customer service specialist Jobs in Karachi

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global compliance & reporting - consultant/senior consultant - karachi - pakistan Jobs in Karachi

global compliance & reporting - consultant/senior consultant - karachi - pakistan

key account analyst – compliance Jobs in Karachi

key account analyst – compliance

manager, rider compliance Jobs in Karachi

manager, rider compliance

regulatory co ordinator(evening shift) Jobs in Karachi

regulatory co ordinator(evening shift)

regulatory compliance specialist

California Chemical

<div>
 
 Are you a detail-oriented professional with a background in
 
 Chemical Regulatory Documentations and Compliance
 
 ?
 
 
 
 California Chemical
 
 is looking for a dedicated specialist to join our team for a crucial
 
 on-site, night shift
 
 role focused on regulatory compliance and document control.
 
 
 
 About California Chemical
 
 
 
 We are a leading company in the chemical industry (US-based), committed to safety, quality, and compliance across all our operations of Supply Chain Management.
 
 
 
 
 
 
 Key Responsibilities &amp; Job Details
 
 
 
 This role is a unique mix of regulatory compliance and department management, perfect for someone who thrives on structure and accuracy.
 
 
 
 1. Chemical Regulatory &amp; Documentation
 
 
 <ul>
 <li>
 
 Sanitize and Review Documents:
 
 Carefully examine and refine
 
 Chemical Products documents
 
 (like SDS, COA, etc.) to ensure absolute accuracy and clarity before they are approved for use.
 </li>
 <li>
 
 Approval Process:
 
 Officially
 
 review and approve
 
 finalized chemical products documentation, confirming it meets all company and regulatory standards.
 </li>
 <li>
 
 Compliance Checks:
 
 Ensure all chemical products documentation complies with relevant local, state, and federal
 
 chemical safety and regulatory requirements
 
 .
 </li>
 </ul>
 
 
 2. Document Control Management
 
 
 <ul>
 <li>
 
 Department Oversight:
 
 Manage and maintain the
 
 Document Control Department
 
 , ensuring all documents are stored, tracked, and easily retrievable.
 </li>
 <li>
 
 Inquiry Handling:
 
 Be the primary contact for internal and external inquiries related to
 
 chemical product documentation
 
 and its control, providing clear, accurate, and timely information.
 </li>
 </ul>
 
 
 Requirements
 
 
 <ul>
 <li>
 
 Experience:
 
 A minimum of
 
 2 years of professional work experience
 
 in a chemical, regulatory, or documentation-focused environment, and the Candidate should be
 
 Chemical Engineering
 
 .
 </li>
 <li>
 
 Language:
 
 Must be
 
 fluent in English
 
 (written and verbal).
 </li>
 <li>
 
 Skills:
 
 Exceptional attention to detail, strong organizational skills, and a commitment to maintaining confidentiality and accuracy.
 </li>
 </ul>
 
 
 
 
 
 Role Logistics
 
 
 <ul>
 <li>
 
 Schedule:
 
 
 Full-Time, On-Site, Night Shift
 
 (8:00 PM to 5:00 AM).
 </li>
 <li>
 
 Location:
 
 Karachi Based.
 </li>
 <li>
 
 Salary:
 
 Competitive compensation package ranging from
 
 200,000 to 250,000
 
 PKR, Plus One Annual Bonus.
 
 The salary package is negotiable based on your specific knowledge and experience.
 
 </li>
 </ul>
 
 
 
 <ul>
 <li>
 
 Growth:
 
 An opportunity to be a key part of the growing
 
 California Chemical
 
 team.
 </li>
 <li>
 
 Inclusion:
 
 We encourage both
 
 Male and Female candidates
 
 to apply.
 </li>
 </ul>
 
 
 
 
 
 How to Apply
 
 
 
 Through linkedin or Share your resume at: saddy.mehar@californiachemical.com
 
</div>

Chemical Regulatory & Document Control Specialist

UTOPIA INDUSTRIES PVT LTD

Regulatory Compliance Officer/ Specialist &ndash; Dietary SupplementsEducation: Bachelor&rsquo;s/Master&rsquo;s degree in Pharmacy, Food Science, Nutrition, Biotechnology, or Regulatory Affairs.Experience: Minimum 3&ndash;5 years in product regulatory compliance, preferably in dietary supplements, cosmetics, or nutraceuticals.KeyResponsibilities:<ul><li>Ensure all dietary supplements comply with U.S. FDA Dietary Supplement regulations under the FD&amp;C Act and 21 CFR 111 (cGMP).</li><li>Review and verify supplier documentation, including Certificates of Analysis (COA), GMP certificates, NDI notifications, product dossiers, permitted ingredients, prohibited or restricted ingredients and formulation specifications.</li><li>Ensure scientific substantiation of ingredient functions and claims.</li><li>Review all product labels, claims and Amazon listings for compliance with FDA labeling guidelines (identity statement, net quantity, Supplement Facts, ingredient declaration, warnings).</li><li>Communicate with suppliers to ensure documentation completeness, GMP certification, facility registration, and FDA establishment listing and product conformity.</li><li>Evaluate supplier test data for microbial, heavy metals, and purity compliance.</li><li>Ensure all required premarket notifications (e.g., NDIN, if applicable) are filed or confirmed by the supplier, manage product listing on Amazon and FDA notification (via SPL) if needed.</li><li>Oversee post-market vigilance, including consumer complaint tracking, recall coordination, and adverse event reporting.</li><li>Work closely with QA/QC, Procurement, and Marketing teams to integrate regulatory compliance early in product selection.</li><li>Support packaging and labeling approval cycles before production.</li></ul>Job Type: Full-timeWork Location: In person

Regulatory Affairs Specialist

Datamatics Global Services Ltd

<div>Location: Riyadh, KSA 
Duration: 6 Months (Extendable) 
Work Mode: Onsite 
Experience: 6+ Years<h3 class="jobSectionHeader">
Job Summary:</h3>
We are seeking a Data Compliance Specialist to support and oversee compliance with the NDMO (National Data Management Office) and PDPL (Personal Data Protection Law) frameworks in Saudi Arabia. The candidate will ensure all data management and privacy practices align with local regulations and corporate governance policies.<h3 class="jobSectionHeader">
Key Responsibilities:</h3><ul><li>
Implement and monitor compliance with NDMO and PDPL data governance requirements.</li><li>
Develop and maintain data protection policies, frameworks, and documentation.</li><li>
Conduct data classification, privacy risk assessments, and compliance audits.</li><li>
Work with IT and business teams to enforce data protection measures.</li><li>
Monitor data access, sharing, and storage practices for compliance.</li><li>
Support incident management and reporting of data breaches.</li><li>
Conduct awareness sessions and provide compliance training.</li></ul><h3 class="jobSectionHeader">
Qualifications:</h3><ul><li>
Bachelor&rsquo;s or Master&rsquo;s degree in Information Security, Data Governance, or related field.</li><li>
5+ years of experience in data compliance, privacy, or governance.</li><li>
In-depth knowledge of NDMO and PDPL regulatory frameworks.</li><li>
Experience in data protection audits, risk management, and documentation.</li><li>
Strong analytical, communication, and stakeholder management skills.</li><li>
Certifications like CIPP/E, CIPM, or ISO 27001 Lead Implementer preferred.</li></ul>
It9iHXDAO2</div>

Data Compliance Specialist – NDMO / PDPL

The Citizens Foundation (TCF)

The role is responsible for ensuring regulatory and legal compliance of TCF&rsquo;s international country partners. This includes overseeing documentation, completion, and filing requirements to ensure smooth and compliant operations of TCF&rsquo;s legal entities abroad.The individual will also liaise with the TCF Board and management to understand compliance expectations related to foreign legal entities and provide timely updates and feedback to management.Key Responsibilities<ul><li>Ensure compliance with all regulatory and legal requirements for TCF&rsquo;s international country partners.</li><li>Oversee documentation and filing processes related to foreign entities.</li><li>Liaise with the TCF Board and management to align on compliance requirements.</li><li>Provide regular updates and feedback on regulatory matters to management.</li><li>Coordinate and maintain effective communication with:</li></ul>- Country partners - Law firms abroad and in Pakistan - Regulatory authorities abroadRequired Skills<ul><li>Good communication skills and command over English.</li><li>Ability to communicate effectively both verbally and in writing.</li><li>Ability to use the computer and internet resources effectively</li><li>Ability to research and learn quickly</li><li>Ability to proactively identify challenges and propose solutions</li><li>Self-driven and able to work with minimum supervision</li><li>Courteous</li></ul>EducationA Bachelor of Laws (LLB) degree is required.ExperienceThe ideal candidate should have legal experience, preferably gained from working in a law firm, and possess 5 to 10 years of relevant professional experience.Job Type: Full-timeApplication Question(s):<ul><li>What is your current salary?</li><li>What is your expected salary?</li></ul>Work Location: In person

Manager Compliance

<div>Site Name: Pakistan - Sindh - Karachi 
Posted Date: Nov 7 2025 
Job Purpose
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.
Education, Experience &amp; Skills<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>
Key Responsibilities<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>
Job Purpose
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.
Education, Experience &amp; Skills<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>
Key Responsibilities<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>
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
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.
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.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Site Regulatory Compliance Head

Alibaba

<div><div>Basic Infomation<div><div><div>
Department:
Daraz</div><div>
Degree:
Master</div><div>
Work Experience:
6 year</div></div></div></div><div>
Job Description<div>
Financial Compliance and AML Manager
&#12304;Job Description&#12305;&#65306;
1&#12289;Lead and oversee the development and implementation of AML (Anti-Money Laundering) and financial compliance policies, procedures, and controls for Daraz Pakistan-Karachi operations.
2&#12289;Ensure compliance with local and international regulations, including monitoring and reporting suspicious transactions to relevant authorities.
3&#12289;Conduct regular risk assessments to identify potential vulnerabilities and propose mitigation strategies in the financial operations.
4&#12289;Provide training and guidance to the finance team on AML regulations and compliance best practices, ensuring a culture of compliance within the organization.
5&#12289;Collaborate with internal stakeholders and external partners, such as banks and legal advisors, to stay updated on regulatory changes and industry trends.
&#12304;Job Requirements&#12305;&#65306;
1&#12289;Master's degree in Finance, Law, or a related field, with a focus on compliance or AML.
2&#12289;Minimum of 6 years of experience in financial compliance and AML, preferably in an e-commerce or banking environment.
3&#12289;In-depth knowledge of AML laws and regulations, including local Pakistani AML/CFT requirements and international standards.
4&#12289;Strong analytical skills to investigate complex financial transactions and identify potential money laundering activities.
5&#12289;Excellent communication and interpersonal skills to effectively engage with various teams and external parties.
6&#12289;Proven ability to lead and manage compliance projects, ensuring timely completion and adherence to regulatory standards.
7&#12289;Certification in AML or compliance, such as CAMS (Certified Anti-Money Laundering Specialist) or ICA, is highly desirable.</div></div><div>
Position Requirement<div>
Financial Compliance and AML Manager
&#12304;Job Description&#12305;&#65306;
1&#12289;Lead and oversee the development and implementation of AML (Anti-Money Laundering) and financial compliance policies, procedures, and controls for Daraz Pakistan-Karachi operations.
2&#12289;Ensure compliance with local and international regulations, including monitoring and reporting suspicious transactions to relevant authorities.
3&#12289;Conduct regular risk assessments to identify potential vulnerabilities and propose mitigation strategies in the financial operations.
4&#12289;Provide training and guidance to the finance team on AML regulations and compliance best practices, ensuring a culture of compliance within the organization.
5&#12289;Collaborate with internal stakeholders and external partners, such as banks and legal advisors, to stay updated on regulatory changes and industry trends.
&#12304;Job Requirements&#12305;&#65306;
1&#12289;Master's degree in Finance, Law, or a related field, with a focus on compliance or AML.
2&#12289;Minimum of 6 years of experience in financial compliance and AML, preferably in an e-commerce or banking environment.
3&#12289;In-depth knowledge of AML laws and regulations, including local Pakistani AML/CFT requirements and international standards.
4&#12289;Strong analytical skills to investigate complex financial transactions and identify potential money laundering activities.
5&#12289;Excellent communication and interpersonal skills to effectively engage with various teams and external parties.
6&#12289;Proven ability to lead and manage compliance projects, ensuring timely completion and adherence to regulatory standards.
7&#12289;Certification in AML or compliance, such as CAMS (Certified Anti-Money Laundering Specialist) or ICA, is highly desirable.</div></div></div>

Financial Compliance and AML Manager-Financial Compliance and AML Manager-Anti Money Laundering & Compliance

Amros Pharmaceuticals

CMA Finalist - Audit &amp; Compliance Specialist (Male) - Amros Pharmaceutical Amros Pharmaceutical is seeking a highly motivated and skilled CMA Finalist to join our team, specifically to focus on Audit and Compliance. This is a pivotal role for an ambitious professional looking to accelerate their career in the pharmaceutical sector.Key Responsibilities:Assist in planning, executing, and reporting on internal audit assignments.Verify the accuracy of financial records and transactions for audit purposes.Ensure strict compliance with internal controls, accounting standards (IFRS/local GAAP), and regulatory requirements relevant to the pharmaceutical industry.Analyze financial data to identify risks and recommend improvements to control systems.Prepare detailed audit working papers and reports for management review.Coordinate with external auditors and regulatory bodies as required.Required QualificationsCMA Finalist from a recognized institute.1-2 years of relevant experience, ideally in internal or external audit, or a management accounting traineeship.Sound knowledge of auditing standards, internal controls, and corporate governance.Strong analytical and problem-solving skills.Excellent written and verbal communication abilities.This is a role designated for a male candidate.Job Type: Full-timeWork Location: In person

Sr. Account Executive (Male)

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