Aggregate Report Writer Pharmacovigilance Jobs at Lambda Therapeutics for BPharm MPharm professionals with 1–3 years experience.
Company Overview
Lambda Therapeutics is a well-established pharmaceutical and research-driven organization known for its contribution to drug development, clinical research, and regulatory compliance. The company works across multiple therapeutic areas and follows international quality and pharmacovigilance standards. With a strong presence in India and exposure to global regulatory systems, Lambda Therapeutics provides professionals with an environment focused on compliance, learning, and long-term career development in regulatory and safety domains. Aggregate Report Writer Pharmacovigilance Jobs
As part of its expanding pharmacovigilance operations, the organization is inviting skilled professionals to join its safety and regulatory writing team.
Job Location & Employment Type
- Location: Ahmedabad, Gujarat
- Employment Type: Full-time, Work from Office
- Department: Pharmacovigilance / Drug Safety
Open Positions / Department Details
- Position Title: Aggregate Report Writer – Pharmacovigilance
- Number of Openings: Not disclosed
- Reporting Function: Pharmacovigilance & Regulatory Writing Team
This role is designed for professionals who already have experience in aggregate safety reporting and are looking to strengthen their expertise in global pharmacovigilance documentation. Aggregate Report Writer Pharmacovigilance Jobs
Key Roles & Responsibilities
Selected candidates will be responsible for handling end-to-end activities related to aggregate safety report writing and regulatory compliance. The major responsibilities include: Aggregate Report Writer Pharmacovigilance Jobs
- Preparation, review, and finalization of aggregate safety reports such as PSUR, PADER, DSUR, and Risk Management Plans
- Compilation and interpretation of safety data from various sources for periodic reporting
- Ensuring all safety reports comply with international pharmacovigilance guidelines and regulatory expectations
- Performing medical review and benefit-risk evaluation as part of periodic safety assessments
- Coordinating with internal stakeholders including safety, regulatory affairs, data management, and medical teams
- Managing report timelines to ensure submissions are completed within defined regulatory deadlines
- Maintaining documentation, version control, and records as per internal SOPs and quality standards
- Supporting internal audits, client audits, and regulatory inspections when required
- Keeping up to date with evolving global pharmacovigilance regulations and safety reporting requirements
Eligibility Criteria
Education
- Bachelor’s Degree in Pharmacy (B.Pharm)
- Master’s Degree in Pharmacy (M.Pharm)
Candidates with a strong academic background in pharmacovigilance, regulatory affairs, or clinical research will be preferred.
Experience
- Minimum 1 year of hands-on experience in aggregate safety report writing
- Maximum 3 years of relevant experience in pharmacovigilance or regulatory writing roles
Experience in handling global submissions will be considered an added advantage.
Skills Required
- Practical knowledge of pharmacovigilance systems and processes
- Hands-on exposure to PSUR, PADER, DSUR, and RMP preparation
- Understanding of ICH guidelines, EMA requirements, and US FDA safety reporting standards
- Strong medical writing and data interpretation skills
- Ability to analyze safety data and present conclusions clearly
- Good communication and coordination skills for cross-functional collaboration
- Capability to work independently with minimal supervision
- Strong attention to detail and ability to manage multiple deadlines
Aggregate Report Writer Pharmacovigilance Jobs
Salary & Benefits
- Salary Range: ₹4,00,000 to ₹7,00,000 per annum (CTC)
- Structured work environment with defined processes
- Opportunity to work on global pharmacovigilance submissions
- Professional exposure to international regulatory standards
- Stable full-time role based in Ahmedabad
Aggregate Report Writer Pharmacovigilance Jobs
Selection Process
The selection process will generally include:
- Profile shortlisting based on experience and skill relevance
- Technical interview focused on pharmacovigilance and aggregate reporting
- Final HR discussion
The exact selection stages may vary depending on company requirements.
How to Apply
- Mode of Application: Online Application Only
- Interested candidates should apply through the official application link provided by the company
- Immediate joiners or candidates with a short notice period may be given preference
Important Dates
- Job Posted On: January 30, 2026
- Application Deadline: Not specified (apply as early as possible)
Why Apply for This Pharma Job?
This opportunity is ideal for pharmacovigilance professionals who want to specialize further in aggregate safety reporting. Working with Lambda Therapeutics allows candidates to gain hands-on exposure to global regulatory submissions, strengthen their medical writing expertise, and grow within a structured pharmacovigilance framework. The role offers long-term learning, regulatory exposure, and career stability in one of the most in-demand domains of the pharmaceutical industry. Aggregate Report Writer Pharmacovigilance Jobs
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical job information platform. We are not associated with, authorized by, or officially connected to Lambda Therapeutics or any other company. Job details are shared strictly for informational purposes. Candidates are advised to verify all information directly from the official company sources before applying. Aggregate Report Writer Pharmacovigilance Jobs
Final Call-to-Action
If you have experience in pharmacovigilance aggregate report writing and are looking for growth in regulatory safety roles, apply now and take the next step in your pharmaceutical career. Aggregate Report Writer Pharmacovigilance Jobs
