Orcapod Consulting Services Pvt. Ltd. is recruiting experienced professionals for Senior Professional Executive (SPE) and Subject Matter Expert (SME) roles in Pharmacovigilance and Drug Safety for a client described as a Top MNC. The advertised positions focus on safety case processing, medical coding, case quality review and pharmacovigilance database operations.
The vacancies are listed across Pune, Mumbai and Bengaluru, with 100 openings mentioned in the recruitment listing. Candidates with qualifications in Life Sciences, Pharmacy, Medical Sciences or equivalent disciplines and practical experience with pharmacovigilance safety databases such as Veeva Safety and Argus are encouraged to review the requirements.
The SPE role focuses on end-to-end safety case processing, while the SME position involves quality review of serious and fatal cases, defect tracking and monitoring case-processing quality. These positions are intended for experienced candidates rather than freshers.
Orcapod Pharmacovigilance Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Recruitment Partner | Orcapod Consulting Services Pvt. Ltd. |
| Hiring Client | Top MNC; name not disclosed |
| Job Category | Pharmacovigilance / Drug Safety |
| Available Positions | SPE – Case Processing Associate; SME – Quality Review Associate |
| Job Locations | Pune, Mumbai and Bengaluru |
| Experience | Requirements vary by position |
| Education | Graduate, postgraduate or doctorate degree in a relevant discipline |
| Required Databases | Veeva Safety and Argus |
| Employment Type | Full-time, permanent |
| Number of Openings | 100 stated in the listing |
| Salary | Not disclosed |
| Application Mode | Contact recruitment representative |
| Recruitment Contact | Sonali Chattopadhyay |
| sonali.chattopadhyay@orcapod.work | |
| Listing Date | October 23, 2026 |
About Orcapod Pharmacovigilance Hiring
Orcapod Consulting Services is handling recruitment for pharmacovigilance positions on behalf of a client identified in the listing as a Top MNC. The end employer’s name has not been disclosed.
Pharmacovigilance teams process, document and review information relating to the safety of medicinal products. These activities can include individual case intake, data entry, medical coding, narrative preparation, quality checks and case routing.
The advertised positions are designed for professionals with prior experience in safety case processing or quality review.
1. SPE – Case Processing Associate
Experience: The listing mentions 2–5 years for the SPE grade, while the detailed eligibility section specifies 1–2 years of pharmacovigilance safety case-processing experience. Candidates should confirm the applicable requirement with the recruiter.
The SPE position involves processing individual safety cases using pharmacovigilance databases and following established case-processing procedures.
Key Responsibilities
- Book in incoming safety cases.
- Perform complete safety case data entry.
- Prepare case narratives and I-Narratives.
- Carry out medical coding and product coding.
- Perform self-checks using online quality control tools.
- Handle unblinding when required by the applicable process.
- Route cases through the appropriate workflow.
- Complete case locking and closure where applicable.
- Perform product labelling activities, including USPI labelling.
Eligibility Criteria
| Requirement | Details |
|---|---|
| Educational Qualification | Graduate, postgraduate or doctorate degree |
| Relevant Fields | Life Sciences, Pharmacy, Medical Sciences or equivalent |
| Experience | 1–2 years specified in the detailed criteria; 2–5 years listed for the grade |
| Technical Experience | Pharmacovigilance safety case processing |
| Safety Databases | Veeva Safety and/or Argus |
| Language | Fluency in English |
Candidates should highlight their hands-on experience with safety case intake, data entry, narrative writing, coding and case-processing workflows.
2. SME – QC/Post-Lock Case Processing Quality Review Associate
Experience: 2+ years of safety case processing or quality review experience.
The SME role focuses on reviewing the quality of pharmacovigilance case-processing deliverables, particularly fatal and serious cases. The role also involves monitoring quality metrics, communicating defects and supporting corrective actions.
Key Responsibilities
- Conduct quality checks of fatal and serious safety cases.
- Track daily quality metrics associated with case-processing defects.
- Communicate quality metrics and identified issues to case-processing associates.
- Discuss corrective actions to address errors and prevent recurring defects.
- Review deliverables to ensure they meet expected quality standards.
- Support consistent and accurate case-processing operations.
Eligibility Criteria
| Requirement | Details |
|---|---|
| Educational Qualification | Graduate, postgraduate or doctorate degree |
| Relevant Fields | Life Sciences, Pharmacy, Medical Sciences or equivalent |
| Experience | 2+ years |
| Relevant Work | Safety case processing or quality review |
| Safety Databases | Veeva Safety and Argus |
| Language | Fluency in English |
Candidates with experience reviewing serious or fatal cases, tracking quality metrics and identifying case-processing defects may be suitable for this position.
Educational Qualifications
The vacancy listing accepts candidates with a graduate, postgraduate or doctorate degree in Life Sciences, Pharmacy, Medical Sciences or an equivalent discipline.
Candidates should ensure that their degree and professional experience match the requirements for the selected position. Additional eligibility criteria may be confirmed directly with the recruitment representative.
Skills Required for Pharmacovigilance Jobs
The following skills are relevant to the advertised positions:
- Pharmacovigilance and drug safety operations.
- Individual safety case processing.
- Medical coding and product coding.
- Case narrative and I-Narrative writing.
- Case routing, locking and closure.
- Familiarity with Veeva Safety and Argus databases.
- Quality control and post-lock quality review.
- Review of serious and fatal cases.
- Quality metrics monitoring and defect tracking.
- USPI labelling.
- English communication and accurate documentation.
The precise combination of skills required will depend on whether the candidate applies for the SPE or SME role.
Salary and Employment Details
The vacancy listing does not disclose a salary range for either position.
The advertised employment type is full-time and permanent. Candidates should contact the recruitment representative to confirm compensation, shift timings, work arrangements, project allocation and other employment conditions.
How to Apply for Orcapod Recruitment 2026
Interested candidates can contact the recruitment representative using the details in the vacancy listing.
Recruitment Contact: Sonali Chattopadhyay, Associate People Success
Recruitment Company: Orcapod Consulting Services Pvt. Ltd.
Email: sonali.chattopadhyay@orcapod.work
Before applying:
- Prepare an updated CV with your relevant pharmacovigilance experience.
- Clearly state whether you are applying for the SPE Case Processing Associate or SME Quality Review Associate role.
- Highlight your experience with Veeva Safety, Argus, safety case processing or quality review.
- Mention your total relevant experience and educational qualification.
- Confirm the exact eligibility requirements and hiring process with the recruiter.
Privacy and safety note: Verify the recruitment representative and opportunity before sharing sensitive personal information, including PAN details or identity documents. Never pay a recruitment fee to secure a job.
Frequently Asked Questions (FAQs)
1. Is Orcapod recruiting for pharmacovigilance jobs in 2026?
A vacancy listing published on October 23, 2026, advertises SPE and SME Drug Safety positions through Orcapod Consulting Services.
2. Which cities have openings?
The listed locations are Pune, Mumbai and Bengaluru.
3. How many vacancies are mentioned?
The recruitment listing states that there are 100 openings. Candidates should confirm the current number of available positions with the recruiter.
4. Can freshers apply?
No. The listed positions require prior experience in pharmacovigilance case processing or quality review.
5. What experience is required for the SPE position?
The detailed criteria mention 1–2 years of safety case-processing experience, while the grade summary lists 2–5 years. Candidates should clarify this discrepancy with the recruiter.
6. What experience is required for the SME position?
The SME role requires at least two years of safety case processing or quality review experience.
7. Which pharmacovigilance databases are mentioned?
The listing mentions Veeva Safety and Argus.
8. What is the salary for these positions?
The salary has not been disclosed in the available vacancy details.
9. Is this a permanent job?
The listing describes the employment type as full-time and permanent. Candidates should confirm the employment terms during the recruitment process.
10. How can candidates apply?
Candidates can email Sonali Chattopadhyay at sonali.chattopadhyay@orcapod.work with an updated CV and details of their relevant experience.
Disclaimer
This article is based on a third-party vacancy listing published on October 23, 2026. The hiring client is described as a Top MNC, but its name has not been disclosed. The vacancy has not been independently verified as an official announcement from the end employer. Experience requirements for the SPE position differ between sections of the listing. Candidates should confirm the job details, recruiter identity and eligibility criteria before applying.