What Jobs are available for Regulatory Compliance in Pakistan?

Position Title: Regulatory & Compliance Executive

Location: Main Shahra-e-Faisal, Karachi

Shift Timings: 06:00 PM to 03:00 AM PKT

Working Days: Monday to Friday

Employment Type: Full Time and Onsite

Position Overview:

The Regulatory & Compliance Executive will be responsible for assisting in the implementation, monitoring, and documentation of compliance programs to ensure the organization meets all industry regulations and standards. This role requires strong attention to detail, excellent communication skills, and the ability to work effectively with internal teams and external stakeholders.

Key Responsibilities:

• Assist in monitoring adherence to local, regional, and international regulatory requirements.
• Support the development and implementation of compliance policies and procedures.
• Participate in compliance audits and risk assessments.
• Prepare drafts of regulatory reports for submission to relevant authorities.
• Maintain accurate, updated documentation of compliance activities.
• Assist in tracking and reporting compliance metrics and potential issues.

Requirements:

• Graduate degree with 1–2 years of relevant experience (fresh graduates with strong skills may also be considered).
• Excellent written and verbal communication skills.
• Strong attention to detail and organizational abilities.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Ability to document, proofread, and maintain compliance records.
• Willingness to communicate with clients in the United States.
• Knowledge of U.S. regulatory requirements such as HIPAA, will be considered a strong plus.

Benefits:

• OPD and IPD Health facility for self, dependents, and parents
• Life Insurance Coverage for self
• Fuel Card for Male Employees
• Free Pick & Drop for Female Employees
• In-House Gym Facility
• Paid Leaves & US Holidays
• Referral Bonus

Job Type: Full-time

Application Question(s):

• Residential Area in Karachi?
• What is your current salary?
• What is your expected salary?
• Are you comfortable working in the evening shifts? 6:00 PM - 3:00 AM
• If selected? Would you be able to join immediately?

Work Location: In person

Department: Administration / Legal Affairs

Location: Rehmanabad, Rawalpinid

Employment Type: Full-Time, Rotational Shift / On-site

Report to: BOD's Chairman

CloudRexpo is seeking a Retired Colonel to oversee the company's legal, compliance, and administrative operations. The ideal candidate will uphold the highest standards of discipline, integrity, and professionalism while ensuring all company activities are conducted in accordance with legal requirements and internal policies.

This role demands a strategic thinker with strong leadership, administrative control, and legal acumen to safeguard the company's interests and maintain regulatory compliance.

Key Responsibilities:

• Oversee and manage all legal and compliance matters within the organization.
• Draft, review, and vet contracts, agreements, and official documents.
• Ensure compliance with all labor laws, corporate regulations, and government requirements.
• Represent the company in legal proceedings and liaise with external legal advisors.
• Maintain and update the company's legal records, documentation, and correspondence.
• Advise senior management on risk management, disciplinary procedures, and legal exposure.
• Ensure proper enforcement of company policies and SOPs across all departments.
• Handle property-related and contractual legal affairs when required.
• Provide legal and compliance training to relevant staff to ensure awareness and accountability.
• Foster a disciplined, transparent, and compliant organizational environment.

Qualifications & Experience:

• Retired Colonel (Pakistan Army) with strong administrative, disciplinary, or legal experience.
• Bachelor's or Master's degree in Law (LLB/LLM) preferred but not mandatory if relevant experience is proven.
• Minimum 5–10 years of professional experience, including leadership or compliance-related roles.
• Solid understanding of corporate, labor, and civil law.
• Excellent communication, negotiation, and documentation skills.
• High integrity, confidentiality, and attention to detail.

***Competitive market salary (to be finalized during the initial selection phase)

Job Type: Full-time

Pay: From Rs1.00 per month

Education:

• Bachelor's (Required)

Experience:

• Legal Complanice : 10 years (Required)

Language:

• English (Required)

Location:

• Rawalpindi (Required)

Work Location: In person

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 Responsibilities

Assist 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.

Requirements

PharmD degree.

6-12 months of relevant pharma industry experience.

Strong attention to detail and excellent communication skills.

Job Type: Full-time

Work Location: In person

Company Description

Founded in 2006, Novamed Pharmaceuticals is a leader in the pharmaceutical industry, known for its dedication to trust, excellence, and high-quality generic drugs. Our mission is to enhance the quality of life for our customers by manufacturing top-notch products, adhering to CGMP and Quality standards. We foster a result-oriented culture that promotes professional growth and well-rounded development for our employees. Novamed continuously invests in upgrading our facilities and systems, ensuring efficiency, productivity, and strong alliances with both national and multinational pharmaceutical companies. We are committed to providing safe and effective medicines while encouraging healthier lives worldwide.

Role Description

This is a full-time on-site role located in Lahore for a Manager of Regulatory Affairs. The Manager will be responsible for overseeing and ensuring regulatory compliance, preparing and submitting regulatory documents, and liaising with regulatory authorities. Daily tasks include managing regulatory submissions, ensuring product compliance with local and international regulations, and staying updated on regulatory changes. The Manager will also collaborate closely with Quality Control and Quality Assurance departments to achieve quality compliance goals.

Qualifications

• Regulatory Affairs knowledge and experience in the pharmaceutical industry
• Experience in preparing and submitting regulatory documents
• Strong understanding of CGMP and Quality standards
• Excellent communication and interpersonal skills
• Ability to work independently and collaboratively in a team setting
• Bachelor's degree in Pharmacy, Chemistry, or a related field
• Relevant certifications in Regulatory Affairs are a plus

Regulatory Affairs Officer - Karachi
The Regulatory Affairs Officer ensures compliance with
DRAP regulations
for licensing, registration, and marketing of medical devices, acting as the key link between Rech International and regulatory authorities.

Job Type: Full time - Onsite
Working hours: 9am - 6pm
Working Days: Monday - Saturday
Market Competitive Salary & Benefits
Key Responsibilities:

• Prepare, submit, and follow up on DRAP registration/notification dossiers.
• Manage licensing of medical devices (Orthopedic Implants, OMF, Neuro, Spine, Knee & Hip Joints).
• Liaise with DRAP officials and internal stakeholders to ensure timely approvals.
• Monitor and implement changes in DRAP regulations, keeping records updated.
• Ensure compliance of product portfolio with DRAP guidelines and legislation.
• Provide regulatory input, reporting, and support for internal teams and external partners.

Qualifications & Experience:

• Bachelors degree in Sciences; Masters preferred.
• 3-4 years experience in Regulatory Affairs with DRAP submissions.
• Strong knowledge of DRAP laws and guidelines for medical devices.
• Proficiency in MS Office & Google Apps.
• Excellent communication, analytical, and documentation skills.

Company Description

Epoch Pharmaceuticals, established in 1998, is located in the Korangi Industrial Area, Karachi, Pakistan. With a commitment to providing quality and affordable medicines, the company has obtained GMP quality standards and registrations from the Ministry Of National Health Pakistan. Epoch Pharmaceuticals specializes in the development, manufacturing, and sales of pharmaceutical products. The company collaborates with healthcare providers, government, and local communities to expand access to reliable and affordable healthcare worldwide. With over 170 registered products, Epoch Pharmaceuticals aims to help people do more, feel better, and live longer.

Role Description

This is a full-time, on-site role for a Regulatory Affairs Manager based in Karachi Division. The Regulatory Affairs Manager will be responsible for ensuring compliance with regulatory requirements, preparing and submitting regulatory documents, and managing quality systems. The role includes continuous monitoring and application of regulatory trends and ensuring that all products meet the necessary legal and regulatory standards.

Qualifications

• Experience in Regulatory Compliance and understanding of Regulatory Requirements
• Expertise in Regulatory Affairs, including preparing Regulatory Submissions
• Knowledge of establishing and maintaining Quality Systems
• Strong analytical and problem-solving skills
• Ability to work collaboratively with cross-functional teams
• Bachelor's degree in a relevant field such as Pharmacy, Biomedical Sciences, or a related discipline
• Experience in the pharmaceutical industry is a plus
• Excellent written and verbal communication skills

Responsibilities

• Prepare and submit CTD / ACTD dossiers for international markets, handle queries and follow up till registration.
• Ensure that all product registrations and submissions comply with applicable laws, guidelines, and industry standards.
• Prepare other supporting regulatory documents as required by foreign regulatory agencies.
• Collaborate with QA, QC, Production, and Export departments to gather accurate and up-to-date technical and manufacturing data for dossier completion.
• Maintain clear and continuous communication with international stakeholders regarding dossier status and updates.
• Maintain accurate and updated records of all submitted dossiers, correspondence, and regulatory approvals.

Qualifications

• Education: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences.
• 6 months to 1 year in regulatory affairs for the pharmaceutical industry.
• Proficiency in CTD format preparation and dossier compilation.
• Excellent written and verbal communication skills.
• Ability to work effectively under tight deadlines

Location:

18km Multan Road Lahore Pakistan

Email:

Job Type: Full-time

Pay: From Rs50,000.00 per month

Application Question(s):

• How much Relevant experience you have in Regulatory Affairs.

Education:

• Bachelor's (Preferred)

Location:

• Lahore (Preferred)

Work Location: In person

Job Title: Pharmacovigilance Officer

Department: Drug Safety / Regulatory Affairs

Location: Karachi, Korangi

Key Responsibilities:

• Collect, review, and assess adverse drug reaction (ADR) reports.
• Ensure timely entry and reporting of safety data to regulatory authorities.
• Maintain pharmacovigilance databases and documentation.
• Prepare periodic safety reports (e.g., PSURs, PBRERs).
• Monitor product safety and escalate risk signals as needed.
• Support audits, inspections, and compliance with global PV regulations.
• Collaborate with cross-functional teams on safety-related issues.

Requirements:

• Degree in Pharmacy
• Knowledge of pharmacovigilance processes and regulatory requirements.
• Strong attention to detail and documentation skills.

Job Type: Full-time

Application Question(s):

• Are you from karachi?
• Doo you have 2-3 years of experience in pharmacovigilance only?

Work Location: In person

We Are Hiring | Assistant Manager / Deputy Manager – Regulatory Affairs Efroze Chemical Industries (Pvt.) Ltd.

Location: Korangi Industrial Area, Karachi

Qualification: Doctor of Pharmacy (Pharm-D)

Experience: 4–6 years in Pharmaceutical

Key Responsibilities:

Preparation and submission of regulatory dossiers.

Coordination with DRAP and other regulatory bodies.

Ensuring product compliance with regulatory requirements.

Job Type: Full-time

Work Location: In person