"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya." (Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers) Introduction If you are a fresher or early-career professional aiming to build a strong career in Medical Device Regulatory Affairs and Quality Assurance , this opportunity can be a perfect starting point. ELEXES Medical Consulting Pvt. Ltd. has announced hiring for the position of Project Associate I – Regulatory Affairs & Quality Assurance (RA/QA) . This role is specially designed for fresh graduates and candidates with up to 6 months of experience who want hands-on exposure to global medical device regulations , including US FDA, EU MDR, CDSCO, Health Canada , along with ISO 13485 quality systems . The position offers real project experience under expert mentorship, making it ideal for long-term growth in the medical device regulatory domain. About The Company – ELEXES Medical Consulting Pvt. Ltd. EL...
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"Latest Mega Lifesciences Hiring Pharmacovigilance Executive / Sr Executive in Thane | Pharma PV Jobs"
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"Latest Mega Lifesciences Hiring Pharmacovigilance Executive / Sr Executive in Thane | Pharma PV Jobs"
Pharmacovigilance has become one of the most stable and high-growth career options in the pharmaceutical industry due to increasing global regulatory scrutiny and patient safety requirements. Companies are actively hiring skilled pharmacovigilance professionals who can manage aggregate safety reports, global compliance, and ICSR case processing.
In this direction, Mega Lifesciences has announced a new hiring opportunity for Executive / Senior Executive – Pharmacovigilance at its Thane (Maharashtra) location. This role is ideal for candidates with 2–4 years of hands-on pharmacovigilance experience, especially those skilled in PSUR, PBRER, RMP, AddCo authoring, and ICSR processing.
If you are looking to grow your career in global pharmacovigilance operations, this job can be a strong next step.
ABOUT THE COMPANY – MEGA LIFESCIENCES
Mega Lifesciences is a globally recognized pharmaceutical and healthcare company with a strong presence across Asia-Pacific, Europe, Africa, and CIS regions. The company focuses on branded generics, nutraceuticals, and specialty healthcare products, serving millions of patients worldwide.
🔹 Company Highlights
Founded: 1978
Headquarters: Bangkok, Thailand
Employees: 10,000+ globally
Presence: 30+ countries
Business Areas: Pharmaceuticals, Consumer Healthcare, Nutraceuticals
Mega Lifesciences is recognized for its quality-driven culture, strict regulatory compliance, and patient-centric approach, making it a preferred employer in the pharmaceutical and life sciences sector.
JOB OVERVIEW SUMMARY
The Executive / Senior Executive – Pharmacovigilance role at Mega Lifesciences involves handling both aggregate safety reporting and ICSR case processing in compliance with global pharmacovigilance regulations. The selected candidate will work closely with international affiliates, safety teams, and regulatory stakeholders.
This role offers exposure to global PV operations, scientific writing, and safety risk management, making it an ideal fit for professionals seeking to specialize further in pharmacovigilance.
As a Pharmacovigilance Executive / Senior Executive, you will be responsible for ensuring continuous safety monitoring of pharmaceutical products throughout their lifecycle.
🔹 Major Responsibilities Include:
Authoring and reviewing aggregate safety reports, such as:
PSUR (Periodic Safety Update Reports)
PBRER (Periodic Benefit Risk Evaluation Reports)
RMP (Risk Management Plans)
Addenda and safety variations
Handling ICSR data entry, processing, and follow-up in global safety databases
Conducting literature searches for individual case safety reports and periodic reports
Ensuring strict compliance with ICH guidelines, GVP modules, FDA, EMA, and local PV regulations
Coordinating with global pharmacovigilance affiliates and internal cross-functional teams
Supporting signal detection, safety evaluations, and ongoing risk management activities
This role demands high regulatory accuracy, scientific understanding, and strong documentation skills.
ELIGIBILITY CRITERIA (OFFICIAL)
Candidates must meet the following eligibility requirements:
Educational Qualification:
B.Pharm / M.Pharm
Experience:
Minimum 2–4 years of relevant pharmacovigilance experience
Mandatory Experience In:
PSUR, PBRER, RMP, AddCo authoring
ICSR case processing
Literature review and safety signal support
SKILLS REQUIRED
To succeed in this pharmacovigilance role, candidates should have:
Strong knowledge of global pharmacovigilance operations
Excellent scientific writing and regulatory documentation skills
Thorough understanding of ICH, GVP, FDA, and EMA requirements
High attention to detail and a compliance mindset
Ability to handle multiple deliverables under tight timelines
Good communication and collaboration skills
Experience working with global stakeholders and affiliates
SALARY ESTIMATE
Expected Salary Range: ₹6,00,000 – ₹9,00,000 per annum
Salary may vary depending on:
Total PV experience
Expertise in aggregate report authoring
Interview performance and technical knowledge
Mega Lifesciences also offers professional growth, learning exposure, and a stable work environment.
LOCATION & EXPERIENCE SUMMARY
Job Location: Thane, Maharashtra, India
Experience Required: 2–4 Years
Work Environment: Regulated, global pharmacovigilance operations
INTERVIEW DETAILS (OFFICIAL)
Interview Mode: As per the company selection process
Shortlisting: Based on CV and pharmacovigilance experience
Interview Focus:
Aggregate safety reports
ICSR handling
Regulatory compliance knowledge
REQUIRED DOCUMENTS
Candidates should keep the following documents ready:
Updated Resume / CV
Educational certificates (B.Pharm / M.Pharm)
Experience letters
Last salary slips (if applicable)
ID proof
APPLY METHOD (OFFICIAL)
Interested and eligible candidates can apply online through the official Mega Lifesciences career portal:
No, this role requires 2–4 years of pharmacovigilance experience.
Q2. Is aggregate report authoring mandatory?
Yes, experience in PSUR, PBRER, RMP, and AddCo is essential.
Q3. What is the job location?
The position is based in Thane, Maharashtra.
Q4. What background is required?
Candidates must have a B.Pharm or M.Pharm degree.
Q5. Is this a global pharmacovigilance role?
Yes, the role involves global PV operations and affiliate coordination.
FINAL CONCLUSION
The Executive / Senior Executive – Pharmacovigilance role at Mega Lifesciences is an excellent opportunity for experienced PV professionals looking to strengthen their expertise in aggregate safety reporting and global drug safety operations.
With strong exposure to international regulations, scientific writing, and compliance-driven work, this position offers long-term career growth in one of the most stable pharma domains.
If you meet the eligibility criteria and want to advance your pharmacovigilance career, this opportunity is worth applying for.
DISCLAIMER
Note:Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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Agar aap pharma interviews ki preparation kar rahe ho ya actively QA, QC, Pharmacovigilance, Clinical Research jobs search kar rahe ho, to niche diye gaye trusted resources zaroor padhein 👇
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