Global life sciences company ProductLife Group (PLG) is hiring experienced professionals for multiple remote Pharmacovigilance, Drug Safety, Medical Review, and Regulatory Affairs positions in India. These permanent work-from-home opportunities are ideal for candidates with experience in pharmacovigilance case processing, medical review, regulatory submissions, and safety database management.
The latest PLG jobs in India include openings for PV Specialists, Data Officers, Regulatory Affairs Specialists, RA Officers, and Medical Advisors. Candidates with B.Pharm, M.Pharm, PharmD, MBBS, MD, or Life Sciences backgrounds can apply depending on the role.
Open Positions at PLG India
1. PV Specialist โ Safety & Vigilance
Experience: 4โ5 Years
Qualification: Pharmacist / Doctor in Pharmacy
Location: India (Remote Possible)
Key Responsibilities
- Quality control of vigilance cases
- Medical evaluation and case assessment
- MedDRA coding and causality assessment
- Safety database management
- Follow-up requests and case closure
- Identification of reporting requirements
- Reviewing medical information and quality complaints
- Supporting pharmacovigilance operations
Skills Required
- Knowledge of global PV regulations
- Safety database experience
- Strong communication and analytical skills
- Microsoft Office proficiency
- Ability to multitask and work in teams
2. Data Officer โ Pharmacovigilance
Experience: 1โ3 Years
Qualification: B.Pharm / M.Pharm
Location: India (Remote Possible)
Key Responsibilities
- Vigilance case intake and triage
- MedDRA coding and narrative writing
- Duplicate search in safety databases
- Regulatory submissions and reporting
- Case follow-up through email and phone
- Maintenance of tracking tools and line listings
Skills Required
- Pharmacovigilance case processing
- Safety database handling
- Regulatory reporting knowledge
- Attention to detail and client communication
3. RA Officer (Associate Consultant)
Department: Regulatory Affairs & Operations
Experience: Minimum 3 Years
Qualification: Pharmaceutical Sciences / Life Sciences
Location: India (Remote Possible)
Key Responsibilities
- Regulatory submissions for Australia & New Zealand
- eCTD publishing support
- Preparation of TGA and Medsafe dossiers
- GMP clearance applications
- Lifecycle maintenance activities
- Regulatory documentation and client support
Preferred Skills
- TGA & Medsafe regulations knowledge
- Regulatory dossier preparation
- Project management and communication skills
4. Regulatory Affairs Specialist โ UK Legislation
Experience: 3โ7 Years
Qualification: Pharmacy / Life Sciences
Location: India (Remote Possible)
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
Required Skills
- Experience with MHRA & EMA regulations
- Veeva Vault, LorenZ, Trackwise knowledge
- Product lifecycle management expertise
- Strong regulatory compliance understanding
5. Medical Advisor โ Drug Safety & Medical Review
Experience: 10+ Years
Qualification: MBBS / MD
Location: India (Remote Possible)
Key Responsibilities
- Medical monitoring for clinical trials
- SUSAR assessments and medical review
- Pharmacovigilance leadership
- Benefit-risk evaluation
- Training and mentoring PV teams
- Client communication and audit support
Required Skills
- Strong GCP, GVP, FDA knowledge
- Clinical phase monitoring experience
- Safety database expertise
- Leadership and stakeholder management
Why Join PLG?
- Permanent remote opportunities
- Work with global pharmaceutical clients
- Exposure to international regulatory markets
- Career growth in Pharmacovigilance and Regulatory Affairs
- Collaborative global work environment
How to Apply
Application Link For PV Specialist โ Safety & Vigilance
Application Link For Data Officer โ Pharmacovigilance
Application Link For RA Officer (Associate Consultant)
Application Link For Regulatory Affairs Specialist โ UK Legislation
Application Link For Medical Advisor โ Drug Safety & Medical Review
