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manager it risk assurance

L'Oréal

<div>
 <strong>
  Overview
  <br/>
  <br/>
 </strong>
 The Quality Assurance Manager assures quality products and processes by establishing and enforcing quality standards; testing materials and product that assures proper adherence to company requirements and global standards.
 <br/>
 <br/>
 <strong>
  Key Job Accountabilities
  <br/>
  <br/>
 </strong>
 Strategic Contribution:
 <br/>
 <br/>
 <ul>
  <li>
   Drives the Quality Assurance agenda to support the manufacturing strategy for providing high quality products to customers.
  </li>
  <li>
   Functional Policies and Controls:
  </li>
  <li>
   Monitors the effectiveness of the Quality function establishing Quality Assurance and control programs, policies and procedures which ensure product integrity and compliance with group standards and specifications.
  </li>
  <li>
   Set up and maintain quality controls and documentation procedures.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Analytics
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Responsible for product and process quality reports by collecting, analyzing, and summarizing information and trends.
  </li>
  <li>
   Preparing and analyzing reports on design, pre-production, and production to check on the quality status of the product at all stages of production and inform the production team.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Quality Assurance
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensuring all Finished Goods, Raw Material and Packaging Material lab testing is done as per L&rsquo;Oreal methods and specifications in the following labs:
  </li>
  <li>
   Testing of cosmetics related products in Micro-biological lab
  </li>
  <li>
   Packaging material parameters testing in Physical lab
  </li>
  <li>
   Raw material testing - Chemical Lab
  </li>
  <li>
   Bulk testing or To be filled products testing in In-process testing lab
  </li>
  <li>
   Ensure the timely and accurate evaluations of raw materials, packaging components, manufactured batches, in process materials and finished products.
  </li>
  <li>
   Ensures production record documentation is accurate.
  </li>
  <li>
   Creating batch making records to guarantee quality from stage one.
  </li>
  <li>
   Recommends the acceptance or blocking of deliveries or production in accordance with L&rsquo;Or&eacute;al specifications.
  </li>
  <li>
   Drive efficiency and implement quality as part of Operational excellence pillar.
  </li>
  <li>
   Works with production manager to understand the root causes of the problems in the operations.
  </li>
  <li>
   Coordinate with Unit Production to lead and monitor RTFT (Right the first time) for all local manufacturing.
  </li>
  <li>
   Formalizing methods of manufacturing for all new Fla&rsquo;s (Formulas) to guarantee quality from stage one and getting it validated from Zone Quality team for processing.
  </li>
  <li>
   Lead raw material diversification/localization process in coordination with local purchasing team and zone quality team.
   <br/>
   <br/>
  </li>
 </ul>
 Quality Audits
 <br/>
 <br/>
 <ul>
  <li>
   Responsible for leading all investigations or audits concerning product quality.
  </li>
  <li>
   Ensure supplier quality audits are conducted to gauge performance and share feedback for improvement.
  </li>
  <li>
   Ensure quarterly quality audits are happening of all critical processes and share feedback for improvement.
   <br/>
   <br/>
  </li>
 </ul>
 Continuous Improvement
 <br/>
 <br/>
 <ul>
  <li>
   Liaise with other managers and staff and provide training, tools and techniques to enable others to achieve quality standards.
  </li>
  <li>
   Implementing improvements to production processes that lead to overall increases in product quality.
  </li>
  <li>
   Look at ways to reduce waste and increase efficiency in production line.
  </li>
  <li>
   Measure performance and identify any areas of weakness, recommending and implementing improvements
  </li>
  <li>
   Utilizing extensive knowledge of the product's inner workings to diagnose problems.
  </li>
  <li>
   Continuing education on newly developing Quality Assurance techniques.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  People Development
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Supervises Quality engineers and Lab team in their day-to-day tasks. Provide recommendations to the Line Manager and Human Resources on hiring and promotions.
  </li>
  <li>
   Consistently promotes high standards through personal example and roll out through the team so that each member of the team understands the standards and behaviors expected of them.
  </li>
  <li>
   Setting individual objectives, conduct periodic performance reviews, providing feedback and appraisal to maximize subordinates and departmental performance.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  KEY STAKEHOLDERS
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Internal: Manufacturing, Supply Chain, Marketing, Commercial and other departments within L&rsquo;Or&eacute;al
  </li>
  <li>
   External: 3rd Party Manufacturing team, Suppliers, Auditors, Quality Assurance Institutes
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 Minimum Qualifications:
 <br/>
 <br/>
 <ul>
  <li>
   BSc Engineering (any discipline)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   6- years of experience in Quality Assurance in FMCG/Process industry
  </li>
  <li>
   At least 3 years in managing role
  </li>
  <li>
   Extensive knowledge of Quality Assurance/Quality Control systems and procedures, chemistry, biological sciences, statistics, managerial disciplines, Federal Regulations (cosmetic, drug, food).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Behavioral Skills
  <br/>
  <br/>
 </strong>
 <strong>
  EXPERIENCE &amp; SKILLS
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Creative problem-solving skills and ability to thrive in an entrepreneurial environment are a must
  </li>
  <li>
   Dynamic &amp; Resilient and happy to do business at fast pace
  </li>
  <li>
   Able to manage team effectively
  </li>
  <li>
   Demonstrate a strong power of analytical reasoning that can drive the business forward
  </li>
  <li>
   Highly conscientious and diligent.
  </li>
  <li>
   Data analysis and statistical aptitude
  </li>
  <li>
   Ability to facilitate change
  </li>
  <li>
   Team Management
  </li>
  <li>
   Leadership Skills
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Competencies
  <br/>
  <br/>
 </strong>
 Technical Competencies
 <br/>
 <br/>
 <ul>
  <li>
   Hands-on knowledge of Inspection Equipment
  </li>
  <li>
   Thorough knowledge of Good Manufacturing Practices (GMP)
  </li>
  <li>
   Commitment to the quality function
  </li>
  <li>
   Ability to make effective and efficient use of financial resources to achieve objectives
  </li>
  <li>
   Knowledge of manufacturing and filling of bulk, and the operation of various types of manufacturing and packaging equipment
  </li>
 </ul>
</div>


Quality Assurance Manager

<div><div><b>OVERVIEW</b></div><div></div><div><br>
The Quality Assurance Manager assures quality products and processes by establishing and enforcing quality standards; testing materials and product that assures proper adherence to company requirements and global standards.</div><div></div><div><b><br>
KEY JOB ACCOUNTABILITIES</b></div><div>
Strategic Contribution:</div><div><ul><li>
Drives the Quality Assurance agenda to support the manufacturing strategy for providing high quality products to customers.</li><li>
Functional Policies and Controls:</li><li>
Monitors the effectiveness of the Quality function establishing Quality Assurance and control programs, policies and procedures which ensure product integrity and compliance with group standards and specifications.</li><li>
Set up and maintain quality controls and documentation procedures.</li></ul></div><div>
Analytics:</div><div><ul><li>
Responsible for product and process quality reports by collecting, analyzing, and summarizing information and trends.</li><li>
Preparing and analyzing reports on design, pre-production, and production to check on the quality status of the product at all stages of production and inform the production team.</li></ul></div><div>
Quality Assurance:</div><div><ul><li>
Ensuring all Finished Goods, Raw Material and Packaging Material lab testing is done as per L&rsquo;Oreal methods and specifications in the following labs:</li><li>
Testing of cosmetics related products in Micro-biological lab</li><li>
Packaging material parameters testing in Physical lab</li><li>
Raw material testing - Chemical Lab</li><li>
Bulk testing or To be filled products testing in In-process testing lab</li><li>
Ensure the timely and accurate evaluations of raw materials, packaging components, manufactured batches, in process materials and finished products.</li><li>
Ensures production record documentation is accurate.</li><li>
Creating batch making records to guarantee quality from stage one.</li><li>
Recommends the acceptance or blocking of deliveries or production in accordance with L&rsquo;Or&eacute;al specifications.</li><li>
Drive efficiency and implement quality as part of Operational excellence pillar.</li><li>
Works with production manager to understand the root causes of the problems in the operations.</li><li>
Coordinate with Unit Production to lead and monitor RTFT (Right the first time) for all local manufacturing.</li><li>
Formalizing methods of manufacturing for all new Fla&rsquo;s (Formulas) to guarantee quality from stage one and getting it validated from Zone Quality team for processing.</li><li>
Lead raw material diversification/localization process in coordination with local purchasing team and zone quality team.</li></ul></div><div>
Quality Audits</div><div><ul><li>
Responsible for leading all investigations or audits concerning product quality.</li><li>
Ensure supplier quality audits are conducted to gauge performance and share feedback for improvement.</li><li>
Ensure quarterly quality audits are happening of all critical processes and share feedback for improvement.</li></ul></div><div>
Continuous Improvement</div><div><ul><li>
Liaise with other managers and staff and provide training, tools and techniques to enable others to achieve quality standards.</li><li>
Implementing improvements to production processes that lead to overall increases in product quality.</li><li>
Look at ways to reduce waste and increase efficiency in production line.</li><li>
Measure performance and identify any areas of weakness, recommending and implementing improvements</li><li>
Utilizing extensive knowledge of the product's inner workings to diagnose problems.</li><li>
Continuing education on newly developing Quality Assurance techniques.</li></ul></div><div>
People Development:</div><div><ul><li>
Supervises Quality engineers and Lab team in their day-to-day tasks. Provide recommendations to the Line Manager and Human Resources on hiring and promotions.</li><li>
Consistently promotes high standards through personal example and roll out through the team so that each member of the team understands the standards and behaviors expected of them.</li><li>
Setting individual objectives, conduct periodic performance reviews, providing feedback and appraisal to maximize subordinates and departmental performance.</li></ul></div><div></div><div><b><br>
KEY STAKEHOLDERS</b></div><div></div><div><br>
<ul><li>
Internal: Manufacturing, Supply Chain, Marketing, Commercial and other departments within L&rsquo;Or&eacute;al</li><li>
External: 3rd Party Manufacturing team, Suppliers, Auditors, Quality Assurance Institutes</li></ul></div><div></div><div><b><br>
QUALIFICATIONS</b></div><div></div><div><br>
Minimum Qualifications:</div><div><ul><li>
BSc Engineering (any discipline)</li></ul></div><div>
Minimum Experience:</div><div><ul><li>
6- years of experience in Quality Assurance in FMCG/Process industry</li><li>
At least 3 years in managing role</li><li>
Extensive knowledge of Quality Assurance/Quality Control systems and procedures, chemistry, biological sciences, statistics, managerial disciplines, Federal Regulations (cosmetic, drug, food).</li></ul></div><div></div><div><br>
 <b>EXPERIENCE &amp; SKILLS</b></div><div></div><div><br>
Behavioral Skills:</div><div><ul><li>
Creative problem-solving skills and ability to thrive in an entrepreneurial environment are a must</li><li>
Dynamic &amp; Resilient and happy to do business at fast pace</li><li>
Able to manage team effectively</li><li>
Demonstrate a strong power of analytical reasoning that can drive the business forward</li><li>
Highly conscientious and diligent.</li><li>
Data analysis and statistical aptitude</li><li>
Ability to facilitate change</li><li>
Team Management</li><li>
Leadership Skills</li></ul></div><div></div><div><b><br>
COMPETENCIES:</b></div><div>
Technical Competencies</div><div><ul><li>
Hands-on knowledge of Inspection Equipment</li><li>
Thorough knowledge of Good Manufacturing Practices (GMP)</li><li>
Commitment to the quality function</li><li>
Ability to make effective and efficient use of financial resources to achieve objectives</li><li>
Knowledge of manufacturing and filling of bulk, and the operation of various types of manufacturing and packaging equipment</li></ul></div></div>

NOW HR

<p><b>Role Overview</b></p><p>The manager Networking/IT will be responsible for developing and executing the company&rsquo;s technology strategy while ensuring the integrity, security, and efficiency of all IT systems across the head office and branch network. This role involves managing IT infrastructure, overseeing hardware and networking operations, and ensuring compliance with regulatory standards and cyber security protocols.</p><p><b>Key Responsibilities:</b></p><p><b>1. Technology Strategy &amp; Implementation</b></p><p>&middot; Design and implement technology solutions to enhance operational efficiency.</p><p>&middot; Plan and manage the integration, upgrading, and alignment of core IT systems.</p><p><b>2. IT Operations &amp; Infrastructure</b></p><p>&middot; Oversee the performance, availability, and security of the organization&rsquo;s IT infrastructure.</p><p>&middot; Ensure the reliability of servers and platforms with proactive performance monitoring and risk mitigation.</p><p>&middot; Lead procurement processes, vendor negotiations, and contract management.</p><p><b>3. Governance, Policy &amp; Compliance</b></p><p>&middot; Develop and enforce IT governance policies, procedures, and standards.</p><p>&middot; Ensure alignment with legal and regulatory requirements related to data privacy, cyber security, and IT systems.</p><p><b>4. Information Security &amp; Risk Management</b></p><p>&middot; Design and maintain a comprehensive IT security and risk management framework.</p><p>&middot; Establish and implement an Information Security Management Framework (ISMF).</p><p>&middot; Conduct regular risk assessments, vulnerability scans, and implement appropriate safeguards.</p><p>&middot; Lead the organization's incident response, including forming an Emergency Response Team and conducting post-incident evaluations.</p><p>&middot; Continuously adapt the cyber security strategy in line with emerging threats and technologies.</p><p><b>5. Reporting &amp; Additional Duties</b></p><p>&middot; Provide strategic technology insights and regular reports to senior leadership.</p><p>&middot; Undertake special assignments and projects as directed by the functional head or top management.</p><p><b>Qualifications &amp; Experience</b></p><p>&middot; Bachelors or Master&rsquo;s degree in Computer Science, Information Technology, or a related field.</p><p>&middot; Professional certifications such as CISSP, CISM, PMP, or ITIL are preferred.</p><p>&middot; Minimum 10 years of progressive experience in IT leadership roles, preferably within the insurance or financial services sector.</p><p>&middot; Strong understanding of cyber security, system integration, and infrastructure management will be an added advantage.</p><p>Job Type: Full-time</p><p>Pay: Rs150,000.00 - Rs200,000.00 per month</p><p>Work Location: In person</p>

Manager IT Support

<div>
 At EY, we&rsquo;re all in to shape your future with confidence.
 <br/>
 <br/>
 We&rsquo;ll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.
 <br/>
 <br/>
 Join EY and help to build a better working world.
 <br/>
 <br/>
 <strong>
  The opportunity
  <br/>
  <br/>
 </strong>
 As an Account Support Associate (ASA), you&rsquo;ll be a key member of our Business Support Services (BSS) team . The ASA program supports a wide range of service lines (Assurance, Consulting, Tax, Strategy and Transactions), making this a great place to gain exposure to new skills and progress your career. You will work directly with high-level client-serving professionals (partners/principals, executive directors, senior managers and managers) to drive project management and engagement coordination for EY&rsquo;s key account client-serving teams. You will drive efficiencies for the account teams and reduce time to provide services to clients, with a focus on maintaining the applicable professional standards.
 <br/>
 <br/>
 <strong>
  Your Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Manage stakeholder expectations, project plans and communications, and provide status updates as needed to continuously advance service delivery
  </li>
  <li>
   Act as the knowledge manager for the engagement team, managing internal databases and/or portals designed to facilitate global team communications and coordination of go-to-market strategy
  </li>
  <li>
   Take complete ownership of engagement economics (e.g., hours/budgets/estimates to complete, fees, billings, Work in Process spreadsheets), proactively collaborating with relevant team members to resolve any issues that arise
  </li>
  <li>
   Collaborate with the account team, business development and resource management teams to achieve team goals
  </li>
  <li>
   Coordinate risk management processes, such as engagement letters, client continuance, independence, family tree, preapproval and other regulatory requirements
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Skills And Attributes For Success
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Minimum of 1&ndash;2 years of experience in account or project management, customer service, or a related support role
  </li>
  <li>
   A degree in Business Administration, Marketing, Communication, or a related field is preferred
  </li>
  <li>
   Proficiency in Microsoft Office Suite
  </li>
  <li>
   Excellent verbal and written communication skills to interact effectively with clients and team members
  </li>
  <li>
   Strong analytical and problem-solving abilities to address challenges proactively
  </li>
  <li>
   High attention to detail with the ability to manage multiple tasks accurately
  </li>
  <li>
   Strong organizational and time management skills to handle a high volume of work efficiently
  </li>
  <li>
   Client-focused mindset with a commitment to delivering exceptional service and building long-term relationships
  </li>
  <li>
   Collaborative team player with the ability to work effectively in a team environment
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We Offer
  <br/>
  <br/>
 </strong>
 At EY, we&rsquo;ll develop you with future-focused skills and equip you with world-class experiences. We&rsquo;ll empower you in a flexible environment, and fuel you and your extraordinary talents in a diverse and inclusive culture of globally connected teams. Learn more.
 <br/>
 <br/>
 Are you ready to shape your future with confidence? Apply today.
 <br/>
 <br/>
 To help create the best experience during the recruitment process, please describe any disability-related adjustments or accommodations you may need.
 <br/>
 <br/>
 <strong>
  EY
 </strong>
 |
 <strong>
  Building a better working world
  <br/>
  <br/>
 </strong>
 EY is building a better working world by creating new value for clients, people, society and the planet, while building trust in capital markets.
 <br/>
 <br/>
 Enabled by data, AI and advanced technology, EY teams help clients shape the future with confidence and develop answers for the most pressing issues of today and tomorrow.
 <br/>
 <br/>
 EY teams work across a full spectrum of services in assurance, consulting, tax, strategy and transactions. Fueled by sector insights, a globally connected, multi-disciplinary network and diverse ecosystem partners, EY teams can provide services in more than 150 countries and territories.
</div>


Account Support Associate - Rapid Innovation - Karachi

<div><b>Site Name:</b> Pakistan - Sindh - Karachi<br>
<b>Posted Date:</b> Nov 7 2025<p><b><br>
Job Purpose
</b></p><p>The Site Regulatory Compliance Head at GSK is responsible for ensuring that all company operations, products, and processes comply with relevant regulatory requirements. The role involves developing, implementing, and managing regulatory compliance programs and procedures to ensure adherence to laws, regulations, and guidelines set by regulatory bodies. The Regulatory Compliance Manager will play a critical role in maintaining the company's reputation and protecting it from GMP and regulatory compliance risks. The role ensures the risks are identified, escalated and mitigation plans In-place. This position ensures that all critical Quality Regulatory Compliance activities at the site comply with applicable regulatory authority guidelines, QMS requirements, cGMP standards, and applicable local standard operating procedures.</p><p></p><p><b>
Education, Experience &amp; Skills</b></p><ul><li>
Science Graduate/Pharm D/ /Pharmacist</li><li>
Minimum 8 years of Experience in Quality Assurance, Regulatory Compliance, Quality Control, or a related field, including a position of significant leadership and decision-making authority within Quality or Regulatory functions.</li><li>
Strong knowledge of QMS, GMP and Regulatory requirements and guidelines</li></ul><p></p><p><b>
Key Responsibilities</b></p><ul><li>
Manage Quality Regulatory Compliance and systems on site by creating and executing regulatory compliance strategies and programs.</li><li>
Ensure to monitor changes in global and local regulatory environment/regulatory requirements and ensure GSK processes and products comply with applicable laws and regulations.</li><li>
Establish, review, and update site procedures to align with regulatory requirements.</li><li>
Accountable for timely communication, correspondence with Regulators, government officials for warrantors, queries, cases and any other correspondence in liaison with Site, Legal and Regulatory team.</li><li>
Responsible for attending meetings and hearings with government officials and regulators in liaison with Site Quality Head</li><li>
Proactive engagement with regulator, where possible e.g. DTL, PQCB to expediate the current ongoing regulatory queries</li><li>
Investigate and resolve compliance issues, including conducting root cause analysis and implementing corrective actions.</li><li>
Identify Internal and external risks, where applicable develop risk mitigation plan and monitor the implementation plan.</li><li>
Governance of regulatory KPIs and processes and identify and assess compliance risks to develop effective mitigation strategies.</li><li>
Engage and communicate effectively with internal stakeholders and senior management to ensure alignment on compliance matters.</li><li>
Ensure compliance of the site-specific regulatory process for Management of Regulatory authority letters notifications and statutory regulatory orders (SROs).</li><li>
Ensure the Inspection readiness at Site, escalates any issues which impacting inspection readiness to site senior management.</li><li>
Represent the site during regulatory inspections in coordination with site relevant team.</li><li>
Develop and maintain accurate records of site product registration details, regulatory submissions and correspondence with regulatory agencies.</li><li>
Ensures compliance with QMS Implementation on site to comply with the requirements of the QMS, company internal policies, Global SOPs, and all related regulatory guidelines.</li><li>
Engages with the site to promote a culture of awareness and understanding of regulatory compliance.</li><li>
Provide training to employees on regulatory compliance topics to enhance their understanding and adherence to applicable regulations.</li><li>
Ensure to maintain accurate and up-to-date records of regulatory activities, decisions, and communications.</li><li>
Ensure reporting of compliance risks and issues to Site Quality Head, Site Director and at governance forum i.e. Site Quality Council, Site Leadership Team meetings.</li><li>
Permanent member of Site Quality Council and Risk Management Council Board meetings.</li><li>
This role may require traveling to attend regulatory meetings, conferences, visits or inspections.</li></ul><p><b>
Job Purpose
</b></p><p></p><p>The Site Regulatory Compliance Head at GSK is responsible for ensuring that all company operations, products, and processes comply with relevant regulatory requirements. The role involves developing, implementing, and managing regulatory compliance programs and procedures to ensure adherence to laws, regulations, and guidelines set by regulatory bodies. The Regulatory Compliance Manager will play a critical role in maintaining the company's reputation and protecting it from GMP and regulatory compliance risks. The role ensures the risks are identified, escalated and mitigation plans In-place. This position ensures that all critical Quality Regulatory Compliance activities at the site comply with applicable regulatory authority guidelines, QMS requirements, cGMP standards, and applicable local standard operating procedures.</p><p></p><p><b>
Education, Experience &amp; Skills</b></p><ul><li><p>
Science Graduate/Pharm D/ /Pharmacist</p></li><li><p>
Minimum 8 years of Experience in Quality Assurance, Regulatory Compliance, Quality Control, or a related field, including a position of significant leadership and decision-making authority within Quality or Regulatory functions.</p></li><li><p>
Strong knowledge of QMS, GMP and Regulatory requirements and guidelines</p></li></ul><p></p><p><b>
Key Responsibilities</b></p><ul><li><p>
Manage Quality Regulatory Compliance and systems on site by creating and executing regulatory compliance strategies and programs.</p></li><li><p>
Ensure to monitor changes in global and local regulatory environment/regulatory requirements and ensure GSK processes and products comply with applicable laws and regulations.</p></li><li><p>
Establish, review, and update site procedures to align with regulatory requirements.</p></li><li><p>
Accountable for timely communication, correspondence with Regulators, government officials for warrantors, queries, cases and any other correspondence in liaison with Site, Legal and Regulatory team.</p></li><li><p>
Responsible for attending meetings and hearings with government officials and regulators in liaison with Site Quality Head</p></li><li><p>
Proactive engagement with regulator, where possible e.g. DTL, PQCB to expediate the current ongoing regulatory queries</p></li><li><p>
Investigate and resolve compliance issues, including conducting root cause analysis and implementing corrective actions.</p></li><li><p>
Identify Internal and external risks, where applicable develop risk mitigation plan and monitor the implementation plan.</p></li><li><p>
Governance of regulatory KPIs and processes and identify and assess compliance risks to develop effective mitigation strategies.</p></li><li><p>
Engage and communicate effectively with internal stakeholders and senior management to ensure alignment on compliance matters.</p></li><li><p>
Ensure compliance of the site-specific regulatory process for Management of Regulatory authority letters notifications and statutory regulatory orders (SROs).</p></li><li><p>
Ensure the Inspection readiness at Site, escalates any issues which impacting inspection readiness to site senior management.</p></li><li><p>
Represent the site during regulatory inspections in coordination with site relevant team.</p></li><li><p>
Develop and maintain accurate records of site product registration details, regulatory submissions and correspondence with regulatory agencies.</p></li><li><p>
Ensures compliance with QMS Implementation on site to comply with the requirements of the QMS, company internal policies, Global SOPs, and all related regulatory guidelines.</p></li><li><p>
Engages with the site to promote a culture of awareness and understanding of regulatory compliance.</p></li><li><p>
Provide training to employees on regulatory compliance topics to enhance their understanding and adherence to applicable regulations.</p></li><li><p>
Ensure to maintain accurate and up-to-date records of regulatory activities, decisions, and communications.</p></li><li><p>
Ensure reporting of compliance risks and issues to Site Quality Head, Site Director and at governance forum i.e. Site Quality Council, Site Leadership Team meetings.</p></li><li><p>
Permanent member of Site Quality Council and Risk Management Council Board meetings.</p></li><li><p>
This role may require traveling to attend regulatory meetings, conferences, visits or inspections.</p></li></ul><p></p><p><b>
Why GSK?</b><br>
<b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.</p><p></p><p>
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p></p><p><b>
Contact information:</b><br>
You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>
Important notice to Employment businesses/ Agencies</b></p><p>
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Site Regulatory Compliance Head

Standard Chartered

<div>
 <strong>
  Job Summary
  <br/>
  <br/>
 </strong>
 This position is responsible to analyse comprehensive impact of financial crime related regulatory matters on the relevant business area and its operations.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Providing governance and oversight over the implementation of Financial Crime Compliance related policies and procedures in Country to ensure compliance with such policies and procedures
  </li>
  <li>
   Support relevant stakeholders to make decisions based on current and possible future policies, practices and trends on the interpretation and application of regulatory expectations
  </li>
  <li>
   Execute activities as part of the Financial Crime Post Investigations &amp; Counter Finance Terrorism Desk team (including but not limited to Quality Control Outcome reviews for Act, Quality Assurance reviews, Controls Checks, Health checks)
  </li>
  <li>
   Provide advice to relevant stakeholders on compliance with Group standards relating to Financial Crime Compliance related matters.
  </li>
  <li>
   Perform Public domain search for identification and reporting of terrorist incidents/ attack to the Head Post Investigations.
  </li>
  <li>
   Ensure Financial Monitoring Unit queries are addressed timely complying with the provision of information.
  </li>
  <li>
   Provide advice on the application of risk management frameworks
  </li>
  <li>
   Apply Group and Financial Crime Compliance policies and processes (Anti Money Laundering surveillance, client screening, risk assessment) to manage risks.
  </li>
  <li>
   Inform senior management of any regulatory breaches (or where risk tolerances have been breached) and ensure that actions are taken quickly to remediate and/or activities are ceased.
  </li>
  <li>
   Support line manager in conducting Country risk assessment.
  </li>
  <li>
   Map risks, quantify the potential impact and escalate where necessary.
  </li>
  <li>
   Provide intelligent input (where applicable) to support calibration of bank&rsquo;s Risk Methodologies (including aggregate client risk, product risk and country risk assessments).
  </li>
  <li>
   Understand technical aspects of systems relevant to Customer Due Diligence, Client Risk Assessments, Name and Transaction Screening, Anti Money Laundering Monitoring and Case Management.
  </li>
  <li>
   Ensure timely completion of the Post Investigation (follow up) actions related to Transaction Monitoring/Name Screening cases as and when these are assigned.
  </li>
  <li>
   Align/support with the alignment of relevant systems and controls to industry best practice and close out any compliance gaps
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About Standard Chartered
  <br/>
  <br/>
 </strong>
 We're an international bank, nimble enough to act, big enough for impact. For more than 170 years, we've worked to make a positive difference for our clients, communities, and each other. We question the status quo, love a challenge and enjoy finding new opportunities to grow and do better than before. If you're looking for a career with purpose and you want to work for a bank making a difference, we want to hear from you. You can count on us to celebrate your unique talents and we can't wait to see the talents you can bring us.
 <br/>
 <br/>
 Our purpose, to drive commerce and prosperity through our unique diversity, together with our brand promise, to be here for good are achieved by how we each live our valued behaviours. When you work with us, you'll see how we value difference and advocate inclusion.
 <br/>
 <br/>
 <strong>
  Together We
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Do the right thing and are assertive, challenge one another, and live with integrity, while putting the client at the heart of what we do
  </li>
  <li>
   Never settle, continuously striving to improve and innovate, keeping things simple and learning from doing well, and not so well
  </li>
  <li>
   Are better together, we can be ourselves, be inclusive, see more good in others, and work collectively to build for the long term
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We Offer
  <br/>
  <br/>
 </strong>
 <strong>
  In line with our Fair Pay Charter,
 </strong>
 we offer a competitive salary and benefits to support your mental, physical, financial and social wellbeing.
 <br/>
 <br/>
 <ul>
  <li>
   Core bank funding for retirement savings, medical and life insurance, with flexible and voluntary benefits available in some locations.
  </li>
  <li>
   Time-off including annual leave, parental/maternity (20 weeks), sabbatical (12 months maximum) and volunteering leave (3 days), along with minimum global standards for annual and public holiday, which is combined to 30 days minimum.
  </li>
  <li>
   Flexible working options based around home and office locations, with flexible working patterns.
  </li>
  <li>
   Proactive wellbeing support through Unmind, a market-leading digital wellbeing platform, development courses for resilience and other human skills, global Employee Assistance Programme, sick leave, mental health first-aiders and all sorts of self-help toolkits
  </li>
  <li>
   A continuous learning culture to support your growth, with opportunities to reskill and upskill and access to physical, virtual and digital learning.
  </li>
  <li>
   Being part of an inclusive and values driven organisation, one that embraces and celebrates our unique diversity, across our teams, business functions and geographies - everyone feels respected and can realise their full potential.
  </li>
 </ul>
</div>


Associate, Financial Crime Post Investigations & Counter Finance Terrorism Desk

Minerva Research Solutions

<div><p><b>JOB DESCRIPTION:</b><br>
<br>
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.</p><p>
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.<br>
<br>
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.<br>
<br>
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.</p><p><b>
Responsibilities:</b></p><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><p><b>
Knowledge, Education, and Experience:</b></p><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><p><b>
Skills and Abilities:</b></p><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><b>
Benefits:</b><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><b>
Openings:</b><p>
04 positions<br>
Full-time<br>
On-site job<br>
<br>
<b>Work Schedule Timings:</b><br>
Monday to Friday<br>
Evening Shift (07 PM to 03 AM)<br>
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)</p><p>
</p><p>vapSso9DaM</p></div>

Clinical Trials Quality Assurance Associate (Night)

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