Baxter has announced a new Intake Associate, PV job opening in Gurgaon for candidates interested in building their careers in pharmacovigilance, drug safety, adverse event reporting, and safety operations.
The Intake Associate, PV will join Baxter’s Safety Operations team and support country-level pharmacovigilance activities. The position primarily involves the collection, documentation, triage, and processing of local adverse event (AE) reports from different sources.
Candidates with a degree in science, pharmacy, or a related field may be considered for this Baxter pharmacovigilance job. The official requirement also provides an alternative pathway of a minimum of two years of pharmacovigilance experience.
This opportunity may be particularly relevant for candidates searching for pharmacovigilance jobs in Gurgaon, Baxter PV jobs, drug safety jobs, adverse event reporting jobs, and life sciences jobs in India.
Key Responsibilities
As an Intake Associate, PV at Baxter, the selected candidate will support local pharmacovigilance and safety operations. Major responsibilities include:
- Collect, document, and process local adverse event reports received from different sources.
- Handle AE reports according to applicable national legislation and Baxter procedures.
- Conduct surveillance activities to identify new or potentially important safety information.
- Escalate potential safety information according to established procedures.
- Perform local case triage and assess cases for validity.
- Conduct duplicate checks for adverse event cases.
- Forward safety cases to appropriate internal and external partners when required.
- Perform case intake within the Pharmacovigilance Safety System (PSS).
- Respond to queries received from the global case processing team.
- Perform source document redaction when necessary.
- Ensure relevant source documentation is accurately captured within PSS.
- Conduct local quality checks as required.
- Perform Health Authority case downloads where applicable.
- Support other pharmacovigilance and safety operations activities as assigned.
Qualification and Eligibility
Baxter specifies the following educational and professional eligibility:
Education: Degree in Sciences, Pharmacy, or a related field, or a minimum of two years of pharmacovigilance experience.
Relevant educational backgrounds may therefore include pharmacy, pharmaceutical sciences, life sciences, biological sciences, or other science-related disciplines, subject to Baxter’s final screening criteria.
Candidates should carefully review the official job posting before applying, as the employer makes the final determination regarding degree equivalency and eligibility.
Skills Required
Candidates applying for the Baxter Intake Associate PV position should demonstrate:
- Excellent attention to detail
- Strong written communication skills
- Strong verbal communication skills
- Medical and clinical knowledge
- Ability to work effectively within a team
- Ability to work under strict timelines and deadlines
- Strong workload prioritization skills
- Ability to multitask in a changing work environment
- Ability to develop proficiency in the Pharmacovigilance Safety System (PSS)
- Understanding of adverse event documentation and safety processes is advantageous
What Does an Intake Associate in Pharmacovigilance Do?
An Intake Associate in Pharmacovigilance generally works at the initial stages of the drug safety case lifecycle.
In this Baxter role, the associate receives and documents adverse event information, checks whether cases contain the required information, identifies possible duplicate reports, performs case intake in the safety system, maintains supporting source documents, and forwards cases for further processing when required.
The role therefore provides exposure to important pharmacovigilance concepts including AE intake, case validity, duplicate checking, case triage, safety databases, source documentation, quality checks, and safety surveillance.
Why Consider This Baxter PV Opportunity?
This role offers an opportunity to work within the Safety Operations function of a global healthcare organization.
Potential professional benefits include:
- Exposure to country-level pharmacovigilance operations
- Experience with adverse event intake and documentation
- Exposure to pharmacovigilance safety systems
- Experience with local case triage and duplicate checking
- Interaction with global case processing teams
- Exposure to safety surveillance activities
- Experience working within structured PV procedures and regulatory requirements
- Development of practical drug safety and case management skills
Specific compensation, employee benefits, working arrangements, and other employment terms should be confirmed directly with Baxter during the recruitment process.
Estimated Salary
Baxter has not provided a salary range in the supplied job posting.
For structured-data purposes, a reasonable market estimate for this type of pharmacovigilance position in Gurgaon is approximately ₹3.5 lakh to ₹6.5 lakh per year.
Important: This is an editorial market estimate and not an officially disclosed Baxter salary range. Actual compensation may vary depending on qualifications, relevant experience, internal compensation policies, and the final offer.
How to Apply
