Life Science Job at ProductLife Group | Apply Now
ProductLife Group is currently seeking a specialized professional for a Life Science Job as an Information & Documentation Officer, focused on Literature Monitoring. This role is based in India and is an essential component of the company’s pharmacovigilance operations. By identifying and documenting adverse events reported in scientific literature, you will play a critical role in maintaining drug safety standards. If you are looking to launch or advance a Pharmacovigilance Career, this position offers exposure to international databases and rigorous quality control systems.
- Job Position: Information & Documentation Officer (Literature Monitoring)
- Location: India
About The Company
ProductLife Group is a specialized organization focused on high-level regulatory and safety services within the pharmaceutical industry. The company serves as a critical partner for global clients, ensuring that drug safety data is meticulously monitored and documented according to international standards. A Pharmacovigilance Career at ProductLife Group involves working within a rigorous quality-controlled environment to protect public health through proactive literature surveillance.
Key Responsibilities Of This Life Science Job
In this role, you will be responsible for the systematic monitoring of scientific literature to support global safety data collection.
- Database Monitoring: Perform comprehensive literature searches in international databases and prepare detailed output reports.
- Database Proficiency: Utilize the PubMed and ADIS international literature databases to list cases found in scientific publications.
- Local Surveillance: Conduct periodic literature watches in local journals to ensure no regional safety data is missed.
- Quality Assurance: Contribute to the implementation of the quality control system for all performed tasks and follow up on results.
- Audit Participation: Engage in client audits to verify that literature monitoring processes meet regulatory and contractual requirements.
- Document Management: Receive, store, and formally acknowledge receipt of documents provided by clients.
Qualification and Experience: Pharmacovigilance Career
ProductLife Group is looking for candidates with a strong foundational knowledge of pharmacology and drug safety regulations.
- Educational Background: You must be a Master or Bachelor of Pharmacy or a Life Science graduate.
- Professional Experience: Candidates should have 1 to 3 years of experience in Pharmacovigilance. Freshers with specific Pharmacovigilance knowledge are also encouraged to apply.
- Regulatory Knowledge: A good understanding of GVP Module VI is essential for this Life Science Job.
- Technical Training: Formal training in Pharmacovigilance (PV) and an understanding of literature writing or publishing are required.
- Communication Skills: Proficiency in English, both oral and written, is mandatory for global reporting.
- Software Proficiency: Advanced knowledge of Microsoft Office, including Outlook, Teams, Excel, PowerPoint, Word, and SharePoint, is necessary.
In summary, the Information & Documentation Officer position at ProductLife Group is a definitive step for those committed to a Pharmacovigilance Career. This Life Science Job provides the opportunity to master complex databases like PubMed and ADIS while ensuring compliance with international GVP modules. Because the role involves direct participation in client audits and quality control, it serves as an excellent platform to build expertise in the regulatory aspects of drug safety. If you have a passion for pharmacology and a detail-oriented mindset, this position in India is the perfect place to grow your career.
