Macleods Pharma Hiring for RMP Reviewer in Mumbai for pharmacovigilance roles. Check eligibility, responsibilities, salary, and full application process here.
Introduction
Macleods Pharmaceutical Ltd, one of India’s leading research-driven pharmaceutical companies, is inviting applications for the position of RMP Reviewer in its Pharmacovigilance (PV) and Risk Management division located in Andheri East, Mumbai. This role is ideal for candidates with an M.Pharm in Pharmacology and 1–2 years of hands-on experience in reviewing risk management plans, periodic safety update reports, and other regulatory safety documents. Macleods Pharma Hiring for RMP Reviewer
With a strong global presence across Europe, the UK, India, and several ROW (Rest of the World) markets, Macleods Pharma offers an excellent platform for professionals looking to advance their careers in pharmacovigilance, regulatory submissions, and global safety compliance. This long-format post provides complete details about the job, including responsibilities, required qualifications, skills, work environment, salary insights, and the exact steps to apply. Macleods Pharma Hiring for RMP Reviewer
About Macleods Pharmaceutical Ltd
Founded in 1986, Macleods Pharmaceutical Ltd has grown into a respected global pharmaceutical organization with significant contributions in formulations, R&D, and commercial operations across more than 120 countries. Known for its commitment to quality and safety, the company invests heavily in research and innovation, particularly in complex therapeutic areas. Macleods Pharma Hiring for RMP Reviewer
The Pharmacovigilance and Risk Management division plays a crucial role in ensuring that all Macleods products meet stringent international safety requirements. The RMP Reviewer position is a key role in this department, supporting regulatory compliance across multiple regions. Macleods Pharma Hiring for RMP Reviewer
Overview of the RMP Reviewer Job in Mumbai
The RMP Reviewer is responsible for performing comprehensive quality checks on safety documents such as PSURs, PBRERs, ACOs, and Risk Management Plans. These documents are central to ensuring drug safety through continuous monitoring, evaluation, and mitigation of risks associated with pharmaceutical products. Macleods Pharma Hiring for RMP Reviewer
Job Highlights
- Job Title: RMP Reviewer
- Department: Pharmacovigilance / Pharma Covigilance RND Department
- Company: Macleods Pharmaceutical Ltd
- Location: Andheri East, Mumbai
- Qualification Required: M.Pharm in Pharmacology
- Experience Required: 1–2 years
- Job Type: Full-time
- Application Mode: Email
- Salary Range: INR 4.5–6.5 LPA (based on experience)
- Eligibility: Only experienced candidates; freshers should not apply
Why This Role Is Important
Risk management planning is an essential component of pharmacovigilance. Regulatory authorities such as EMA, MHRA, CDSCO, and other global agencies expect pharmaceutical companies to maintain active and transparent safety reporting systems. Macleods Pharma Hiring for RMP Reviewer
As an RMP Reviewer, you will play a central role in:
- Enhancing patient safety
- Ensuring product compliance with national and international regulatory standards
- Supporting global submissions
- Improving overall quality of safety documentation
This makes the role highly responsible, impactful, and valuable for long-term growth in the field of drug safety.
Roles and Responsibilities
The RMP Reviewer position involves detailed analysis, quality review, and timely submission of pharmacovigilance documents. Below are the key responsibilities associated with the role:
1. Quality Review of Safety Documents
The RMP Reviewer will be responsible for conducting high-quality reviews of the following:
- PSUR (Periodic Safety Update Report)
- PBRER (Periodic Benefit-Risk Evaluation Report)
- ACO (Addendum to Clinical Overview)
- RMP (Risk Management Plan)
These reports are reviewed for accuracy, completeness, regulatory compliance, formatting, and alignment with safety data. Macleods Pharma Hiring for RMP Reviewer
2. Preparation of Submission Calendars
The reviewer must prepare:
- Submission timelines
- PBRER/PSUR calendars
- Task allocation schedules
This ensures on-time submission of safety documents to the Regulatory Affairs (RA) team, Lead Responsible Person (LRP), or respective global authorities.
3. Tracking and Monitoring Reports
The role requires tracking:
- Report progress
- Submission timelines
- Outstanding tasks
- Queries from authorities
The reviewer must maintain accurate documentation throughout the process.
4. Preparation and Training for SOPs and SGDs
Candidates will be involved in:
- Preparing Standard Operating Procedures (SOPs)
- Preparing Standard Guideline Documents (SGDs)
- Training the pharmacovigilance team on updated guidelines
This ensures alignment with current regulatory expectations.
5. Responding to Regulatory Queries
Handling questions from authorities such as:
- European agencies
- UK regulatory bodies
- CDSCO (India)
- ROW markets
You must prepare accurate and timely responses to queries regarding safety submissions. Macleods Pharma Hiring for RMP Reviewer
6. Technical Skill Usage
Candidate must be proficient in:
- MS Word (report formatting, editing)
- Microsoft Excel (tracking tables, calendars)
- PowerPoint (presentations, training material)
Qualifications and Eligibility Criteria
1. Educational Qualification
- M.Pharm in Pharmacology is mandatory.
Other specializations are not eligible for this role.
2. Experience Required
- 1 to 2 years of experience in pharmacovigilance, specifically in reviewing:
- PSUR
- PBRER
- ACO
- RMP
Freshers or candidates without document review experience should not apply.
3. Domain Knowledge Required
Applicants must demonstrate knowledge of:
- EU/UK regulatory frameworks
- RMP structure and content requirements
- Safety reporting guidelines
- Global submission standards
- Risk minimization measures (RMMs)
4. Additional Requirements
- Strong attention to detail
- Ability to understand scientific literature
- Good communication and writing skills
- Ability to work under deadlines
- Experience in a pharma covigilance setup is preferred
Salary and Benefits
Macleods Pharma offers competitive compensation within the range of:
Salary:
INR 4.5–6.5 Lakhs per annum
Salary is offered based on: Macleods Pharma Hiring for RMP Reviewer
- Total experience
- Expertise in safety document review
- Exposure to international submissions
- Performance in interview rounds
Benefits of Working at Macleods
- Strong learning environment
- Exposure to global regulatory submissions
- Growth opportunities in pharmacovigilance and safety writing
- Experience working with R&D and RA teams
- Stable long-term career path
Work Environment and Career Growth
The position is based in Andheri East, Mumbai, a major hub for pharmaceutical operations. Employees in the pharmacovigilance RND team get exposure to: Macleods Pharma Hiring for RMP Reviewer
- Global PV guidelines
- Multidepartment collaboration
- New drug development processes
- International audits and compliance requirements
Career paths from this role include:
- Senior RMP Reviewer
- PV Scientist
- Aggregate Report Writer
- Regulatory Writing Specialist
- Safety Lead / Team Lead
FAQs
1. What experience is required for the RMP Reviewer job?
Applicants need 1–2 years of experience in pharmacovigilance with practical exposure to PSUR, PBRER, ACO, or RMP review. Freshers are not eligible.
2. Where is the job located?
The job is located in the Pharma Covigilance RND Department, Andheri East, Mumbai.
How to Apply
Experienced candidates who meet the eligibility criteria can apply by following the steps below: Macleods Pharma Hiring for RMP Reviewer
Step-by-Step Application Process
- Prepare your updated resume in PDF format.
- Ensure your resume highlights experience in PSUR, PBRER, ACO, and RMP review.
- Write a professional email mentioning your interest in the RMP Reviewer role.
- Add the subject line:
“Application for RMP Reviewer – Mumbai” - Attach your resume and any relevant certifications.
- Send your application to the official email ID:
Email ID to Apply:
Application Deadline:
Applications are open for 30 days from the published date.
For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.
Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
