MSN Laboratories hiring Medical Writer in Hyderabad
- Medical Writer – PharmD/M.Pharm – Hyderabad (PV Role)
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Background
- Experience Requirements
- Required Skills
- Location & Employment Details
- Job Location
- Employment Type
- Application Process
- FAQs
- Who can apply for the Medical Writer role at MSN Laboratories?
- Is this role focused on pharmacovigilance?
- Is prior experience mandatory?
- Where is the job location?
- Is this a work-from-home role?
Medical Writer – PharmD/M.Pharm – Hyderabad (PV Role)
MSN Laboratories hiring Medical Writer in Hyderabad. PharmD, M.Pharm eligible with PV experience in PSUR, PADER, RMP writing.
MSN Laboratories has announced a full-time, on-site opening for the position of Medical Writer at its Hyderabad facility. This role is positioned within the pharmacovigilance and drug safety function and is ideal for professionals with hands-on experience in regulatory medical writing, aggregate report preparation, and safety documentation across the product lifecycle. The opportunity offers direct involvement in global pharmacovigilance operations, regulatory compliance, and patient safety activities, making it a high-value career move for PharmD and M.Pharm professionals aiming to grow in high-demand, high-CPC drug safety and medical writing domains.
Company Overview
MSN Laboratories is one of India’s fastest-growing pharmaceutical companies with a strong presence across APIs, formulations, and contract research and manufacturing services. The company supplies affordable, high-quality medicines to regulated and semi-regulated markets worldwide and maintains strict compliance with global regulatory standards.
With dedicated investments in research, quality systems, and pharmacovigilance infrastructure, MSN Laboratories plays a critical role in ensuring drug safety, regulatory compliance, and lifecycle risk management. Working with MSN offers long-term stability, strong technical exposure, and hands-on experience in global safety reporting and regulatory medical writing.
Job Role & Responsibilities
The Medical Writer role at MSN Laboratories combines medical writing, pharmacovigilance operations support, and quality review responsibilities. The position contributes directly to regulatory submissions, aggregate safety reporting, and risk management activities.
Key Responsibilities
- Authoring regulatory medical writing documents across the product lifecycle
- Preparation of aggregate safety reports including:
- Periodic Safety Update Reports (PSURs)
- Periodic Adverse Drug Experience Reports (PADERs)
- Development Safety Update Reports (DSURs)
- Risk Management Plans (RMPs)
- Medical and quality review of pharmacovigilance documents prepared by peers
- Ensuring accuracy, consistency, and regulatory compliance of safety documents
- Supporting pharmacovigilance operations linked to medical writing activities
- Reviewing case narratives, safety data, and signal management reports
- Active participation in trainings, audits, and quality system maintenance
- Continuous self-learning on regulatory guidelines, safety reporting standards, and medical writing best practices
This role aligns strongly with high CPC search categories such as medical writer jobs in pharmacovigilance, drug safety medical writing roles, regulatory affairs documentation, and aggregate report writing careers.
Eligibility / Qualifications
Educational Background
Candidates must possess one of the following qualifications:
PharmD, M.Pharm (Pharmacology, Pharmaceutics, Clinical Pharmacy, Regulatory Affairs), MBBS, MD (Pharmacology)
Experience Requirements
- Prior experience in pharmacovigilance medical writing is preferred
- Hands-on exposure to PSURs, PADERs, DSURs, RMPs, and Signal Management Reports
- Experience in drug safety documentation and regulatory submissions will be a strong advantage
Required Skills
- Strong understanding of pharmacovigilance and drug safety processes
- Excellent written and verbal communication skills
- Advanced proficiency in MS Word, Excel, and PowerPoint
- Strong time management, multitasking, and attention to detail
- Fluency in English for regulatory documentation and global submissions
Location & Employment Details
Job Location
- Hyderabad, Telangana
Employment Type
- Full-time
- On-site role
Salary is aligned with industry standards for experienced pharmacovigilance medical writers and depends on qualifications and prior experience.
Application Process
Interested candidates can apply directly through the official LinkedIn job posting using the link below:
Apply here: https://www.linkedin.com/jobs/view/4329979549/
Shortlisted candidates will be contacted by the MSN Laboratories talent acquisition team for further evaluation.
FAQs
Who can apply for the Medical Writer role at MSN Laboratories?
Candidates with PharmD, M.Pharm, MBBS, or MD Pharmacology qualifications and relevant medical writing or pharmacovigilance experience can apply.
Is this role focused on pharmacovigilance?
Yes. The role is heavily focused on aggregate safety reports, risk management plans, and pharmacovigilance medical writing.
Is prior experience mandatory?
Relevant experience in drug safety medical writing is preferred and gives candidates a strong advantage.
Where is the job location?
The position is based in Hyderabad, Telangana.
Is this a work-from-home role?
No. This is a full-time, on-site position.
| Company | MSN Laboratories |
|---|---|
| Vacancies | Not Disclosed |
| Required Education | PharmD, M.Pharm (Pharmacology, Pharmaceutics, Clinical Pharmacy, Regulatory Affairs), MBBS, MD Pharmacology |
| Experience | Relevant PV Medical Writing Experience Preferred |
To apply for this job please visit www.linkedin.com.
