Looking for remote Pharmacovigilance jobs in India or Regulatory Affairs jobs for pharmacy graduates? ProductLife Group (PLG) has announced hiring for three exciting positions in its Safety & Vigilance and Regulatory Affairs divisions. The company is inviting applications from Pharmacy and Life Science professionals for Information and Documentation Officer, Case Specialist, and RA Officer (Associate Consultant) positions.
These work-from-home pharmaceutical jobs offer excellent opportunities for professionals interested in Pharmacovigilance, Literature Monitoring, Drug Safety, and Regulatory Affairs.
About ProductLife Group
ProductLife Group (PLG) is a global life sciences consulting company providing regulatory affairs, pharmacovigilance, quality compliance, and medical information services to pharmaceutical, biotechnology, and medical device companies worldwide.
The organization supports the complete product lifecycle, helping healthcare companies ensure regulatory compliance and patient safety.
1. Information and Documentation Officer (India)
Job Location
- India
- Remote Work Available
Department
Safety and Vigilance
Employment Type
Permanent
Key Responsibilities
- Perform literature searches using international databases.
- Conduct literature monitoring in local journals.
- Search and review scientific publications using PubMed and ADIS databases.
- Prepare literature outputs and case listings.
- Participate in client audits.
- Support quality control activities.
- Receive and acknowledge documentation from clients.
- Maintain documentation records accurately.
Eligibility
- Bachelor’s or Master’s degree in Pharmacy
- Life Science graduates may also apply
Experience Required
- 1โ3 years of Pharmacovigilance experience
OR
- Freshers with Pharmacovigilance knowledge are eligible.
Required Skills
- Good understanding of GVP Module VI
- Pharmacovigilance training
- Literature review and scientific publication knowledge
- Knowledge of PubMed and ADIS databases
- Excellent English communication
- Microsoft Office (Excel, Word, Outlook, Teams, SharePoint)
- Pharmacology knowledge
2. Case Specialist (India)
Job Location
- India
- Remote Work Available
Department
Safety and Vigilance
Employment Type
Permanent
Key Responsibilities
- Quality control of vigilance cases
- Medical evaluation of Individual Case Safety Reports (ICSRs)
- Data entry into pharmacovigilance databases
- Follow-up of safety cases
- Medical assessment of adverse event reports
- Coding using standard dictionaries
- Causality assessment
- Seriousness evaluation
- Submission requirement identification
- Review medical information and product complaints
- Support medical information teams
- Prepare quality documents
- Customer communication
Eligibility
- Doctor of Pharmacy (PharmD) or Pharmacist by training
Experience Required
- 4โ5 years of Pharmacovigilance experience
Required Skills
- Pharmacovigilance database experience
- Current regulatory knowledge
- Excellent communication
- Microsoft Office
- Multitasking ability
- Teamwork
- Process-oriented mindset
3. RA Officer (Associate Consultant)
Job Location
- India
- Remote Work Available
Department
Regulatory Affairs & Operations
Employment Type
Permanent
Key Responsibilities
- Support pharmaceutical registrations
- Regulatory submissions for Australia, New Zealand and JAPAC region
- eCTD publishing
- Prepare regulatory dossiers
- Submit applications to TGA and Medsafe
- Support GMP Clearance applications
- Client management
- Regulatory documentation review
- Quality document preparation
Eligibility
- Undergraduate degree in Pharmaceutical Sciences or related Life Sciences
Experience Required
- Minimum 3 years in Regulatory Affairs
- Australian or New Zealand Regulatory Affairs experience preferred
Required Skills
- TGA regulations
- Medsafe regulations
- eCTD publishing
- Regulatory dossier preparation
- Project management
- Strong written communication
- Computer proficiency
Why Join ProductLife Group?
- Permanent employment
- Remote work opportunity across India
- Global pharmaceutical projects
- Career growth in Pharmacovigilance
- Exposure to international regulatory agencies
- Collaborative global team
- Learning and professional development
Who Should Apply?
These openings are ideal for:
- B.Pharm graduates
- M.Pharm graduates
- PharmD professionals
- Life Science graduates
- Pharmacovigilance professionals
- Regulatory Affairs professionals
- Drug Safety Associates
- Literature Monitoring Specialists
How to Apply
Application Link For Information and Documentation Officer (India)
Application Link For Case Specialist (India)
Application Link For RA Officer (Associate Consultant)