17 Clinical Affairs jobs in 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.

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.

The QA & RA manager will be responsible for development and effective implementation of the company’s quality management system to fulfill requirements of ISO 9001:2008, ISO 13485 quality management systems and FDA’s 21CFR, Section 820 (GMP) quality system regulation for Medical Devices. Trainings will be provided by the company to the selected candidate for further understanding of ISO 13485 quality management system.

The candidate should preferably have a master's in Total Quality Management and a B.Sc. in Mechanical Engineering and should be a lead auditor for ISO 9001:2008/ISO 13485 quality management system. The applicant must have a minimum work experience of 5 years in system development, implementation, and audit of ISO 9001:2008/ISO 13485 quality management system in a manufacturing industry. The applicant should also have good IT skills, be highly motivated & result-oriented, and should have strong leadership qualities.

The compensation package will be attractive, based on qualification, experience and linked to Key Performance Indicators (KPI) which will be determined by the Board of Directors.