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regulatory affairs specialist

Medichem Enterprises

Regulatory Affairs Officer &mdash; Job DescriptionLocation: Karachi Reports To: Regulatory Affairs ManagerRole OverviewResponsible for maintaining DRAP compliance, supporting regulatory submissions, and providing key documentation and technical support for tenders and commercial operations.Key Responsibilities<ul><li>Prepare &amp; submit DRAP product registration, renewals, variations, and import permissions, NOC's</li><li>Maintain regulatory documents: certificates, technical files, IFUs, CEO declarations, etc.</li><li>Support tender submissions by providing updated DRAP certificates, import history, and compliance forms</li><li>Coordinate regulatory requirements with principals/manufacturers</li><li>Support Sales &amp; Procurement with regulatory status for institutional approvals and import planning</li><li>Maintain compliance to GDP and assist in audits/inspections</li></ul>Qualifications<ul><li>Degree in Pharm-D / Biomedical / Life Sciences</li><li>1&ndash;3 years relevant experience preferred</li><li>Knowledge of DRAP &amp; Medical Devices Rules 2017</li></ul>Skills<ul><li>Strong documentation &amp; communication skills</li><li>Proficient in MS Office</li><li>Detail-oriented and organized</li></ul>Job Type: Full-timePay: Rs40,000.00 - Rs65,000.00 per monthWork Location: In person

Regulatory Affairs Officer

K-Electric

<div>
 
 
 Purpose
 
 :
 
 
 To facilitate Regulatory Affairs team in day-to-day operations.
 
 
 
 
 
 
 Areas Of Responsibility:
 
 
 
 &bull; Assist in preparation of regulatory submissions and correspondence related to NEPRA based on detailed assessment of regulatory changes and its possible implications for KE.
 
 
 &bull; Provide support in addressing queries / drafting responses regarding on-going regulatory proceedings.
 
 
 &bull; Provide support to the line manager in ensuring regulatory compliance in consultation with internal stakeholders.&bull; Ensure timely and correct submission of Generation Concurrence cases to NEPRA after thorough scrutiny of received cases from Net Metering team
 
 
 &bull; Provide support to line manager / HoD on ad hoc assignments
 
 
 
 
 
 
 Required Education:
 
 
 
 &bull; Bachelors in relevant field
 
</div>

Project Trainee

<div>
 
 Purpose
 
 
 
 To facilitate Regulatory Affairs team in day to day operations.
 
 
 
 Areas Of Responsibility
 
 
 
 <ul>
 <li>
 Assist in preparation of regulatory submissions and correspondence related to NEPRA based on detailed assessment of regulatory changes and its possible implications for KE.
 </li>
 <li>
 Provide support in addressing queries / drafting responses regarding on-going regulatory proceedings.
 </li>
 <li>
 Provide support to the line manager in ensuring regulatory compliance in consultation with internal stakeholders.
 </li>
 <li>
 Ensure timely and correct submission of Generation Concurrence cases to NEPRA after thorough scrutiny of received cases from Net Metering team
 </li>
 <li>
 Provide support to line manager / HoD on ad hoc assignments
 
 
 </li>
 </ul>
 
 Required Education
 
 
 
 <ul>
 <li>
 Bachelors in relevant field
 </li>
 </ul>
</div>

AEG Consulting

Industry: Medical DevicesAbout the RoleWe are seeking a detail-oriented Regulatory Compliance Officer responsible for ensuring full compliance with the requirements of the Drug Regulatory Authority of Pakistan (DRAP).The ideal candidate will maintain an in-depth and continuously updated understanding of DRAP regulations, ensure internal systems align with regulatory standards, and prepare the organization for successful external audits.This role is critical in maintaining licensing integrity, operational compliance, and audit readiness across all relevant functions.Key Responsibilities<ul><li>Maintain up-to-date knowledge of all DRAP regulations, guidelines, and compliance updates</li><li>Ensure organizational processes, documentation, and operations meet regulatory requirements</li><li>Conduct regular internal compliance audits to identify gaps and non-conformities</li><li>Develop and implement corrective and preventive actions (CAPA) for audit findings</li><li>Prepare all documentation and systems for external regulatory inspections and audits</li><li>Liaise with internal departments to ensure adherence to SOPs and regulatory frameworks</li><li>Maintain complete and audit-ready compliance documentation and records</li><li>Monitor regulatory changes and communicate updates to relevant stakeholders</li><li>Support quality assurance functions in maintaining compliance standards</li></ul>Required Skills &amp; Knowledge<ul><li>Strong understanding of DRAP regulatory framework and pharmaceutical compliance systems</li><li>Knowledge of Good Manufacturing Practices (GMP) and audit procedures</li><li>Experience in internal audits, compliance checks, or regulatory inspections</li><li>Strong documentation, reporting, and analytical skills</li><li>Ability to interpret regulatory guidelines and translate them into operational requirements</li><li>High attention to detail and structured thinking</li><li>Experience in pharmaceutical or medical device industries</li></ul>Preferred Experience<ul><li>1&ndash;5 years in regulatory affairs, quality assurance, or compliance roles</li></ul>Work Environment<ul><li>Professional, compliance-driven organizational setting</li><li>Cross-functional coordination with QA, production, and management teams</li></ul>Why Join Us<ul><li>Direct involvement in regulatory compliance and audit readiness</li><li>Exposure to DRAP inspection processes and industry best practices</li><li>Opportunity to strengthen expertise in pharmaceutical regulatory systems</li></ul>Pay: Rs70,000.00 - Rs90,000.00 per monthWork Location: In person

Regulatory Compliance Officer (DRAP Compliance Specialist)

Pakistan Single Window

<div>This position is being recruited by Pakistan Single Window (PSW) on behalf of the National Agri-Trade and Food Safety Authority (NAFSA). NAFSA is being established as a strategic national initiative to strengthen Pakistan&rsquo;s agri-trade ecosystem through enhanced regulatory oversight, facilitation, and modernization of food safety and trade processes. The selected candidate will be part of NAFSA&rsquo;s foundational team, contributing to the development of systems, processes, and institutional capabilities.
Responsibilities:<ul><li>
Manage pesticide product registration processes, including new registrations, amendments, renewals, and regulatory actions as notified.</li><li>
Implement scientific review of efficacy, toxicology, environmental fate, residues, and labelling data received from risk assessment and pesticide studies experts.</li><li>
Ensure product registration decisions are science-based and risk-informed, with appropriate documentation and rationale.</li><li>
Maintain national pesticide product registers, approval records, and decision histories with strong version control.</li><li>
Coordinate with risk assessment and pesticide studies functions to resolve data gaps and ensure completeness of dossiers.</li><li>
Prepare decision briefs, regulatory notices, and communication to applicants and stakeholders on product registration outcomes.</li><li>
Support post-registration reviews and regulatory updates based on surveillance, studies, or emerging risks.</li><li>
Perform any other responsibilities assigned by the reporting officer in support of NAFSA's mandate.</li></ul> 

Requirements 
Education:<ul><li>
M.Sc. (Hons.) / MPhil (minimum eighteen years of education) in Agriculture (Plant Protection/Entomology/Plant Pathology, Weed Science), Chemistry/Toxicology, Environmental Sciences, or equivalent.</li></ul> 
Experience:<ul><li>
Minimum 8 years of relevant experience in pesticide product evaluation, regulatory review, risk assessment support, or related fields.</li></ul>
For contact, kindly reach out to hr.support@psw.gov.pk.</div>

Deputy Director (Product Registration - Pesticides) | NAFSA

Yousuf Adil (Chartered Accountants)

Job Title: Senior Manager &ndash; Corporate Affairs Location: KarachiDepartment: Tax and LegalJob Summary:Yousuf Adil, Chartered Accountants is seeking a competent and experienced Senior Manager &ndash; Corporate Affairs to lead and manage corporate secretarial and legal compliance functions. The role requires hands-on expertise in statutory requirements and corporate advisory under the Companies Act, 2017 and other related Rules and Regulations and other applicable laws related to the Listed/ Unlisted/Private companies/ Liaison and Branch offices and making representations before the Securities and Exchange Commission of Pakistan (SECP), Board of Investment (BOI) and Stock Exchange (PSX).The incumbent will be responsible for managing end-to-end corporate matters along with liaising with regulatory authorities and ensuring adherence to corporate governance best practices.Key Responsibilities:<ul><li>Manage and oversee statutory and regulatory compliances, handling end-to-end corporate secretarial matters for listed and unlisted entities, including regulatory filings and documentation.</li><li>Liaise and represent clients before regulatory authorities including SECP, PSX, and other relevant bodies.</li><li>Advise clients on corporate governance, compliance frameworks, and regulatory requirements.</li><li>Execute and manage complex corporate transactions and restructuring assignments, including but not limited to:</li></ul>-Incorporation of companies-Merger/Amalgamation/Reconstruction of companies-Winding up and De-registration of companies-Establishment of Branch and Liaison Offices of Foreign entities-Closure and De-registration of Branch and Liaison Offices of Foreign entities-Various modes of Winding up of companies-Issuance of Right Shares-De-listing of shares of companies-Conversion of status of companies-Change of management of companies-Any other corporate related assignment.<ul><li>Prepare and review legal documentation, resolutions, and regulatory submissions.</li><li>Stay updated with changes in corporate laws and ensure timely implementation within client engagements.</li></ul>Requirements:<ul><li>Strong knowledge and understanding of the Companies Act, 2017, and other related Rules and Regulations and other regulatory frameworks.</li><li>Hands-on experience in corporate secretarial functions, particularly for listed companies.</li><li>Proven expertise in handling regulatory filings, corporate restructuring, and corporate advisory.</li><li>Experience in representing matters before SECP, BOI, and PSX.</li><li>Excellent drafting, analytical, and communication skills.</li><li>Ability to manage multiple assignments and work independently in a fast-paced environment.</li></ul>Education &amp; Experience:<ul><li>Education: ACMA / ACCA / LLB / ACS or equivalent qualification.</li><li>Experience: 7+ years of relevant experience in corporate affairs, corporate secretarial, or legal roles, preferably within professional services or consulting firms.</li></ul>Job Type: Full-timePay: From Rs200,000.00 per monthApplication Question(s):<ul><li>Have you completed your qualification in ACMA / ACCA / LLB / ACS or equivalent field?</li><li>How many years of experience you have as a Company Secretary? </li><li>Do you have experience working with listed Companies? </li><li>Have you ever represent matters before SECP, BOI, and PSX?</li><li>What is your current salary? </li><li>What is your expected salary?</li><li>What will be your notice period? </li></ul>Experience:<ul><li>Corporate Secretary: 6 years (Required)</li></ul>Location:<ul><li>Karachi (Required)</li></ul>Work Location: In person

Senior Manager - Corporate Affairs

TAQWA PHARMA

We are seeking a highly organized and detail-oriented Program Coordinator to manage the complete operational and regulatory workflow of our healthcare access program. This role is strictly compliance-based and operational in nature; it does not involve direct selling, sales target achievement, or demand generation. The ideal candidate will be the central operational point of contact ensuring smooth regulatory approvals, documentation, and supply chain tracking.Key Responsibilities:<ul><li>Registration Management: Manage the end-to-end registration process for partnering hospitals and medical consultants.</li><li>Regulatory Compliance: Oversee the processing and securing of No Objection Certificates (NOCs) through the Drug Regulatory Authority of Pakistan (DRAP) and maintain all necessary regulatory documentation.</li><li>Financial Operations: Coordinate payment processing with finance department and ensure the timely submission of final banking documentation for import/clearance purposes.</li><li>Supply Chain Tracking: Handle pre-clearance procedures, monitor shipment statuses, and ensure accurate delivery tracking to the final destination.</li><li>Workflow Coordination: Actively follow up with internal teams, regulatory bodies, and external partners to prevent delays and ensure strict compliance with program guidelines.</li></ul>Required Skills &amp; Qualifications:<ul><li>Communication: Excellent verbal and written communication skills to effectively interact with consultants, banks, and regulatory authorities.</li><li>Technical Proficiency: Highly proficient in Microsoft Office (Excel, Word, PowerPoint) and professional email correspondence.</li><li>Time Management: Strong ability to prioritize tasks, meet strict regulatory deadlines, and manage time effectively.</li><li>Follow-Up &amp; Diligence: Exceptional follow-up skills with a proactive approach to resolving operational bottlenecks.</li><li>Prior experience in pharmaceutical administration, regulatory affairs, or supply chain operations is highly preferred.</li></ul>Location : Near Karachi Chamber of Commerce &amp; IndustryPay: Rs40,000.00 - Rs70,000.00 per monthEducation:<ul><li>Bachelor's (Required)</li></ul>Work Location: In person

Patient Program Coordinator

Explore 350+ Regulatory affairs specialist in Karachi this May. Find roles across top companies and apply now to boost your career.

350 regulatory affairs specialist jobs In Karachi

Regulatory Affairs Officer

Project Trainee

Project Trainee

Regulatory Compliance Officer (DRAP Compliance Specialist)

Deputy Director (Product Registration - Pesticides) | NAFSA

Senior Manager - Corporate Affairs

Patient Program Coordinator