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aml senior compliance manager (uae market) Jobs in Karachi

aml senior compliance manager (uae market)

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assistant manager - corporate affairs Jobs in Karachi

assistant manager - corporate affairs

regulatory affairs manager

HRCONSOL

HRCONSOL is Hiring | Regulatory Affairs Specialist (Cosmetics, Skincare &amp; Nutraceuticals)HRCONSOL is hiring for a leading E-Commerce company in Karachi and we are looking for a highly skilled Regulatory Affairs Specialist with strong expertise in Cosmetics, Skincare, and Nutraceuticals.Location: Karachi (On-site) Salary: PKR 100,000 &ndash; 300,000 + Benefits Apply at: jobs@hrconsol.comJob ResponsibilitiesCosmetics &amp; Skincare Regulatory Compliance<ul><li>Evaluate suppliers to ensure compliance with U.S. FDA MoCRA, ISO 22716 (Cosmetic GMP), and ingredient safety standards.</li><li>Review &amp; approve supplier documentation including COA, SDS, CPSR, GMP certificates, test reports, ingredient lists, MoCRA filings, and marketing claims.</li><li>Maintain complete compliance documentation for each product (formulation data, safety assessments, labeling proofs, MoCRA listings).</li><li>Validate Responsible Person (RP) arrangements and import compliance as per FDA rules.</li><li>Verify supplier labeling and artwork according to MoCRA &amp; FTC advertising guidelines.</li><li>Coordinate with suppliers for adverse event monitoring, recall readiness, risk communication protocols, and reporting duties under MoCRA.</li><li>Liaise with FDA, Regulatory Consultants, and RPs for submissions &amp; resolving compliance issues.</li><li>Track and interpret updates in MoCRA, FDA guidance, and global cosmetic regulations; advise management on potential impacts and compliance requirements.</li></ul>Nutraceuticals (Plus Point)<ul><li>Review compliance documentation as per dietary supplement regulations (FDA/USP standards).</li><li>Support import approvals, labeling validation, ingredient verification, and claim assessments.</li></ul>Who Should Apply?Candidates with strong experience in Cosmetic Regulatory Affairs, US FDA MoCRA, ISO 22716, labeling compliance, and supplier documentation review are highly encouraged to apply.Apply Now: jobs@hrconsol.com Be part of a top-tier e-commerce brand scaling globally!Job Type: Full-timePay: Rs100,000.00 - Rs300,000.00 per monthWork Location: In person

Regulatory Affairs Specialist (Cosmetics, Skincare & Nutraceuticals)

Amros Pharmaceuticals

We're Hiring: Regulatory Affairs ExecutiveAmros Pharmaceuticals is looking for a highly skilled and detail-oriented RA Executive to manage the preparation, review, and submission of regulatory dossiers for both local and international markets while ensuring full compliance with regulatory guidelines.Qualification:<ul><li>Pharm-D from a recognized institution.</li><li>2 to 3.5 years of experience in Regulatory Affairs.</li><li>Proficiency in MS Office, DRAP Portal, and PSW.</li></ul>Key Responsibilities:<ul><li>Prepare and review CTD and ACTD dossiers for local and international submissions.</li><li>Prepare CPI applications and quota applications as per regulatory requirements.</li><li>Submit documents and ensure timely query compliance for export-related submissions.</li><li>Handle hardship cases by preparing and reviewing necessary documentation.</li><li>Maintain, review, and ensure the accuracy of all regulatory records and data.</li><li>Correspond with internal and external stakeholders regarding dossier requirements, updates, and submissions.</li><li>Ensure compliance with regulatory frameworks and support continuous improvement in dossier quality.</li></ul>Location: Ahsanabad, SITE Area II, Karachi.Timings: 8:30 AM &ndash; 5:30 PMApply Now:Send your updated profile to hr.recruitment@amrospharma.comJob Type: Full-timeWork Location: In person

Regulatory Affairs Executive

COLOR STUDIO PROFESSIONAL

Position: Regulatory, Compliance &amp; Factory Operations ManagerLocation: Karachi Type: Full-time Industry: Cosmetics &amp; Skincare Manufacturing1. Regulatory &amp; Compliance Responsibilities Pakistan (Local).<ul><li>Manage GMP (ISO 22716) implementation and documentation.</li><li>Handle PSQCA standards compliance.</li><li>Maintain MSDS, batch records, product dossiers, QC reports.</li><li>Submit documentation for compliance.</li><li>Handle new factory projects, documentations and regulatory matters for the factory and brands.</li></ul>International (Exports)<ul><li>Prepare dossiers for:</li><li>Dubai Municipality Product Registration (UAE)</li><li>Saudi Food &amp; Drug Authority (SFDA) cosmetic e-registration</li><li>UK SCPN (Cosmetic Product Notification Portal)</li><li>Create &amp; maintain Technical Files (PIF) for global compliance.</li><li>Obtain Certificates of Free Sale, Halal certification, or GMP certificates as needed for exports.</li></ul>2. Factory Management Responsibilities<ul><li>Oversee day-to-day production flow &amp; ensure SOPs are followed.</li><li>Coordinate with procurement for raw materials &amp; packaging.</li><li>Monitor inventory, stock levels, and reorder points.</li><li>Supervise packing, labeling, batch coding, and QC checks.</li><li>Ensure workplace safety, cleanliness, and compliance with Factories Act.</li><li>Train workers on hygiene, safety, and production standards.</li><li>Manage day to day factory operations and maintain GMP standards and protocols</li></ul>3. Documentation &amp; Quality Responsibilities<ul><li>Maintain all regulatory files, licensing documents, and audit records.</li><li>Prepare product specifications, COAs, batch records, and quality documentation.</li><li>Ensure proper labeling compliance for each country of export.</li><li>Prepare monthly and annual compliance reports.</li></ul>4. Orders, Sales &amp; Export Coordination<ul><li>Process local manufacturing orders &amp; plan production resources with the production management and operations teams to ensure deadlines are met.</li><li>Coordinate dispatch, invoicing, delivery notes.</li><li>Prepare export documentation:</li><li>Commercial Invoice</li><li>Packing List</li><li>COO (Chamber of Commerce)</li><li>Certificates required by destination countries</li><li>Communicate with international distributors &amp; clients on documentation needs.</li><li>Assist the sales team with product details, compliance copies, and marketing documentation.</li></ul>Skills &amp; Qualifications Needed Education<ul><li>BSc / MSc in Chemistry, Biochemistry, Pharmacy, or Industrial Engineering preferred.</li><li>OR strong experience in cosmetics, FMCG, pharma, or chemical industry.</li></ul>Experience<ul><li>3&ndash;7 years in:</li><li>Regulatory affairs</li><li>Cosmetics/pharma manufacturing</li><li>Operations &amp; compliance</li><li>Export documentation (bonus)</li></ul>Key Skills<ul><li>Strong documentation abilities</li><li>Familiarity with Pakistan&rsquo;s regulatory authorities (DRAP, PSQCA, SEPA)</li><li>Understanding of GMP / ISO 22716 standards</li><li>Good command of English for international submissions</li><li>Ability to manage workers &amp; factory routines</li><li>Organized, proactive, and detail-oriented</li></ul>Job Type: Full-timePay: Rs60,000.00 - Rs95,000.00 per monthWork Location: In person

Regulatory, Compliance & Factory Operations Manager

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

Bayer

<div>
 <ul>
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 Executing complex field trials across corn and rice and multiple sites to deliver high-quality data to enable accurate and timely decisions in the advancement of products through the pre-commercial and breeding pipelines.
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 Ensure field testing innovation strategy and plans in place to enable and advance data science driven Precision Breeding.
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 Support evaluate mission team outcomes linked to Product Unit outcomes on all aspects related to field testing - field selection, grower management, field plot management, data collection, contribute to highest data quality.
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 Support end to end activities related to Mechanisation to support the team with timely deployment of breeding equipment for supporting field operations which involves procurement, maintenance, breakdown handling etc.
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 Actively lead and execute an innovative project/strategies developed by collaborating with stakeholders exhibiting defined LIFE attributes.
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 </ul>
 
 
 
 
 
 YOUR TASKS &amp; RESPONSIBILITIES:
 
 
 
 
 
 
 
 
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 Geographies to cover: Okara, Depalpur, Pakpathan with a plot load of ~9 K.
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 Responsible for implementation of product characterization strategy and Implementation of field testing (FT) operations and support services to deliver product pipelines in alignment with global and regional FT strategy.
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 Serve as a member of Pakistan Breeding delivering the pre-commercial Corn seed pipelines and product advancement processes and decision in Pakistan.
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 Execute field testing activities as per aligned trial plan - Trials, Data capture and Data return etc. through mechanisation and automation, contributing to efficient data driven advancement decisions. Deliver the highest data quality through the work of the employees in the organization with the use of new technology and processes. Strategically implement new technologies that drive a step-change in Breeding phenotyping, planting and harvesting processes through a partnership with automated engineering, IT, data science, and external vendors.
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 Responsible for all day-to-day operations of the testing program as well as the general operations of a multi-location testing programs. Support ineffective administration of testing responsibility, including temporary/contract employee hiring, development, training and retention; budget management; and care of assets.
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 Support end to end activities related to Mechanisation at Depalpur Equipment hub to support the team with timely deployment of breeding equipment for supporting field operations which involves procurement, maintenance, breakdown handling etc.
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 Overnight travel during the planting and harvest season is possible, wherever needed. Several 2-3 days of travel for training and other meetings are likely during the year.
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 Implementation and ensuring compliance of company/functional polices on Environment, Safety and Health, Quality Management Systems and stewardship across testing locations.
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 Partner closely with Field Testing Technical unit mission teams to implement new technologies that drive a step-change in Breeding phenotyping, planting and harvesting processes through a partnership with automated engineering, IT, data science, and external vendors to improve operational efficiencies in coordination with FT Technical Unit to advance Precision Breeding.
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 Manage hybrid import, set creation, logistics, Trait Hybrid Registration process and DUS characterization, IT tools &amp; new platforms for Breeding, plant health projects, DEKALB and Coordinate trainings. Coordinate with Govt. Scientific officers for Knowledge &amp; Learning center their visit.
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 Transfer knowledge of new deployments to Market Development, Marketing, Product Management &amp; sales colleagues and ensure information flow on commercial inputs and gaps to internal breeding teams.
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 </ul>
 
 
 
 
 
 
 
 
 WHO YOU ARE:
 
 
 
 
 
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 MS in Agriculture or related field of study with 2-5 years of significant people and project management experience in an agricultural-related researchposition.
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 Relavant field experience in trialing of agricultural/horticultural crops.
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 Advanced computer skills and excellent knowledge of software related to data acquisition and analysis.
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 Expertise in handling handling equipment, tools and technologies contributing to data management, acquisition, organization, analysis.
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 Expected attributes: Coordination, Communication, Planning, Proactiveness, Interpersonal relationship.
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 </ul>
 
 
 
 
 
 YOUR APPLICATION:
 
 
 
 
 
 
 Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer.
 
 
 
 
 
 To all recruitment agencies: Bayer does not accept unsolicited third-party resumes.
 
 
 
 
 
 Bayer is an Equal Opportunity Employer/Disabled/Veterans
 
 
 
 
 
 Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below.
 
 
 
 
 
 
 Location:
 
 Depalpur, Okara, Punjab, Pakistan
 
 
 
 
 
 
 Division:
 
 Crop Science
 
 
 
 
 
 
 Deadline:
 
 December 07, 2025
 
</div>

Territory Operation Manager

PerksHR

OB DESCRIPTIONPurpose of the Role:The Chief Compliance Officer (CCO) is responsible for ensuring that the organization&rsquo;s operations and processes are fully compliant with all applicable laws, regulations, and internal policies. The role ensures that departmental objectives are achieved in a timely manner, aligned with the organization&rsquo;s strategic goals. The CCO also provides strategic compliance guidance to the Board, CEO, and senior management while fostering a culture of ethics, integrity, and responsible business conduct.Key Responsibilities :1. Strategic Compliance Leadership<ul><li>Develop and execute the enterprise-wide compliance strategy and roadmap aligned to corporate objectives</li><li>Provide strategic guidance to Board, CEO, and senior management on compliance trends, regulatory changes, and</li></ul>risk exposure2. Regulatory Liaison &amp; Governance<ul><li>Act as primary contact with regulators; manage regulatory audits, inspections, and reporting</li><li>Ensure full compliance with regulatory frameworks, laws, and industry standards</li><li>Support Board Governance and ensure strong relationships with regulatory bodies</li></ul>3. Policy &amp; Framework Development<ul><li>Develop, implement, and regularly update compliance policies, SOPs, and ethical standards</li><li>Establish company-wide governance and compliance standards and processes</li></ul>4. Monitoring, Audits &amp; Risk Management<ul><li>Oversee compliance monitoring, audits, testing, and control reviews</li><li>Lead enterprise compliance risk assessment and controls evaluation programs</li><li>Ensure identification, escalation, and timely remediation of compliance issues</li></ul>5. Ethics &amp; Culture<ul><li>Promote a culture of legal, ethical, and responsible business conduct</li><li>Drive ethics, anti-bribery, AML, data privacy, and whistleblower programs</li></ul>6. Training &amp; Capacity Building<ul><li>Develop compliance capability across all departments through structured training</li><li>Build and lead a high-performing compliance team; mentor department heads</li></ul>7. Reporting<ul><li>Present compliance reports, dashboards, and risk updates to Board Committees</li><li>Maintain documentation and reporting cycles aligned to regulatory and internal needs</li></ul>Requirements:<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in a relevant field.</li><li>10&ndash;15 years of experience in governance or legal roles (preferably in Insurance/Financial Services).</li><li>Strong interpersonal and negotiation skills.</li><li>Conflict management and critical thinking abilities.</li><li>High integrity and professional ethics.</li><li>Internal coordination with all departments.</li><li>External coordination with relevant regulatory authorities.</li><li>Decision-making as per management approval.</li></ul>Job Type: Full-timePay: Rs400,000.00 - Rs409,500.00 per monthWork Location: In person

Chief Compliance Officer

AEG Consulting

Position: Regulatory Officer Industry: Pharmaceutical Location: Karachi Job Type: Full-timeWe are seeking a knowledgeable and detail-oriented Regulatory Officer to support regulatory affairs and ensure full compliance with national and international pharmaceutical guidelines.Key Responsibilities<ul><li>Prepare, compile, and submit regulatory dossiers for drug registration, renewals, and variations.</li><li>Ensure compliance with DRAP (Drug Regulatory Authority of Pakistan) and other relevant global regulatory guidelines (FDA, WHO, ICH where applicable).</li><li>Maintain and update regulatory documentation, product files, and technical records.</li><li>Coordinate with R&amp;D, Quality Assurance, Quality Control, and Production teams to gather required data.</li><li>Track and manage timelines for submissions, approvals, and regulatory commitments.</li><li>Review and approve product labels, packaging, leaflets, and promotional materials to ensure regulatory accuracy.</li><li>Support internal and external audits, including GMP inspections.</li><li>Monitor changes in pharmaceutical regulations and communicate updates to relevant teams.</li><li>Ensure timely renewal of registrations, licenses, certifications, and regulatory submissions.</li></ul>Requirements<ul><li>Bachelor&rsquo;s/Master&rsquo;s degree in Pharmacy (Pharm-D preferred).</li><li>Minimum 1&ndash;3 years of experience in Regulatory Affairs within the pharmaceutical industry.</li><li>Strong knowledge of DRAP rules, GMP guidelines, and ICH standards.</li><li>Excellent documentation, dossier preparation, and technical writing skills.</li><li>Ability to manage deadlines and work cross-functionally.</li><li>Strong communication and attention to detail.</li></ul>Job Type: Full-timePay: Rs80,000.00 - Rs100,000.00 per monthWork Location: In person

Regulatory Officer – Pharmaceutical Industry

Explore 706+ Regulatory affairs manager in Karachi this December. Find roles across top companies and apply now to boost your career.