quality assurance preferred.</div><div></div><div><br>
Proven experience in application/software testing or software development required, two years preferred. Experience in insurance domain preferred.</div><div></div><div><br>
Certification in quality assurance or testing methodologies preferred.</div><div></div><div><b><br>
Note:</b> Farm Bureau offers a full benefit package including medical, dental, vision, and 401K.</div><div></div><div><br>
PM19</div></div>

Quality Assurance Analyst

PharmEng Technology

<div>
 <strong>
  About The Job Quality Assurance Consultant
  <br/>
  <br/>
 </strong>
 <strong>
  Job Summary:
 </strong>
 The Quality Assurance Consultant is responsible for the implementation, maintenance, and oversight of the Quality Management System (QMS) in local affiliates. This role ensures compliance with regulatory requirements, quality standards, and company policies. The Quality Assurance Consultant will manage quality risk, complaints, change controls, deviations, CAPA, authority inspections, self-inspections, GxP surveillance, product quality reviews, training, local product release, and oversight of GDP requirements for local warehousing and distribution.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   QMS implementation, maintenance, and oversight in local affiliates.
  </li>
  <li>
   Maintenance of the local Quality Manual and Site Master File.
  </li>
  <li>
   Quality risk management in local affiliate, including risk identification, analysis, communication, control, and escalation as required.
  </li>
  <li>
   Complaint management, acting as the Local Complaint Coordinator for reporting, local assessment, and local investigation.
  </li>
  <li>
   Change control management, QA assessment, site change control, QA review for change implementation and closure.
  </li>
  <li>
   Deviation management for internal, external, and transport deviations.
  </li>
  <li>
   CAPA management from deviations, internal audits, external audits, and self-inspections.
  </li>
  <li>
   Management of authority inspections and self-inspections.
  </li>
  <li>
   Local GxP surveillance and assessment.
  </li>
  <li>
   Product quality review (PQR).
  </li>
  <li>
   Training management, including maintenance of training matrix, training of local staff, annual GxP refresher training, and handling of training assignments in the LMS.
  </li>
  <li>
   Local product release (local QP), shipment review of transport performance, goods receipt check, and deviation handling.
  </li>
  <li>
   Oversight of GDP requirements for local warehousing and distribution.
  </li>
  <li>
   Shipping lane qualification and local transport performance of secondary distribution.
  </li>
  <li>
   Secondary distribution transport performance review.
  </li>
  <li>
   Return management, including QA evaluation against return criteria and collaboration with distributors.
  </li>
  <li>
   Product recall management, including local recall execution, communication with customers, communication with HA, recall reconciliation, and local product destruction.
  </li>
  <li>
   GxP suppliers management, including supplier identification, qualification, approval, annual compliance status evaluation, quality audit planning, conduct quality audits, and CAPA approval and closure.
  </li>
  <li>
   Local repackaging and relabeling, including change management, protocol, execution, QA review, and release.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in Quality Management, Life Sciences, or a related field.
  </li>
  <li>
   Minimum of 5 years of experience in Quality Assurance within the pharmaceutical or healthcare industry.
  </li>
  <li>
   Strong knowledge of GxP regulations and quality standards.
  </li>
  <li>
   Excellent analytical, problem-solving, and communication skills.
  </li>
  <li>
   Ability to work independently and collaboratively in a team environment.
  </li>
  <li>
   Proficiency in using Quality Management Systems and Learning Management Systems (LMS).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Competencies
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Attention to detail and accuracy.
  </li>
  <li>
   Strong organizational and time management skills.
  </li>
  <li>
   Effective leadership and team management abilities.
  </li>
  <li>
   Proactive and results-oriented mindset.
  </li>
 </ul>
</div>


Quality Assurance Consultant

Alimentiv

<div>
 <p>
  Responsible for providing senior support in planning, organizing and/or evaluating the day-to-day delivery of global quality assurance (QA) services. Responsible for supporting the business in quality assurance, policy planning and development, ongoing quality improvement through clinical audit and liaison with other business units and external partners. Will also provide support, expertise, and industry best practice guidance.
 </p>
 <p>
  <p>
   <br/>
  </p>
  <strong>
   Quality Assurance Implementation
  </strong>
  <ul>
   <li>
    Implement quality assurance plans and processes and identify indicators needed to assess product/service quality levels.
   </li>
   <li>
    Collaborating with management/functional experts or Sponsors to identify requirements of the organization in order to conduct internal audits, site audits, vendor assessments and vendor audits.
   </li>
   <li>
    Oversee the development of Quality System documents including policy, procedure, instruction, guidance and form and template development in collaboration with departments and senior management.
   </li>
   <li>
    Develop QA processes, train and oversee junior QA staff.
   </li>
   <li>
    Liaise with the Human Resources department to ensure that all staff are qualified.
   </li>
   <li>
    Remain current on and ensure internal awareness of regulatory trial conduct standards and requirements.
   </li>
   <li>
    Identify changes to standards and regulations governing Clinical Research and provide recommendations for implementation as required
    <br/>
   </li>
  </ul>
  <p>
   <br/>
  </p>
  <strong>
   Regulatory, Ethical Conduct and Audit Monitoring
  </strong>
  <ul>
   <li>
    Remain current on, interpret and communicate changes to regulatory trial conduct standards and requirements.
   </li>
   <li>
    Identify, implement and/or develop policies, processes, and/or training to meet these standards.
   </li>
   <li>
    Plan/lead/facilitate Sponsor and regulatory inspections and audit activities including preparation of staff, oversight of proceedings and ensure findings addressed are resolved.
   </li>
   <li>
    Perform internal audits and vendor assessments, ensuring that all observations are appropriately addressed and resolved.
   </li>
   <li>
    Communicate audit findings to internal stakeholders and provide guidance to teams regarding the development of Root Cause Analysis and Corrective Preventive Actions.
   </li>
   <li>
    Liaise with other departments in the completion of Sponsor requests for information.
   </li>
   <li>
    Support internal departments with privacy related questions or inquiries
    <br/>
   </li>
  </ul>
  <p>
   <br/>
  </p>
  <strong>
   Product/Service Consulting
  </strong>
  <ul>
   <li>
    Provide guidance during product/service enhancements cycles or during times of  organizational change around quality compliance and cross-functional process  requirements and organization efficiency gains.&nbsp;
    <br/>
   </li>
  </ul>
  <p>
   <br/>
  </p>
  <strong>
   Qualifications
  </strong>
  <ul>
   <li>
    The successful candidate will possess either an undergraduate degree with 4-6 years of related experience and on the go training, or a College Diploma with 7-9 years of related experience and training.
   </li>
   <li>
    Life Sciences, Clinical Research, Information Technology or Clinical Quality Assurance specialty preferred. Strong analytical, critical thinking and problem-solving skills required. Knowledge of ICH GCP, global regulations governing Clinical Research and global privacy regulations
    <br/>
   </li>
  </ul>
 </p>
 <p>
  <br/>
 </p>
 <br/>
 <p>
  We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
 </p>
</div>


Quality Assurance Specialist

<div>
 <strong>
  About The Job Quality Assurance Specialist
  <br/>
  <br/>
 </strong>
 <strong>
  Quality Assurance Specialist
  <br/>
  <br/>
 </strong>
 <strong>
  Washington, DC
  <br/>
  <br/>
 </strong>
 <strong>
  Contract
  <br/>
  <br/>
 </strong>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 Experience: 2-3 years in Quality Assurance (QA) or a strong background in process/manufacturing
 <br/>
 <br/>
 Industry: Pharmaceutical, GMP environment
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 Manage documentation processes to ensure compliance with Good Manufacturing Practices (GMP)
 <br/>
 <br/>
 Handle Corrective and Preventive Actions (CAPA), change control, and deviation management
 <br/>
 <br/>
 Develop and maintain controlled environments and ensure compliance with industry standards
 <br/>
 <br/>
 Support the client in managing and streamlining documentation to enhance efficiency and compliance
 <br/>
 <br/>
 Work towards reducing on-site quality documentation by 80%Collaborate with cross-functional teams to ensure consistent quality standards
 <br/>
 <br/>
 <strong>
  Skills and Qualifications:
 </strong>
 2-3 years of experience in Quality Assurance or a strong background in process/manufacturing within the pharmaceutical industry
 <br/>
 <br/>
 Expertise in documentation management, CAPA, change control, deviations, and complianceStrong understanding of GMP regulations and standards
 <br/>
 <br/>
 Excellent attention to detail and problem-solving skills
 <br/>
 <br/>
 Ability to work effectively in a controlled environment
 <br/>
 <br/>
 Strong communication and interpersonal skills
 <br/>
 <br/>
 <strong>
  Key Objectives
  <br/>
  <br/>
 </strong>
 Reduce 80% of on-site quality documentation
 <br/>
 <br/>
 Streamline processes to enhance efficiency and compliance
 <br/>
 <br/>
 Support Client in documentation management
</div>


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