Apply for Pharmacovigilance Officer Jobs in New Delhi at Alde Medi Impex. Explore eligibility, salary and responsibilities today.
Introduction
Alde Medi Impex is inviting applications for the position of Pharmacovigilance Officer in New Delhi. This opportunity is ideal for experienced pharmacy and life sciences professionals who wish to build their careers in drug safety, adverse event reporting, regulatory compliance, and risk management. Candidates with relevant pharmacovigilance experience and strong knowledge of safety reporting processes are encouraged to apply. The role offers exposure to safety case processing, signal detection, literature surveillance, and regulatory reporting activities. Professionals searching for Pharmacovigilance Jobs, Pharma Jobs 2026, Regulatory Affairs Jobs, and Latest Pharma Jobs can explore this excellent career opportunity.
About Company
Alde Medi Impex is a pharmaceutical and healthcare organization involved in delivering quality healthcare solutions while maintaining compliance with industry regulations and safety standards. The company focuses on ensuring patient safety through effective pharmacovigilance systems, regulatory compliance programs, and quality management practices.
With a commitment to maintaining high standards of drug safety monitoring and risk management, Alde Medi Impex actively supports healthcare professionals, regulatory agencies, and patients through robust pharmacovigilance operations. The organization works closely with medical, regulatory affairs, clinical research, and quality assurance teams to ensure product safety throughout the lifecycle of pharmaceutical products.
The company provides opportunities for skilled professionals to contribute to patient safety initiatives while gaining valuable experience in the pharmaceutical and life sciences industry.
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Job Details / Job Summary
| Particulars | Details |
|---|---|
| Company Name | Alde Medi Impex |
| Job Role | Pharmacovigilance Officer |
| Department | Risk Management & Compliance |
| Qualification Required | B.Pharm, B.Tech/B.E. in Biotechnology or Biochemistry |
| Experience Required | 3 – 4 Years |
| Salary Package | ₹4.25 LPA – ₹4.75 LPA |
| Job Location | Kirti Nagar, New Delhi |
| Employment Type | Full-Time, Permanent |
| Industry Type | Pharmaceutical & Life Sciences |
| Shift Timing | General Shift |
| Gender Eligibility | Male & Female |
| Application Mode | Online |
| Selection Process | Resume Screening, Technical Interview, HR Discussion |
| Skills Required | ADR Processing, Safety Reporting, Signal Detection, Regulatory Compliance |
| Official Notification Status | Active |
| Application Last Date | Apply As Soon As Possible |
Eligibility Criteria
Candidates applying for this Pharmacovigilance Officer position should meet the following requirements:
- B.Pharm degree from a recognized institution.
- B.Tech/B.E. in Biotechnology or Biochemistry may also apply.
- Minimum 3 to 4 years of relevant pharmacovigilance experience.
- Strong understanding of adverse drug reaction reporting processes.
- Knowledge of pharmacovigilance regulations and compliance requirements.
- Experience in safety database management and case processing.
- Good communication and analytical skills.
- Ability to work with cross-functional teams.
Required Skills
The ideal candidate should possess:
- Adverse Drug Reaction (ADR) Case Processing
- Pharmacovigilance Operations
- Safety Data Entry and Management
- Literature Surveillance and Review
- PSUR Preparation
- Regulatory Reporting
- Signal Detection and Risk Assessment
- Drug Safety Monitoring
- Compliance Management
- Data Analysis and Documentation
- Quality Assurance Coordination
- Medical and Regulatory Communication
- Clinical Safety Reporting
- Problem-Solving Skills
- Attention to Detail
Roles and Responsibilities
Selected candidates will be responsible for:
- Managing adverse drug reaction (ADR) case processing activities.
- Performing safety data entry and maintaining pharmacovigilance databases.
- Conducting literature reviews for safety-related information.
- Preparing Periodic Safety Update Reports (PSURs).
- Supporting regulatory reporting requirements.
- Performing signal detection and risk evaluation activities.
- Ensuring compliance with pharmacovigilance regulations and company procedures.
- Coordinating with Medical Affairs, Regulatory Affairs, Clinical Research, and Quality Assurance teams.
- Monitoring product safety information and identifying potential risks.
- Maintaining accurate documentation of safety-related activities.
- Supporting inspections, audits, and compliance reviews.
- Contributing to continuous improvement of pharmacovigilance processes.
Salary Details
Alde Medi Impex offers a competitive salary package for qualified pharmacovigilance professionals.
Expected Salary
- Annual CTC: ₹4.25 LPA – ₹4.75 LPA
Additional Benefits
- Career growth opportunities in Pharmacovigilance
- Exposure to regulatory and safety reporting activities
- Professional development programs
- Collaborative work environment
- Experience in risk management and compliance operations
- Opportunities to work with multidisciplinary healthcare teams
Salary may vary depending on candidate experience, skills, and interview performance.
Selection Process
The hiring process generally includes the following stages:
Step 1: Online Application
Interested candidates submit their applications through the company recruitment platform.
Step 2: Resume Screening
Applications are reviewed based on educational qualifications and pharmacovigilance experience.
Step 3: Technical Interview
Shortlisted candidates undergo an evaluation of pharmacovigilance knowledge, ADR processing, and regulatory compliance expertise.
Step 4: HR Discussion
Selected candidates participate in discussions regarding compensation, benefits, and joining timelines.
Step 5: Final Selection
Successful applicants receive an official offer letter and onboarding information.
How to Apply
Interested and eligible candidates can apply through the company’s official recruitment process.
Application Tips
- Update your resume with pharmacovigilance experience and relevant achievements.
- Highlight expertise in ADR processing, PSUR preparation, and regulatory reporting.
- Include details of safety database experience and compliance activities.
- Submit the application before the vacancy is filled.
Candidates are encouraged to apply early due to limited openings.
Frequently Asked Questions
1. What qualification is required for the Pharmacovigilance Officer role?
Candidates should possess a B.Pharm degree or B.Tech/B.E. in Biotechnology or Biochemistry.
2. Can freshers apply for this position?
No. The company requires candidates with 3–4 years of relevant pharmacovigilance experience.
3. What salary is offered for this role?
The salary package ranges between ₹4.25 LPA and ₹4.75 LPA.
4. What are the major responsibilities of a Pharmacovigilance Officer?
The role involves ADR case processing, literature review, PSUR preparation, regulatory reporting, signal detection, and pharmacovigilance compliance activities.
