Are you looking for Pharmacovigilance jobs in Ahmedabad and have a background in pharmacy, medical sciences, or dentistry? Lambda Therapeutics has openings across multiple drug-safety functions that may be relevant for qualified candidates.
The current opportunities cover areas such as Medical Information, Regulatory Case Processing, and Global Literature Screening. These roles can provide exposure to important Pharmacovigilance activities, including adverse event processing, medical information management, safety data review, and literature surveillance.
Candidates with qualifications including B.Pharm, M.Pharm, Pharm.D, BDS, and MDS can explore these opportunities.
📌 Lambda Therapeutics Recruitment 2026 – Job Highlights
| Category | Details |
|---|---|
| Company | Lambda Therapeutics |
| Industry | Pharmacovigilance / Life Sciences / Clinical Research |
| Job Functions | Medical Information, Regulatory Case Processing, Global Literature Screening |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, BDS, MDS |
| Job Location | Ahmedabad, Gujarat |
| Work Mode | Work from Office / Onsite |
| Employment Type | Full-time |
| Experience | Refer to the official recruitment details |
| Application Mode | Online Application |
💼 1. Medical Information Specialist
The Medical Information function plays an important role in providing accurate and scientifically supported information about pharmaceutical products.
Professionals working in this area may interact with healthcare professionals and other stakeholders to handle medical information requests.
Key Responsibilities
Depending on the specific position, responsibilities may include:
- Handling unsolicited medical information inquiries.
- Reviewing and documenting medical questions.
- Providing accurate responses based on approved information and company procedures.
- Recording product complaints and relevant safety information.
- Identifying and documenting potential adverse events.
- Following established Standard Operating Procedures (SOPs).
- Maintaining appropriate records and documentation.
- Working with internal teams when additional medical or safety information is required.
This type of position can be useful for candidates interested in Medical Information, Pharmacovigilance, and drug-safety operations.
📝 2. Regulatory Case Processing Analyst
Individual Case Safety Report (ICSR) processing is one of the major operational areas within Pharmacovigilance.
Professionals involved in case processing work with safety information received from different sources and help ensure that relevant information is accurately documented and processed.
Possible Responsibilities
The role may involve:
- Receiving and performing initial assessment of adverse event reports.
- Performing case intake and triage.
- Entering safety information into relevant databases.
- Reviewing patient and event information.
- Coding medical terminology using standardized dictionaries such as MedDRA.
- Preparing or updating medical narratives.
- Following Pharmacovigilance procedures and quality requirements.
- Supporting the preparation of safety reports.
- Maintaining accurate case documentation.
- Working according to applicable regulatory and company requirements.
Candidates interested in developing a career in drug safety case processing can gain valuable exposure through this type of role.
📚 3. Global Literature Screening
Scientific literature is an important source of information for ongoing drug-safety surveillance.
The Global Literature Screening function involves reviewing scientific publications and identifying information that may be relevant to the safety profile of pharmaceutical products.
Possible Responsibilities
Candidates working in this area may be involved in:
- Searching scientific and biomedical literature databases.
- Screening published research articles.
- Reviewing publications for potentially relevant safety information.
- Identifying adverse drug reactions and other safety-related information.
- Assessing publications according to established screening criteria.
- Documenting relevant findings.
- Escalating potentially important safety information for further evaluation.
- Following internal procedures for literature surveillance.
This can be a suitable career path for candidates who enjoy scientific literature review, medical research, and Pharmacovigilance.
🎓 Educational Qualification
According to the vacancy information, candidates from the following educational backgrounds can explore these opportunities:
- B.Pharm – Bachelor of Pharmacy
- M.Pharm – Master of Pharmacy
- Pharm.D – Doctor of Pharmacy
- BDS – Bachelor of Dental Surgery
- MDS – Master of Dental Surgery
Candidates should carefully check the official recruitment information for any additional eligibility requirements, experience criteria, or role-specific conditions before applying.
📍 Job Location – Ahmedabad, Gujarat
These opportunities are based in Ahmedabad, Gujarat.
The positions mentioned in the vacancy information are onsite/work-from-office roles, meaning candidates should be prepared to work from the company’s Ahmedabad location.
Candidates currently living in Ahmedabad or nearby areas may find the location more convenient for regular office attendance.
🏢 Why Consider a Pharmacovigilance Career?
Pharmacovigilance is an important part of the pharmaceutical and healthcare industry. The field focuses on identifying, evaluating, documenting, and monitoring information related to the safety of medicines.
Depending on the role, professionals can develop experience in areas such as:
- Individual case safety report processing
- Adverse event documentation
- Medical terminology
- MedDRA coding
- Safety database operations
- Medical information
- Literature surveillance
- Regulatory safety requirements
- Quality and compliance processes
Experience in these areas can be relevant when exploring future opportunities in Pharmacovigilance, Clinical Research, Medical Information, Drug Safety, and Regulatory Affairs.
👨💼 Who Can Apply?
This opportunity may be relevant for candidates who:
- Have a degree in Pharmacy, Dental Science, or a related eligible discipline.
- Are interested in Pharmacovigilance and drug safety.
- Want to build a career in clinical research or life sciences.
- Are comfortable working from an Ahmedabad office.
- Have good attention to detail and documentation skills.
- Are interested in scientific and medical information.
Candidates should verify the exact eligibility criteria for the specific position before submitting their application.
📲 How to Apply for Lambda Therapeutics Jobs
Interested and eligible candidates can submit their details through the recruitment application form provided for these openings.
👉 Apply Here:
If you’re looking to develop your knowledge alongside your Pharmacy, Life Sciences, or Clinical Research education, you can check out the course here:
👉 Learn More & Enroll on Udemy
Note: Please verify the application link and vacancy details before submitting your personal information. Recruitment conditions can change, and candidates should rely on the latest information provided by the hiring organization.
📌 Important Note for Job Seekers
Before applying, candidates should:
- Keep an updated resume ready.
- Check their educational eligibility.
- Verify the job location.
- Review the specific position they are applying for.
- Provide accurate information in the application form.
- Never pay money to anyone in exchange for a job or interview.
🔎 Frequently Asked Questions
Is Lambda Therapeutics hiring for Pharmacovigilance jobs in Ahmedabad?
The vacancy information provided indicates openings in Pharmacovigilance-related functions in Ahmedabad, including Medical Information, Regulatory Case Processing, and Global Literature Screening.
What qualifications are eligible?
The listed qualifications include B.Pharm, M.Pharm, Pharm.D, BDS, and MDS, subject to the specific requirements of the position.
Is this a work-from-home opportunity?
No. The vacancy information indicates that these positions are onsite/work-from-office roles in Ahmedabad.
What type of work is involved in Regulatory Case Processing?
Regulatory case processing generally involves activities such as adverse event intake, case triage, safety data entry, medical terminology coding, narrative preparation, and quality review.
What is Global Literature Screening?
Global Literature Screening involves systematically reviewing scientific publications to identify information potentially relevant to pharmaceutical product safety.
🚀 Final Words
For pharmacy, dental, and life-science professionals interested in building a career in Pharmacovigilance and drug safety, these Lambda Therapeutics openings in Ahmedabad cover several important areas of the industry.
Whether your interest is Medical Information, ICSR processing, or Global Literature Screening, these functions can provide exposure to different aspects of pharmaceutical safety operations.
Eligible candidates should review the vacancy information carefully and submit their application through the provided recruitment channel.