Alvotech has announced 4 Pharmacovigilance and Safety Data Management vacancies for its Clinical and Medical Research (iCMR) function in India. The openings include Pharmacovigilance Specialist and Pharmacovigilance Associate positions, with opportunities based at the Bangalore Office and India Home Office under a partially remote work arrangement.
The roles focus on clinical trial safety, post-marketing pharmacovigilance, ICSR/SAE management, regulatory submissions, literature monitoring, safety systems and global PV compliance.
Application deadline: September 29, 2026
Work arrangement: Partially Remote
Location: Bangalore Office / India Home Office
Job type: Full Time
Alvotech Pharmacovigilance Vacancies 2026
| Position | Experience | Job Requisition |
|---|---|---|
| Pharmacovigilance Specialist – Safety Data Management | 3+ years | JR100100 |
| Pharmacovigilance Specialist – Safety Data Management | 3+ years | JR100092 |
| Pharmacovigilance Associate – Safety Data Management | 2+ years | JR100088 |
| Pharmacovigilance Associate – Safety Data Management | 2+ years | JR100089 |
Although the four vacancies have different requisition IDs, the supplied job descriptions indicate substantially similar responsibilities and requirements.
About Alvotech
Alvotech is a specialty biopharmaceutical company focused on the development and manufacturing of biosimilar medicines.
The positions are part of the company’s Global Safety Data Management team, within the integrated Clinical and Medical Research function. The team supports safety activities associated with clinical trials and post-marketing programs.
Alvotech Pharmacovigilance Job Responsibilities
Selected candidates may be responsible for:
- Managing assigned clinical safety and post-marketing PV activities
- Performing ICSR and SAE management
- Supporting regulatory safety submissions
- Conducting literature monitoring
- Supporting digital platform monitoring
- Performing safety data reconciliations
- Working with EV and XEVMPD activities
- Supporting safety-system setup, configuration and validation
- Participating in PV system lifecycle management
- Maintaining and optimizing global pharmacovigilance processes
- Ensuring compliance with FDA, EMA and ICH requirements
- Working with Clinical, Benefit-Risk Management and Partner Compliance teams
- Collaborating with Quality, Regulatory, IT and other internal functions
- Coordinating with external PV service providers and business partners
- Delivering training on pharmacovigilance processes and standards
- Supporting audits and inspections related to Safety Data Management
Alvotech Pharmacovigilance Specialist – Eligibility
For the Pharmacovigilance Specialist positions, applicants should have:
- A Master’s degree in pharmaceutical sciences or a related field
- Relevant backgrounds may include Pharmacy, Medicine or Life Sciences
- 3+ years of experience in Pharmacovigilance/Drug Safety
- Hands-on experience in Safety Data Management
- Experience with both clinical trial safety and post-marketing PV
- Experience with safety systems such as Argus or ARISg
- Experience with Veeva Safety Vault is an advantage
- Experience working with global products and clinical trials
- Knowledge of biologics and combination products is advantageous
- Strong knowledge of PV regulations and guidelines
Alvotech Pharmacovigilance Associate – Eligibility
For the Pharmacovigilance Associate positions, candidates should have:
- A Master’s degree in pharmaceutical sciences or a related field
- Background in Medicine, Pharmacy or Life Sciences
- 2+ years of Pharmacovigilance/Drug Safety experience
- Hands-on experience in Safety Data Management
- Clinical trial safety and post-marketing PV experience
- Experience with Argus or ARISg
- Veeva Safety Vault experience is an advantage
- Knowledge of global PV processes and regulatory requirements
- Experience with global products and clinical trials
Regulatory Knowledge Required
The positions specifically call for knowledge of major pharmacovigilance and clinical research frameworks, including:
- 21 CFR
- ICH guidelines
- GVP
- GCP
- CIOMS
- FDA requirements
- EMA requirements
- Clinical safety and post-marketing PV requirements
Key Skills for These Pharmacovigilance Jobs
Candidates applying for these Alvotech jobs should be comfortable with:
Pharmacovigilance: ICSR processing, SAE management, post-marketing safety, clinical trial safety and regulatory reporting.
Safety Data Management: Data reconciliation, safety databases, case management and safety-system lifecycle activities.
Safety Systems: Argus, ARISg and preferably Veeva Safety Vault.
Regulatory Compliance: 21 CFR, ICH, GVP, GCP and CIOMS.
Professional Skills: Communication, organization, time management, independent working and cross-functional collaboration.
Who Can Apply?
The stated educational requirement is a Master’s degree in pharmaceutical sciences or a related discipline, including Pharmacy, Medicine and Life Sciences.
For experienced candidates, the most relevant backgrounds include:
- Pharmacovigilance
- Drug Safety
- Safety Data Management
- Clinical Safety
- Post-Marketing Safety
- Clinical Research with substantial safety-data responsibilities
The Specialist vacancies require 3+ years, while the Associate vacancies require 2+ years of relevant experience.
Alvotech Job Location & Work Mode
The vacancies list:
Bangalore Office, India
India Home Office
The work arrangement is listed as Partially Remote, making these positions relevant to candidates seeking hybrid pharmacovigilance opportunities in India.
How to Apply
