quality assurance manager Jobs in Karachi

quality assurance manager

regulatory co ordinator(evening shift) Jobs in Karachi

regulatory co ordinator(evening shift)

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assistant manager industry affairs Jobs in Karachi

assistant manager industry affairs

assistant manager, risk and compliance (mergers and acquisitions ) -night shift Jobs in Karachi

assistant manager, risk and compliance (mergers and acquisitions ) -night shift

regulatory affairs manager

Amros Pharmaceuticals

Regulatory Affairs Officer.We seek a highly motivated individual with a Doctor of Pharmacy (PharmD) degree and 6 months to 1 year of experience in the pharmaceutical industry (Regulatory Affairs or a related function preferred).Key ResponsibilitiesAssist in compiling and submitting CTD/eCTD dossiers to health authorities.Support the coordination of responses to regulatory agency queries.Research and monitor global regulatory guidelines (ICH, FDA, EMA) for compliance.Maintain accurate regulatory documentation and archives.RequirementsPharmD degree.6-12 months of relevant pharma industry experience.Strong attention to detail and excellent communication skills.Job Type: Full-timeWork Location: In person

Regulatory Affairs Officer

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

<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

ACCA Careers

<div>
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 Manage statutory filings with the Securities and Exchange Commission of Pakistan (SECP), corporate compliance, and regulatory reporting.
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 Facilitate Board of Directors&rsquo; meetings, including drafting agendas, circulating board packs, and recording minutes.
 </li>
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 Ensure compliance with the Companies Act, Corporate Governance Regulations, and SECP directives.
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 Maintain and update corporate records, including Memorandum &amp; Articles of Association, bylaws, statutory registers, and board resolutions.
 </li>
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 Act as a liaison between the Company, the SECP, and other government authorities.
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 Manage and conduct Annual General Meetings (AGMs) and Extraordinary General Meetings (EGMs), including preparation of notices, proxy statements, and statutory documents.
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 Oversee timely preparation of financial statements in accordance with International Financial Reporting Standards (IFRS) and regulatory requirements. Monitor audit processes and coordinate with internal and external auditors.
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 Ensure compliance with tax laws, including filing income tax and withholding statements, and manage liaison with tax authorities.
 </li>
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 Develop and implement financial controls, standard operating procedures (SOPs), and risk management frameworks.
 </li>
 </ul>
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Company Secretary

PPT Square

K4 Global is the back-office service provider, we make sure company provides the best services to our customer that encourage them to focus on growth. This is the one of the key position in the company, the person will be responsible not just to meet the UK compliances but also will ensure that we have implemented that in our operations.<ul><li>Manage regulatory filings, licenses, renewals, and other corporate documentation.</li><li>Liaise with government departments, external agencies, and industry associations.</li><li>Support the preparation and review of legal documents, contracts, and governance records.</li><li>Coordinate and manage internal and external audits from regulatory agencies.</li><li>Monitor, interpret, and report on new regulations impacting the automotive industry.</li><li>Implement existing SOPS and create new if needed in coordination of departmental heads.</li><li>Continue audit all the departments to make sure SOPs are being followed</li><li>Prepare compliance reports and recommend corrective or preventive actions where required</li></ul>Job Type: Full-timePay: Rs100,000.00 - Rs130,000.00 per monthEducation:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>Compliance: 2 years (Required)</li></ul>Language:<ul><li>English (Required)</li></ul>Work Location: In person

Complaince and Quality Control officer

Simpaisa

<div>
 Simpaisa a global consumer fintech firm, is looking for a Regulatory Affairs Analyst who will support the Global Head of Regulatory Affairs by researching, analyzing, and tracking changes in global regulations that impact Simpaisa operations. The analyst will play a critical role in ensuring that the companys policies are up-to-date and aligned with evolving regulatory requirements. This role will also assist in managing relationships with regulatory bodies.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Regulatory Research and Analysis:
 </li>
 <li>
 Conduct research on global regulatory developments in key jurisdictions.
 </li>
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 Monitor legislative and regulatory developments across key regions and fintech verticals.
 </li>
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 Analyze the impact of new and updated regulations on Simpaisa's operations and suggest the Global Head on necessary adjustments to compliance frameworks.
 </li>
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 Regulatory Risk Assessment:
 </li>
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 Assess potential regulatory risks and develop recommendations for mitigation strategies.
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 Collaborate with internal teams to ensure the companys operations are adaptable to new regulatorychanges.
 </li>
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 Regulatory Reporting and Documentation:
 </li>
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 Assist in preparing regulatory reports, submissions, and filings required by government bodies and financial authorities.
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 Ensure that all regulatory documentation is accurate, comprehensive, and in compliance with legal requirements.
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 Track and report on the progress of regulatory matters and compliance projects.
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 Support in Regulatory Affairs Initiatives:
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 Assist in preparing presentations and reports for senior management on regulatory matters.
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 Draft consultation responses, regulatory briefings, white papers, and position notes for internal and external audiences.
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 Provide support for compliance audits, meetings with regulators, and policy discussions.
 </li>
 <li>
 Stakeholder Communication:
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 Support the Global Head of Regulatory Affairs in liaising with policymakers, regulators, government agencies, and industry groups.
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 Assist in managing Simpaisas regulatory relationships with external regulatory bodies and stakeholders.
 </li>
 <li>
 Regulatory Knowledge Management:
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 Maintain a knowledge base of relevant regulatory frameworks and guidelines.
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 Maintain a global regulatory watch-list and internal updates for executive and product teams.
 </li>
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 Ensure the company is aware of emerging regulatory trends and developments.
 
 
 
 </li>
 </ul>
 
 Key Performance Indicators (KPIs):
 
 
 
 1. Accuracy and timeliness of regulatory research and analysis.
 
 
 2. Number of regulatory changes tracked and reported.
 
 
 3. Number of successful regulatory submissions made on time.
 
 
 4. Stakeholder satisfaction with regulatory reports and communication.
 
 
 5. Number of risks identified and documented.
 
 
 
 Key Qualifications:
 
 
 
 Education: Bachelors degree in Law, or Master in Public Policy, Business, Economics, Finance,or a related field.
 
 
 
 Experience:
 
 
 
 <ul>
 <li>
 3+ years of experience in regulatory affairs, compliance, or legal analysis, preferably in the fintech or financial services industries.
 </li>
 <li>
 Experience drafting public policy papers and working with financial regulatory stakeholders.
 
 </li>
 </ul>
</div>

Regulatory Policy Analyst

Minerva Research Solutions

<div>
 
 Company Overview:
 
 
 
 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.
 
 
 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.
 
 
 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.
 
 
 
 Job Purpose:
 
 
 
 The Coordinator - Regulatory Affairs is responsible for working as a team member of regulatory professionals in ensuring regulatory compliance of company products and activities, including the preparation and submission of regulatory documents, the management of regulatory inspections, and the development and implementation of regulatory strategies.
 
 
 
 Key Responsibilities:
 
 
 
 <ul>
 <li>
 Working as a regulatory professional to ensure effective and efficient regulatory support for the company's products and activities
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 Develop and implement regulatory strategies that support the company's business objectives and ensure compliance with relevant regulations and guidelines
 </li>
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 Manage the preparation and submission of regulatory documents, including regulatory filings, registrations, and certifications
 </li>
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 Coordinate and manage regulatory inspections and audits, and ensure appropriate corrective and preventive actions are taken in response to any findings
 </li>
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 Keep abreast of changes in regulatory requirements and guidelines, and communicate these changes to relevant stakeholders in a timely manner
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 Build and maintain positive relationships with regulatory authorities and other external stakeholders
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 Provide regulatory guidance and support to cross-functional teams, including product development, clinical research, manufacturing, and quality assurance
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 Collaborate with internal and external stakeholders to develop and implement regulatory policies and procedures that support the company's overall goals and objectives
 </li>
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 Ensure timely and accurate reporting of regulatory activities and metrics
 
 
 </li>
 </ul>
 
 Qualifications:
 
 
 
 <ul>
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 Bachelor's degree in a scientific discipline, preferably in life sciences, chemistry, or pharmacy
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 01 years of experience in regulatory affairs, fresh graduates will also be preferred
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 In-depth knowledge of global regulatory requirements and guidelines for pharmaceuticals, medical devices, or other regulated products
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 Excellent communication, interpersonal, and problem-solving skills
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 Ability to work independently and manage multiple projects simultaneously
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 Strong attention to detail and accuracy
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 Experience working in a fast-paced, deadline-driven environment
 
 
 </li>
 </ul>
 
 Benefits:
 
 
 
 <ul>
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 Competitive salary and performance-based bonuses
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 Medical health insurance coverage
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 Employees Old-age benefits coverage
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 Professional learning and development support
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 Generous vacation and paid time off
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 Employee assistance programs for mental health
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 Company-sponsored events and team-building activities
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 Diverse, professional, and inclusive work environment
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 Opportunities for career growth
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 Cutting-edge technology and tools
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 Family-friendly policies, including parental leave
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 Commuter benefits or transportation assistance
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 Social responsibility and community involvement programs
 
 
 </li>
 </ul>
 
 Openings:
 
 
 
 04 positions
 
 
 Full-time
 
 
 On-site job
 
 
 
 Work Schedule Timings:
 
 
 
 Monday to Friday
 
 
 Evening Shift (07 PM to 03 AM)
 
 
 (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
 
 
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Regulatory Co Ordinator(Evening Shift)

Explore 612+ Regulatory affairs manager in Karachi this November. Find roles across top companies and apply now to boost your career.