PLG Hiring Multiple Pharmacovigilance & Regulatory Affairs Roles | Remote
ProductLife Group (PLG) is hiring multiple professionals for remote Pharmacovigilance, Drug Safety, Medical Review, and Regulatory Affairs positions across India.
These opportunities are ideal for candidates interested in Pharmacovigilance Case Processing, Drug Safety Operations, Medical Review, Regulatory Submissions, Safety Databases, and Global Regulatory Affairs.
📋 PLG Recruitment Overview
- Company: ProductLife Group (PLG)
- Work Mode: Permanent Remote / Work From Home
- Industry: Pharmacovigilance / Regulatory Affairs / CRO
- Job Type: Full-Time
- Qualification: B.Pharm / M.Pharm / Pharm.D / MBBS / MD / Life Sciences
- Experience: 1–10+ Years
💊 PV Specialist – Safety & Vigilance
🎓 Qualification:
Pharmacist / Doctor in Pharmacy
🧑💻 Experience:
4–5 Years
📌 Key Responsibilities
- Quality control of vigilance cases
- Medical evaluation and case assessment
- MedDRA coding and causality assessment
- Safety database management
- Case follow-up and closure
- Review medical information and complaints
- Support global pharmacovigilance operations
📊 Data Officer – Pharmacovigilance
🎓 Qualification:
B.Pharm / M.Pharm
🧑💻 Experience:
1–3 Years
📌 Key Responsibilities
- Vigilance case intake and triage
- MedDRA coding and narrative writing
- Duplicate search in safety databases
- Regulatory submissions and reporting
- Maintain tracking tools and line listings
- Follow-up through email and phone
📑 RA Officer (Associate Consultant)
🎓 Qualification:
Pharmaceutical Sciences / Life Sciences
🧑💻 Experience:
Minimum 3 Years
📌 Key Responsibilities
- Regulatory submissions for Australia & New Zealand
- eCTD publishing support
- Preparation of TGA and Medsafe dossiers
- Lifecycle maintenance activities
- GMP clearance applications
- Regulatory documentation and client support
🌍 Regulatory Affairs Specialist – UK Legislation
🎓 Qualification:
Pharmacy / Life Sciences
🧑💻 Experience:
3–7 Years
📌 Key Responsibilities
- UK & EU MAA submissions
- Lifecycle management activities
- CTD/eCTD compilation and maintenance
- Variations, renewals, and MAH transfers
- Artwork and labeling updates
- Coordination with MHRA and EMA
🩺 Medical Advisor – Drug Safety & Medical Review
🎓 Qualification:
MBBS / MD
🧑💻 Experience:
10+ Years
📌 Key Responsibilities
- Medical monitoring for clinical trials
- SUSAR assessments and medical review
- Benefit-risk evaluation activities
- Training and mentoring PV teams
- Client communication and audit support
- Pharmacovigilance leadership activities
🌍 Why Join PLG?
- Permanent remote work opportunities
- Exposure to international pharmaceutical clients
- Career growth in Pharmacovigilance and Regulatory Affairs
- Global collaborative work culture
- Experience with international regulatory markets
- Opportunity to work on global drug safety projects
📄 Resume & Interview Tips
- Highlight Pharmacovigilance or Regulatory Affairs experience
- Mention MedDRA, safety databases, and eCTD knowledge
- Add global regulatory exposure and SOP handling
- Use ATS-friendly resume formatting
- Showcase communication and compliance expertise
🚀 Select Role & Apply
Kindly read the complete job description carefully before applying. Make sure your Pharmacovigilance, Regulatory Affairs, or Drug Safety experience aligns with the selected role requirements before proceeding.
.png)
