Pharmacovigilance Work From Home Hiring -ProductLife Group

ProductLife Group Hiring Information and Documentation Officer | Pharmacovigilance Jobs in India

ProductLife Group (PLG) is currently hiring for the position of Information and Documentation Officer in India. This is an excellent opportunity for pharmacy and life sciences professionals looking to build or advance their careers in pharmacovigilance, drug safety, literature monitoring, medical information management, and regulatory compliance.

The role is part of ProductLife Group’s Safety and Vigilance division and offers the flexibility of remote work. Candidates with experience in pharmacovigilance activities, literature surveillance, adverse event monitoring, and safety documentation will find this opportunity particularly relevant. Freshers with pharmacovigilance knowledge and training are also encouraged to apply.

For candidates searching for pharmacovigilance jobs in India, drug safety associate careers, literature monitoring specialist vacancies, remote PV jobs, pharmaceutical safety officer positions, and healthcare compliance opportunities, this opening offers valuable exposure to global safety operations and regulatory processes.

Company Overview

ProductLife Group is a global consulting and outsourcing organization specializing in regulatory affairs, pharmacovigilance, quality compliance, medical information, and product lifecycle management services for the pharmaceutical, biotechnology, medical device, and healthcare industries.

The company supports healthcare organizations throughout the entire product lifecycle, helping clients maintain regulatory compliance, patient safety, product quality, and market access across international markets.

With growing regulatory requirements and increased focus on drug safety surveillance, ProductLife Group continues to expand its pharmacovigilance and safety operations by recruiting professionals skilled in literature review, adverse event reporting, regulatory documentation, and safety monitoring.

Job Role & Responsibilities

Information and Documentation Officer Responsibilities

The selected candidate will support literature monitoring and pharmacovigilance activities within the Safety and Vigilance team.

Key responsibilities include:

• Conducting literature searches using international scientific databases
• Performing routine literature monitoring activities
• Reviewing local and international medical journals
• Using PubMed and ADIS databases for literature surveillance
• Identifying and documenting safety-related literature cases
• Supporting pharmacovigilance literature review processes
• Maintaining accurate literature monitoring records
• Receiving, storing, and acknowledging client documentation
• Participating in client audits and compliance activities
• Supporting implementation of quality control procedures
• Monitoring quality metrics and follow-up actions
• Ensuring compliance with pharmacovigilance procedures and global safety standards
• Supporting documentation management activities within the pharmacovigilance function

Skills Required

Candidates should possess:

• Pharmacovigilance knowledge
• Literature monitoring experience
• Drug safety and adverse event awareness
• Medical literature review skills
• Understanding of GVP Module VI
• Knowledge of pharmacology principles
• Documentation management skills
• Quality compliance understanding
• Scientific data interpretation abilities
• Strong written and verbal communication skills
• Attention to detail and analytical thinking
• Microsoft Office proficiency

Technical Knowledge Preferred

• PubMed database
• ADIS database
• Pharmacovigilance systems
• Literature surveillance processes
• Safety reporting workflows
• Regulatory compliance requirements

Eligibility / Qualifications

Educational Qualification

Candidates with pharmacy and life sciences backgrounds are eligible.

Relevant courses include:

B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacology, Clinical Research, Pharmaceutical Sciences.

Experience Requirement

• 1–3 years of pharmacovigilance experience preferred
• Freshers with pharmacovigilance training or knowledge can also apply
• Experience in literature monitoring will be an added advantage

Suitable candidates include:

• Pharmacovigilance Associates
• Drug Safety Associates
• Safety Surveillance Professionals
• Literature Review Specialists
• Regulatory Affairs Professionals
• Clinical Research Associates
• Pharmacy Graduates
• Life Science Graduates

Location & Salary

Location

India (Remote)

Salary

₹4.5 LPA – ₹8.5 LPA (Approximate)

Application Process

Interested candidates can apply through the official ProductLife Group careers portal.

Apply Here:

https://www.productlifegroup.com/jobs/information-and-documentation-officer-vaf-580/

Employment Type

Permanent Contract

Department

Safety and Vigilance

Work Mode

Remote

Frequently Asked Questions (FAQs)

1. Who can apply for the Information and Documentation Officer role?

Candidates with Pharmacy or Life Sciences qualifications can apply.

2. Are freshers eligible for this opportunity?

Yes. Freshers with pharmacovigilance knowledge or training are encouraged to apply.

3. What pharmacovigilance knowledge is preferred?

Knowledge of GVP Module VI, literature monitoring, drug safety processes, and pharmacology is preferred.

4. Is this a remote opportunity?

Yes. This position offers remote work flexibility within India.

5. What databases should candidates be familiar with?

Knowledge of PubMed and ADIS databases is preferred.

6. What is the estimated salary for this role?

The expected salary range is approximately ₹4.5 LPA to ₹8.5 LPA depending on experience and pharmacovigilance expertise.

Summary Table

Company	ProductLife Group
Department Vacancies	Information and Documentation Officer – Safety & Vigilance
Qualification	B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Biotechnology, Pharmacology
Experience	Freshers with PV Knowledge or 1–3 Years Experience
Location	India (Remote)