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Pharmaceutical Lahore

Key Responsibilities:<ul><li>Prepare, review and compile regulatory submission dossiers for new product registrations and renewals.</li><li>Ensure compliance with national drug regulatory authority guidelines, packaging &amp; labelling requirements, and pharma regulations.</li><li>Maintain regulatory filings, track regulatory changes and proactively update internal teams on implications.</li><li>Liaise with QA/RA, production, marketing and external regulatory agents/distributors as required.</li><li>Support post-approval changes, variations, and ensure documentation is maintained and audit-ready.</li></ul>Requirements:<ul><li>Pharm-D from a recognized institution.</li><li>2&ndash;5 years&rsquo; experience in regulatory affairs or business development in the pharmaceutical industry.</li><li>Good understanding of regulatory submission formats (ACTD/CTD preferred) and life-cycle management.</li><li>Strong organizational, analytical and communication skills; able to work with cross-functional teams.</li><li>Proficient in MS Office (Word, Excel, PowerPoint) and able to maintain regulatory databases/tracking systems.</li></ul>Job Type: Full-timeApplication Question(s):<ul><li>Please mention your current monthly salary.</li><li>What is your expected monthly salary for this position?</li><li>How many years of relevant work experience do you have in related field?</li><li>Where are you currently residing (city and area)?</li><li>If selected, how soon can you join?</li></ul>Work Location: In person

Regulatory Executive

Star Laboratories (Pvt.) Ltd.

Position: Senior Regulatory Officer (CTD &amp; ACTD) Experience: 1&ndash;2 Years Gender: Female Education: Pharm-D Location: Multan Chung Road, Lahore<ul><li>Preparation and compilation of CTD &amp; ACTD dossiers for product registration.</li><li>Coordination with R&amp;D, QA, and Production teams for required documents and technical data.</li><li>Review and ensure compliance with regulatory guidelines.</li><li>Maintain up-to-date knowledge of DRAP and international regulatory requirements.</li><li>Assist in responding to regulatory queries and variations.</li></ul>Job Type: Full-timeWork Location: In person

Sr. Regulatory Officer

Education &amp; Experience:<ul><li>MSc (Chemistry) or Pharm-D (Doctor of Pharmacy) from HEC-recognized institution.</li><li>Minimum Experience 3 to 4 years</li><li>Candidates with pharmaceutical experience preferred; must not be currently enrolled in studies</li></ul>Responsibilities:<ul><li>Responsible for CTD dossier preparation, method validation and verification, and ensuring compliance with QC protocols and regulatory standards in pharmaceutical analysis.</li><li>Also responsible about CTD Dossiers and Reports</li></ul>Job Locations: Multan Road, Chung LahoreJob Type: Full-timeWork Location: In person

Sr. QC Analyst (Validation)

Pacific Pharmaceuticals

Pacific Pharmaceuticals has been producing and marketing quality pharmaceuticals strictly in compliance with GMP Rules and Regulations and WHO Standards, for more than three decades and serving the nation with world class medicines.Requirements:<ul><li>Doctor of Pharmacy (Pharm-D)</li><li>Up to 1 year experience in a pharmaceutical company.</li><li>Basic knowledge of GMP, SOPs, cGMP, documentation standards, and regulatory requirements.</li><li>Good attention to detail, ability to identify discrepancies.</li><li>Good communication skills (verbal &amp; written).</li><li>Willingness to learn, adapt, and maintain integrity &amp; quality mindset.</li></ul>Job Type: Full-timeWork Location: In person

QA Officer

A.S Global HR Services & Solutions

Job type: In-office Job Locatio: Our client have thier head office in Kharian but after intial 2-3 months training candidates can continue from Islamabad or Lahore officeGlobal Expansion Executives - Basic Job Description:<ul><li>Project Management for all Projects related to the Expansion of the Company's Business</li></ul>into New Countries.<ul><li>Research on the Regulatory Requirements for the Licensing &amp; Running Company</li></ul>Operations.<ul><li>Research and Engagement with Various Consultancy Firms and Legal Firms.</li><li>Comparative Analysis / Feasibility Reports for Internal Approvals.</li><li>Preparation of Business Plan Documents for Visibility on New Business Operations.</li><li>Documentation related to Licensing &amp; Acquisitions.</li><li>Research in multiple countries for New Ventures and Acquisitions.</li><li>Project Management and Trackers to present ongoing performance.</li><li>Strong Relationship Management with the affiliated business partners.</li><li>Perform other duties in the Relationship &amp; Development Department as assigned</li></ul>Skills Required:<ul><li>Excellent Project Management</li><li>Research &amp; Analytical Reporting</li><li>Business Communication</li><li>Excellent Command of the English Language.</li><li>Presentation Skills</li></ul>Fill the following form &quot;https://forms.gle/ihBV2vHUGWQfAE3a6&quot;Job Type: Full-timeApplication Question(s):<ul><li>Have you filled the form whose link is given in job detail?</li></ul>https://forms.gle/ihBV2vHUGWQfAE3a6<ul><li>As mentioned in job details &quot;Our client have thier head office in Kharian but after intial 2-3 months training candidates can continue from Islamabad or Lahore office&quot; so are you ok with that?</li></ul>Work Location: In person

Global Expansion Executive

The Design Logic

Job Description Position Title: Manager &ndash; Policy, Advocacy &amp; Government Relations Location: Johar Town, J Block, Lahore Timings: 10:00 AM to 6:00 PM (Monday to Saturday) Salary Range: PKR 150,000 &ndash; 200,000 per monthAbout the Role Pakistan Solar Association (PSA) is seeking a dynamic and experienced professional to lead its policy, regulatory, and government affairs initiatives. The ideal candidate will drive PSA&rsquo;s engagement with key stakeholders including NEPRA, AEDB, FBR, DISCOs, and relevant government ministries, advocating for sustainable solar energy policies in Pakistan.Key Responsibilities<ul><li>Lead PSA&rsquo;s policy engagement and representation with government and regulatory bodies.</li><li>Draft policy papers, position statements, and regulatory submissions.</li><li>Represent PSA in official meetings, government forums, and industry discussions.</li><li>Build and maintain strong relationships with stakeholders in government, regulatory authorities, and the energy sector.</li><li>Monitor and analyze energy sector regulations, policies, and reforms relevant to solar energy.</li><li>Collaborate with internal teams and industry members to align advocacy goals.</li><li>Prepare reports, summaries, and communication material to support policy initiatives.</li></ul>Requirements<ul><li>Bachelor&rsquo;s or master&rsquo;s degree in public policy, Law, Political Science, or related field.</li><li>5&ndash;7 years of proven experience in public policy, regulatory affairs, or legal advisory, preferably in the energy or renewable sector.</li><li>Strong understanding of Pakistan&rsquo;s energy, regulatory, and policy environment.</li><li>Excellent communication, drafting, and stakeholder engagement skills.</li><li>Demonstrated ability to represent organizations at senior government and industry levels.</li></ul>Why Join PSA<ul><li>Opportunity to shape the future of Pakistan&rsquo;s renewable energy sector.</li><li>Work in a leading national association representing the solar industry.</li><li>Competitive salary package and professional growth opportunities.</li><li>Growth your career and face a different new challenge</li></ul>To Apply: Send your updated CV to contact.hirewithar@gmail.com with the subject line: &ldquo;Manager &ndash; Policy, Advocacy &amp; Government Relations &ndash; PSA&rdquo;Job Type: Full-timePay: Rs150,000.00 - Rs200,000.00 per monthApplication Question(s):<ul><li>Have you read the job description carefully?</li><li>You should apply for this position only if you have 5 to 7 years of relevant experience. if yes then apply</li><li>This position is entirely on-site and does not offer a work-from-home option. Are You agree?</li></ul>Work Location: In person

Manager – Policy, Advocacy & Government Relations

Byonyks Pvt Ltd

We&rsquo;re Hiring! - Quality Engineer (Mechanical) (02 Positions)Location: DHA Phase 3, LahoreExperience: Fresh to 2 yearsDepartment: QA/RA DepartmentPosition Summary:We are seeking a highly motivated and detail-oriented Quality Engineer (Mechanical) to join our Quality Assurance and Regulatory Affairs Department. The ideal candidate will ensure that our medical devices comply with applicable ISO 13485 and FDA 21 CFR Part 820 quality management system (QMS) requirements. This role focuses on process and product quality assurance&mdash;not quality control or calibration activities.Key Responsibilities:<ul><li>Develop, implement, and maintain quality system processes in alignment with ISO 13485 and FDA 21 CFR Part 820 requirements.</li><li>Support the creation, review, and continuous improvement of Standard Operating Procedures (SOPs), work instructions, and quality documentation.</li><li>Participate in risk management activities (e.g., per ISO 14971), including FMEA and design risk analysis.</li><li>Collaborate with cross-functional teams (R&amp;D and Manufacturing) to ensure design and process validation are compliant with regulatory standards.</li><li>Lead and support internal audits and prepare for external audits by regulatory authorities and certification bodies.</li><li>Manage CAPA (Corrective and Preventive Actions), non-conformance investigations, and root cause analyses to prevent recurrence of issues.</li><li>Ensure change control processes are effectively implemented and documented in compliance with regulatory requirements.</li><li>Support document control and ensure that device history records (DHR), design history files (DHF), and technical files are maintained properly.</li><li>Contribute to supplier quality management activities, including supplier qualification, performance monitoring, and audits.</li><li>Participate in post-market surveillance and complaint handling processes as required.</li><li>Assist in regulatory submissions and compliance reviews related to product development and lifecycle management.</li></ul>Qualifications:<ul><li>Bachelor&rsquo;s degree in Mechanical Engineering or a related engineering discipline.</li><li>Fresh to 3 years of experience in quality assurance within the medical device or regulated manufacturing industry.</li></ul>Skills and Competencies:<ul><li>Excellent documentation skills with the ability to prepare, review, and maintain quality records in compliance with regulatory standards.</li><li>Highly proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) for data analysis, reporting, and documentation.</li><li>Strong analytical and logical thinking capabilities to identify issues, interpret data, and propose effective solutions.</li><li>Highly detail-oriented with exceptional accuracy in reviewing technical and quality-related documentation.</li><li>Excellent attention to detail and organizational skills to ensure compliance with ISO 13485 and FDA 21 CFR Part 820 requirements.</li><li>Logical thinker with the ability to approach problems methodically and ensure sound decision-making based on evidence and data.</li></ul>Why Join Us?<ul><li>Work on cutting-edge R&amp;D projects with real-world impact</li><li>Collaborative and innovation-driven engineering environment</li><li>Fuel Card provided for commuting support</li><li>Comprehensive Health Coverage &ndash; including OPD, IPD, and Life Insurance</li><li>Leave Encashments every quarter</li><li>Opportunities for continuous learning, growth, and cross-functional exposure</li></ul>Job Type: Full-timePay: Rs70,000.00 - Rs110,000.00 per monthEducation:<ul><li>Bachelor's (Required)</li></ul>Location:<ul><li>Lahore (Required)</li></ul>Work Location: In person

Quality Engineer (Mechanical)

Explore 315+ Regulatory affairs specialist in Lahore this November. Find roles across top companies and apply now to boost your career.