Last Updated on October 10, 2024 by The Health Master
Govt Job
Govt Job: The Indian Pharmacopoeia Commission (IPC), an autonomous institution under the Ministry of Health and Family Welfare, Govt. of India, plays a pivotal role in establishing and maintaining standards for drugs in the country.
Created with the primary aim of ensuring the quality of medicines, IPC constantly updates and publishes the Indian Pharmacopoeia (IP) – an official document containing monographs that improve the quality of medicines.
Objective and Function of IPC
IPC’s fundamental objective is to set and regularly update standards for drugs necessary for treating prevalent diseases in the region.
The commission strives to enhance the quality of medicines by prescribing standards for identity, purity, and strength of drugs from a healthcare perspective for both humans and animals.
Role in Setting Drug Standards
One of IPC’s core functions is setting and updating the standards of drugs, aligning with the evolving needs of healthcare.
By doing so, IPC contributes significantly to the healthcare system’s efficiency and effectiveness, ensuring the availability of high-quality medications.
Creation and Update of Indian Pharmacopoeia (IP)
The IP is a cornerstone in IPC’s efforts to improve the quality of medicines.
It serves as a comprehensive reference guide that includes new monographs and updates existing ones.
This continual enhancement ensures that the medical community has access to the latest and most reliable information on pharmaceutical standards.
Promotion of Rational Use of Generic Medicines
In addition to its role in drug standards, IPC actively promotes the rational use of generic medicines.
It achieves this by publishing the National Formulary of India, encouraging the use of cost-effective generic alternatives without compromising on quality.
Job Opportunity: Sr Pharmacovigilance Associate
In its pursuit of maintaining drug safety and efficacy, IPC announces a job opportunity for the position of Sr Pharmacovigilance Associate.
Qualifications and Requirements
To be eligible for this position, candidates must possess a Pharm.D/MBBS/BDS from a recognized university or institute.
Alternatively, a Master’s degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice, or Clinical Research is also acceptable.
The candidate should have a minimum of 5 years’ experience in Pharmacovigilance activities and excellent verbal and written communication skills in English.
Responsibilities of Sr Pharmacovigilance Associate
The selected candidate will work as a team member/leader, managing the Collection, Collation & Analysis of Adverse Events associated with Medical Products.
Additionally, they will be responsible for implementing Quality & Safety Management System under PvPI, coordinating with different stakeholders for program expansion, and handling any other duties assigned by the Competent Authority.
Period of Engagement and General Instructions
The tenure of the contract for Sr Pharmacovigilance Associate is one year. However, if the work and conduct are unsatisfactory, services may be terminated without assigning any reason.
General instructions include the authority’s right to adjust the number of vacancies, select/cancel applications, and the relaxation of experience/age at their discretion.
Application Process
Interested candidates must submit their applications online through a Google Form, with the submission deadline set for January 15, 2024.
Interview Process
The interview will be conducted at IPC, Ghaziabad, and no TA/DA shall be provided for attending the interview. Shortlisted candidates must produce original documents for verification during the interview.
Salary and Benefits
The selected Sr Pharmacovigilance Associate will receive a salary of 40,000/- and will be posted at the Indian Pharmacopoeia Commission.
Conclusion
In conclusion, the Indian Pharmacopoeia Commission stands as a beacon for ensuring the quality and safety of medicines in India.
The announcement of the Sr Pharmacovigilance Associate position emphasizes IPC’s commitment to pharmacovigilance and maintaining the highest standards in drug safety.
The last date for submitting the application form is 15th January 2024.
Disclaimer: This article contains information derived from the source mentioned below. Our team utilized an AI language model to rewrite and present the news or article in a unique format.
FAQs
- How can I apply for the Sr Pharmacovigilance Associate position?
- Interested candidates should submit their applications online through a Google Form. The link is provided in the official announcement.
- What are the qualifications required for the Sr Pharmacovigilance Associate position?
- Eligibility includes a Pharm.D/MBBS/BDS or a Master’s degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice, or Clinical Research, along with a minimum of 5 years’ experience in Pharmacovigilance activities.
- What is the tenure of the contract for the Sr Pharmacovigilance Associate position?
- The contract period is one year, with the possibility of termination if the work and conduct are found unsatisfactory.
- Is there an age limit for applying to the Sr Pharmacovigilance Associate position?
- The maximum age limit is 40 years.
- When and where will the interview be conducted for the Sr Pharmacovigilance Associate position?
- The interview will take place at IPC, Ghaziabad. The date will be communicated to shortlisted candidates, and no TA/DA will be provided.
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