15 Regulatory Affairs jobs in Pakistan
Regulatory Affairs Executive
Posted 7 days ago
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Job Description
Epharm Laboratories, Pakistan
We are a pharmaceutical company with our head office at PECHS, seeking young and energetic officers for regulatory affairs with sound knowledge and experience.
Candidates must have at least 2-3 years of experience. Pharmaceutical experience and residency in the nearby area will be preferred.
Job SpecificationResponsibilities include ensuring compliance with regulatory requirements, preparing and submitting documentation to regulatory agencies, and maintaining knowledge of industry regulations.
Qualifications include a degree in pharmacy or a related field, strong communication skills, and the ability to work independently and as part of a team.
#J-18808-LjbffrRegulatory Affairs Manager
Posted 7 days ago
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Job Description :
Med Lab Services, a leading provider of clinical diagnostic solutions in Pakistan, is looking for an experienced Regulatory Affairs Manager to join our team in Rawalpindi.
Responsibilities :
- Ensure compliance with all regulatory requirements for medical devices and laboratory products.
- Prepare and submit applications for product registrations and renewals.
- Liaise with regulatory authorities and act as the point of contact.
- Monitor and interpret regulatory changes.
- Conduct audits to ensure compliance with industry standards.
- Strong knowledge of regulatory guidelines in the healthcare industry.
- Excellent communication and interpersonal skills.
- Detail-oriented with strong analytical skills.
- Ability to work collaboratively within a team.
- Proficiency in regulatory documentation and reporting.
Incentive Bonus
#J-18808-LjbffrRegulatory Affairs Manager
Posted 9 days ago
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Job Description : Med Lab Services, a leading provider of clinical diagnostic solutions in Pakistan, is looking for an experienced Regulatory Affairs Manager to join our team in Rawalpindi.
Responsibilities : Ensure compliance with all regulatory requirements for medical devices and laboratory products. Prepare and submit applications for product registrations and renewals. Liaise with regulatory authorities and act as the point of contact. Monitor and interpret regulatory changes. Conduct audits to ensure compliance with industry standards. Job Specification :
Strong knowledge of regulatory guidelines in the healthcare industry. Excellent communication and interpersonal skills. Detail-oriented with strong analytical skills. Ability to work collaboratively within a team. Proficiency in regulatory documentation and reporting. Job Rewards and Benefits :
Incentive Bonus
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Regulatory Affairs & Pharmacovigilance Officer
Posted 2 days ago
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Regulatory Affairs & Pharmacovigilance OfficerLocation:
Lahore, PK
About Us
Chiesi Pharmaceuticals Pvt. Ltd., headquartered in Lahore, Pakistan, was established on June 2, 1987 , and is the second international affiliate of the group. With the Best HR Practices Certifications of Top Employer 2025 for 3rd consecutive year and Great Place to Work since 2021, it is a wholly owned subsidiary of Chiesi Farmaceutici S.p.A, a global R&D-focused pharmaceutical company based in Parma, Italy.
The mission of Chiesi Pakistan is to provide the Pakistani nation with state-of-the-art, high-quality products that are used in the most developed countries of the world. As a result, almost all the group’s products are promoted and marketed by Chiesi Pakistan, ranging from respiratory diseases, cardiovascular diseases, and central nervous system disorders to musculoskeletal pain and special care areas like neonatology.
Main ResponsibilitiesWe are looking for a dynamic Regulatory Affairs & Pharmacovigilance Officer with at least 2 years of experience in the pharmaceutical industry. The ideal candidate will be responsible for ensuring compliance with regulatory requirements and overseeing drug safety monitoring.
Experience RequiredMinimum 2 years of relevant experience in regulatory affairs and pharmacovigilance.
Knowledge of Local regulatory guidelines and PV systems.
EducationPharm-D
- Proficiency in maintaining records and documents.
- Excellent communication, organization, and time management.
- Accuracy and attention to detail.
- Ability to understand complex frameworks
What we offer
You would join a dynamic, fast-growing, challenging and friendly environment.
In Chiesi we firmly believe that our people are our most valuable asset, that is why we invest in continuous training, learning and development. Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and to collective well-being.
We want our people to come to work happy every day, and we know how important it is to find the right work-life balance in order to be able to give our best. That is why we offer flexible working approach, support in the relocation process, and many other people-care services.
#J-18808-LjbffrDeputy Manager – Regulatory Affairs
Posted 3 days ago
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MBA preferably in Finance / ACCA with 02 Years of qualification experience.
Knowledge of Regulatory Framework, Tariff determination and revenue requirement will be considered as an added advantage.
Responsibilities:
- Assist in coordination and collection of data from relevant departments at the beginning of each financial year to prepare and file tariff petitions (Revenue) with OGRA for determination of estimated revenue requirement of SSGC along with technical reports to justify the pricing.
- Supervise preparation of Transmission and Distribution (T&D) annexures for revenue requirement petitions.
- Assist in preparation of annual reports including Capital Expenditures (CAPEX) for submission to OGRA.
- Assist in preparing historical / current scenarios for Human Resource (HR) cost benchmarking.
- Assist in analyzing SSGC’s doubtful debts as per prescribed guidelines of OGRA.
- Assist in preparing points against Board of Directors and Managing Director’s recommendations regarding OGRA’s petitions and revenue requirements.
- Undertake any other assignment as instructed by user department.
Deputy Manager – Regulatory Affairs
Posted 7 days ago
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Join to apply for the Deputy Manager – Regulatory Affairs role at Sui Southern Gas Company Limited .
Experience and Qualifications: MBA preferably in Finance / ACCA with 2 years of relevant experience. Knowledge of Regulatory Framework, Tariff determination, and revenue requirements will be considered an added advantage.
Key Responsibilities:
- Assist in preparing comprehensive reports regarding Gas Distribution System (GDS) for Revenue Requirements Petitions.
- Prepare detailed reports and include necessary details as per Regulatory framework for GDS & LPG Air Mix Projects.
- Manage Licensing Requirements of LPG Air Mix Projects.
- Coordinate with Accounts department to prepare reports on other assets for Actual Revenue Petition.
- Compile feasibility studies for LPG project approvals by OGRA.
- Support Board of Directors and Managing Director’s recommendations regarding OGRA’s petitions and revenue requirements.
- Ensure timely filing of tariff petitions following OGRA’s guidelines.
- Assist senior management in preparing tariff-related petitions.
- Maintain backup of historical revenue requirement data for SSGC.
- Perform other tasks as instructed by senior management.
- Seniority level: Mid-Senior level
- Employment type: Full-time
- Job function: Legal
- Industries: Utilities
Referrals can increase your chances of interview invitations at Sui Southern Gas Company Limited by 2x.
Get notified about new Regulatory Affairs Manager jobs in Karachi Division, Sindh, Pakistan .
#J-18808-LjbffrRegulatory Affairs & Pharmacovigilance Officer
Posted 1 day ago
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Job Description
Location: Lahore, PK
About Us Chiesi Pharmaceuticals Pvt. Ltd.,
headquartered in Lahore, Pakistan, was established on
June 2, 1987 , and is the second international affiliate of the group. With the
Best HR Practices Certifications
of
Top Employer 2025
for 3rd consecutive year and
Great Place to Work
since 2021, it is a wholly owned subsidiary of
Chiesi Farmaceutici S.p.A,
a global R&D-focused pharmaceutical company based in Parma, Italy. The mission of
Chiesi Pakistan
is to provide the
Pakistani nation
with state-of-the-art, high-quality products that are used in the most developed countries of the world. As a result, almost all the group’s products are promoted and marketed by Chiesi Pakistan, ranging from
respiratory diseases, cardiovascular diseases, and central nervous system disorders to musculoskeletal pain and special care areas like neonatology. Main Responsibilities
We are looking for a dynamic Regulatory Affairs & Pharmacovigilance Officer with at least 2 years of experience in the pharmaceutical industry. The ideal candidate will be responsible for ensuring compliance with regulatory requirements and overseeing drug safety monitoring. Experience Required
Minimum 2 years of relevant experience in regulatory affairs and pharmacovigilance. Knowledge of Local regulatory guidelines and PV systems. Education
Pharm-D Proficiency in maintaining records and documents. Excellent communication, organization, and time management. Accuracy and attention to detail. Ability to understand complex frameworks What we offer You would join a dynamic, fast-growing, challenging and friendly environment. In Chiesi we firmly believe that our people are our most valuable asset, that is why we invest in continuous training, learning and development. Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and to collective well-being. We want our people to come to work happy every day, and we know how important it is to find the right work-life balance in order to be able to give our best. That is why we offer flexible working approach, support in the relocation process, and many other people-care services.
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Deputy Manager – Regulatory Affairs
Posted 3 days ago
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Deputy Manager – Regulatory Affairs
Posted 7 days ago
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Job Description
Deputy Manager – Regulatory Affairs
role at
Sui Southern Gas Company Limited . Experience and Qualifications:
MBA preferably in Finance / ACCA with 2 years of relevant experience. Knowledge of Regulatory Framework, Tariff determination, and revenue requirements will be considered an added advantage. Key Responsibilities: Assist in preparing comprehensive reports regarding Gas Distribution System (GDS) for Revenue Requirements Petitions. Prepare detailed reports and include necessary details as per Regulatory framework for GDS & LPG Air Mix Projects. Manage Licensing Requirements of LPG Air Mix Projects. Coordinate with Accounts department to prepare reports on other assets for Actual Revenue Petition. Compile feasibility studies for LPG project approvals by OGRA. Support Board of Directors and Managing Director’s recommendations regarding OGRA’s petitions and revenue requirements. Ensure timely filing of tariff petitions following OGRA’s guidelines. Assist senior management in preparing tariff-related petitions. Maintain backup of historical revenue requirement data for SSGC. Perform other tasks as instructed by senior management. Additional Information:
Seniority level:
Mid-Senior level Employment type:
Full-time Job function:
Legal Industries:
Utilities Referrals can increase your chances of interview invitations at Sui Southern Gas Company Limited by 2x. Get notified about new Regulatory Affairs Manager jobs in
Karachi Division, Sindh, Pakistan .
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Officer / Sr. Officer Regulatory Affairs
Posted today
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Job Description
We are seeking a dedicated Senior Officer Regulatory Affairs to prepare and manage the compilation of CTD and ACTD dossiers, as well as Certificates of Pharmaceutical Product (COPP) and Free Sale Certificates (FSC). The ideal candidate will ensure compliance with regulatory requirements and support the approval and registration of our products.
Job Specification- Strong knowledge of regulatory guidelines and requirements.
- Excellent organizational and documentation skills.
- Strong attention to detail and ability to work under tight deadlines.
- Effective communication and interpersonal skills.