17 Medical Affairs jobs in Pakistan

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 :

1. Ensure compliance with all regulatory requirements for medical devices and laboratory products.
2. Prepare and submit applications for product registrations and renewals.
3. Liaise with regulatory authorities and act as the point of contact.
4. Monitor and interpret regulatory changes.
5. 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

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.

Responsibilities 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.

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 .

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.

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.

• 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.