What Jobs are available for Corporate Governance in Pakistan?

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

Hiring Alert

Position:
Regulatory Affairs Manager

Location: Lahore

• Pharm-D
• 5-6 years experience at same position in a reputable pharmaceutical company.

Please send your resume on

, or ,

Position:
Regulatory Affairs Officer

Department:
Regulatory Affairs Officer

Location:
Shahrah e Faisal, SMCHS, Karachi

Working Days:
Monday to Friday

Timings:
9 am to 6 pm

Al-Habib Pharmaceuticals is seeking a detail-oriented and proactive
Regulatory Affairs Officer
to join our team. The ideal candidate will be responsible for preparing, compiling, and submitting regulatory documentation to ensure compliance with national and international requirements. This role will involve close collaboration with regulatory authorities, internal teams, and external stakeholders to achieve timely product approvals and renewals.

Key Responsibilities

• Prepare and compile
  Common Technical Document (CTD)
  and
  ASEAN Common Technical Dossier (ACTD)
  submissions for pharmaceutical products in compliance with local and international regulatory standards.
• Apply for
  CoPPs (Certificates of Pharmaceutical Product), NOCs (No Objection Certificates), and drug registrations
  through
  Pakistan Single Window (PSW)
  .
• Prepare, compile, and submit
  new drug applications, renewals, and post-approval variations (Type I/II)
  .
• Act as a liaison between the company and regulatory agencies to ensure
  timely approvals
  .
• Support
  internal audits
  and
  regulatory inspections
  .
• Handle product
  labelling updates
  in line with regulatory feedback.
• Ensure timely renewal of
  Drug Manufacturing Licenses (DML)
  and
  product registration certificates
  in compliance with
  DRAP
  regulations.
• Manage
  post-registration changes
  , including composition, manufacturing site, and packaging materials.
• Liaise with
  DRAP
  and other regulatory authorities to stay updated on
  guidelines, checklists, and procedural changes
  .
• Review
  artwork and labeling
  to ensure alignment with approved data and regulations.
• Respond effectively to
  regulatory actions and queries
  .

Qualification and Skills:

• Bachelor's or Master's degree in
  Pharmacy, Life Sciences, or a related field
  .
• 1–3 years of proven experience in
  regulatory affairs
  within the pharmaceutical industry.
• In-depth knowledge of
  DRAP regulations
  and international regulatory frameworks.
• Strong organizational and documentation skills.
• Excellent communication and liaison abilities.
• Proficiency in
  regulatory submission systems
  (e.g., PSW).

Interested candidates can share their resume

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.

Job Type: Full-time

Pay: Rs40, Rs80,000.00 per month

Application Question(s):

• What is your current salary ?
• How soon can you join?
• What is your salary expectation?
• Do you have experience of DRAP?

Education:

• Bachelor's (Required)

Experience:

• Regulatory affairs: 2 years (Required)

Work Location: In person