Aptita Services has announced new Pharmacovigilance job openings for experienced professionals in ICSR Case Processing, Drug Safety, and Case Quality Review. Two positions are currently listed: Case Processing Associate (Pharmacovigilance) and QC Post Lock Case Processing Quality Review Associate/SME.

These openings may be suitable for candidates with hands-on experience in ICSR case processing, Oracle Argus Safety, Veeva Safety, medical coding, narrative writing, product coding, and pharmacovigilance quality review.

The Case Processing Associate role offers a listed salary of ₹6–8 LPA, while the QC/Quality Review position offers ₹10–12 LPA.

Aptita Pharmacovigilance Jobs – Overview

Role 1: Case Processing Associate – Pharmacovigilance

Aptita is hiring candidates with previous experience in ICSR case processing and pharmacovigilance operations. The professional will be responsible for processing safety cases from initial data entry through case completion while maintaining regulatory and quality standards.

Key Responsibilities

• Perform end-to-end ICSR case processing activities.
• Enter and review adverse event and safety case information.
• Prepare accurate and medically relevant case narratives.
• Perform medical coding and product coding.
• Complete appropriate case routing and workflow activities.
• Perform case lock and case closure activities.
• Handle USPI labeling requirements as applicable.
• Work with pharmacovigilance databases such as Oracle Argus and Veeva Safety.
• Maintain case-processing quality and regulatory compliance.
• Ensure safety information is processed accurately and within applicable timelines.

Qualifications & Experience

The official listing specifies UG: Any Graduate. Candidates with relevant pharmacovigilance experience and appropriate graduate qualifications may apply.

Degrees commonly relevant to pharmacovigilance include B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Life Sciences, B.Sc Biotechnology, M.Sc Biotechnology, B.Sc Microbiology, M.Sc Microbiology, B.Sc Biochemistry, M.Sc Biochemistry, Nursing and other relevant graduate degrees. However, these specific degrees are not separately mandated in the supplied listing; the stated requirement is Any Graduate.

Candidates should have approximately 1–2 years of relevant experience, particularly in ICSR case processing.

Preferred Skills

Knowledge or hands-on experience in ICSR Case Processing, Pharmacovigilance, Drug Safety, Medical Coding, Narrative Writing, Product Coding, Oracle Argus Safety and Veeva Safety will be particularly relevant.

Role 2: QC Post Lock Case Processing Quality Review Associate/SME

The second opening focuses on pharmacovigilance case quality review and QC. Candidates should have prior ICSR case-processing knowledge along with the ability to identify errors, monitor quality metrics, and provide feedback to improve case-processing compliance.

Key Responsibilities

• Review and perform quality checks on ICSR cases.
• Evaluate completed safety cases for accuracy and completeness.
• Identify case-processing defects and quality issues.
• Monitor relevant pharmacovigilance quality metrics.
• Provide constructive feedback to case-processing teams.
• Support improvements in overall case quality.
• Ensure cases meet applicable pharmacovigilance requirements.
• Apply knowledge of Oracle Argus Safety, medical coding and product coding during quality review.
• Support consistent compliance with established safety procedures and quality standards.

Qualifications & Experience

The official job listing states UG: Any Graduate.

Candidates with B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Nursing or other relevant graduate qualifications may have an academic background aligned with pharmacovigilance work, but applicants should note that the supplied advertisement itself lists the eligibility broadly as Any Graduate.

Approximately 2–5 years of relevant experience is listed for this position.

Skills Required for Aptita Pharmacovigilance Jobs

Candidates applying for these Aptita Pharmacovigilance jobs should particularly highlight relevant experience with:

• ICSR Case Processing
• Pharmacovigilance / Drug Safety
• Oracle Argus Safety
• Veeva Safety
• Medical Coding
• Product Coding
• Narrative Writing
• Case Quality Review
• Case Lock and Closure
• Quality Metrics
• Regulatory Compliance

Applicants should ensure that their resume clearly describes the types of safety cases processed or reviewed and the pharmacovigilance databases they have used.

Salary

According to the supplied job listings, the salary ranges are:

Case Processing Associate – Pharmacovigilance: ₹6–8 LPA

QC Post Lock Case Processing Quality Review Associate/SME: ₹10–12 LPA

Actual compensation offered to an individual candidate may depend on relevant experience, existing compensation, interview performance, skills and the employer’s final selection process.

Why Consider These Pharmacovigilance Openings?

These opportunities provide experienced drug-safety professionals with exposure to core ICSR case processing and pharmacovigilance quality activities. The positions may be especially relevant to candidates looking to strengthen their experience in safety databases such as Oracle Argus and Veeva Safety.

The QC opening can also be relevant for experienced case processors seeking progression into case quality review, QC or SME-level pharmacovigilance responsibilities.

How to Apply

Application Link For Case Processing Associate – Pharmacovigilance

Application Link For QC Post Lock Case Processing Quality Review Associate/SME